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How NIH Misread Hormone Study in 2002 Print E-mail
SciMed - Healthcare
TS-Si News Service   
Sunday, 08 July 2007 07:59
no input in the final paper by investigators who worked for nearly a decade
 
How could the heart risks of menopause hormones for this crucial cohort change so dramatically in just five years?New York City, NY, USA. On July 9, 2002, health officials from the US federal government announced that they had halted a major study of menopause hormones, saying the drugs increased a woman's risk of heart attack by 29%.

But in the five years since, it's become clear that some aspects of what was initially reported from the $725 million Women's Health Initiative (WHI) study were either misleading or just wrong.
 
 
 
Although the government initially said the findings applied to all women, regardless of age or health status, additional data published in recent months show that the age of a woman and the timing of hormone use dramatically changes the risk and benefits.
 
WHI data published in the Journal of the American Medical Association showed that women in their 50s who took a combination of estrogen and progestin or estrogen alone had a 30% lower risk of dying than women who didn't take hormones.

The New England Journal of Medicine reported that 50-59-year-old women in the WHI who regularly used estrogen alone showed a 60% lower risk for severe coronary artery calcium, an important risk factor for heart attack.

How could the heart risks of menopause hormones for this crucial cohort change so dramatically in just five years? Officials from the National Institutes of Health, which directed the study of more than 27,000 women, say the interpretation of the WHI has simply evolved as researchers have used different methods to analyze the voluminous body of data.

The average age of women in the study was 63. While older women in the study did show a heart risk, researchers eventually focused on women in their 50s who were closer to menopause, finding that hormones were more likely to protect those women's hearts than harm them.
 
But critics including some of the WHI's own investigators, speaking out for the first time, say that NIH officials initially overgeneralized in large part because they excluded many of the study's own investigators and physicians from the first review. As a result, key questions that could have clarified the data far sooner weren't asked.

Just 11 days before the public announcement in July 2002, the WHI's 40 investigators met in Chicago, where they were told the study had been stopped early. Several people who attended the meeting say several WHI researchers were stunned and angry when they were given final page proofs of the study report for the Journal of the American Medical Association. Although some researchers expressed concern that the results were too broadly interpreted, it was too late to make meaningful changes to the JAMA article. Many investigators who had spent nearly a decade working on the WHI had no input in the final and most important paper.

"I think that had the initial report been written by a broader group, as almost all of our later papers have been, it would have been framed differently," says Robert D. Langer, the former principal investigator for the WHI's clinical center at University of California, San Diego, who was among those who protested at the time. He has since served as an expert witness for hormone maker Wyeth. Dr. Langer says he remains concerned that the interpretation of the WHI has unnecessarily scared a generation of women from the treatment.

Jacques Rossouw, a physician with the National Heart Lung and Blood Institute who has overseen the WHI since its inception, confirms that some investigators were upset that they weren't included in writing the first WHI report. "That was an NIH decision supported by the WHI executive committee to keep it to a small group because we realized it was a sensitive paper," he says.
 
Still, he defends the government's handling of the study results "based on what we knew at the time," and says that study officials wanted to make a dramatic statement. "Our main job at the time was to turn around the prevailing notion that hormones would be useful for long-term prevention of heart disease," he says. "That was our objective. That was a worthy objective which we achieved."

But many in the medical community disagree, saying key questions about long-term use still aren't answered. Although the WHI data clearly show that starting hormones at an older age is risky, what's not clear is whether the heart protection women get starting at a younger age will continue with long-term use.

That was the question that the WHI was supposed to answer when it was launched in 1991 after data from an ongoing trial of nurses showed that women who used menopause hormones have as much as a 50% lower risk of heart attack. But the WHI designers didn't take into account that the timing of hormone use might affect the results and recruited mostly older, symptom-free women. Some of the study participants were already 20 years past menopause when the WHI began.
 
Historical TimelineSince mostly older women were recruited, there weren't enough recently menopausal women under 60 to generate conclusive data in some of the findings. But the trends were provocative. Among recently menopausal women who used estrogen and progestin, heart attack risk fell 11%. By comparison, women who started taking hormones 10 or more years past menopause had a 22% to 71% higher risk of heart problems.
 
