Meds

February 8, 2010

Combo Treatment Beneficial in Biliary-Tract Cancer Study

Filed under: Uncategorized — admin @ 9:21 am

A new combination drug therapy shows promise in treating patients with advanced biliary-tract cancers, researchers say.

The study from the Massachusetts General Hospital Cancer Center in Boston found that survival and tumor response in patients treated with bevacizumab (Avastin), an angiogenesis inhibitor that has helped slow the growth of other cancers, in addition to the chemotherapy regimen of gemcitabine and oxaliplatin — a combined treatment called GEMOX-B — was comparable to findings in previous studies in which patients were treated with gemcitabine and oxaliplatin alone.

In the new phase 2 trial, 35 biliary-tract cancer patients were given all three drugs intravenously (bevacizumab at 10 milligrams per kilogram, followed by gemcitabine at 1,000 milligrams per square meter, and oxaliplatin at 85 milligrams per square meter) on days 1 and 15, every 28 days. Whole-body PET scans were used to assess patients at the start of the study and at the end of the second cycle of treatment.

The researchers found that the overall tumor response rate was 40 percent (14 patients with confirmed partial responses) and stable disease was noted in another 10 patients (29 percent). The overall survival was found to be 12.7 months, with a median progression-free survival of seven months. However, progression-free survival at six months was below the targeted rate at 63 percent, they noted.

The most common negative side effects of GEMOX-B therapy were fatigue, an abnormally low number of white blood cells, peripheral neuropathy, high blood pressure and gastrointestinal problems, but the therapy was generally well-tolerated, the study authors pointed out.

The findings add to increasing evidence “supporting the combination of molecularly targeted agents with chemotherapy to further improve treatment outcomes in patients with biliary-tract cancers,” the researchers wrote.

January 31, 2010

How long does hepatitis B vaccine protection last?

Filed under: Health — Tags: , — admin @ 2:53 am

The hepatitis B vaccine – given to protect against infection by a virus that can cause severe liver damage and cancer – may protect for more than two decades, according to a new study.

In 1981, Dr. Brian J. McMahon, from the Alaska Native Medical Center, Anchorage, and his colleagues gave more than 1500 Alaska Native adults and children over age 6 months three doses of hepatitis B vaccine. Before the hepatitis B vaccine was licensed for U.S. use in 1981, as many as one in 12 Alaskan Natives were infected.

In 2003, the team checked with almost 500 of those given the shots and had a response to them at the time to see who was still showing evidence of an immune system response. Blood tests found that more than half – 60 percent — were still considered immune to the virus.

To test whether the other 40 percent were immune, they were given a booster dose of the vaccine, to simulate infection. Most of those people – more than 80 percent – showed a response.

Overall, the researchers estimate that more than 90 percent of the original group was protected. There were no long-term hepatitis B infections in the group, which also suggests a high level of protection, they note in a report in the Journal of Infectious Diseases.

They conclude, “in light of the strong evidence we present here, hepatitis B vaccine booster doses are not currently indicated.”

January 25, 2010

Nicotine Patch Plus Lozenge Best for Quitting Smoking

Filed under: Health — Tags: , — admin @ 2:51 am

The first head-to-head comparison of different quit-smoking products finds that a nicotine patch combined with a nicotine lozenge had the most success.

More than other methods, including antidepressants, this combination best mimics the actual highs and lows of smoking to help smokers kick their habit, experts said.

“The study shows that, yes, one therapy came out on top, the patch and the lozenge [together],” said Dr. Jonathan H. Whiteson, co-director of the Joan and Joel Smilow Cardiopulmonary Rehabilitation and Prevention Center at NYU Langone Medical Center in New York City.

“The reasoning behind it is that the patch supplies a steady supply of nicotine replacement and the lozenges give a boost of nicotine which you can use when you have an extra craving. It gives people control,” said Whiteson, who was not involved in the research.

“If you combine these different types of nicotine replacement you’re going to get the best bang for your buck,” added Megan E. Piper, lead author of the new study and an assistant professor at the Center for Tobacco Research and Intervention at the University of Wisconsin, Madison. “But also remember that in this study people got a lot of counseling. It was that combination that resulted in a 40 percent quit rate [at six months out].”

In fact, coupling the patch with the lozenge was the only intervention that performed better than a placebo, reported the study, which appears in the November issue of the Archives of General Psychiatry.

