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Saturday, 28 February 2009

[beasiswa] [OOT] Careers in Life Sciences & International Talent Programe

Dear All,

Cuman mau forward info ttg International Programme for Life Science and Health pd 29 Mei 2009. Program ini secara khusus dirancang bagi talented researchers dari luar Belanda yg tertarik menjajaki kesempatan karier di lembaga-lembaga penelitian Belanda. Siapa tahu ada yg berminat.

kind regards,
Agus

Agustinus R. Uria
Kekulé-Institut für Organische Chemie und Biochemie

Universität Bonn

Gerhard-Domagk-Str. 1

53121 Bonn, Germany

--- On Tue, 2/3/09, YEBN - the Young European Biotech Network <debora.keller@yebn.org> wrote:
From: YEBN - the Young European Biotech Network <debora.keller@yebn.org>
Subject: Careers in Life Sciences & International Talent Programe
To: biotech49@yahoo.com
Date: Tuesday, February 3, 2009, 7:32 AM








Dear Agustinus



Don't miss the opportunity to participate in shaping your career in European Life Sciences!


You also have the chance to take part in an International Talent Programme in Life Sciences!






Your career in European Life Sciences












 


Dear Life Scientist,


 


please take
a moment to look into your future with us: What can your career be like?
Talking to friends and colleagues, we find that there's a huge level of
uncertainty when confronted with this question. What can you do to have a
clearer and more optimistic view of the career that lies in front of you?


 


Discuss
with us on http://btmag.eu to find out more
about Life Science careers in Europe ! Use this
opportunity to tell students, professors and entrepreneurs what they can do to help
young scientists prepare for the job market.


 


We want to
take up as much input as possible in preparation of the first Conference on
European Life Science Careers. Please inform all your colleagues and friends so
that they can make their voice heard!


 


Yours,


 


Peter
Kaiser


Project
Manager


1st
Youth Conference on European Life Sciences Careers 2009


Feb 11th
- 13th, 2009


Frankfurt, Germany

























International Talent Programme for Life Sciences & Health











 


The Dutch Life Sciences sector is
developing fast. The need for talented scientists is strong,
despite worldwide economic downturn. We welcome talented researchers from
outside the Netherlands
to explore the opportunities in the Dutch Life Sciences sector and to find
their next job here.   


Up to 50 persons will be selected for a 5-day VIP
programme that will allow them to explore the many career opportunities at
Dutch research institutes and companies.


The participants will receive a travel
bursary and a free stay (hotel + meals) during 25 to 29 May 2009 in the Netherlands.



Read more...




















 






 
























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[PozHealth] Re:Black

It is relevant what race they are referring to.  Unfortunately, HIV/AIDS DOES affect different races differently.  Don't be too quick to judge what intentions the person that posted had in mind.

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[PozHealth] Information on EECP

Recent data documenting the effectiveness of Enhanced External Counterpulsation (EECP) for the treatment of angina has failed to bring this apparently effective procedure into the mainstream of cardiology practice. In this article, DrRich discusses what EECP is, how it works, and why cardiologists are avoiding this FDA approved, insurance and Medicare reimbursable, safe, noninvasive treatment like the plague.

What is EECP?

EECP is a mechanical procedure in which long inflatable cuffs (like blood pressure cuffs) are wrapped around both of the patient’s legs. While the patient lies on a bed, the leg cuffs are inflated and deflated with each heartbeat. This is accomplished by means of a computer, which triggers off the patient’s ECG so that the cuffs deflate just as each heartbeat begins, and inflate just as each heartbeat ends. When the cuffs inflate they do so in a sequential fashion, so that the blood in the legs is “milked” upwards, toward the heart.

EECP has two potentially beneficial actions on the heart. First, the milking action of the leg cuffs increases the blood flow to the coronary arteries. (The coronary arteries, unlike other arteries in the body, receive their blood flow after each heartbeat instead of during each heartbeat. EECP, effectively, “pumps” blood into the coronary arteries.) Second, by its deflating action just as the heart begins to beat, EECP creates something like a sudden vacuum in the arteries, which reduces the work of the heart muscle in pumping blood into the arteries. Both of these actions have long been known to reduce cardiac ischemia (the lack of oxygen to the heart muscle) in patients with coronary artery disease. Indeed, an invasive procedure that does the same thing, intra-aortic counterpulsation (IACP, in which a balloon-tipped catheter is positioned in the aorta, which then inflates and deflates in time with the heartbeat), has been in widespread use in intensive care units for decades, and its effectiveness in stabilizing extremely unstable patients is well known.

While a primitive form of external counterpulsation has also been around for a long time, it has not been very effective until recently. Thanks to new computer technology that allows the perfect timing of the inflation and deflation of the cuffs, and produces the milking action, modern EECP has been greatly enhanced.

EECP is administered as a series of outpatient treatments. Patients receive 5 one-hour sessions per week, for 7 weeks (for a total of 35 sessions). The 35 one-hour sessions are aimed at provoking long lasting beneficial changes in the circulatory system.

How effective is it?

EECP now appears to be quite effective in treating chronic stable angina. A randomized trial with EECP, published in the Journal of the American College of Cardiologyin 1999, showed that EECP significantly improved both the symptoms of angina (a subjective measurement) and exercise tolerance (a more objective measurement) in patients with coronary artery disease. EECP also significantly improved “quality of life” measures, as compared to placebo therapy.

More recent data show that this improvement in symptoms following a course of EECP seems to persist for up to five years.

Furthermore, there is also preliminary data suggesting that EECP may be useful for treating unstable angina, as adjunctive therapy after revascularization (i.e., with angioplasty, stent, and/or bypass surgery), and even as first-line (instead of last resort) therapy for more routine forms of angina. (Read about EECP as early therapy for angina here.)

Who is likely to benefit from EECP?

Based on what is already known, EECP should be considered in anybody who still has angina despite maximal medical therapy and prior revascularization. No cardiologist could argue logically against this. And, frankly, if a patient insisted on trying EECP prior to agreeing to purely elective revascularization for chronic stable angina, the cardiologist might not like it, but would be hard pressed to give anything beyond a purely emotional reason as to why this should not be tried.

Why does EECP work?

The mechanism for the sustained benefits seen with EECP still amount to speculation. Everyone can agree that there are good reasons for EECP (just as for IACP) to benefit the heart while the therapy is actually taking place. But as to why the benefit of EECP persists even after the therapy is finished, no one can say for sure.

There are preliminary data suggesting that EECP can help induce the formation of collateral vessels in the coronary artery tree, by stimulating the release of nitric oxide and other growth factors in within the coronary arteries. There is also evidence that EECP may act as a form of “passive” exercise, leading to the same sorts of persistent beneficial changes in the autonomic nervous system that are seen with real exercise.

Can EECP be harmful?

EECP can be somewhat uncomfortable (it is said to be more difficult to watch – what with the patient being noticeably jostled due to the milking action of the inflatable leg cuffs – than it is to actually have it done), but is not painful. In fact, it is apparently very well tolerated by the large majority of patients.

But not everyone can have it. People probably should not have EECP if they have certain types of valvular heart disease (especially aortic insufficiency), or if they have had a recent cardiac catheterization, an irregular heart rhythm, severe hypertension, significant blockages in the leg arteries, or a history of deep venous thrombosis (blood clots in the legs). For anyone else, however, the procedure appears to be quite safe.

Despite its increasingly apparent potential usefulness, EECP is hardly taking the cardiology world by storm. In fact, it seems that for most cardiologists EECP is not even on the list of potential treatments for coronary artery disease. Why is that?

There are several possible reasons. Let us dispense with the most obvious first, namely, that EECP doesn’t pay well. A series of 35 treatments costs $5000 to $6000 dollars. That’s not chicken feed, but keep in mind that we’re talking about 35 hours of therapy over 7 weeks, which involves not only the doctor’s time but also the time of office staff, nursing personnel, etc., etc. Still not a terrible return, but when you consider that a cardiologist can often bill that much by spending a morning in the cath lab, well - - -.

 

Then there’s the fact that EECP remains somewhat intellectually unsatisfying. To your average cardiologist, there’s no reason at all that anyone should have thought it would work in the first place – that temporarily providing counterpulsation would have lasting effects. And the fact that it apparently does work is merely blind luck, and leaves investigators scrambling ridiculously to explain why it does. This is a less than satisfying way to advance science.

 

In addition, to most cardiologists, EECP is logistically difficult. To accommodate patients for EECP, they would not only have to purchase expensive equipment, but also would have to radically change the organization of their offices, their office staff, and their space.

 

Finally, and most importantly, EECP has nothing in common with what cardiologists do. Cardiologists study and treat the heart, for goodness sake. They stress it, image it, measure it, pace it, shock it, stent it, ablate it, revascularize it, and bathe it in drugs. What they do takes years of specialized training and expertise, millions of dollars of high-tech equipment, and tremendous manual dexterity, and it brings them significant prestige, even within the medical community. 

 

Now they’re supposed to drop all that? In order to attach fancy balloons to peoples’ legs, throw a switch, watch them bounce around for an hour, then say, “See you tomorrow?” That’s not cardiology. That’s glorified physical therapy.

 

This, in DrRich’s estimation, is the real reason the average cardiologist is completely ignoring EECP, as if it doesn’t even exist. They simply can’t believe anyone really expects them to do this.

 

In any case, you may need to raise your cardiologist’s consciousness. If you have coronary artery disease that has proved difficult to treat, then you need to bring EECP up yourself.

 

Once enough patients show themselves to be aware of this new therapy and to be expecting it, suddenly EECP will no longer be beneath cardiologists, and they’ll eagerly find a way to incorporate it into their practices.

 

How can you receive EECP?

If you are a candidate for EECP and wish to pursue it, start with your doctor. If your doctor discourages you from pursuing EECP, make sure he/she gives you a good reason for discouraging it. Good reasons would include: you don’t have the sort of coronary artery disease or angina that would benefit from EECP; your coronary artery disease is of the type that requires revascularization; or you have one of the contraindications (listed above) for having EECP. (Good reasons would not include: it’s unproven; it doesn’t work; it’s voodoo; or I’ve never heard of it.)