In a second part of the study, in which women who had undergone hysterectomy took estrogen without progestin, women who started hormones after the age of 70 had an 11% higher risk of heart problems. But women below 60 in the estrogen-only study had a 37% lower heart risk.
 
In a bid to draw a more definitive conclusion, the WHI in April 2007 published a report in JAMA combining the data from both hormone trials. That paper showed that the timing of hormone use matters: Younger women appear to receive heart protection, while older women are at risk.
 
"We now have a refined understanding of the benefits and risks of hormone therapy, and there has been so much reassuring evidence for younger women over the last few years," says Harvard professor and WHI investigator JoAnn Manson, who has no ties to drug firms.
 
Despite the recent data, questions about long-term use of hormones are far from resolved. While most people now agree that hormones are a reasonable option for women to treat menopause symptoms like hot flashes, the bigger question is whether hormones should be considered in the armamentarium of drugs used for heart protection, along with blood pressure medications and cholesterol-lowering drugs called statins.
 
The National Heart, Lung and Blood Institute, which oversaw the WHI, firmly believes that menopause hormones shouldn't be used to prevent heart disease because of potential risk of blood clot, stroke and breast cancer.
 
Indeed, the WHI showed that hormones have a range of risks and benefits. On the plus side, they may protect younger women's hearts, they definitely protect against hip fractures, they lower the risk for diabetes and may lower the risk for colon cancer.
 
On the other hand, menopause hormones do increase the risk for blood clots and stroke. Women in the WHI who used both estrogen and progestin were at 24% higher risk for breast cancer. But women who regularly use estrogen without progestin had a 33% lower risk of breast cancer.
 
"Hormone therapy long term has these other adverse events hanging around. It doesn't fit the paradigm of what you are looking for in a viable long-term prevention strategy," says Dr. Rossouw. "If you're going to use something to prevent atherosclerosis, your choice is statins, not hormones."
 
The data on women who use statins are mixed, but suggest that they lower a woman's heart risk by 15% to 20%. Statins carry their own risks, including liver effects, muscle pain, memory problems and in rare cases a life-threatening muscle disease call rhabdomyolysis. There are no studies showing the risks and benefits of long-term use of statins.
 
Many doctors now believe that for younger women without a uterus, estrogen should be an option for long-term prevention of heart disease. (The progestin is added to protect against uterine cancer.)
 
"If this is preventing heart disease and saving lives, I think it's really wrong not to consider it," says Yale associate professor Hugh Taylor, a principal investigator for the Kronos Early Estrogen and Prevention Study (KEEPS), a study of estrogen and heart disease funded by Arizona billionaire John Sperling, an education entrepreneur who was upset with the way the WHI study was initially interpreted. "Some of the other drugs we use for cardiovascular disease don't have the evidence that we have for hormone therapy."
 
Two important ongoing studies will further illuminate the role estrogen plays in heart disease. The KEEPS study is recruiting 720 women, ages 42 to 58, to study the effects of oral or transdermal estrogen as well as progesterone on the coronary arteries of healthy women. An NIH-funded Early Versus Late Intervention Trial will study 500 women and the effects of hormone therapy given within six years of menopause compared to treatment given 10 or more years after menopause. Both studies will also test whether using natural progesterone, instead of the synthetic progestin used in the WHI, lowers or eliminates the risk of breast cancer associated with combination therapy.
 
Even though the long-term heart issue is unresolved, some critics say the NIH's handling of the WHI data scared away younger women who might want to use hormones for menopause symptoms. "We've gone to considerable efforts to reassure women and gynecologists that it's okay [to use hormones] in the short term," to treat the symptoms of menopause, Dr. Rossouw says.
 
Still, since the WHI results were announced in 2002, hormone sales have plummeted 30% to $1.9 billion, according to IMS Health, a health-care information company.
 
"I don't think it's fair to extrapolate from the data that women should be put on this as a preventative treatment for heart disease," says Michael E. Mendelsohn, a Tufts University professor who recently wrote an NEJM editorial about estrogen and heart disease. "What the data do support is that women who use hormones to treat menopause symptoms can feel reassured that they are not increasing their cardiovascular risk and may be providing some long-term benefit."
 