The study adds insight to a field that’s long suffered from too little research. “As each medication comes out, it is tested against a placebo,” but not against other methods, Piper explained. “There just hasn’t been the funding or the availability of a program to do something like that.”

This research was funded by the U.S. National Institutes of Health. Medication was provided free by drug maker GlaxoSmithKline. Several of the study authors reported financial ties to different pharmaceutical companies.

For this study, 1,504 adults who had smoked at least half a pack a day for the past six months and wanted to quit were randomly assigned to a placebo or one of five different quit-smoking interventions: nicotine lozenge, nicotine patch, bupropion (Wellbutrin, an antidepressant), nicotine patch plus nicotine lozenge, and bupropion plus nicotine lozenge. All groups received six individual counseling sessions with a case manager.

The nicotine patch, which has been available for more than two decades, is currently the most widely used pharmacotherapy to help people quit smoking.

However, only the combination of the nicotine patch and the lozenge performed significantly better than placebo six months after the person smoked their last cigarette, the team found.

People taking the patch-lozenge combination were also more likely to have sworn off cigarettes after one week and were more likely to have attained one full day without smoking, the researchers said.

The 40 percent (at six months) success rate reported here will decline as time goes on, Whiteson noted. He added, however, that in the smoking cessation arena, “even the 30 percent range is very good.”

Another expert said the study raised some key concerns. “The question is, how many of them had to continue on the lozenge in order to stay off cigarettes? I always tell people not to do the lozenge alone because it mimics the very thing that smoking does, which gives you a spike. Then, when you reach a trough, you pick up a lozenge — or cigarette,” said Dr. Len Horovitz, a pulmonary specialist with Lenox Hill Hospital in New York City. “Once they stopped everything, could they do without the spikes and troughs [of the lozenge], which mimics physiologically everything the cigarette is doing? Smoking is a two-pronged problem. There’s nicotine dependence and a behavioral aspect to it.”

Dr. Elliot Wineburg, assistant clinical professor of psychiatry at Mount Sinai School of Medicine in New York City, felt the study suffered from some limitations, namely lack of individual attention to individual smokers’ habits.

“The authors said that they gave the patients lozenges according to the company’s [instructions],” he said. But this doesn’t take into account how much people smoke or how strong their cigarettes are. “They don’t even look into the amount of nicotine a person takes.”

January 18, 2010

NIH-Supported Trial to Study Testosterone Therapy in Older Men

Filed under: Uncategorized — Tags: — admin @ 2:47 am

Low serum testosterone may contribute to a number of problems affecting older men, including decreased ability to walk, loss of muscle mass and strength, decreased vitality, decreased sexual function, impaired cognition, cardiovascular disease and anemia. While testosterone normally decreases with age, in some men, low levels of testosterone may contribute to these debilitating conditions. A new national clinical trial will test whether these conditions can be favorably affected by testosterone therapy.

The National Institute on Aging (NIA), part of the National Institutes of Health, today announced the start of a large-scale clinical trial to evaluate the effect of testosterone therapy on older men. Led by the University of Pennsylvania School of Medicine and conducted at 12 sites across the nation, the Testosterone Trial will involve 800 men age 65 and older with low testosterone levels.

“We know that, as men get older, a significant proportion are unable to carry out activities of daily living and experience decreased physical and cognitive function and decreased independence,” said NIA Director Richard J. Hodes, M.D. “We do not know the extent to which low levels of testosterone may contribute to these conditions.”

A 2004 report by the Institute of Medicine, “Testosterone and Aging: Clinical Research Directions,” noted several important unanswered questions about the effects of testosterone therapy. The NIA is aiming to answer these questions by testing the effectiveness of testosterone therapy in older men with low testosterone levels and one of the following conditions: impaired walking, low vitality, sexual or cognitive dysfunction. A key consideration is the use of testosterone as a therapy for certain conditions, rather than as a preventive measure.

The NIA is the primary source of support for this trial. Additional funding is being provided by the National Heart, Lung, and Blood Institute (NHLBI); the National Institute on Neurological Disorders and Stroke (NINDS); the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and Solvay Pharmaceuticals, which is also supplying the study drug.