There are fewer than 200 places today performing EECP, though the number is growing rapidly. If your doctor can’t think of a place to refer you for EECP, go online. The best place to start online would be EECP.com. This is a website run by Vasomedical, Inc., the company that makes the equipment for EECP, so it is not unbiased. But it does offer an excellent means of finding a place where you can get EECP in your area.

 

Your insurance carrier should cover EECP, though these fine humanitarians might well deny coverage initially. Medicare has approved EECP for reimbursement, and once Medicare approves a new treatment, insurance companies normally fall in line quite quickly. In the case of EECP, however, many insurance companies are still balking at paying, perhaps because their cardiology consultants are telling them it’s not really a serious therapy. Don’t let this discourage you. If you are turned down for reimbursement, appeal the decision. Most insurance companies count on patients failing to appeal (which is why they so frequently deny therapy that is obviously needed), and with Medicare supporting your contention that EECP ought to be covered, odds are that if you appeal you’ll win.

 

 

 




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[PozHealth] Fw: NATAP/CROI: Vitamin D Supplementation in HIV+

First Report of Dose/Response Data of HIV-infected Men Treated with Vitamin D3 Supplements


Reported by Jules Levin
CROI 2009 Feb 8-12 Montreal

from Jules: one should consider researching safety of such high dose vitamin D before embarking on such high dosing.

Kathryn Childs*, S Fishman, S Factor, D Dieterich, M Mullen, and A Branch

Mt Sinai Sch of Med, New York, NY, US


Background:  Among the general public, low vitamin D levels have many adverse health effects including enhanced inflammation. HIV infection causes inflammation and may increase the importance of optimal vitamin D, defined as 30 to 60 ng/mL of 25-hydroxyvitamin D (25[OH]D). Studies are needed to determine the doses of vitamin D3 (VD3) required by HIV patients.


Methods:  With investigational review board (IRB) approval, 25(OH)D status was assessed in 74 HIV-infected men during the winter in New York of whom 51 with 25(OH)D <30 ng/mL were prescribed daily oral VD3 at doses based on the baseline 25(OH)D level:  2800 IU for <10 ng/mL (severe deficiency); 1800 IU for 10 to 20 ng/mL (deficiency); 800 IU for 20 to 30 ng/mL (insufficiency). All subjects were prescribed 1 g of calcium, as calcium citrate. The level of 25(OH)D was measured at a median follow up of 16 weeks, during summer.


Results:  Most of the 74 men (84%) were Caucasian. The median CD4 count was 444 cells/µL. Among the 51 (69%) prescribed VD3, 25(OH)D increased by a median of 7.2 ng/mL (from 15 to 23 ng/mL) on an intention-to-treat basis (p <0.001; table). Among the 20 subjects who reported 100% adherence, 25(OH)D rose by 15 ng/mL (from 15 ng/mL to 30 ng/mL), allowing 8 of 20 (40%) to achieve optimal 25(OH)D status. As expected, the greatest increases in serum 25(OH)D occurred in the men with the lowest baseline levels. These men were prescribed 2800 IU VD3/day, the highest dose (figure). Only 1 of the 12 non-adherent men (8%) achieved an optimal 25(OH)D level in the summer. Serum calcium remained below the ULN in all subjects prescribed VD3. Surprisingly, no winter to summer seasonal increase occurred among the 23 men with 25(OH)D>30 ng/mL at baseline (who were not prescribed VD3). Rather, median winter and summer levels were 42 and 41 ng/mL, respectively; the median change was –7.3 ng/mL. Of 23 (65%) men, 15 with 25(OH)D levels >30 at baseline had a winter-to-summer decrease.


Conclusions:  To our knowledge, our study provides the first dose/response data for oral VD3 in HIV patients. Doses as high as 14 times the Recommended Daily Allowance were safe and did not lead to hypercalcemia in any subject. VD3 increased 25(OH)D levels, allowing 8 of 20 (40%) fully adherent subjects to achieve 25(OH)D levels in the optimal range. The dose/response effects we observed indicate that many HIV patients can achieve optimal vitamin D status by using oral VD3.  Of note for future dose/response studies, minimal seasonal variation in 25(OH)D occurred in untreated patients. 


Picture 9.png

Picture 10.png


[PozHealth] In defence of anger

 

Funny that the work of Dr. George Solomon, my mentor, the father of

psycho-neuro-immunology and a man who has a chair at UCLA and also
the man who coined the term PTSD (Post Traumatic Stress Disorder), felt
differently about this issue...the data from his Long Term
survivors clinical study I participated in showed that anger and
aggressiveness are a big part in improved immune function, elevated
NK cells and present in ALL long term survivors of HIV. We have a
lot to be pissed at.
 
Those who do not have that anger, or are so repressed that that cannot 
show anger and then get over it, are the ones most likely to die sooner and
turn to drugs to dull the pain of their insufferably frustrating existence.
 
In Los Angeles I know Boxer who is perhaps the angriest man alive
(my closest friend). He buried several lovers and lost virtually
everything important in his life. But he is an angry cuss and NEVER
let HIV destroy him and he bounced back to hit new highs in his
life. He shows anger every day and is healthy as a horse teaching
boxing for 8-9 hours daily.
 
Those who chose to let a smile be their umbrella and take sedatives
and go with the flow will prove to be living examples of evolution
in action...that is, as Dr. Solomon showed, they won't live as long
or live as well. (by 'well' I am not talking about owning a Lexus
or a condo, but the ability to feel the powerful joy of being alive
instead of a victimized lost soul.
 
Remember: ANGER IS AN ENERGY...rock on!

 

 




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[PozHealth] Re:Anger and hostility hurt those who participate

"The more hostile a man's personality, the more his body mass index
(BMI) increased over the following two decades, Dr. Hermann Nabi of
Hopital Paul Brousse in Villejuif, France and his colleagues found.
BMI is the ratio of height to weight, used to determine if someone is
within a normal weight range or is underweight, overweight or obese."


This is fascinating.   It begins to suggest that the "anger hormones" do something very basic.............

JB

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[PozHealth] Re:Black

"Why is it necessary to mention race?
What difference does it make knowing the race of the person you are talking about?"


Well, what harm does it do?   I see what you are saying, but 

1.  medical people are used to giving patient histories, which always include age, gender, and race.  I think it was normal for Charles to introduce race in a "medical" note.

2.  I would bet that this list is overwhelmingly male and white.   Perhaps, even here, it's not a bad thing to be reminded from time to time how many millions of women and people of color are affected and infected, around the world.  

We do live in a world where race is difficult to address, but I don't find it inappropriate to mention it.

JB

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[beasiswa] [INFO] PhD position in Development and Food Policy at KU Leuven, Belgium

website link:
http://www.econ.kuleuven.be/licos/Staff/documents/LICOS_PhD_Vacancy_Development_FoodPolicy.pdf

PhD Vacancy in Development and Food Policy

LICOS - Centre for Institutions and Economic Performance at the
Faculty of Business and Economics, Katholieke Universiteit Leuven, is
seeking to appoint a PhD student/Research Assistant for 4 years as of
Fall 2009, to support current research on Food Policy, Development and
related fields. Field work in any of the geographic regions of focus
(Eastern Europe, China, India, Africa) is possible. The supervisor of
the project is Prof. J. Swinnen, Director of LICOS.

Selection Criteria
University degree in economics or applied economics, preferably at
MPhil level
Strong analytic and technical capabilities in modern economic methods
Proficiency in statistical and econometric methods Interest in
developing collaborative research within the research project
A GRE test will be required for admission
Fluency in spoken and written English (a TOEFL or IELTS test will be
required for non-native speakers)

About LICOS
LICOS is a research centre of Excellence at the Faculty of Business
and Economics that focuses on theoretical and empirical research of
macro- and micro-economic aspects of transition, institutional changes
and economic performance. LICOS belongs to the 12 "Centres of
Excellence" of K.U. Leuven. The research at LICOS is organized around
four main research themes, each under the auspices of a Research Director:
Development and Food Policy (Prof. J. Swinnen)
Labour Markets and Industrial Restructuring (Prof. J. Konings)
Market Structure and Performance (Prof. P. Van Cayseele)
International Trade and Fiscal Policy (Prof. Hylke Vandenbussche)
(for more info: www.econ.kuleuven.be/licos/)

PhD Program at the Faculty
The research project will allow the student to simultaneously pursue a
PhD in (Applied) Economics. The University of Leuven (KUL) has an
extensive Ph.D. program: about 160 researchers are currently pursuing
a Ph.D. in Applied Economics/Business studies or PhD in Economics.
Usually, a PhD program takes 4 years, with the first year including
important course work in advanced economics.
(for more info: www.econ.kuleuven.be/lsbe)

How to Apply
Candidates must send their curriculum vitae, together with a statement
outlining expression of interest in the position, to
conny.schuurmans@econ.kuleuven.be. There is no application form.
Applications must reach us no later than 15 April 2009.

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[PozHealth] NATAP/CROI: HIV Drug Pipeline....not what it was

HIV Drug Pipeline at CROI

--for patients with extensive drug resistance a little is ongoing.......