— Tara Parker Pope (WSJ)
 

Reprinted by permission. This main body of this article is not subject to TS-Si's Creative Commons policy and can not be reprinted or redistributed for commercial use. The information sidebar is availble for reprint under the standard TS-Si licensing terms.
 
 
Last Updated on Wednesday, 27 February 2008 14:18
 
Should Medical Implants React With Your Body? Print E-mail
SciMed - Healthcare
TS-Si News Service   
Thursday, 05 July 2007 20:00
Use implant materials that engage with biological processes
 
Professor Buddy Ratner, Director of the University of Washington Engineered Biomaterials (Seattle, USA).Seattle, WA, USA. A world leader in medical implants has called for new approach to building medical implants. Currently so-called biomaterials are chosen because they are reasonably successful at hiding from the body’s immune system, and are consequently not rejected.
 
All the same, within a month of implanting them, the body isolates implants by wrapping them in a collagenous, avascular sac. Materials are considered to be ‘biocompatible’ if this sac is not too thick.
 
Professor Buddy Ratner says “That’s not very clever.” Ratner is the Director of the University of Washington Engineered Biomaterials (Seattle, USA). In a Polymer International commentary, he calls for a more intelligent approach.
 
Rather than building implants out of materials that try to hide from the body’s systems, he believes that we should be creating them from materials that are specifically designed to engage with biological processes. This could take the form of materials made with specifically sized pores that encourage small blood vessels to actively grow through the implant, or implants coated with DNA that specifically prevents formation of the collagenous capsule.
 
Both of these let the implant and the body actively work together, rather than simply try to prevent them fighting against each other.
 
Ratner looks forward to an exciting future. “These sorts of ideas will lead to a new biomaterials science that will permit us to make materials for medical devices that function better, last longer, encourage healing and provide enhanced patient satisfaction,” says Ratner.
 
Last Updated on Wednesday, 19 September 2007 01:58
 
Study: Estrogen Boosts Aging Brain Cells Print E-mail
SciMed - Healthcare
TS-Si News Service   
Monday, 25 June 2007 20:00
". . . our study suggests that if we jump before it’s too late, we may possibly prevent memory loss.”
 
In a multi-center study comparing older rhesus monkeys with younger female monkeys, researchers found that estrogen significantly improved cognitive function in older animals but not in young monkeys.New York City, NY, USA. Cyclical, long-term estrogen injections protected brain cells from age-related deterioration, according to a new study conducted at the Mount Sinai School of Medicine.
 
The study suggests that age is a factor in estrogen treatment and sheds light on the intricate relationship between mind, age, and hormones. The study is published in the online edition of Proceedings of the National Academy of Sciences.
 
In a multi-center study comparing older rhesus monkeys with younger female monkeys, researchers found that estrogen significantly improved cognitive function in older animals but not in young monkeys.
 

The study was led by Jiandong Hao, MD, PhD, & senior co-author John H. Morrison, PhD. Peter Rapp, PhD, Interim Chair of the Department of Neuroscience & Associate Professor of Neuroscience, & Geriatrics & Adult Development, led the behavioral phase of the study.  

 
Working with colleagues from the University of Toronto and the University of California-Davis, Drs. Morrison, Rapp, and Hao compared the outcomes of four groups of female monkeys that were ovarectomized, which induced menopause: old monkeys that received estrogen, old monkeys that did not receive estrogen, young monkeys that received estrogen, and young monkeys that did not receive estrogen. The treated animals received pure estradiol injections every 21 days while being tested on a series of cognitive tasks over the course of more than two years.
 
Cognitive performance tests showed the older treated animals performed almost as well as the younger animals, whereas older untreated animals displayed dramatic cognitive decline. Surprisingly, the younger animals performed equally well with or without estrogen treatments. The aged animals had their ovaries removed around the time of perimenopause—before the onset of full menopause—and began treatment within months of ovariectomy.
 
Peter Rapp, PhD, Interim Chair of the Department of Neuroscience and Associate Professor of Neuroscience, and Geriatrics and Adult Development, Mt. Sinai.Rapp's microscopic studies, conducted after completing the cognitive testing, revealed that in the prefrontal cortex — a region of the brain associated with cognitive tasks — the older estrogen-treated animals showed a greater density of synaptic spines. The latter are tentacle-like structures that link brain cells to one another and aid in brain cell communication. The older untreated animals showed no such neuronal growth. These spines are critically important for learning and memory.
 
