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Saturday, September 10, 2011



Chondroitin sulfate improves hand function, relieves morning stiffness caused by osteoarthritis


New research shows that chondroitin sulfate significantly decreased pain and improved hand function in patients with osteoarthritis (OA) of the hand compared with those in the placebo group. Results of the clinical trial available today in Arthritis & Rheumatism, a journal published by Wiley-Blackwell on behalf of the American College of Rheumatology (ACR), also report that chondroitin sulfate improves grip strength and relieves morning stiffness.



The ACR estimates that OA—the most common form of —affects more than 27 million adults in the U.S., causing joint pain and stiffness. Approximately 10% of the world population, 60 years and older, have symptomatic osteoarthritis according to the Global Burden of Disease 2000 report from the World Health Organization (WHO). Prior studies have found that 20% to 30% of adults have OA of the hand, with the prevalence rising to more than 50% after 60 years of age.
"Although hand OA is highly prevalent among adults and can significantly impact the quality of life for suffers, therapeutic options are still limited," said Cem Gabay, M.D., with University Hospitals of Geneva in Switzerland and lead investigation of the Finger   Treatment Study (FACTS). "There are few trials examining therapeutic approaches specific to hand OA and much of the available evidence has been extrapolated from studies investigating other forms of OA."
The single-center, placebo-controlled FACTS trial included 162 patients with radiographic hand OA who met inclusion criteria—spontaneous hand pain on the visual analogue scale (VAS) of 40 mm (scale 0-100) or more and Functional Index for Hand OA (FIHOA) level of 6 (scale 0-30). Participants received either 800 mg of chondroitin sulfate (80 patients) or placebo (82 patients) once daily for 6 months.
Results showed that patients in the chondroitin sulfate group had significant decrease in global hand pain compared with the , reflecting an 8.7 decrease on the VAS. Hand function also improved significantly for those taking chondroitin sulfate, decreasing more than 2 points on the FIHOA. Researchers also reported significantly improved hand function and reduction in morning stiffness for participants taking chondroitin sulfate versus placebo.
"Our findings show chondroitin sulfate is a safe and effective treatment for patients with hand OA," concluded Dr. Gabay. "Alternative therapies, such as nonsteroidal anti-inflammatory drugs (NSAIDs), provide similar pain reducing effects, but with considerably more long-term toxicities." Chondroitin sulfate is a naturally occurring molecule and a main component of joint cartilage. The chondroitin sulfate agent used in this study (Chondrosulf®) is licensed as a drug in Europe and not as a nutripharmaceutical; in the U.S. chondroitin  is sold as a supplement and often paired with glucosamine.
More information: Symptomatic Effect of Chondroitin Sulfate 4&6 in Hand Osteoarthritis: The Finger osteoArthritis Chondroitin Treatment Study (FACTS): A Randomized Double-Blind Placebo Controlled Clinical Trial." Cem Gabay, Carole Medinger-Sadowski, Danielle Gascon, Frank Kolo, Axel Finckh. Arthritis & Rheumatism; Published Online: September 6, 2011. DOI:10.1002/art.30574
Provided by Wiley (news : web)

Friday, September 9, 2011

Killer Hospital Bug




A fungus that has become a major threat to hospital patients may have a hidden weakness, according to research published on Monday that highlights the bug's ability to bind to human tissue.



But in , C. albans is a peril for sick people or individuals whose immune system has been compromised by cancer, HIV or organ transplant.
It accounts for one in every four hospital-acquired infections, often through plastic surfaces implanted in the body such as catheters, prosthetic joints or heart devices.
In the severest cases, nearly half of those infected die.
Adding to the problem is that C. albicans is a stealthy foe, able to change the structure of its cell wall to outsmart .
The latest research, published in a PNAS journal on Monday, highlights a promising target: the mechanism that the yeast uses to latch on to  and colonise them, thanks to a tiny part of a protein call Als adhesin.
"Als adhesin proteins give the yeast an ability to thrive throughout the human body, which is what makes it such a dangerous infections," said Ernesto Cota, a medical biologist at Imperial College London.
Cota's team used hi-tech scanners to probe the structure of the elusive protein.
The next step is to test experimental compounds on lab-dish samples of the fungus to see whether this will block the binding action.
The study appears in  (PNAS).
(c) 2011 AFP