The Testosterone Trial will include five separate studies. At each of the 12 sites, men 65 and older with low serum testosterone and at least one of the following conditions — anemia, decreased physical function, low vitality, impaired cognition or reduced sexual function — will be randomly assigned to participate in a treatment group or a control group. Treatment groups will be given a testosterone gel that is applied to the torso, abdomen, or upper arms; control groups will receive a placebo gel. Serum testosterone will be measured monthly for the first three months and quarterly thereafter up to one year. Participants will be tested on a wide range of measures to evaluate physical function, vitality, cognition, cardiovascular disease, and sexual function.

“This study is important because testosterone products have been marketed for many years as treatments for a variety of conditions,” said Evan C. Hadley, M.D., director of NIA’s Division of Geriatrics and Clinical Gerontology, which is the primary funder of the trial. “”We hope this trial will establish whether testosterone therapy results in clear benefits for older men.”

The University of Pennsylvania School of Medicine is the lead institution for the trial and will serve as coordinating center for the study sites. Peter J. Snyder, M.D., professor of medicine in the Division of Endocrinology, Diabetes and Metabolism at Penn, is the principal investigator and will oversee trial activities. “This is an unprecedented opportunity for older men to learn more about themselves and at the same time help find out if testosterone will improve some of the afflictions of old age,” said Dr. Snyder.

Recruitment of study participants will begin in November of 2009. Men age 65 and older who are interested in participating should call the site closest to them. Men living within a 50-mile radius of the study centers, listed below, are especially encouraged to participate.

Participating institutions and their phone numbers include:
University of California, Los Angeles; 310-222-5297
University of California, San Diego; 877-219-6610
Boston University; 617-414-2968
University of Pittsburgh; 800-872-3653
Albert Einstein College of Medicine, Bronx, N.Y.; 718-405-8271
Baylor College of Medicine, Houston, Texas; 713-798-8343
University of Minnesota, Minneapolis; 612-625-4449
Yale University, New Haven, Conn.; 203-737-5672
University of Alabama at Birmingham; 205-934-2294
VA Puget Sound Health Care System and University of Washington School of Medicine, Seattle; 206-768-5408
Northwestern University, Evanston, Ill.; 877-300-3065
University of Florida, Gainesville; 866-386-7730, 352-273-5919

January 11, 2010

Radiation After Surgery Lowers Chances of Melanoma Recurrence

Filed under: Health — Tags: — admin @ 3:36 am

Patients whose melanoma has spread to one or more lymph nodes face a decreased risk of the deadly skin cancer returning if they have radiation treatment following the removal of the nodes, a new Australian study shows.

In a paper to be presented Monday at the American Society for Radiation Oncology annual meeting in Chicago, lead researcher Dr. Bryan Burmeister, a radiation oncologist at Princess Alexandra Hospital in Brisbane, reported the hopeful findings from the five-year study.

“Results of this trial now confirm the place of radiation therapy in the management of patients who have high-risk features following surgery for melanoma involving the lymph nodes,” Burmeister said in a news release. “In some institutions, radiation treatment is routine protocol, while in others, the protocol has been either for patients to just be observed or receive some type of adjuvant chemotherapy or immunotherapy. I encourage patients with melanoma to talk to their doctors about whether radiation should be added to their treatment plan.”

External beam radiation involves the use of a beam (or beams) of radiation directed through the skin to the cancer and the tissue in its immediate vicinity. This targeted radiation destroys the tumor while helping to mop up nearby cancer cells that might remain after surgery. The therapy is usually painless and performed on an outpatient basis.

Burmeister’s study followed 217 patients with melanoma, a deadly skin cancer, between 2002 and 2007. All had at least one lymph node removed after doctors determined that the cancer had spread into the nodes. The surgery, called a lymphadenectomy, is standard treatment for metastasized melanoma.

About half the patients underwent postoperative radiation treatment, while the other half followed-up with their physicians to see if their cancer had returned. By the end of the study, 19 percent of the radiation patients had experienced a local nodal relapse of their melanoma, compared with 31 percent of patients who did not undergo postoperative radiation treatment. Overall survival was not affected, however.

Melanoma starts in the melanocytes, which are cells found in the top layer of skin that are responsible for producing the pigment melanin. Melanoma can arise anywhere there is pigmented tissue, including the eyes, sinuses, anus and a woman’s vulva.