John H. Morrison, PhD, Dean of Basic Sciences and the Graduate School of Biological Sciences, Mt Sinai.The findings indicate that the debate on the potential benefits of postmenopausal hormone therapy is not yet over, says Dr. Morrison. “There’s been a great deal of confusion as to whether estrogen helps or harms post-menopausal women, and our findings tell us is that there is a very critical window of opportunity in which estrogen therapy may be helpful.”
 
Dr. Morrison notes that this critical window may be around the time of perimenopause, in which cyclical estrogen treatments as used in this study may be particularly effective in protecting the brain from age-related decline.
 
“We found that this increase in synaptic spines in the prefrontal cortex in the older estrogen-treated monkeys appears to have prevented age-related cognitive decline,” Dr. Morrison explains. “Importantly, the increase was most pronounced among the small spines that are highly plastic and particularly important for learning and memory.
 
Young monkeys retain a high number of these small spines even without estrogen, which explains their ability to perform well on the cognitive tasks. Estrogen levels decline in old age, so the brain may need a certain amount of circulating estrogen to remain supple. Timing may be everything.”
 
“The increase we observed in small, thin spines suggests that estrogen allows for greater neuroplasticity, says Dr. Morrison. “Synaptic spines are lost during aging, and interestingly, it is the dynamic nature of the small-headed spines that are critical to the formation of new memories.”
 
The younger animals retain neural plasticity in the absence of estrogen, Dr. Morrison explains, “but what’s happening with the older animals is this double hit of both age and estrogen decline. These particular brain cells are not resilient enough anymore to endure this kind of double hit.”
 
Rhesus monkeys undergo menstrual cycles and a menopause that closely mimics those of humans. Although it is well known that estrogen affects brain function, what is unclear is what form of estrogen works best, when estrogen should be given, and how much is needed to be effective. It is possible, the researchers note, that administering the same cyclical estradiol treatments to very old monkeys would result in less benefit.
 
“It’s possible a middle-aged brain reacts differently to estrogen than a young brain, and that a very old brain might not react to estrogen at all,” Dr. Morrison explains, “so this window of opportunity may be fairly narrow—we just don’t know yet. If the brain is too old, then age-related decline may be difficult to reverse. However, our study suggests that if we jump before it’s too late, we may possibly prevent memory loss.” What is also unclear, Dr. Morrison adds, is at what point the natural course of aging trumps the effects of any estrogen treatment.
 
Drs. Rapp and Morrison plan to extend their research through similar behavioral and microscopic studies in monkeys that have not been ovarectomized, so that the aging process is more natural and not acutely induced.
 

 
The study was led by Jiandong Hao, MD, PhD, Assistant Professor of Neuroscience, and senior co-author John H. Morrison, PhD, Dean of Basic Sciences and the Graduate School of Biological Sciences, and the W.T.C. Johnson Professor of Geriatrics and Adult Development (Neurobiology of Aging). Peter Rapp, PhD, Interim Chair of the Department of Neuroscience and Associate Professor of Neuroscience, and Geriatrics and Adult Development, led the behavioral phase of the study.
 
Partrick Hof, MD, the Irving and Dorothy Regenstreif Research Professor Neuroscience, and William Janssen, a researcher in Neurobiology of Aging, also contributed to the research.
 
 
Last Updated on Tuesday, 15 January 2008 02:14
 
Experts Question Risk Of Planned U.S. Uterus Transplant Print E-mail
SciMed - Healthcare
TS-Si News Service   
Monday, 15 January 2007 09:28
". . . some even wonder whether the procedure, if successful, could theoretically lead to men being able to bear children."
 
Giuseppe Del Priore, center, and colleagues transplant a monkey uterus. Photo by Jeanetta Stega, courtesy of the New York Downtown Hospital.Washington, DC, USA. First came kidney, liver and heart transplants. Then a few doctors started transplanting hands. French surgeons even did a face.
 
Now, doctors are planning the first womb transplant in the United States.
 
A team based in Manhattan [New York City] has begun screening women left barren by cancer, injuries or other problems who want a chance to bear their own children.
 