Thursday, September 8, 2011



Research indicates certain probiotics may influence brain functioning


(Medical Xpress) -- It was just last year that a certain company selling a special probiotic enhanced yogurt was ordered by a U.S. court to stop suggesting in its advertisements that it's product had health benefits that went beyond the norm. Now, new evidence by Javier Bravo and colleagues at University College Cork, suggests the company may have been on to something. In their paper, published in the Proceedings of the National Academy of Science, the team describes how mice given the prbiotic Lactobacillus rhamnosus, showed signs of being less anxious and depressed and even had lowered levels of stress hormones.

Wednesday, September 7, 2011

Gut Reaction to Arthritis Drugs



Study finds more gut reaction to arthritis drugs
Patients often take drugs to lower stomach acid and reduce the chances they will develop ulcers from taking their anti-inflammatory drugs for conditions such as arthritis, but the combination may be causing major problems for their small intestines, McMaster researchers have found.

A team from the Farncombe Family Digestive Health Research Institute has found those stomach acid-reducing drugs, known as , may actually be aggravating damage in the  caused by the non-steroidal anti-inflammatory drugs, also known as NSAIDs.

In a study published in the medical journal Gastroenterology, principal investigator John Wallace says the extent of the hard-to-detect damage caused to the small intestine has only recently been discovered through use of small video cameras swallowed like pills.
"Suppressing acid secretion is effective for protecting the stomach from damage caused by NSAIDs, but these drugs appear to be shifting the damage from the stomach to the small intestine, where the ulcers may be more dangerous and more difficult to treat," said Wallace. He is director of the Farncombe institute and professor of medicine of the Michael G. DeGroote School of Medicine at McMaster.
He added that the use of  is being investigated as a potential cure for the small intestine damage.
Provided by McMaster University 