Reported by Jules Levin
CROI 2009 Feb 8-12 Montreal

For early-line therapy there are several new twists. For patients with pan-class HIV drug resistance as I see there are a few but limited promising new developments, there is GSK's 2 integrase inhibitors, if they are active against raltegravir resistance, which in vitro they appear to be but this has to be tested in patients, so these integrase inhibitors could also be for early therapy, perhaps firstline. There is the Tanox drug which is an infusion, there is PRO140 which is in reality a CCR5 inhibitor which may be active against CCR5 drug maraviroc resistance which I don't think has been tested yet in patients but still PRO140 is an infusion even if perhaps subcutaneous; there are the 2 Ardea NNRTIs, in the poster it says RDEA427 retains activity against "many of the recently identified etravirine mutations" which is a key question so they will have to prove this in patients. There is also the Idenix NNRTI which was bought recently by GSK, and again a key question is can they prove it's activity against etravirine resistance mutations. There is CMX 157 which is merely a new perhaps improved of tenofovir, yet to be proven. There is the Merck RNase program which displayed its first poster at a major conference, see link below, but is in preclinical and in very early development; as they identified a series of compounds with HIV activity in cell culture, I don't know how close this could be. Then there are the maturation inhibitors, Panacos' bevirimat now at Myriad and the back up maturation inhibitors at Myriad and at Panacos. Bevirimat appears to be a reasonable candidate but whether it can be used by a patient appears to require a lab test to see if a patient has certain polymotphism mutations, so the drug will be active for about 50% of patients. Myriad has an additional maturation inhibitor program that includes MPC-9055 which is early clinical development and Myriad said they plan to start a new bevirimat study and develop MPC-9055 as well. In sum, there are several possibilities for patients with extensive HIV drug resistance and with pan-class resistance. The most promise at this time for the near future is that the GSK integrase inhibitors, they have 2 in early clinical patient studies, will be active against raltegravir resistance. And if they prove the new NNRTIs from Idenix/GSK and Ardea are active against etravirine mutations in patients with etravirine resistance these are promising.  There still is CCR5 maraviroc and soon vicriviroc, for CCR5-tropic patients. If the maturation inhibitors work out that would provide helpful therapy but bevirimat has limited promise, for 50% of patients, if it gets developed. The Myriad maturation inhibitors are further behind and perhaps that will work out. Panacos has a second generation maturation inhibitor program and an oral fusion inhibitor, but as you know the company is almost bankrupt and looking to sell its assets. Several years ago we had an exciting and explosive new drug development situation for pan-resistant patients with several very good drugs in development-- darunavir, etravirine, raltegravir, maraviroc and prior to that T-20 and tipranavir. Don't lose these drugs, adherence is the key. Right now future options appears limited for bright and novel developments. The only new class in clinical development is maturation inhibitors. Why? Coming up with new ideas is not easy. It's much harder to develop new drugs, it's expensive and the field of available drugs is very crowded, so there is limited opportunity to make much profit. J&J and Tibotec displayed guts, a big commitment to HIV, and were fortunate to be able to develop their new drugs including TMC278 out of the Belgium labs co-founded by Rudi Pauwels and Paul Stoffels in the 1990s, where J&J got these drugs, thank them all for their foresight and skills. Both Virco & Tibotec co-founded by Pauwels & Stoffels in the 1994/1995 were acquired by J&J in 2002. I recall participating in the early scientific meetings in Europe during the 1990s organized by Pauwels and other resistance scientists before they discovered darunavir (TMC114) and etravirine (TMC125), where resistance testing was first discussed. These meetings were in the pre-discovery days of resistance testing, they helped to develop and promote resistance testing. Merck as well displayed guts & determination & a big commitment. The Merck integrase program started at least 10 years ago hit a wall many times over the years appearing to be stalled. The development team at Merck deserves much credit for sticking this out. There have been a number of big drug companies that discovered but sold new HIV drugs because they did not want to get into HIV, or did not want to make any commitment to invest at all in HIV drug discovery. As well Pfizer and Schering have demonstrated commitment to their CCR5 programs. A full new drug development program is very expensive and in order to make a commitment you need a drug or a new class of drugs with great promise, and it has become much harder to find these.. Patients who still have not used Fuzeon can still use it. We can hope that novel major breakthroughs might occur but right now the future has a few hopeful opportunities for new therapy, but it's not like it was several years ago with the explosion of new potent drugs from Merck & Tibotec.. But don't forget Pfizer's CCR5 drug maraviroc and Schering Plough's vicriviroc. For the CCR5-tropic patient this remains a viable treatment option, particularly pan-class resistant.. CCR5 drugs are a new class with no cross-resistance with other HIV drug classes. It was a big discovery and promise for patients. Recently Pfizer reported positive safety data and are following through with their 5-year safety data commitment. As well, Schering will provide similar safety data. Sure you have to take a test, the Tropism assay to see if a patients is CCR5-tropic to see if you can use the drug, but if you need a new drug and you are CCR5-tropic these drugs are potent and maraviroc has demonstrated a good side effects and clean lipids profile in patients in Phase 3. Here are links to reports from CROI with more detailed reports forthcoming for Myriad maturation inhibitor and Ardea NNRTI programs. Jules

New HIV Agents - written by Joe Eron, MD, University of North Carolina - (02/25/09)

Weekly and Biweekly Subcutaneous PRO 140 Demonstrates Potent, Sustained Antiviral Activity: 2-week study - (02/26/09)

New HIV Drug Candidates in Pre-Clinical Development - (02/24/09)

TNX-355 survives Tanox: new Phase 2 Dose-Finding StudyStudy

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Re: [PozHealth] Black

It does make a difference, as it does whether someone is straight or LGBT, male, female or third gender.


I know what you mean though. Shouldn't we be color blind? In some essential ways, yes, of course. We exist with equal potential, regardless of ethnic background, gender, sexual orientation and we should be accorded the same rights, respect and sense of dignity.

Yet at the same time, we celebrate our differences. Our cultural differences in the traditions of music, food, clothing that an ethnic background brings us--or the gay culture created here in the United States (but that exists around the world in its own forms). This diversity can make us strong.

It is also what is used to divide us into "better" and "inferior" through constructs exploited by jerks like Hitler, Pol Pot and slave owners. 

But it is also a physiologically relevant issue. For example, African Americans and Latinos with type 1 Hepatitis C virus infection have about half the sustained viral response rate as Caucasians or Asians. So there are differences in metabolism of which a good clinician should be aware. 

Note that I avoided the use of the term "race" as this is part of the construct of division that embeds political or eugenic superiority in its meaning and is thus arbitrary. What is the Black Race? Does it include Hutus and Tutsis? How about Tamil Indians? Or Australian Aboriginals? Are Caucasians just Norwegians and English? How about Italians? Or Iranians? 

Race is a stupid notion. We all have the capacity to excel! We all have the capacity to exhibit bigotry and hate because of the FEAR of difference and diversity that characterizes some individuals (e.g., homophobes, white supremacists, repugnicans).

George M. Carter

On Feb 27, 2009, at 3:35 PM, Mister wrote:


Why is it necessary to mention race?
What difference does it make knowing the race of the person you are talking about?

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Friday, 27 February 2009

[Dokter Umum] Re: alergi sperma (maaf)

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[PozHealth] Anger and hostility hurt those who participate

Get over it or it'll get you!
-------------------------------

Hostile men more prone to weight gain, study shows
Fri Feb 27, 2009 3:33pm EST

NEW YORK (Reuters Health) - Hostile men may pack on more pounds over
time than their less hostile, more laid-back peers, new research shows.

The more hostile a man's personality, the more his body mass index
(BMI) increased over the following two decades, Dr. Hermann Nabi of
Hopital Paul Brousse in Villejuif, France and his colleagues found.
BMI is the ratio of height to weight, used to determine if someone is
within a normal weight range or is underweight, overweight or obese.

The researchers looked at data on 6,484 men and women participating in
a UK study of socioeconomic status and health. Study participants
ranged in age from 35 to 55 at the study's outset. They completed a
standard scale measuring hostility at the beginning of the study,
while their BMI was determined at four points over 19 years.

At the beginning of the study, the researchers found, both men and
women with higher hostility levels also had higher BMIs. BMIs rose
over time.

While the relationship between BMI and hostility remained constant for
women, hostility seemed to accelerate weight gain over time in the men.

Hostility could affect BMI in many ways, Nabi and his colleagues note
in a report of the study appearing in the American Journal of
Epidemiology. For example, hostile people may be less likely to follow
health guidelines on diet and exercise, or be more likely to be depressed.

Prior studies have linked hostility to heart disease, high blood
pressure, and a greater overall mortality risk, the researchers also note.

SOURCE: American Journal of Epidemiology, February 1, 2009.

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Re: [Konsultasi-Kesehatan] Re: (Tanya) Menggugurkan Kandungan Usia < 1 Bulan

Saya jd ingat diri saya sendiri Pak, saya dan kakak saya beda 11 bulan
jadi pas kakak saya berumur 3 bulan Ibu saya mengandung saya. Sekarang
saya 25 tahun, normal dan anal laki2 satu2nya dr 3 bersaudara.