"The desire to have a child is a tremendous driving force for many women," said Giuseppe Del Priore of the New York Downtown Hospital, who is leading the team. "We think we could help many women fulfill this very basic desire."
 
But the planned operation, which Del Priore and his colleagues could attempt later this year, is stirring objections among some transplant experts, fertility specialists and medical ethicists. They question whether the procedure has been tested sufficiently on animals and whether the benefit of being able to carry a pregnancy outweighs the risks for the woman and fetus.
 
"This raises a set of very difficult medical and ethical questions," said Thomas H. Murray, who heads the Hastings Center, a bioethics think tank in Garrison, N.Y. "I think it's very questionable. This would be very hard to justify."
After the birth of her first child in 1996, hemorrhaging forced removal of a 20-year-old woman's womb. In 2002, a 46-year-old woman with an ovarian condition that required removal of her ovaries and uterus donated her womb to the other woman. Blood clots resulted in removal of the organ after 99 days, but the doctors and surgeons involved considered the procedure a technical success.
The operation marks a confluence of two medical specialties -- transplant surgery and reproductive medicine -- that frequently spark controversy.
"It is the convergence of two fields that are already embedded in large ethical disputes," said Lori B. Andrews, a bioethicist at the Chicago-Kent College of Law. "This represents the worst of both worlds."
 
Several experts said the plans highlight the unique status that childbearing holds in the United States and elsewhere, and the lengths to which some women will go to experience it, even with the availability of such options as adoption and surrogacy.
 
"I'm not convinced that science and medicine and society as a whole should be putting so much emphasis on having this particular nine-month experience," said Adrienne Asch, who studies family life at Yeshiva University. "Why is that the sine qua non of being a parent? The real work of parenting is in the time after a child is born and is in someone's home."
 
 
 
Last Updated on Wednesday, 19 September 2007 01:50
 
Helping Artificial Skin Fight Lethal Infection Print E-mail
SciMed - Healthcare
TS-Si News Service   
Thursday, 11 January 2007 19:00
Genetically altered cells hold potential for skin grafting
 
Dorothy Supp, PhD, is an adjunct research professor at the University of Cincinnati and researcher at Cincinnati Shriners Hospital for Children. Photo courtesy of the University of Cincinnati Academic Health Center (D. Davenport)Cincinnati, Ohio, USA. Burn researchers have created genetically modified skin cells that, when added to cultured skin substitutes, may help fight off potentially lethal infections in patients with severe burns.
 
Dorothy Supp, PhD, and her team found that skin cells that were genetically altered to produce higher levels of a protein known as human beta defensin 4 (HBD4) killed more bacteria than normal skin cells.
 
HBD4 is one in a class of proteins that exist throughout the body as part of its natural defense system. Researchers have only recently begun targeting these tiny molecules as a way to combat infections.
 
"If we can add these genetically modified cells to bioengineered skin substitutes, it would provide an important defense system boost during the initial grafting period, when the skin is most susceptible to infection," explains Supp, an adjunct research associate professor at the University of Cincinnati (UC) and researcher at the Cincinnati Shriners Hospital for Children.
 
Supp says defensins could become an effective alternative method for burn wound care and infection control. Using them in cultured skin substitutes, she adds, could also decrease a patient's risk for infection, improve skin graft survival and reduce dependence on topical antibiotics.
Cells that were genetically modified to produce higher levels of a protein known as human beta defensin 4 are shown in green.
A modified skin cell may help protect cultured skin substitutes from infection.
 
Here, cells that were genetically modified to produce higher levels of a protein known as human beta defensin 4 are shown in green.
Cultured skin substitutes are grown in a laboratory using cells from a burn patient's own skin. These cells are cultured, expanded and combined with a spongy layer of collagen to make skin grafts that are reattached to the burn wound.
 
"Cultured skin substitutes are improving the lives of many burn patients, but they also have limitations--including an increased susceptibility to infection," says Supp. "Because cultured skin grafts aren't connected to the circulatory system at the time of grafting, they aren't immediately exposed to circulating antibiotic drugs or antibodies from the body's immune system to fight off infection."
 
Currently, physicians manage cultured skin graft infections during the early healing period by continually wrapping the wound in dressings soaked in antimicrobial drugs. Although this protects the grafts, Supp says, it can also contribute to the emergence of drug-resistant strains of bacteria.
 