Tuesday, September 6, 2011

Studies About Medications Frequently Designed In Misleading or Confusing Resuts


UCLA-Harvard study highlights 3 types of confusing outcome measures
Studies about medications published in the most influential medical journals are frequently designed in a way that yields misleading or confusing results, new research suggests.
Investigators from the medical schools at UCLA and Harvard analyzed all the randomized medication trials published in the six highest-impact general medicine journals between June 1, 2008, and Sept. 30, 2010, to determine the prevalence of three types of outcome measures that make data interpretation difficult.
In addition, they reviewed each study's abstract to determine the percentage that reported results using relative rather than absolute numbers, which can also be a misleading.
The findings are published online in the Journal of General Internal Medicine.
The six journals examined by the investigators— the New England Journal of Medicine, the Journal of the American Medical Association, The Lancet, the Annals of Internal Medicine, the British Medical Journal and the Archives of Internal Medicine — included studies that used the following types of outcome measures, which have received increasing criticism from scientific experts:
Surrogate outcomes (37 percent of studies), which refer to intermediate markers, such as a heart medication's ability to lower blood pressure, but which may not be a good indicator of the medication's impact on more important clinical outcomes, like heart attacks.
Composite outcomes (34 percent), which consist of multiple individual outcomes of unequal importance lumped together — such as hospitalizations and mortality — making it difficult to understand the effects on each outcome individually.
Disease-specific mortality (27 percent), which measures deaths from a specific cause rather than from any cause; this may be a misleading measure because, even if a given treatment reduces one type of death, it could increase the risk of dying from another cause, to an equal or greater extent.
"Patients and doctors care less about whether a medication lowers blood pressure than they do about whether it prevents heart attacks and strokes or decreases the risk of premature death," said the study's lead author, Dr. Michael Hochman, a fellow in the Robert Wood Johnson Foundation Clinical Scholars Program at the David Geffen School of Medicine at UCLA's division of general internal medicine and health services research, and at the U.S. Department of Veterans Affairs' Los Angeles Medical Center.
"Knowing the effects of a medication on blood pressure does not always tell you what the effect will be on the things that are really important, like heart attacks or strokes," Hochman said. "Similarly, patients don't care if a medication prevents deaths from heart disease if it leads to an equivalent increase in deaths from cancer."
Dr. Danny McCormick, the study's senior author and a physician at the Cambridge Health Alliance and Harvard Medical School, added: "Patients also want to know, in as much detail as possible, what the effects of a treatment are, and this can be difficult when multiple outcomes of unequal importance are lumped together."
The authors also found that trials that used surrogate outcomes and disease-specific mortality were more likely to be exclusively commercially funded — for instance, by a pharmaceutical company.
While 45 percent of exclusively commercially funded trials used surrogate endpoints, only 29 percent of trials receiving non-commercial funding did. And while 39 percent of exclusively commercially funded trials used disease-specific mortality, only 16 percent of trials receiving non-commercial funding did.
The researchers suggest that commercial sponsors of research may promote the use of outcomes that are most likely to indicate favorable results for their products, Hochman said.
"For example, it may be easier to show that a commercial product has a beneficial effect on a surrogate marker like blood pressure than on a hard outcome like heart attacks," he said. "In fact, studies in our analysis using surrogate outcomes were more likely to report positive results than those using hard outcomes like heart attacks."
The new study also shows that 44 percent of study abstracts reported study results exclusively in relative — rather than absolute — numbers, which can be misleading.
"The way in which study results are presented is critical," McCormick said. "It's one thing to say a medication lowers your risk of heart attacks from two-in-a-million to one-in-a-million, and something completely different to say a medication lowers your risk of heart attacks by 50 percent. Both ways of presenting the data are technically correct, but the second way, using relative numbers, could be misleading."
Still, the authors acknowledge that the use of surrogate and composite outcomes and disease-specific mortality is appropriate in some cases. For example, these outcomes may be preferable in early-phase studies in which researchers hope to quickly determine whether a new treatment has the potential to help patients.
To remedy the problems identified by their analysis, Hochman and McCormick believe that studies should report results in absolute numbers, either instead of or in addition to relative numbers, and that committees overseeing research studies should closely scrutinize study outcomes to ensure that lower-quality outcomes, like surrogate makers, are only used in appropriate circumstances.
"Finally, medical journals should ensure that authors clearly indicate the limitations of lower-quality endpoints when they are used — something that does not always occur," McCormick said.
###
The authors did not receive any internal or external funding for this research.
The Robert Wood Johnson Foundation focuses on the pressing health and health care issues facing our country. As the nation's largest philanthropy devoted exclusively to improving the health and health care of all Americans, the Foundation works with a diverse group of organizations and individuals to identify solutions and achieve comprehensive, meaningful and timely change. For more than 35 years, the Foundation has brought experience, commitment, and a rigorous, balanced approach to the problems that affect the health and health care of those it serves. When it comes to helping Americans lead healthier lives and get the care they need, the Foundation expects to make a difference in your lifetime.
General Internal Medicine and Health Services Research is a division within the Department of Medicine at the David Geffen School of Medicine at UCLA. It provides a unique interactiveenvironment for collaborative efforts between health services researchers and clinical experts with experience in evidence-based work. The division's 100-plus clinicians and researchers are engaged in a wide variety of projects that examine issues related to access to care, quality of care, health measurement, physician education, clinical ethics and doctor/patient communication. The division's researchers have close working relationships with economists, statisticians, social scientists and other specialists throughout UCLA and frequently collaborate with their counterparts at the RAND Corp and Charles Drew University.
Cambridge Health Alliance is an innovative, award-winning health system that provides high quality care in Cambridge, Somerville, and Boston's metro-north communities. It includes three hospital campuses, a network of primary care and specialty practices, the Cambridge Public Health Dept., and the Network Health plan. CHA is a Harvard Medical School teaching affiliate and is also affiliated with Harvard School of Public Health, Harvard School of Dental Medicine, and Tufts University School of Medicine.
For more news, visit UCLA Newsroom and UCLA News|Week and follow us on Twitter.
Contact: Enrique Rivero
erivero@mednet.ucla.edu
310-794-2273
University of California - Los Angeles Health Sciences
Posted: August 2011