According to the Memorial Sloan-Kettering Cancer Center in New York City, skin melanomas often look asymmetrical, have a ragged or blurred border and are dark in color. But rare forms of melanoma contain no pigment and can appear as pink nodules on the skin.

The disease is less common than other skin cancers, but if untreated, melanoma can spread and be difficult to cure. In the United States, more than 67,000 people annually are diagnosed with melanoma, and more than 8,000 will die, according to the American Cancer Society.

Given the severity of the disease, U.S. melanoma experts said they found the study intriguing.

“This is the first randomized study that tested the question whether postoperative radiation therapy offered any advantage in terms of loco-regional control to patients with loco-regionally advanced melanoma,” said Dr. Nancy Lee, a radiation oncologist at Memorial Sloan-Kettering. “The authors are to be congratulated for finally completing an important study in our field. This is particularly important as [local] recurrence can be devastating and often is difficult to salvage with additional therapy.”

Dr. David Fisher, of Boston’s Massachusetts General Hospital, praised the study but said he wanted more data on overall survival.

“This is an important study, since decisive data on the value of adjuvant radiation therapy have been lacking,” said Fisher, director of the melanoma program at Mass General. “It will be important to learn additional details, but the study appears to provide important supportive evidence for adjuvant radiation therapy.”

December 27, 2009

Social Isolation Adversely Affects Breast Cancer

Filed under: Uncategorized — admin @ 10:16 am

A socially isolated, stressful environment can speed up the growth of breast cancer, researchers studying the effects of stress in animal models reported Tuesday.

Social isolation can actually change the expression of genes important in the growth of mammary gland tumors, according to Dr. Suzanne D. Conzen, an associate professor of medicine at the University of Chicago and the study’s lead author.

“As far as we know, this is the first assessment of gene expression in mammary glands, looking at the molecular basis for differences in tumor development under the setting of social stress,” Conzen said at a news conference Tuesday.

The findings, published in the October issue of Cancer Prevention Research, follow other studies, some in humans, that showed stress can adversely impact cancer. One study, for instance, found that stressful marriages are bad for breast cancer recovery.

Conzen and her colleagues randomly assigned mice that were genetically susceptible to breast cancer to live either in isolation or in group housing.

“We separated the mice at a very young age, just a few days after they had been weaned from their mothers’ milk,” Conzen said. “Mice are social animals. In the wild, they live in groups of three or four. They have dramatic responses to isolation.”

“What we found was the isolated mice developed larger and more breast cancers than the group-housed mice,” she added.

Three and a half weeks into the isolation, Conzen’s team measured gene expression in the animals’ mammary glands, the equivalent of the human breast. “We found very reproducible changes in gene expression [in the isolated mice]. We found genes that were turned on and turned off that had to do with metabolism,” she said. These pathways are known to contribute to increased growth of breast cancer, she added.

The isolated mice also had a higher corticosterone stress hormone response than did the group-housed mice.

The changes in the expression levels of metabolic pathway genes occurred in the isolated mice even before the tumor size differences were able to be measured, Conzen said.

So what are the practical applications of the research?

The findings may suggest molecular biomarkers, or targets, for preventive intervention in breast cancer, she said.

“Many questions remain,” Conzen added. “One of the things we did note is that the isolated animals were much more vigilant, less exploratory. They released more of a stress hormone when we added another stressor to the situation [besides the isolation].”

Thea Tisty, a pathology professor at the University of California, San Francisco, who is familiar with the findings, called the research “a very exciting beginning.”

The implication is that perceived or actual stress from outside can affect which genes get turned on or off. If the research findings bear out, it could lead to a way to catch tumors in their formation before they become tumors and suppress them, she said.

Another expert speaking at the briefing cautioned that the findings, while exciting, are only preliminary and based only on animal studies.

“This is an area that has a long way to go in terms of understanding how these factors play out in humans,” said Caryn Lerman, the Mary W. Calkins Professor of Psychiatry at the Abramson Cancer Center at the University of Pennsylvania in Philadelphia.

December 20, 2009

Scientists Discover How Chemo Can Make Women Infertile

Filed under: Women — admin @ 9:15 am

Italian researchers say they have identified the mechanism by which chemotherapy can rob a woman of her ability to have children.

Intriguingly, the scientists also found that another anti-cancer drug might counteract the negative effects of the chemotherapy drug cisplatin.

