Saturday, May 28, 2011

Mystified by Menopause? A Major Life Transition

Mystified by Menopause?
A Major Life Transition


Menopause—it’s a transition that looms large in the minds of many women as they approach age 50. It’s sometimes called the “change of life.” Menopause marks the end of menstrual periods and fertility.

It can be a challenging time, physically and mentally. Familiar concerns include hot flashes, trouble sleeping and mood changes, but symptoms can vary greatly for each woman. Many women don’t need treatment. For those bothered by symptoms, choosing the best treatment can be confusing. Different therapies have benefits and risks that need to be weighed carefully.

Knowledge about menopause has grown significantly over the last 2 decades. Large NIH-funded studies of women before, during and after menopause have given new insights into how menopause proceeds. New treatment options are being developed, and long-standing therapies are under more thorough evaluation.

“This ongoing research is necessary because there are 40 million menopausal or postmenopausal women right now in this country, and a growing number are entering menopause each year,” says Dr. Howard N. Hodis, a cardiovascular and menopause researcher at the University of Southern California.

Menopause is defined as the final menstrual period. On average, women have their last period around age 51, but it can also occur in their 40s or late 50s. Symptoms usually begin to appear several years before menopause. This time of change—called the menopausal transition, or perimenopause—extends to 1 year after your final period.

During perimenopause, levels of estrogen and progesterone—2 female hormones made in the ovaries—go up and down irregularly. This leads to changes in menstrual periods. The fluctuation in hormone levels that begins during perimenopause can affect many different parts of the body.

Dr. Gail Greendale of the University of California, Los Angeles, is one of the lead researchers in an NIH-funded study that’s looking at the many shifts women face during the transition. The study’s been following more than 3,000 women for over 15 years, from before menopause to well after. The researchers are monitoring bone health, the heart and blood vessels, the brain, cancer and a variety of symptoms.

“Part of our mission is to let women know what’s coming—the range of common experiences—because it can help them understand what’s going on during the transition,” says Greendale.

Among the study’s many findings, the researchers discovered that thinking can become temporarily muddled during perimenopause. “Our study found that women were not learning information as efficiently as they had before. There was a subtle decline in cognitive performance during the transition,” says Greendale. But the learning deficits went away once women hit postmenopause. “So there’s light at the end of the tunnel,” she says.

Another part of the study looked at mood and found that depressive symptoms—such as feelings of hopelessness, loss of appetite and a persistent sad mood—increase during the transition and continue into postmenopause. During that same period, hot flashes and night sweats also tend to increase.

“Hot flashes can be severe and highly disruptive. We used to think that they lasted for 2 or 3 years, but our studies have shown that for some women they can last a lot longer—up to 7 or 10 years,” says Dr. Sherry Sherman, who oversees the menopause research programs funded by NIH’s National Institute on Aging.

For some women, hot flashes and other symptoms can become so troubling that they interfere with daily activities. If this happens, check with your doctor. There are many ways to seek relief. Lifestyle changes, such as exercise or reducing stress, might help. Some women turn to medications—especially menopausal hormone therapy—to reduce symptoms. The therapy may include different hormone combinations and is available in a variety of forms and doses. Some studies, though, have raised questions about the safety of hormone therapy.

Back in the 1990s, hormones were recommended for most women for the rest of lives. Hormones not only relieved symptoms; they were also thought to help prevent heart disease and other conditions. Things changed in 2002, when a large NIH-funded study called the Women’s Health Initiative concluded that the overall risks of hormone therapy outweighed the benefits. The therapy—a particular type of estrogen plus progestin—led to fewer bone fractures and less risk for colon and rectum cancer. But it also raised the risk for breast cancer, heart attack, stroke and blood clots in the legs and lungs. In 2004, the study found a lower risk of bone fractures in women using only estrogen, but an increased risk of stroke.

Further analysis suggested that some health risks may depend on when a woman begins menopausal hormone therapy. “Multiple lines of evidence suggest that if we put women on hormones at a time that is early or close to menopause, there tends to be a benefit to heart health and a reduction in mortality (death rate),” Hodis says. He’s heading an NIH-funded study to explore the idea that vascular health might be improved in women close to menopause. Results are expected by 2013.