Monday, September 5, 2011

A Little Known Disease Cause Venus Williams to Withdraw From U.S. Open


THURSDAY, Sept. 1 -- Venus Williams' surprising withdrawal from the U.S. Open on Wednesday has shifted the spotlight from the tennis star's daunting serve to her diagnosis with a little-known disease known asSjogren's syndrome.
Williams, 31, said the disease has diminished her energy level and caused joint pain, curtailing her ability to continue in the tournament.
More than 4 million Americans have the chronic autoimmune disease, which also causes dry mouth and dry eyes. Ninety percent of those with the disease are women.
Sjogren's syndrome "targets and destroys over time the exocrine glands responsible for tear production and saliva -- and is characterized by dryness of the mouth and eyes," said Dr. Michael Belmont, an associate professor of medicine in the division of rheumatology at NYU Langone Medical Center and medical director for Hospital for Joint Diseases. Less commonly, it can cause severe arthritis involving joint deformity and impaired function, he noted.
The publicity surrounding Williams' announcement is expected to increase awareness of the systemic disease, potentially leading to better diagnostic and treatment options.
"Sjogren's syndrome can occur as a primary disorder or secondary to other autoimmune diseases, principally rheumatoid arthritis or systemic lupus erythematosus [lupus]," Belmont said. Multiple organs, including the kidneys, lungs, gastrointestinal system, blood vessels and the central nervous system, can also be involved.
When Sjogren's progresses to a multi-organ disease, treatment becomes complex, said Dr. Victoria Shanmugam, a rheumatologist at Georgetown University Medical Center.
"Treatment for Sjogren's ranges from therapies to alleviate symptoms, such as topical therapies for dry eyes and dry mouth, to drugs that suppress the immune system, including hydroxychloroquinemethotrexate and steroids," said Shanmugam, who is not involved in Williams' care. "We also use medications that help fight fatigue and fibromyalgia symptoms."
Fibromyalgia is another chronic autoimmune disease.
Sjogren's, first identified in 1933, affects virtually every racial and ethnic group, according to the Sjogren's Syndrome Foundation. It is difficult to diagnose because symptoms mimic other diseases. It takes nearly seven years, on average, for a diagnosis.
How the disease will play out for Williams is unclear. Symptoms can remain mild, worsen or, occasionally, go into remission, Belmont said.
While the exact cause of Sjogren's syndrome is not known, Belmont said genetic factors appear to be involved. "An as-yet unidentified environmental factor likely plays a role, as observation finds that identical twins with the same DNA do not always share the illness," he said.
However, it is found more commonly in families that have members with other autoimmune illnesses, he said, noting this supports the genetic theory.
"Early diagnosis and proper treatment are important -- they may prevent serious complications and greatly improve a patient's quality of life," he said.
More information
To learn more about the disorder, visit the Sjogren's Syndrome Foundation.
Posted: September 2011

Sunday, September 4, 2011

Research Reveals Why Blacks More Prone to Kidney Failure


THURSDAY, Sept. 1 -- Black Americans are more likely than whites to have a condition in which the kidneys spill protein into the urine, which may help explain why blacks are four times more likely than whites to develop kidney failure, a new study suggests.
Emory University researchers analyzed data from about 28,00 people (40.5 percent blacks, 59.5 percent whites) in the United States and found that 133 of them developed kidney failure after an average follow-up of 3.6 years.
There were 96 cases of kidney failure among blacks and 37 cases among whites.
Kidney failure was more common among people who excreted large amounts of protein in their urine, and blacks were more likely than whites to have this problem.
The researchers suggested a number of reasons why blacks are more likely to excrete more protein in their urine, including: blood pressure and other heart-related issues; smoking, vitamin D levels, obesity, income, genetic differences and birth weight.
All these factors can impact kidney health.
Treating urinary protein excretion could reduce racial disparities in kidney failure rates and also slow the rate of progression to kidney failure among patients of all races, the researchers said.
The study appears in an upcoming issue of the Journal of the American Society of Nephrology.
More information
The American Urological Association has more about kidney failure.
Posted: September 2011