The finding, demonstrated in mice and reported in the Sept. 27 online edition of Nature Medicine, raises the hope that there might be a way to protect a woman’s fertility while she undergoes treatment for cancer but, the authors stressed, this is still a long way off.

“The extension of these findings to patients and the design of clinical trials is likely to require the development of targeted drug delivery strategies to avoid any potential interference with anti-cancer systemic therapy,” explained study author Stefania Gonfloni, of the department of biology at the University of Rome.

“I think it’s a great idea. They found a pathway that can be used as a marker to detect which drug would produce cell death as a result of chemotherapy, and they found a repair effect of a drug,” said Dr. George Attia, an associate professor of reproductive endocrinology and infertility at the University of Miami Miller School of Medicine. “[But] it’s very basic science research. It’s still early.”

Because chemotherapy affects the egg cells of the ovary, women often end up with ovarian failure and infertility as a result of cancer treatment.

“We frequently deal with women of childbearing age, and there’s a lot of concern about fertility preservation although as women get older, the chemo induces menopause,” said Dr. Igor Astsaturov, an assistant professor of medical oncology at Fox Chase Cancer Center in Philadelphia. “The standard approach now is egg collection [storing eggs for later use].”

Chemotherapy can also cause genetic defects in offspring. In particular, cisplatin, which was studied in this trial, causes specific types of chromosomal damage.

Cisplatin is primarily usually used to treat ovarian cancer, Attia noted.

In this study, Gonfloni and her colleagues showed that cisplatin promotes the death of oocytes, or female germ cells, by way of the c-Abl enzyme, a protein that, when mutated, can also cause chronic myeloid leukemia (CML).

But targeting the enzyme with imatinib (Gleevec), a drug used to treat CML, protected the oocytes from the ill effects of cisplatin.

“These results raise the possibility of protecting ovarian function during cancer treatments, thereby preserving the fertility in female cancer survivors,” Gonfloni added.

But how to use one drug without compromising the other?

“First, we have to show that imatinib can be used to prevent chemotherapy-induced ovarian toxicity without interfering with anti-cancer treatments,” Gonfloni said. “In other words, we have to prove that tumor-bearing laboratory animals can be cured with a combined cisplatin and imatinib treatment, while at the same time preserving fertility,” she explained.

“Then, for any clinical implications, it will be very important to prove the same protective effect of a specific dosage of imatinib on human oocytes cultured and challenged with chemotherapeutic drugs in vitro,” she added.

And preserving fertility is not always the right thing, Astsaturov said.

“Chemotherapy induces menopause in some hormone-dependent cancers. It has a beneficial effect because it’s withdrawing the stimulants for the cancer cells. Menopause is contributing to the cure,” he said. “It’s still debated whether we should preserve menstrual function at all costs.”

December 13, 2009

Task Force Finds Insufficient Evidence for Screening for Newborn Jaundice To Prevent a More Serious Chronic Condition

Filed under: Health — admin @ 9:14 am

According to a new recommendation from the U.S. Preventive Services Task Force, there is insufficient evidence to assess the balance of benefits and harms of screening infants for hyperbilirubinemia to prevent chronic bilirubin encephalopathy. Hyperbilirubinemia is a condition marked by a high level of bilirubin in the blood, which is often apparent as yellow-colored skin and eyes (jaundice). This recommendation and the accompanying summary of evidence will appear in the October issue of Pediatrics.

About 60 percent of all infants have jaundice, and it generally clears up without any medical treatment. Some infants are more likely to have severe jaundice and higher bilirubin levels than others. In some infants, hyperbilirubinemia may lead to chronic bilirubin encephalopathy, a rare but devastating neurological condition. The brain damage associated with chronic bilirubin encephalopathy, or kernicterus, may result in cerebral palsy, auditory processing problems, gaze and vision abnormalities, and cognitive problems. The number of children who develop chronic bilirubin encephalopathy is unknown and difficult to determine.

“There is inadequate evidence that screening all full-term and near-term infants for elevated bilirubin leads to improved health outcomes,” said Task Force Chair Ned Calonge, M.D., who is also chief medical officer for the Colorado Department of Public Health and Environment. “More research is necessary to understand how often chronic bilirubin encephalopathy occurs, its risk factors, and whether screening is associated with a reduction in chronic bilirubin encephalopathy.”