On 2/21/09, Eko Pujianto <ekopujianto99@yahoo.co.id> wrote:
> Benar yang di katakan Ibu Dewi, Pak. Istri saya satu minggu yang lalu juga
> di kuret karena kondisi jahitan bekas operasi Caesar anak kami yang kedua (1
> tahun) belum memungkinkan untuk hamil lagi dan akhirnya di kuret oleh
> dokter.Tapi terlepas dari itu semua mungkin bapak tidak mencoba untuk
> menggugurkan kandungan baik dengan obat maupun jamu"an. Karena seperti kata
> Ibu Dewi akibatnya justru akan lebih merepotkan bapak di kemudian hari
> (maaf: kondisi anak cacat, atau bahkan lebih extreem lagi bisa merenggut
> nyawa istri bapak)
> Keadaan sekarang ini memang sulit. Tapi tatkala kita mensyukuri apa yang
> diberikan-Nya, dan selalu berusaha pasti selalu ada jalan. Kata orang Jawa,
> yang namanya anak selalu membawa rejekinya masing2.
>
> Semoga bapak dan istri bisa mempertimbangkan lagi semua langkah yang hendak
> di ambil.
> Yang sabar ya pak.
>
> Salam
>
>
>
> Re: (Tanya) Menggugurkan Kandungan Usia < 1 Bulan
> Posted by: "Dewi Indrajani" dewi@tri-wall.co.id
> Thu Feb 19, 2009 8:16 pm (PST)
> Dear,
>
> Saya pernah di kuret karena janin tidak berkembang, bukan karena "tidak
> diinginkan" - tidak sakit dan tidak mahal. Tapi mohon maaf ya, kalau menurut
> pendapat saya jangan pernah punya pikiran untuk kuret, karena "dia" sudah
> ada dan karena Bapak diberi kepercayaan untuk memelihara dia, jadi jangan
> disia-siakan.
>
> Jangan pernah pakai jamu2 tradisional ato obat2an karena belum tentu
> berhasil, nanti malah bisa menjadi anak yang, maaf, cacat bisa mental ato
> fisiknya.
>
> Mohon dipikirkan baik2 ya Pak. Mudah2an Bapak diberi jalan oleh-Nya untuk
> bisa memelihara dan merawat "dia".
>
> Salam
>
> Eko Pujianto
> FAIQ FURNITURE
> Jl. A. Yani 96 Pengkol Jepara 59415
> P : +62291 3368383
> F : +62291 595515
> M : +6281390642727
> www.faiqfurniture.indonetwork.co.id
>
> _____
>
> From: Konsultasi-Kesehata n@yahoogroups. com
> [mailto:Konsultasi-Kesehata n@yahoogroups. com] On Behalf Of Togar
> Sent: Thursday, February 19, 2009 2:14 PM
> To: Konsultasi-Kesehata n@yahoogroups. com
> Subject: [Konsultasi- Kesehatan] (Tanya) Menggugurkan Kandungan Usia < 1
> Bulan
>
> Dear Friends
>
> Minta pendapatnya dunk...
>
> Usia pernikahan kami baru 1 tahun 2 bulan, kami menikah di usia saya 24 th
> dan istri 21 th. Menikah di usia muda Enak tapi tidak mudah apalagi di jaman
> suseh seperti ini. Sekarang istriku telat men's setelah diperiksa ternyata
> hamil usia kandungan 2 minggu, kami belum siap untuk kehadiran anak kedua
> karena anak kami pertama baru berusia 5 bulan. Dokter menyarankan KIRET
> diRumah Sakit Raden Saleh.
>
> Apakah tidak ada cara lain selain kiret, apakah bisa menggunakan jamu2
> tradisional atau obat2 di apotik dan apa bahayanya untuk istri saya bila
> menggunakan kedua cara diatas. Usia kandungan masih muda banget gk papa
> kan?? Seperti apa sih kiret itu, sakitkah dan berapa biayanya?
>
>
>
> __________________________________________________________
> Dapatkan nama yang Anda sukai!
> Sekarang Anda dapat memiliki email di @ymail.com dan @rocketmail.com.
> http://mail.promotions.yahoo.com/newdomains/id/

--
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[PozHealth] LA doctor admits giving diluted AIDS meds

 

LA doctor admits giving diluted AIDS meds

Thursday, February 26, 2009


(02-26) 18:05 PST Los Angeles, CA (AP) --

A doctor has pleaded guilty in Los Angeles to administering diluted doses of medicine to patients with HIV, AIDS or hepatitis and improperly billing Medicare at least $350,000.

Dr. George Kooshian of La Quinta pleaded guilty Tuesday to federal charges of health care fraud.

His assistant, Virgil Opinion of Anaheim, previously pleaded guilty to participating in the scheme to administer watered-down medications and billed patients' insurance companies for the full dose. The treatments were given at four offices in Los Angeles and Orange County.

Kooshian admitted that he and his assistant continued to bill for the treatments even after the patients were no longer taking the drugs.

Prosecutors say the government's losses could be as much as $660,000.

 




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[PozHealth] SOUTH TEXAS volunteers needed!

Whether you personally are HIV+ or not, IF you are a "kind supporter"
of those who are living with HIV/AIDS, please do consider becoming a
member of one, or all of my online groups:

My groups:

FOR SOUTH TEXAS, CORPUS CHRISTI AND RIO GRANDE VALLEY ONLY (OVER 50
MEMBERS):

http://groups.yahoo.com/group/pozitivelyfriendsSTX/

A GROUP TO HELP PEOPLE WITH HIV FIND AFFORDABLE HOUSING OR SHARED
LIVING ARRANGEMENTS (500 MEMBERS- NATIONWIDE):

http://groups.yahoo.com/group/pozhousing/

AN ONLINE SUPPORT GROUP NATION WIDE (150+ MEMBERS):

http://health.groups.yahoo.com/group/pozwithproblems/

A GROUP FOR SINGLES AND DATING WITHIN TEXAS ONLY (100 MEMBERS):

http://groups.yahoo.com/group/texaspozromance/

Thanks for considering joining any or all of my groups. If you aren't
interested, perhaps you might know of friends who would be?

Please send questions or comments to zestymike48@gmail.com. I will
help in any way that I possibly can!

Also, I met personally with Bill Hoelser; Client Services Coordinator
at CBAF (Coastal Bend AIDS Foundation) this past Thursday, and he has
asked me repeatedly to "head up" our new Social Group here in town. I
told him that I wanted to coordinate my online groups to work with the
offline group. CBAF has given US, the clients and members A SUITE ON
THE 3RD FLOOR of the CBAF building, downtown on Mann St. Bill said
that he wants the group to be FOR and RUN BY the clients rather than
by CBAF itself. YOUR COMMENTS AND SUGGESTIONS ARE REALLY NEEDED in
order to plan and make all of this a success and something that you
would want to participate in. I also need a lady volunteer to step up
and head out the "ladies outreach" part of the social group.

Hugz,
Mike

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[PozHealth] tired, weak, loss of muscle

Hey guys..hope all are doin well. Poz since 2001, undetectable and
healthy.. kindof,(couple of herniated discs) Meds I'm taking are
Truvada,Reyataz,and Norvir. My issue is that I'm constantly tired,
especially after a meal. I workout, but cannot gain any muscle, and am
very weak. No matter how much I run and do cardio, I still remain
flabby. I have had my doc check my testosterone level, which he says
is in the normal range. Im so frustrated. My previous doc (now
retired) had me on androgel, which made all the difference in the
world. But the new doc doesnt feel that I need it... any suggestions?
I read posts of members taking Nandrolone, etc. Are these prescribed
or bought 'from a friend'? Im not looking to get huge or look good at
the club, just feel better about myself and make it thru the day
without a couple naps. Thanks for any help.

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[Computershow2] Re: Backup utility info.

Thanks
--- In Computershow2@yahoogroups.com, "IKnowComputers"
<iknowcomputers@...> wrote:
>
> I think you would just image each drive replace the drives that you
> want restore the image and keep going. Even if you are using RAID5
> data is data. Just be sure to restore the proper drives to where they
> were on the new drives.
>
> Ju--- In Computershow2@yahoogroups.com, "georgekid" <georgekid@> wrote:
> >
> > I understand what you guys are saying. What if your drives are RAID
> > 5. The thing is I have a server that the drives are in RAID5. The
> > drives are getting full pretty fast. I'm looking for a way to change
> > the drives to a much bigger ones (they all have to be same size).
> > And I have been scratching my head thinking on how to go about it. I
> > do my backups using Acronis (image) to an external drive. What do
> > you suggest would be the best way to go about this.
> >
> > Thanks for your help,
> >
> > ~~George
> >
> >
> >
> >
> > --- In Computershow2@yahoogroups.com, "Robert A. Gismondi"
> > <RGismondi@> wrote:
> > >
> > > Very interesting, Ken. People do report problems with backup
> > images.
> > > Perhaps they did not do a check on them. One solution is to
> > separately
> > > back up Data. I do that. In fact, if your external drive is large
> > > enough, you can have more than one data backup. And even more than
> > one
> > > image, in Folders.
> > >
> > > As far as the uselessness of an Image that will not work, here is
> > a
> > > story. During WWII, Navy flyers were given a small container of
> > Shark
> > > Repellent, in case they had to ditch. The repellent did not work.
> > But,
> > > it served the purpose of making the fliers more confident, and
> > reducing
> > > anxiety. So, make an Image, anyhow. (But keep the Windows Disk in
> > a safe
> > > place!) :)
> > >
> > > Your system, for those who are willing to go to that much trouble,
> > > sounds like a really good one. What I am about to do is to put an
> > image
> > > on a second internal HDD, and also continue to back up to the
> > external
> > > drive. Just a bit of redundancy; but, not quite as good, perhaps,
> > as
> > > your system. Of course, if in a hurry when the HDD goes kaput,
> > just
> > > switch the jumpers on the secondary, and away I go.
> > >
> > > Your point about the little software installations does ring a
> > bell with
> > > me. I have many scores of programs obtained as free downloads.
> > However,
> > > the Files for virtually all of them reside comfortably in my
> > *Programz
> > > Folder,* ready for instant re-Installation. They are thus backed
> > up when
> > > I do a data backup, or an Image. In a number of cases, the
> > original
> > > source of the program evidently lost interest, and disappeared
> > into the
> > > ether. So, my Files are invaluable, in that sense.
> > >
> > > If you back up with an Image to a second internal drive, you can
> > always
> > > switch the pins, and boot up, to try it out.
> > >
> > > Now, that's a backup!
> > >
> > > ~~Robert
> > >
> > > Ken Clark wrote:
> > > > Hi!
> > > > I am a fan of Acromis 11 (because it works for me!)
> > > > I tried Ghost and could not get it to work. (It would chug away
> > for
> > > > hours--then report some arcane error message and stop.)
> > > >
> > > > Years ago I read a chilling article about how many of these
> > backup programs
> > > > fail when you actually try to recover data. So, many folk are
> > dutifully
> > > > creating useless backup files, because they are never testing
> > the recovery
> > > > part of their plan.
> > > >
> > > > I learned the hard way, what a pain it is to have a drive die
> > suddenly (Is
> > > > there any other way?) So I have two hard drives, and every so
> > often do a
> > > > full clone of the one I am using as the "master" boot drive, to
> > the other.
> > > > Then I switch the cables and use the clone as my work drive
> > until next time.
> > > > For the cost of a hard drive, I have a full redundancy so I have
> > a WORKING
> > > > backup drive, with all my software up to date. This procedure
> > also means
> > > > that I am always testing my latest backup copy, so I know it is
> > functional.
> > > >
> > > > To add to Robert's comment about what a big job it can be to
> > reload all your
> > > > software--I became quite paranoid as I thought it through and
> > realized how
> > > > much software I had bought online and downloaded, so I have
> > no "original
> > > > CD" to reload from! (and how many little useful utilities I had
> > downloaded
> > > > and would have a problem tracking down again.) So a full clone
> > of my drive
> > > > is the way I have chosen to go.
> > > >
> > > > Regards!
> > > > Ken
> > > >
> > > > ----- Original Message -----
> > > > From: "msuffin2" <msuffin2@>
> > > > To: <Computershow2@yahoogroups.com>
> > > > Sent: Monday, February 23, 2009 3:53 PM
> > > > Subject: [Computershow2] Backup utility info.
> > > >
> > > >
> > > >
> > > >> The following is a just in case question.
> > > >> About 5 yrs. ago their was alot written about the necessity to
> > do a
> > > >> backup of ones hard drive,I guess it was pretty much before
> > external
> > > >> HD's were reasonably priced, so I purchased the software
> > utility by
> > > >> Stompsoft called Backup My PC#5 which copies to CD's, as I
> > > >> understand, all folders and files which are on HD. I initially
> > > >> proceeded to copy to about 8 CD's in a compressed mode all that
> > was
> > > >> on drive and periodically I copy to additional cd's the info
> > entered
> > > >> on HD since previous copy, program allows you to do this.
> > Anyway,
> > > >> after quite a few years and a collection of discs, I recently
> > > >> scrapped out this collection and burnt a new set which is the
> > up to
> > > >> date version of drive (cd's are only about 5 cents each) and
> > still
> > > >> only takes 8 in compressed mode.
> > > >> Bottom line question is! If I have a major HD crash, will my 8
> > CD's
> > > >> along with original Windows XP1 CD(XP2 had been downloaded)be
> > > >> applicable in getting a new HD booting up and installing all
> > stored
> > > >> files folders and downloaded programs?
> > > >> My computer is 6yrs old and was built up by an expert Microsoft
> > > >> certified professional repair man in the west S.F. valley with
> > top
> > > >> grade parts,HD is a 40gb Western Digital but with the mileage
> > > >> starting to build ,however, no strange noises. Being that I am
> > not
> > > >> sure where I would be with these backup discs,I am starting to
> > give
> > > >> thought to buying an external HD. Most come with the necessary
> > > >> transfer software. Thanks for comments, Mark
> > > >>
> > > >>
> > > >>
> > > >> ------------------------------------
> > > >>
> > > >> World Famous Links & Files:
> > > >> Links: http://tech.groups.yahoo.com/group/Computershow2/links
> > > >> Files: http://tech.groups.yahoo.com/group/Computershow2/files/
> > > >>
> > > >> Yahoo! Groups Links
> > > >>
> > > >>
> > > >>
> > > >>
> > > >> __________ Information from ESET Smart Security, version of
> > virus
> > > >> signature database 3882 (20090223) __________
> > > >>
> > > >> The message was checked by ESET Smart Security.
> > > >>
> > > >> http://www.eset.com
> > > >>
> > > >>
> > > >>
> > > >>
> > > >
> > > >
> > > >
> > > > ------------------------------------
> > > >
> > > > World Famous Links &
> > Files:
> >
> > > > Links: http://tech.groups.yahoo.com/group/Computershow2/links
> > > > Files:
> > http://tech.groups.yahoo.com/group/Computershow2/files/
> > >
> > >
> > Yahoo! Groups Links
> > > >
> > > >
> > > >
> > > >
> > > >
> > >
> >
>