Today, estrogen remains the most effective medicine approved by the U.S. Food and Drug Administration for treating menopausal symptoms such as hot flashes and night sweats. Because of safety concerns, some experts recommend that physicians prescribe the lowest effective dose for the shortest period necessary.

Animal Diseases and Your Health Also called: Zoonoses

 Animal Diseases and Your Health

Also called: Zoonoses




Animal diseases that people can catch are called zoonoses. About 75 percent of the new diseases affecting humans in the past decade can be traced to animals or animal products. You can get a disease directly from an animal, or indirectly, through the environment.

Farm animals can carry diseases. If you touch them or things they have touched, like fencing or buckets, wash your hands thoroughly. Adults should make sure children who visit farms or petting zoos wash up as well.

Pets can also make you sick. Reptiles pose a particular risk. Turtles, snakes and iguanas can transmit Salmonella bacteria to their owners. You can get rabies from an infected dog or toxoplasmosis from handling kitty litter of an infected cat. The chance that your dog or cat will make you sick is small. You can reduce the risk by practicing good personal hygiene, keeping pet areas clean and keeping your pets' shots up-to-date.

What to do in a Medical Emergency Diabetic Emergencies

What to do in a Medical Emergency
Diabetic Emergencies


It is estimated that more than 20 million people in the United States have diabetes, with an estimated six million people being unaware they have it. The best way to prevent diabetic emergencies is to effectively manage the disease through making health food choices, exercise and frequently checking blood glucose levels.

Diabetics may experience life-threatening emergencies from too much or too little insulin in their bodies. Too much insulin can cause a low sugar level (hypoglycemia), which can lead to insulin shock. Not enough insulin can cause a high level of sugar (hyperglycemia), which can cause a diabetic coma.

Symptoms of insulin shock include:
Weakness, drowsiness
Rapid pulse
Fast breathing
Pale, sweaty skin
Headache, trembling
Odorless breath
Numbness in hands or feet
Hunger

Symptoms of diabetic coma include:
Weak and rapid pulse
Nausea
Deep, sighing breaths
Unsteady gait
Confusion
Flushed, warm, dry skin
Odor of nail polish or sweet apple
Drowsiness, gradual loss of consciousness

First aid for both conditions is the same:
If the person is unconscious or unresponsive, call 911 or your local emergency number immediately.
If an unconscious person exhibits life-threatening conditions, place the person horizontally on a flat surface, check breathing, pulse and circulation, and administer CPR while waiting for professional medical assistance
If the person is conscious, alert and can assess the situation, assist him or her with getting sugar or necessary prescription medication.
If the person appears confused or disoriented, give him or her something to eat or drink and seek immediate medical assistance.

Researchers pool data to search for genetic risks in heart disease

Researchers pool data to search for genetic risks in heart disease
American Heart Association Rapid Access Journal Report

Study highlights:
An international consortium analyzing pooled data from all published whole-genome studies of heart attack and coronary artery disease (CAD) has found multiple genetic mutations, including one that increases heart attack risk by 29 percent.
The collective gene data could provide 10 times more subjects and controls than the largest CAD study to date.

DALLAS, Oct. 5, 2010 — In an unprecedented international project, researchers have found multiple genetic mutations that play a role in heart attack or coronary artery disease (CAD) risk.

The Coronary ARtery DIsease Genome-wide Replication And Meta-Analysis (CARDIoGRAM) — published in Circulation: Cardiovascular Genetics, an American Heart Association journal — consists of data from every published whole-genome study on genetic mutations in heart attack or CAD risk. Researchers are also pooling data from several unpublished genome-wide association studies to see if any new mutations can be uncovered.

The consortium will analyze the complete genetic profiles of more than 22,000 people of European descent with CAD or a heart attack history, and 60,000 healthy people — 10 times more than in the next largest whole-genome study to date.

Investigators have examined an average 2.2 million single nucleotide polymorphisms (SNPs) in each of the whole-genome studies included in the review. SNPs, or “snips,” are genetic variants at specific locations on individual chromosomes. Sometimes these variants manifest themselves as a disease or susceptibility to a disease. Modern technology allows hundreds of thousands of SNPs to be scanned in a person.