There is evidence that screening using risk factor assessment or bilirubin level measurement can identify infants at risk of developing hyperbilirubinemia, but there is no known screening test that will reliably identify all infants at risk of developing chronic bilirubin encephalopathy. Not all infants with chronic bilirubin encephalopathy have a history of hyperbilirubinemia, and not all infants who have extremely high levels of bilirubin develop chronic bilirubin encephalopathy.

In assessing the potential benefits and harms of screening infants for hyperbilirubinemia, the Task Force looked for evidence that screening reduced the number of new cases of chronic bilirubin encephalopathy. No studies have directly addressed whether screening, either risk-factor assessment or bilirubin testing, reduced the number of new cases of chronic bilirubin encephalopathy. The current evidence on screening has evaluated the effectiveness of screening to identify infants for treatment intended to reduce high levels of bilirubin.

The Task Force found that the evidence is currently insufficient regarding whether treating infants with high levels of bilirubin results in fewer children developing chronic bilirubin encephalopathy. There is a critical gap in the evidence regarding the relationship between screening infants without symptoms of hyperbilirubinemia and the desired outcome of reducing cases of chronic bilirubin encephalopathy. When the Task Force finds insufficient evidence to make a recommendation, it does not mean a clinician shouldn’t provide a service but that the evidence is lacking, and if a service is offered, patients should understand the uncertainty about the balance of benefits and harms. The Task Force recognizes that clinical or policy decisions involve more consideration than their recommendations alone, and clinicians and policy makers should understand the evidence but individualize decision-making to the specific patient or situation.

Efforts have been made by clinicians to eliminate this rare disorder by applying measures to screen for and aggressively manage high bilirubin levels. Universal screening for jaundice is widespread in the United States, and clinicians and parents should continue to work together to decide whether to screen in the face of insufficient evidence. Clinicians must remain aware that screening and resulting treatment of hyperbilirubinemia have potential harms such as weight loss, gastrointestinal problems, and disruption of the mother-infant bonding.

The Task Force is the leading independent panel of experts in prevention and primary care. The Task Force, which is supported by the Agency for Healthcare Research and Quality (AHRQ), conducts rigorous, impartial assessments of the scientific evidence for the effectiveness of a broad range of clinical preventive services, including screening, counseling and preventive medications. Its recommendations are considered the gold standard for clinical preventive services.

The recommendations and materials for clinicians are available on the AHRQ Web site at http://www.ahrq.gov/clinic/uspstf/uspshyperb.htm.

December 7, 2009

When Pounds Go, Sleep Apnea May Improve

Filed under: Health — admin @ 3:13 pm

People with sleep apnea who are also obese may triple the chances of eliminating their sleep problems by losing weight, a new study suggests.

Losing about 10 percent of their body weight was enough to bring on total or near-total remission, said Gary Foster, head of the Center for Obesity Research and Education at Temple University in Philadelphia, and lead author of the study.

“It’s been clear that obesity increases the risk of sleep apnea but less clear that if obese people or people with type 2 diabetes lost weight, it would result in significant improvements in their sleep apnea — and it did,” said Foster.

People who are overweight or obese are much more likely to have obstructive sleep apnea, a condition in which a person’s breathing stops or becomes very shallow, sometimes several hundred times a night and sometimes for as long as a minute, according to the American Sleep Apnea Association.

“The soft palate in the back of mouth falls down and blocks the airway,” said Dr. Mitchell Roslin, chief of bariatric surgery at Lenox Hill Hospital in New York City. “When you get to people with serious levels of obesity, it’s virtually impossible to find those without [this type of] sleep apnea.”

The condition can lead to cardiovascular problems, including stroke, and can raise the risk for dying prematurely.

“It really has tremendous detrimental effects on the cardiovascular system,” Roslin said.

The study involved 264 obese men and women who also had type 2 diabetes and obstructive sleep apnea. They were randomly assigned to an intensive behavioral program intended to encourage weight loss or to a less intensive set of group sessions that mainly addressed the issue of diabetes management.

After a year, those in the intensive program had lost an average of about 24 pounds, compared with slightly more than a one-pound average weight loss for the others.

Those who lost the weight also saw a substantial reduction in the number of sleep apnea episodes they experienced, with more than three times as many people in the intensive group experiencing complete remission (13.6 percent versus 3.5 percent).