__._,_.___
World Famous Links & Files:                                                                    
Links: http://tech.groups.yahoo.com/group/Computershow2/links
Files: http://tech.groups.yahoo.com/group/Computershow2/files/       
                                                                       
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[PozHealth] Black

Why is it necessary to mention race?
What difference does it make knowing the race of the person you are talking about?


--- On Fri, 2/27/09, Nutrishn@aol.com <Nutrishn@aol.com> wrote:
From: Nutrishn@aol.com <Nutrishn@aol.com>
Subject: [PozHealth] CD4 Count Still < 100 after 3 years undetectable
To: PozHealth@yahoogroups.com
Date: Friday, February 27, 2009, 4:52 AM

One of my most successful T cell reconstitution patients is a 45 year old Black woman, who had 25 T cells when we met. She has 1125 now. She has just been on what is now Atripla for the past 7 years.

The nutritional elements that I think have generated this stunning rebound are:

1.
     B-complex vitamins. She takes The Perfect Blend multivitamin, 2 pills per day

2.
     L-carnitine , 1 gram per day.

3.
     Co-enzyme Q10, 100 mg per day

4.
     L-glutamine, 5 grams per day.

The reasons for this regime.

1. Rapidly dividing cell systems need more vit B6, B12, and folic acid. The Perfect Blend provides this. The Vitamin Shoppe sells a product: Two Per Day Tablets, made by Life Extension, that works well too.

2. All cells have a "self-kill" switch, (apoptosis switch) that they can activate when they feel like they are not pulling their weight. HIV infection causes healthy T cells to flip that  "self-kill" switch. L-carnitine blocks that suicide switch.

3. Natural Killer cells play a bigger role in managing HIV than previously thought. Coenzyme Q10 is fuel for NK cells. Co Q10 is also fuel for antigen presentation cells. All in all, it improves total immune function.

4. L-glutamine, helps T cells mature, and is fuel for them.

Try this regime, it can take 3 - 6 months to show good support of T cell count, and the full effect can take a year or more to evolve.

(For people with chronic liver disease, we see that T cell recovery can be slower.

Charlie Smigelski RD
www.eatupbooks. com




************ **
Get a jump start on your taxes. Find a tax professional in your neighborhood today. (http://yellowpages .aol.com/ search?query= Tax+Return+ Preparation+ %26+Filing&ncid=emlcntusyelp00 000004)

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[PozHealth] NATAP: Aging Review CROI 2009-Increased Deaths


Begin forwarded message:

From:julev <julev@aol.com>
Subject:NATAP: Aging Review CROI 2009-Increased Deaths
Date:February 27, 2009 9:11:41 AM EST
To:hiv@natap.org, nataphcvhiv@natap.org, natapindustry@natap.org, natapdoctors@natap.org
Aging Summary CROI 2009

Reported by Jules Levin

Isn't it obvious that all these increases in non-AIDS events being reported now for 3 years will translate into increases in early deaths soon. I have spoken with all the drug companies about the aging issues and I don't think any of them really want to take on the challenges I present to them in turns of what studies need to be done. I have also spoken to many researchers and mostly the research community has not yet stepped up to the plate to address the real key questions that need to be studied, I'm not sure they really grasp the real questions that need to be studied. They are too concerned with accumulating more evidence that non-AIDS events are occurring more and patients are dying earlier, and these events are occuring more in HIV+ compared to HIV-negatives. But the questions that are key is how HIV itself is causing these events and how can we intervene, and very few researchers and drug company researchers appear to me to get this or are willing to address these questions. For the very few researchers who are aware & looking at these issues, they are not moving this important research quickly, they are allowing it to just sit there. These questions are a key to addressing aging: inflammation, premature aging of t-cells to make them prematurely senescent, and immune activation-- these are keys to why HIV+ individuals are aging more quickly, thus developing non-AIDS events earlier than HIV-negatives. Patients will start dying earlier as large numbers start getting into their 60s, perhaps then researchers will take note of it then, when its too late.  To their credit NIAIDS recently issued 3 Aging requests for funding for studies. However, I think more commitment is required to what I think will soon be obvious that this is a major problem and very challenging. It is clear to me that earlier death will stat occurring in large numbers soon due to non-AIDS events and then researchers, drug companies and government officials will pay attention, but by then it will be too late.. All available resources should be mobilized now to begin addressing these problems. I forget but something reminds me that all of this is about the patients; sometimes careers, profits, ACTG agenda, politics appear to be more important. NO, this is not about doctors, government, getting published, THIS IS ABOUT THE PATIENTS!!! Jules

Aging with HIV - Lessons from CROI 2009 - Victor Valcour MD - (02/27/09)

Cognitive Impairment & Neuropathy Persist Despite HAART and Are Associated With Metabolic Syndrome - (02/27/09)
Despite a sustained response to cART, neurocognitive disorders are more frequent in old HIV+ patients than in the general aging population, but are underdiagnosed by their physicians....DSPN remains highly prevalent in the era of cART...The prevalence of peripheral neuropathy increases with time after ARV initiation in ARV-naïve patients despite increased virologic control and immune function, and the decline of n-ARV use. Age and n-ARV use are notable risk factors for N and SPN....significant predictors of DSPN included older age (OR 2.1 per 10-year increase, 95%CI 1.8 to 2.4), lower CD4 nadir (OR 1.2 per 100 cell decrease, 95%CI 1.1 to 1.2), current ARV use (OR 1.6, 95%CI 1.5 to 1.7), past dideoxynucleoside-containing drug use (OR 1.9


HIV Infection May Make the Brain 15 to 20 Years Older: HIV slows cerebral blood flow and stimulus response in MRI study - written by Mark Mascolini - (02/23/09)



Immune Senescence, Activation, and Abnormal T Cell Homeostasis despite Effective HAART, a Hallmark of Early Aging in HIV Disease: "HIV-infected subjects (median 56 years) with good immune reconstitution and viral suppression had immune changes comparable to older (median 88 years) HIV-negative subjects" - (02/20/09)


HIV-1 INFECTION IS ASSOCIATED WITH ACCELERATED VASCULAR AGING(02/18/09)


Studies and Cohort Studies Reporting Increased 'Non-AIDS' Comorbidities and Deaths Associated with 'Non-AIDS' Comorbidiries and This is Occurring at Young Ages
If you read through these studies reported at CROI you will note the average ages of patients getting non-AIDS events and death due to them at young ages, in their 40s. So what will happen 5 years from now, what do you think!!!