“Only a small proportion of the inheritability of CAD has been explained,” said Heribert Schunkert, M.D., a professor of medicine at the University of Lübeck in Germany and a spokesman for CARDIoGRAM. “We have to accept that almost all persons of European ancestry carry multiple small genetic defects that mediate some coronary artery disease risk. The main aim of the consortium is to identify new disease mechanisms to improve risk prevention.”

The task is challenging because of the complex nature of atherosclerosis, with multiple genetic factors contributing in small ways to the disease, he said.

Genome-wide association studies provide an unprecedented sensitivity to detect genetic variants affecting disease risk, and researchers rely on the studies’ sample size. However, in a typical genome-wide association study with about 1,000 patients and controls, the power to detect a SNP with a significant effect is low.

“Collectively, our consortium increases the power of these findings 10-fold,” Schunkert said. “By pooling all of the published and unpublished data, we hope to make discoveries that might have been overlooked. Given that up to 2.5 million comparisons are carried out, in parallel, for each whole-genome scan, distinguishing between true and false associations has been difficult.”

The data will be maintained in a central database, and each SNP that appears related to heart disease will be subjected to replication studies to confirm its significance. Numerous SNPs and the proteins they express increase risk of CAD or heart attack. But it’s unknown whether they’re acting alone or with other genetic variables, Schunkert said.

Spotlight on Research 2011 Scientists Correct Genetic Defect in Blistering Skin Disease in Mouse Model

Spotlight on Research 2011

Scientists Correct Genetic Defect in Blistering Skin Disease in Mouse Model


A new study supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) shows it may be possible to grow healthy new skin for people with a rare disfiguring skin disease called recessive dystrophic epidermolysis bullosa (RDEB). Caused by a defect in the gene coding for a protein called type VII collagen, RDEB is characterized by painful blistering of the skin and mucous membranes that leaves people prone to infections, scarring and skin cancer. Currently, the only treatment for the disease is targeted at relieving pain and improving quality of life.

While some scientists have tried using grafts of the patients’ own skin to replace damaged areas of skin in people with RDEB, these grafts have failed because they contain the same genetic defect that causes the disease. The new study, however, used skin grown from cells of patients with RDEB that were modified to express a normal type VII collagen gene.

After taking a small biopsy of skin cells called keratinocytes from people with RDEB, the scientists used a viral vector – a harmless virus engineered to deliver normal genes into cells – to correct the type VII collagen defect in the cells. The modified keratinocytes were then grown into sheets in the lab and transplanted onto laboratory mice.

Twelve months later, when the study was terminated, the skin on the mice was still attached and healthy, and the cells of the transplanted tissue continued to express the normal type VII collagen gene, says Alfred T. Lane, M.D., professor of dermatology and pediatrics at Stanford University School of Medicine, who led the study.

Now that the researchers know they can successfully transplant the modified skin on mice, the next step is to try growing larger sheets of skin and graft them back onto the people affected by RDEB, Dr. Lane says. Such skin-growing technology is already in place, and studies in adults could begin within a few months.

The greatest uncertainty with the procedure is whether the modified grafts will transplant successfully on skin that has been affected with lesions for 20 years or more, as is often the case in adults with the disease, says Dr. Lane. His goal, eventually, is to test the modified grafts on children in hopes of treating the disease before it has caused extensive or long-term damage.

Brain Cancer Also called: Glioma, Meningioma

Brain Cancer

Also called: Glioma, Meningioma




There are two main types of brain cancer. Primary brain cancer starts in the brain. Metastatic brain cancer starts somewhere else in the body and moves to the brain. Brain tumors can be benign, with no cancer cells, or malignant, with cancer cells that grow quickly.

Brain tumors can cause many symptoms.                                       Some of the most common are
Headaches, usually worse in the morning
Nausea and vomiting
Changes in your ability to talk, hear or see
Problems with balance or walking
Problems with thinking or memory
Muscle jerking or twitching
Numbness or tingling in arms or legs

No one knows the exact causes of brain tumors. Doctors can seldom explain why one person develops a brain tumor and another does not.

NIH: National Cancer Institute
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