"When you give the patient the same drug topically and orally, the risk for drug-resistant bacteria to emerge is greatly increased," says Supp. "We need alternative methods for combating infection in burn patients.
 
Dorothy Supp in lab.In this three-year laboratory study, Supp isolated the HBD4 gene from donated tissue samples and transferred it into surface skin cells (keratinocytes) to give them enhanced infection-fighting abilities.
 
These cells were then infected with pseudomonas aeruginosa, a type of bacteria found commonly in hospitals, and allowed to incubate.
 
Analysis revealed that the genetically altered cells containing HBD4 were more resistant to microbial infections than the unaltered cells.
 
"If it proves effective in additional testing," Supp predicts, "this type of gene therapy could be a promising alternative infection control method for burn wounds."
 
Researchers hope to begin testing this approach in an animal model in early 2007.
 
Journal: Burn Care & Research
 
UC researchers reported these findings in the January 2007 issue of the Journal of Burn Care and Research.
 

 
This study was funded by the Cincinnati Shriners Hospital for Children. Collaborators include Andrea Smiley, Jason Gardner, Jennifer Klingenberg of Shriners and Alice Neely, PhD, who is affiliated with both Shriners and UC.
 

 
Supp DM, and Boyce ST: Bioengineering of Human Skin Substitutes. In: Biomedical Engineering Handbook, Fisher JP and Mikos AG, Eds. CRC Press, Boca Raton, FL, In Press.
 
Boyce ST, and Supp DM: Skin Substitutes: Theoretical and Developmental Considerations. In: Functional and Aesthetic Reconstruction of Burn Patients, McCauley RA, Ed. Taylor Francis Group, Boca Raton, FL, 2005.
 
Supp DM, and Boyce ST: Cutaneous Gene Therapy with Cultured Skin Substitutes. In: Tissue Engineering and Novel Delivery Systems, Yaszemski MJ, Wise DL, Trantolo DJ, Altobelli DE, Hasirci V, Lewandrowski K, Eds. Marcel Dekker, Inc., New York, New York, 2003.
 
Supp DM, and Boyce ST: Genetic Modification of Cultured Skin Substitutes. In: Cultured Human Keratinocytes and Tissue Engineered Skin Substitutes—State of the Art, Horch RE, Munster AM, and Achauer B, Eds. J. A. Barth Verlag, Heidelberg, Germany, 2001.
 
Supp DM, Potter SS, McGrath J, and Brueckner M: Motor Proteins and the Development of Left-Right Asymmetry. In: Etiology and Morphogenesis of Congenital Heart Disease: 20 Years of Progress in Genetics & Developmental Biology, Clark EB, Takao A, and Nakazowa A, Eds. Futura, Inc, Armonk, New York, 2000.
 
 
Last Updated on Tuesday, 11 September 2007 10:55
 
No Surgery For Smokers? Print E-mail
SciMed - Healthcare
TS-Si News Service   
Friday, 05 January 2007 19:00
Hmmmn. What about SRS?
 
London, United Kingdom. Last year a primary care trust announced it would take smokers off waiting lists for surgery in an attempt to contain costs. In this week's British Medical Journal (BMJ), two experts go head to head over whether smokers should be refused surgery.
 
Denying operations is justified for specific conditions, argues Professor Matthew Peters, from the Department of Respiratory Medicine, Concord Repatriation General Hospital, in Australia.
 
Professor Peters says that smoking up to the time of any surgery increases cardiac and pulmonary complications, impairs tissue healing, and is associated with more infections.
 
These effects increase the costs of care and also mean less opportunity to treat other patients, he writes. In healthcare systems with finite resources, preferring non-smokers over smokers for a limited number of procedures will therefore deliver greater clinical benefit to individuals and the community.
 
He believes that, as long as everything is done to help patients to stop smoking, it is both responsible and ethical to implement a policy that those unwilling or unable to stop should have low priority for, or be excluded from, certain elective procedures.
 
But Professor Leonard Glantz from Boston University School of Public Health believes it is unacceptable discrimination. "It is astounding that doctors would question whether they should treat smokers," he says.
 
Last Updated on Monday, 27 August 2007 15:22
 
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