Update on Kidney Disease in HIV Infection: CROI 2009 - written by Christina M.. Wyatt and Paul E. Klotman, Mt Sinai Hospital, New York City - (02/26/09)

Two Inflammation Markers (hsCRP & IL-6) Predict Higher Risk of Opportunistic Disease in SMART - written by Mark Mascolini - (02/18/09)

Markers of Inflammation, Coagulation and Renal Function in HIV-infected Adults in SMART and in two Large Population-Based Studies, CARDIA and MESA: HIV+ have higher levels of inflammatory markers on and off HAART, "markers appear to predict mortality & disease progression in HIV" (02/19/09)

Serious Fatal and Non-fatal Non-AIDS-defining Illnesses in Europe: most common no-AIDS events malignancies/CVD/liver in EuroSida - (02/25/09)


Effects of Aging on HIV Pathogenesis: aging is associated with higher t-cell activation in women than men, effects of menopause on inflammation and immune activation...." (02/23/09)



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[PozHealth] Fear of Foreigners: HIV-related restrictions on entry, stay, and residence

http://www.jiasociety.org/content/11/1/8
 
Regards,

Nelson Vergel
powerusa dot org

__._,_.___
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[PozHealth] is a vaccine against HIV possible?

http://www.jiasociety.org/content/12/1/2
 
Regards,

Nelson Vergel
powerusa dot org

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[PozHealth] Fw: NATAP/CROI: Fatigue & Brain Dysfunction

Fatigue in HIV-infected Individuals Enrolled in A5090: Clinical, Laboratory, and Neuroimaging Characteristics:
"Lower cellular energy levels in the basal ganglia, as measured by MRS creatine concentration, suggest that energy dysmetabolism in this brain region may play a role in the central mechanisms of fatigue."


Reported by Jules Levin
CROI 2009

Giovanni Schifitto*1, L Deng2, T-M Yeh2, S Evans2, and D Clifford3

1Univ of Rochester, NY, US; 2Harvard Sch of Publ Hlth, Boston, MA, US; and 3Washington Univ, St Louis, MO, US


Background:  Fatigue is among the most common symptoms reported by HIV-infected individuals. Reports suggest that the prevalence of fatigue varies by disease status with rates near 80% in patients with AIDS. Most studies have not been conducted in the setting of a controlled trial and have not assessed the association of fatigue with cellular markers of brain activity.


Methods:  Data for this study were derived from baseline evaluations in AIDS Clinical Trials Group (ACTG) A5090, a randomized, double-blind, placebo-controlled trial of the selegiline transdermal system (STS) for the treatment of HIV-associated cognitive impairment. Fatigue was assessed using the fatigue severity scale (FSS) with scores of >4 considered "fatigued"; 44 participants underwent brain magnetic resonance spectroscopy (MRS) imaging, an in vivo method for assessing brain metabolites associated with neuronal and glia activity. Differences between fatigued and non-fatigued participants were evaluated with respect to demographics and clinical characteristics, plasma and cerebrospinal fluid (CSF) HIV-1 RNA concentration, CD4 counts, and brain metabolites using Kruskal-Wallis, exact, or score tests for continuous, nominal, and ordinal factors, respectively.


Results:  We enrolled 128 participants (88% male, 51% white, median age 45, median CD4 425, and 55% with HIV-1 RNA ≤50 copies/mL); 82 participants (64%, 95%confidence interval 55%, 72%) were "fatigued" at baseline. Fatigued participants were significantly younger (p = 0.01), had lower Karnofsky scores (p = 0.015), and had higher levels of depressive symptoms on the Center for Epidemiologic Studies Depression Scale (CES-D) (p <0.001), than non-fatigued participants. Statistically significant differences between fatigued and non-fatigued groups were not detected for plasma and CSF HIV-1 RNA concentration, CD4 counts or on neuropsychological tests. MRS revealed significantly lower levels of the cellular energy marker creatine (p = 0.002) in the basal ganglia of fatigued participants. Statistically significant differences in other brain metabolites were not detected.


Conclusions:  Fatigue was present in 64% of A5090 study participants, a rate similar to previous reports. Younger participants were more likely to display fatigue symptoms, possibly reflecting higher functional expectations. Lower cellular energy levels in the basal ganglia, as measured by MRS creatine concentration, suggest that energy dysmetabolism in this brain region may play a role in the central mechanisms of fatigue.

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[beasiswa] [butuh info] Master of Public Health bidang Epidemiologi di Korsel

Salam,

Ada yang tahu info univ di korsel terutama bidang ilmu Public Health peminatan epidemiologi.

Udah nyari-nyari tp utk yg international postgrad koq susah ya....

Mohon bantuannya.

Terima kasih

== eof ==

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INFO, TIPS BEASISWA, FAQ - ADS:
http://id-scholarships.blogspot.com/

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INFO LOWONGAN DI BIDANG MIGAS:
http://www.lowongan-kerja.info/lowongan/oil-jobs/

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RE: [Konsultasi-Kesehatan] referensi dokter kandungan rs hermina bekasi

  Salam,

 

  Kebetulan isteri saya melahirkan dua kali di rumah sakit Hermina Bekasi secara Caesar.

  Dokter yang menangani adalah Abdulah Basalamah.Kami merasa puas konsultasi dan penanganan dia.

  Coba aja dating kesana sekalian biar tahu lebih detailnya.

  Terima kasih

  Salam

 

   Baskami Tarigan

 

-----Original Message-----
From: Konsultasi-Kesehatan@yahoogroups.com [mailto:Konsultasi-Kesehatan@yahoogroups.com] On Behalf Of Dhian
Sent: Thursday, February 26, 2009 8:46 AM
To: Bayi-Kita@yahoogroups.com; Konsultasi-Kesehatan@yahoogroups.com
Subject: [Konsultasi-Kesehatan] referensi dokter kandungan rs hermina bekasi
Importance: High

 

 

Hallo semua.......

 

Ada yang bisa kasih referensi gak,dokter kandungan di Rs.Hermina Bekasi??? kira2 dokternya enak diajak ngomong,bisa diajak sharing,sabar,teliti,gak bikin takut.

 

Trimakasih sebelumnya

dhian

 

 

 


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Notification: As of 27 Mar 2007, PT. Kiani Kertas had changed its name to PT. Kertas Nusantara. In conjunction with the name change, the email address' domain had also changed from @site.kiani.com to @site.kertas-nusantara.com.

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[PozHealth] CD4 Count Still < 100 after 3 years undetectable

One of my most successful T cell reconstitution patients is a 45 year old Black woman, who had 25 T cells when we met. She has 1125 now. She has just been on what is now Atripla for the past 7 years.

The nutritional elements that I think have generated this stunning rebound are:

1.
     B-complex vitamins. She takes The Perfect Blend multivitamin, 2 pills per day

2.
     L-carnitine , 1 gram per day.

3.
     Co-enzyme Q10, 100 mg per day

4.
     L-glutamine, 5 grams per day.

The reasons for this regime.

1. Rapidly dividing cell systems need more vit B6, B12, and folic acid. The Perfect Blend provides this. The Vitamin Shoppe sells a product: Two Per Day Tablets, made by Life Extension, that works well too.

2. All cells have a "self-kill" switch, (apoptosis switch) that they can activate when they feel like they are not pulling their weight. HIV infection causes healthy T cells to flip that  "self-kill" switch. L-carnitine blocks that suicide switch.

3. Natural Killer cells play a bigger role in managing HIV than previously thought. Coenzyme Q10 is fuel for NK cells. Co Q10 is also fuel for antigen presentation cells. All in all, it improves total immune function.

4. L-glutamine, helps T cells mature, and is fuel for them.

Try this regime, it can take 3 - 6 months to show good support of T cell count, and the full effect can take a year or more to evolve.

(For people with chronic liver disease, we see that T cell recovery can be slower.

Charlie Smigelski RD
www.eatupbooks.com




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Get a jump start on your taxes. Find a tax professional in your neighborhood today. (http://yellowpages.aol.com/search?query=Tax+Return+Preparation+%26+Filing&ncid=emlcntusyelp00000004)

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[Konsultasi-Kesehatan] Magic house



----------







 
 

U N B E L I E V A B L E ! ! !

Could you go to sleep at night and not wonder if these houses would be there the next morning?

Take a deep breath and look below...


# 1

DON'T WANT VISITORS? JUST UNHOOK THE CABLE.






# 2

MOST PEOPLE USETREESFOR A WINDBREAK



# 3

CONSIDER THE PANIC IF YOU HEAR A BRANCH CRACK...


# 4

HOW DID THEY GET THAT CAR IN THERE?




# 5

LONG CLIMB AFTER A DAY'S WORK!




# 6

TREE BELOW...FLOWERS ABOVE....SOME PEOPLE ARE JUST WEIRD!




# 7

NOT DURING HURRICANE SEASON, THANK YOU


# 8

GOT A LITTLE PROBLEM WITH DAMPNESS AT YOUR HOUSE?




# 9

I'VE HEARD OF PEOPLE'S BRIDGEWORK BUT THIS IS RIDICULOUS!




# 10

BETTER TALK TO AL GORE ABOUT GLOBAL WARMING!




Selalu bisa chat di profil jaringan, blog, atau situs web pribadi!
Yahoo! memungkinkan Anda selalu bisa chat melalui Pingbox. Coba!

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[Dokter Umum] pengobatan infeksi saluran kencing

thanks buat kesempatannya.
saya mau tanya, berapa hari yang lalu di perut bagian bawah dekat selangkangan rasanya
pegel, n sakit di bagian perut tapi berpindah2, kadang kanan kadang kiri dan sampai
tembus ke punggung. saya priksa ke dokter, katanya infeksi saluran kencing. memang saya
jarang minum n jarang kencing juga (sering menahan) tapi tidak anyang-anyangan.
kemudian saya diberi obat metaneuron metamizole sadium diazepam dari phapros. yang
saya mau tanyakan adalah:
1. benarkah perkiraan dokter kalo penyakit ini adalah infeksi saluran kencing?
2. bisa kah obat tersebut menyembuhkannya? karena setahu saya, ini adalah obat pengurang
rasa nyeri?

dua dulu aja dokter? saya mohon jawabannya..

thanks alot,

evelin

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[Konsultasi-Kesehatan] Fw: Khasiat Buah dan Sayuran dari Bentuknya


 
Grace A. Wijaya
http://www.gracedsign.com
graphic-web designer and illustrator
http://profiles.friendster.com/jualannyagrace
jualan apa aja yg penting halal:
baju esprit murah, penghemat bensin, sabun mandi, rumah, hasil prakarya, souvenir :D



Khasiat Buah dan Sayuran dari Bentuknya
 
Apakah kita menyadari jika Tuhan sudah memberikan petunjuk untuk kesehatan kita melalui makanan sehari-hari??? Buah-buah berikut ini contohnya...