“The greatest benefit was seen in men and those with severe apnea,” Foster said.

Any amount of weight loss brought on an improvement, but those who lost about 10 percent of their original body weight saw the greatest effect. “Any weight loss is good,” Foster said.

Most experts recommend 10 percent as the weight loss needed to improve sleep apnea.

However, the study also found that people whose weight remained stable experienced a worsening in their sleep apnea. Just why that occurred remains unclear.

“This is one of the first and certainly the largest study ever conducted so we’re at the point in the field, unfortunately, where we’re just describing the effect,” Foster said.

The study, published Sept. 28 in the Archives of Internal Medicine, does seem to confirm what common sense and experience have shown.

“We’ve seen that when patients gain five to 10 pounds, their sleep apnea is much worse. If they lose five to 10 pounds, the sleep apnea is much better,” said Dr. Hormoz Ashtyani, director of pulmonary critical care and sleep medicine at Hackensack University Medical Center in New Jersey. “It’s usually not a resolution, but it’s a significant improvement.”

November 30, 2009

Herb Shows Potential for Rheumatoid Arthritis

Filed under: Uncategorized — admin @ 9:30 am

An ancient Chinese herbal remedy called “thunder god vine” helps reduce inflammation in people with rheumatoid arthritis, a new study shows.

The remedy is an extract of the medicinal plant Tripterygium wilfordii Hook F (TwHF) — known in China as “lei gong teng” — and has been used for centuries to treat a variety of inflammatory diseases.

The study compared reduction in joint swelling among people with rheumatoid arthritis who took either the herb or an anti-inflammatory drug.

Rheumatoid arthritis causes chronic and painful inflammation of the joints that, over time, can lead to joint damage and loss of function.

The 121 participants in the study all had at least six swollen joints. One group took 60 milligrams of TwHF root extract three times a day, and the others 1 gram of sulfasalazine (Azulfidine), a prescription anti-inflammatory drug, twice a day.

After 24 weeks, about 65 percent of those taking the herbal extract showed at least a 20 percent improvement in their joints, based on American College of Rheumatology criteria, a standard measure of the effectiveness of arthritis treatments. About 33 percent of those taking sulfasalazine improved to that degree.

A report on the findings is published Aug. 18 in Annals of Internal Medicine.

“This study is a reminder of the potential importance of supplements and herbs in the management of arthritis,” said Dr. John H. Klippel, president and chief executive of the Arthritis Foundation.

Even so, the study involved a relatively small number of people, Klippel noted. Clinical trials for pharmaceuticals typically involve many more participants studied over several years, he said.

“The findings are encouraging, but [TwHF] is not likely to be recommended by rheumatologists based on the findings of this one study alone,” Klippel said.

And, though sulfasalazine used to be very popular as an arthritis treatment, the drug is not used that often today in the United States, according to Dr. Stephen Lindsey, head of rheumatology at Ochsner Health Systems in Baton Rouge, La.

Methotrexate (Rheumatrex, Trexall) is the drug most often used today, he said.

“I would be optimistic that an herbal medicine would play some role in improving rheumatoid arthritis,” Lindsey said. But he added that he “would be a little bit wary since the medicine they compared it to is a fairly mild, anti-rheumatoid agent and not the standard drug used in the U.S.”

Other alternative remedies, he said, have proven helpful for arthritis, including fish oil, though some of them have not held up to more rigorous studies.

Participants in the new study were allowed to continue taking oral prednisone or nonsteroidal anti-inflammatory drugs, but anyone who was taking disease-modifying anti-rheumatic drugs (such as methotrexate), which slow the progression of the disease, had to stop taking them about a month before the study began.

Researchers did not see a statistically significant difference in joint damage on X-rays, Klippel said. But he said that probably was because six months wasn’t long enough for noticeable changes.

The study also had a high dropout rate, with 62 percent of those taking TwHF and 41 percent of the others continuing to the end. According to the study, 17 people taking sulfasalzine and 8 taking TwHF dropped out because of adverse effects — most often gastrointestinal symptoms, including nausea and diarrhea.

Lindsey noted that people should always remember to tell their doctor if they are taking an herbal supplement.

“Just because something is herbal doesn’t mean it’s going to be cheap or safe,” he said.

Older Posts »

Powered by WordPress