Sebuah irisan wortel terlihat seperti mata manusia. Terlihat seperti pupil, iris, dan garis yang sama persis seperti mata manusia. Dan BENAR, sains terkini membuktikan kalau wortel sangat berfungsi untuk meningkatkan aliran darah dan fungsi mata menjadi lebih baik.

Tomat memiliki empat ruang di dalamnya dan berwarna merah. Jantung manusia memiliki empat ruang dan juga berwarna merah. Semua penelitian membuktikan kalau tomat banyak mengandung lycopine yang berfungsi sebagai asupan untuk darah.

Sekumpulan anggur yang menggantung memiliki bentuk seperti jantung. Setiap butir anggur terlihat seperti sel darah dan semua penelitian terkini menunjukkan bahwa anggur juga baik untuk jantung dan sebagai makanan yang dibutuhkan oleh darah.

Kacang kenari terlihat seperti otak berukuran kecil. Bagian kiri dan kanannya berbentuk hemisphere, atasnya seperti cerebrums, da bawahnya seperti cerebellums. Bahkan kerutan dan lipatan di kacang tersebut seperti neo-cortex. Saat ini kita ketahui kacang kenari membantu memberikan lebih dari tiga lusin neuron-transmitters untuk fungsi otak.

Kacang merah, mempunyai fungsi dan melindungi fungsi ginjal dan mata, dan kacang merah berbentuk seperti ginjal manusia.

Seledri, sawi dan batang-batang sayuran lainnya berbentuk seperti tulang. Makanan-makanan ini memang spesialis untuk kekuatan tulang. Tulang terdiri dari 23% sodium dan makanan-makanan ini juga terdiri dari 23% sodium. Jika Anda kurang sodium di diet Anda, tubuh akan mengambilnya dari tulang dan ini menyebabkan tulang menjadi lemah. Makanan-makanan ini menggantikan kebutuhan tulang yang diperlukan tubuh.

Alpukat, terong dan buah pir dibutuhkan untuk kesehatan kandungan dan mulut rahim dari wanita. Makanan-makanan tersebut terlihat mirip dengan organ-organ tersebut. Penelitian terkini menunjukkan bahwa jika wanita makan satu buah alpukat seminggu, akan menyeimbangkan hormon dan mencegah kanker mulut rahim. Alpukat butuh waktu 9 bulan untuk bertumbuh dari kecil hingga siap dipetik. Terdapat lebih dari 14.000 nutrisi kimia di setiap makanan ini (sains modern hanya mempelajari sekitar 141 dari keseluruhannya).

Buah ara adalah buah yang dipenuhi biji dan tergantung berjumlah 2 ketika mereka tumbuh (sama seperti organ laki-laki). Buah ara meningkatkan kelincahan dan mobilitas dari sperma dan juga meningkatkan jumlah sperma untuk mencegah sterilitas pada laki-laki.

Kentang manis atau ubi jalar terlihat seperti pankreas dan mempunyai khasiat untuk menyeimbangkan glysemic index untuk penderita diabetes.

Buah zaitun berkhasiat untuk menambah kesehatan dan fungsi dari sel telur (bentuknya juga sama).

Jeruk, lemon dan buah-buahan citrus lainnya sangat mirip dengan kelenjar susu dari wanita. Dan percaya atau tidak, buah-buah tersebut berkhasiat untuk menambah kesehatan dari kelenjar susu  dan keluar masuknya getah bening.

Bawang bombay terlihat seperti sel tubuh. Riset terkini menunjukkan bahwa bawang bombay membantu membersihkan material-material yang tak terpakai dari seluruh sel tubuh. Bawang bisa membuat mata memproduksi air mata yang bisa mencuci lapisan luar mata. Bawang putih, juga membantu melenyapkan material-material yang tidak berguna dan berbahaya seperti radikal bebas dari tubuh.

 

sumber : jawaban.com




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Thursday, 26 February 2009

[Konsultasi-Kesehatan] rambut rontok

saya mempunyai seorang teman seorang wanita,dia selalu mengeluh kepada saya tentang rambutnya yang rontok dan tipis.sewaktu bangun tidur rambutnya selalu rontok tidak cuma sehelai dua helai,yaaa lumayan banyak

Ada saran untuk penembuhan atau sekedar menguranginya

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[PozHealth] My lecture with Dr Schrader tonight - handout attached

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Re: [Dokter Umum] MERTUA KENA STRUK RINGAN, BAGAIMANA SOLUSI SUPAYA BISA SEMBUH DGN BIAYA MINIM?

Dear Yulian,
 
 Untuk berobat stroke, silahkan konsultasi ke dokter spesialis saraf atau neurologi. Jika di Jakarta, bisa ke RSCM, bagian unit Stroke dengan dr. Salim Harris, SpS.
Lalu tidak semua perawatan stroke harus di opname. Jika sudah konsultasi, maka dokter akan memutuskan bisa atau tidaknya utk berobat jalan saja yang tentunya akan menekan biaya perawatan.
 
Yang pasti, dokter akan mencari penyakit penyebab timbulnya stroke tsb dan kemudian penyakit itulah yang diobati agar tidak terjadi stroke yang kedua kali.
 
Untuk pengobatan alternatif, setahu saya, mereka biasanya melakukan pengurutan pada anggota gerak saja (lengan atau tungkai) , padahal hal kelumpuhan pada anggota gerak bukan disebabkan karena kerusakan pada anggota gerak tsb, tetapi disebabkan karena rusaknya daerah di otak yang mengatur fungsi pergerakan dari anggota gerak tsb.
 
Yang masih bisa diterima adalah pengobatan fisioterapy.
 
Semoga bermanfaat.
 
salam,
 

Melyanti
0818 0868 1974

--- On Thu, 2/26/09, yulian kamil <yuliankml@yahoo.com> wrote:

From: yulian kamil <yuliankml@yahoo.com>
Subject: Re: [Dokter Umum] MERTUA KENA STRUK RINGAN, BAGAIMANA SOLUSI SUPAYA BISA SEMBUH DGN BIAYA MINIM?
To: dokter_umum@yahoogroups.com
Date: Thursday, February 26, 2009, 2:13 AM

Yang kami maksud dengan biaya minim adalah seminimal mungkin hingga pasien bisa sehat seperti sedia kala. Pengalaman paman kami yang merawat mertuanya di RS Pemerintah, biaya sangat besar hingga 25 juta tanpa operasi selama sekitar 3 minggu (penyakit struk menyerang kaki).
 
Pengobatan alternative itu sebetulnya bagus atau tidak? Jujur aja kami lebih suka pengobatan resmi kedokteran karena banyak sekali pengobatan alternative yang beroprasi tanpa ijin yang jelas.
 
Yulian

 

-----Original Message-----
From: dokter_umum@ yahoogroups. com [mailto:dokter_ umum@ yahoogroups. com] On
Behalf Of yuliankml
Sent: 21 Februari 2009 0:30
To: dokter_umum@ yahoogroups. com
Subject: [Dokter Umum] MERTUA KENA STRUK RINGAN, BAGAIMANA SOLUSI SUPAYA
BISA SEMBUH DGN BIAYA MINIM?

Para Member Milis yg terhormat, terutama Para Dokter, kami mohon
bantuan segera.

Mertua laki-laki kami, umur 58 tahun kemungkinan terkena struk
ringan. Gejalanya tidak bisa bicara (seperti orang cadel, semakin
hari semakin cadel) dan sering mengalami kesemutan. Beliau punya
penyakit asam urat mungkin sejak 5 tahun lalu dan ketahuan kadar
gulanya tinggi pada bulan lalu.

Atas inisiative saya dan istri, Rabu (18/2) lalu kami bawa beliau ke
RS Fatmawati langsung ke poli syaraf, oleh dokter si pasien diminta
untuk rawat inap. Namun sayang saat itu semua kamar kelas 1, 2, 3
penuh (mungkin juga kelas VIP) dan kami diminta menunggu sampai jam
14, tapi tetap saja kamar tidak ada hingga akhirnya kami pulang ke
rumah. Hari itu kami sempat lakukan rontgen di dada dan tidak sempat
CT Scan karena antrian sudah banyak. Hasil rontgen diambil esok
harinya dengan hasil paru / jantung kondisi bagus, menurut seorang
dokter ahli radiologi. Untuk info bahwa Bapak Mertua kami berhenti
merokok 15 tahun lalu dan sangat suka makanan berkolesterol tinggi.
Bila terkena serangan asam urat, beliau selalu minum jamu di warung
jamu, lalu sembuh.

Malam harinya kami bawa mertua kami itu ke pengobatan alternative
(atas saran saudara kami). Di sana pasien diurut oleh ahlinya dan
diberikan obat. Kami bayar sejumlah Rp. 100,000. Oleh si ahli
pengobatan alternative ini kami diminta datang kembali satu minggu
kemudian.

Kemudian tadi pagi (20/2) datang lagi seorang ahli pengobatan
alternative lain (atas rekomendasi saudara kami yang lain) dan lagi-
lagi Bapak Mertua kami diurut dan kami membayar Rp. 100,000. Si ahli
pengobatan tradisional ini akan datang intensive setiap hari hingga
pasien sembuh.

Bisakah pengibatan alternative dengan cara diurut seperti history di
atas disebut theraphy? Bagaimana solusinya supaya Bapak Mertua kami
yang sangat kami sayangi ini bisa sembuh dan menjalankan hidupnya
normal kembali seperti minggu-minggu yang lalu? Jujur saja, semula
kami berencana laksanakan pengobatan rawat inap di RS, tapi kami
sekarang berubah pikiran dikarenakan ketakutan kami akan biaya yang
sangat besar, dan tidak ada dari keluarga kami yang bisa menunggui
beliau setiap hari selama rawat inap di RS.

Kami mohon bantuan Para Pembaca untuk solusinya. Sekarang kami
tertarik pada theraphy yang intensive di RS Fatmawati, namun tanpa
harus rawat inap, bisakah? Adakah? Kira-kira berapa biayanya dan
berapa lama? Kami tidak masalah bila harus lakukan CT Scan dulu
sebelum theraphy.

Demikain kami sampaika. dan terima kasih telah sempatkan waktu baca
message ini.

YULIAN

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Re: [Dokter Umum] Pembengkakan kelenjar

Sehubungan dengan pertanyaan ibu dara saya juga ingin menanyakan tentang
pembengkakan kelenjar.
Sahabat baik saya (wanita 24 tahun) yang baru menikah mengalami pembengkakan
di leher, belakang telinga dan kepala bagian bawah belakang.Bentuk
bengkaknya agal menonjol dan keras seperti tulang timbul tapi kadang kempes
dgn sendirinya. Waktu periksa ke dokter specialis dan diambil contoh
kelenjar tersebut hasil lab menyatakan Hasil lab mikroskopik, sediaan
sitologi aspirasi kgb leher kanan mengandung sel epiteloid, fokus nekrotik
dan limfosit. Tidak ditemukan sel tanda ganas.Kesimpulan : limfadenitis
kronik granulomatosa, kemungkinan adanya tuberkolusa belum dapat
disingkirkan.Bahaya tidak ya Dok? Berhubung sahabat baik saya itu ingin
segera mempunyai anak apakah ada indikasi untuk menular turunan? Sekedar
info bahwa jika sahabat saya ini habis dari salon misal untuk creambath maka
cepat memicu bengkaknya kelenjar lagi. Apa dia alergi obat kimia dari salon?
Mohon bantuan dokter. Terimakasih

2009/2/27 dara_psi83 <dara_psi83@yahoo.co.id>

> Dok, di seluruh tubuh suami saya (punggung, tangan dan kaki) terdapat
> benjolan-benjolan. Katanya, dia pernah ke dokter dan divonis
> pembengkakan kelenjar dan cara menghilangkannya hanya dengan operasi
> kecil.
> Pada kelenjarnya terdapat benda-benda kecil sebesar kacang tanah yang
> harus dikeluarkan. Tapi sekarang kelenjarnya kembali membengkak, dia
> bahkan sudah dioperasi 2 kali. Kata dokter jika tidak pecah tidak
> berbahaya.
> Sebenarnya yang diderita suami saya apa ya dok? soalnya pembengkakan
> tersebut tidak berdampak pada berat badan maupun kesehatannya.
> Terima kasih atas jawabannya.
>
>
>

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[Dokter Umum] Harapan Baru Terapi Genetik Bagi Penderita Penyakit Jantung Bawaan

Harapan Baru Terapi Genetik Bagi Penderita Penyakit Jantung Bawaan
Submitted by Taruna Ikrar on Thursday, 26 February 2009 4

SEBUAH penelitian baru membuktikan bahwa KCNQ1 adalah gen utama yang menyandi fungsi jantung. Mutasi yang terjadi pada gen tersebut akan menyebabkan penyakit jantung bawaan pada ratusan ribu anak dan akan menimbulkan gangguan rhytm atau irama jantung dengan penderitaan seumur hidup. Kondisi ini pada akhirnya bisa menyebabkan gagal jantung atau Cardiac suddent dan kematian. Kami bersama Tim peneliti lainnya di Cardiac Research Center, Niigata University Hospital, Jepang telah melakukan uji gene screening pada lebih dari seratus keluarga dengan penderita penyakit jantung bawaan. Penemuan ini dipublikasikan di journal international of BBRC&#12289;Sciences Journal 2009 Jan 16;378(3):589-94 dan J Cardiovasc Electrophysiol 2008 May;19(5):541-9

Penyakit jantung bawaan ini, dalam ilmu kedokteran disebut LQTS (Long QT Syndrome) karena mengalami perlambatan pacu jantung yang diserta dengan pemanjangan jarak QT interval pada Elektrokardigrafi Jantung. Penyakit ini, juga mempunyai ciri-cirinya berupa sinkop (keadaan dimana terdapat kelemahan menyeluruh pada otot-otot tubuh sehingga tidak mampu mempertahankan sikap tegak yang disertai dengan hilangnnya kesadaran). Pada jantung normal, iramanya harus teratur, berdiri sendiri, dan otonom. Pengatur Jantung berdenyut secara otomatis ini dinamakan pacu jantung (Pace macker). Pacu jantung utama adalah di nodus sinus. Bradikardia atau perlambatan denyut jantung dapat terjadi oleh kerusakan dipusat pacu jantung utama yang di sebab oleh gangguan fungsi sinus atau gangguan rangsang jantung..

Dalam penelitan tersebut, pasien yang menderita kelainan jantung bawaan, ditemukan adanya mutasi genetik pada semua penderita. Tepatnya pada gen KCNQ1 dengan lokasi mutant-nya pada residue 313, dan ternyata residue I313K ini merupakan pusat dari kanal Potassium yang tentunya merupakan molekul utama yang sangat dibutuhkan untuk kontraksi otot-otot jantung. Jadi dengan terjadinya mutasi tersebut penderita penyakit ini akan mengalami gangguan kontraksi otot jantung.

Pengujian selanjutnya, pada sel-sel otot jantung secara invitro dengan menggunakan metode Patch Clamping Electrophysiology, Confocal imaging, dan analisa sequencing DNA pada pasien-pasien penderita penyakit herediter ini, membuktikan bahwa terdapat perbedaan bermakna penurunan fungsi sel-sel mutant KCNQ1-I313K bila dibandingkan dengan sel-sel normal. Untuk membuktikan lebih jauh lagi, kami melanjutkan penelitian ini dengan mengganti asam amino pembentuk mutant tersebut dengan menggunakan metode mutagenesis secara invitro. Caranya dengan merubah susunan asam amino residu I313 berdasarkan muatan listrik dari asam amino tersebut menjadi I313V (Valine) bersifat netral, I313G (Glycine) netral dan molekul kecil, I313K (Lysine) bermuatan positif, dan I313E (Glutamide) bermuatan listrik negatif. Hasilnya menggambarkan bahwa asam amino netral yang tidak bermuatan listrik hasilnya sama dengan sel normal, tidak terdapat perbedaan yang bermakna secara statistik jika dibandingkan dengan sel-sel normal. Namun sebaliknya jika dibandingkan dengan fungsi sel-sel yang mengandung muatan listrik positif ataupun negatif akan menyebabkan gangguan fungsi sel yang sangat menurun bahkan sel-sel tersebut tidak berfungsi lagi. Hal yang manakjubkan terjadi pada sel-sel yang mengandung I313G asam amino dengan ukuran kecil, dan tidak bermuatan listrik/netral, memperlihatkan fenomena seba&#65356;iknya, bahkan mengalami kelebihan fungsi. Sehigga dalam ilmu peyakit jantung, fenomena ini dapat menyebabkan penyakit yang berlawanan dari LQTS diatas, yaitu Short QT syndrome (SQTS) dengan pemendekan QT interval Elekrokadiografi jantung.

Harapan Baru, dari hasil penelitian ini menggambarkan sesuatu yang sangat baru dalam ilmu genetika kedokteran, bahwa mutasi gen KCNQ1 menjadi dasar timbulnya kelainan jantung bawaan LQTS, dan diturunkan secara dominan autosomal. Keparahan penyakit tersebut ditentukan bukan hanya oleh lokasi terjadinya mutasi, namun yang lebih penting lagi adalah jenis asam amino pembentuk mutan tersebut. Sehingga tentunya, hasil ini dimasa depan dapat digunakan sebagai dasar ilmiah teknik pengobatan genetik (gene therapy) bagi penderita penyakit jantung bawaan, yaitu dengan cara mentransgenikkan asam amino mutant pada pasien kearah asam amino normal.

Kepustakaan:

1. Ikrar T, Hanawa H, Watanabe H, Aizawa Y, Ramadan MM, Chinushi M, Horie M, Aizawa Y, Evaluation of channel function after alteration of amino acid residues at the pore center of KCNQ1 channel,&#12288; Biochem Biophys Res Commun, 2009;378(3):589-94

2. Ramadan MM, Mahfouz EM, Gomaa GF, El-Diasty TA, Alldawi L, Ikrar T, Limin D, Kodama M, Aizawa Y. Evaluation of coronary calcium score by multidetector computed tomography in relation to endothelial function and inflammatory markers in asymptomatic individuals. Circ J. 2008; 72(5):778-85.

3. Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y.&#12288;A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome. J Cardiovasc Electrophysiol. 2008; 19(5):541-9.

4. Ramadan MM, Tachikawa H, Kodama M, Okawara A, Mitsuma W, Ito M, Kashimura T, Ikrar T, Hirono S, Okura Y, Suzuki K, Aizawa Y.&#12288;A pilot-controlled study of myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody (MPO-ANCA) in the coronary circulation. Int J Cardiol. 2008; 128(1):114-6.

5. Ramadan MM, Kodama M, Mitsuma W, Ito M, Kashimura T, Ikrar T, Hirono S, Okura Y, Aizawa Y.&#12288;Impact of percutaneous coronary intervention on the levels of interleukin-6 and C-reactive protein in the coronary circulation of subjects with coronary artery disease. Am J Cardiol. 2006; 98(7):915-7.

6. Aizawa Y, Mitsuma W, Ikrar T, Komura S, Hanawa H, Miyajima S, Miyoshi F, Kobayashi Y, Chinushi M, Kimura A, Hiraoka M, Aizawa Y. Human cardiac ryanodine receptor mutations in ion channel disorders in Japan. Int J Cardiol. 2007 ;116(2):263-5.

7. Topol EJ, Califf RM, Isner J, Prystowsky EN, Swain J, Thomas J, Thompson P, Young JB, Nissen S. Textbook of Cardiovascular Medicine. Lippincott Williams & Wilkins, 3th Ed.

2006http://beritaiptek.istecs.org/
Harapan Baru Terapi Genetik Bagi Penderita Penyakit Jantung Bawaan
http://beritaiptek.istecs.org/harapan-baru-terapi-genetik-bagi-penderita-penyakit-jantung-bawaan/

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Wassalam
Taruna

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