Friday, July 20, 2012

Health Highlights: July 20, 2012

HealthDay – 1 hr 22 mins ago Here are some of the latest health and medical news developments, compiled by the editors of HealthDay:

Software Simulation of Entire Organism a First

U.S. scientists have created the first software simulation of an entire organism.

The researchers and outside experts said the model of a single-cell bacterium that lives in the human genital and respiratory tracts is a major advance toward developing computerized laboratories that could conduct complete experiments without the need for traditional instruments, The New York Times reported.

The team from Stanford University and the J. Craig Venter Institute said their simulation of the complete life cycle of the pathogen Mycoplasma genitalium was a "first draft," but added that it was the first time that an entire organism was modeled in such detail. The model included all 525 of the organism's genes.

"Where I think our work is different is that we explicitly include all of the genes and every known gene function," team's leader Markus W. Covert, an assistant professor of bioengineering at Stanford, wrote in an e-mail to The Times. "There's no one else out there who has been able to include more than a handful of functions or more than, say, one-third of the genes."

The research was published Friday in the journal Cell.

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European Approval of Gene Therapy Would be a Milestone

A gene therapy called Glybera should be approved to treat a rare genetic disease called lipoprotein lipase deficiency, the European Medicine Agency has recommended.

If the European Commission follows the agency's advice, Glybera would become the first gene therapy to be approved in the Western world, The New York Times reported.

The approval could give a much-needed boost to the struggling field of gene therapy after more than two decades of failed expectations. Glybera was developed by the Dutch company uniQuire.

Lipoprotein lipase deficiency affects only several hundred people in the European Union and a similar number in North America. The disease is caused by a genetic mutation that prevents people from producing an enzyme required to break down certain fat-carrying particles that circulate in the bloodstream after meals, The Times reported.

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'Polypill' Could Slash Heart Attack, Stroke Rates: Study

A "polypill" that combines a cholesterol-lowering statin drug and three blood pressure drugs reduced patients' "bad" LDL cholesterol by 39 percent and their blood pressure by 12 percent, according to a new study.

The U.K. researchers said the pill could prevent a huge number of heart attacks and strokes each year and called for regulators to make the pill available to patients "as a matter of urgency," BBC New reported.

"The health implications of our results are large," Dr. David Wald of Queen Mary, University of London, said."If people took the polypill from age 50, an estimated 28 percent would benefit by avoiding or delaying a heart attack or stroke during their lifetime."

If half of the people over age 50 in the U.K. took the polypill daily, there would be 94,000 fewer heart attacks and strokes each year, according to the researchers.

The results from the study of 84 people over the age of 50 were published in the journal PLoS One.

While the pill's potential is interesting, medicines are not a substitute for healthy lifestyle habits such as exercise, good nutrition and not smoking, Natasha Stewart, senior cardiac nurse at the British Heart Foundation, told BBC News.

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Vitamin D May Delay Deterioration of Smokers' Lungs: Study

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Don't Be Afraid to Talk to Your Kids About Colorado Killings

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U.S. FDA OKs Onyx's Kyprolis for multiple myeloma

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Whoppers of 2012, Early Edition

unfortunately. The contest so far has been nasty all right, and disregard for the truth has been brutish on both sides, in our judgment. But alas, it won’t be over until Nov. 6.

So many false and misleading claims have already surfaced that, once again, we are moving up the clock on our annual wrap-up of the campaign season’s worst political whoppers, as we did four years ago. We’d like to think there would be no need for a

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FDA approves Novartis drug Afinitor for breast cancer

Reuters – 6 mins ago (Reuters) - The U.S. Food and Drug Administration said on Friday it has approved Novartis AG's drug Afinitor to treat women with a certain type of breast cancer.

The drug is the first in a class known as mTOR inhibitors to be approved for post-menopausal women with advanced hormone-receptor positive, HER2-negative breast cancer.

Afinitor, also known as everolimus, is designed to be given in combination with another drug, Aromasin, to treat women whose cancer has recurred or progressed after treatment with two other therapies.

A late-stage trial showed that patients who received Afinitor plus Aromasin had a 4.6 month improvement in the median time to disease progression or death over those receiving Aromasin plus a placebo, the FDA said.

Afinitor is already approved to treat patients with certain other types of cancer.

(Reporting By Toni Clarke; editing by Carol Bishopric)



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FDA approves Onyx blood cancer drug Kyprolis

The Food and Drug Administration said Friday it approved a new blood cancer drug from Onyx Pharmaceuticals Inc. for patients with advanced disease who have not responded to at least two other drugs.

The injectable drug Kyprolis treats multiple myeloma, a form of cancer that causes tumors to grow in the bone marrow, preventing the production of normal blood cells. Patients with the disease have low red blood cell counts and are more likely to experience infections and excessive bleeding.

The FDA approved the drug for patients who have already tried at least two other drugs, including Velcade and various drugs that boost the immune system.

Shares of South San Francisco, Calif.-based Onyx Pharmaceuticals rose $6.34, or 9.3 percent, to $74.74.

The company studied the drug in 266 patients with advanced multiple myeloma who had already been treated with Velcade and thalidomide. About 23 percent of patients experienced a full or partial disappearance of their tumors, with the typical effect lasting about 7.8 months.

Thirty percent of patients experienced side effects from the drug, including fatigue, fever, shortness of breath and diarrhea.

About 21,700 people will be diagnosed with multiple myeloma this year and 10,710 will die from the disease, according to the American Cancer Society.

The drug was approved under the FDA's accelerated approval program, which allows the agency to clear drugs based on promising preliminary data. Drug companies have to submit follow-up studies showing that the drug performed as expected.



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European regulator: Gene therapy treatment OK

The European Medicines Agency is recommending the first-ever approval of a gene therapy treatment in the EU, in a significant move for a type of treatment that has so far failed to deliver on its promise to cure diseases.

In a statement on Friday, the EMA said Glybera, made by Dutch company uniQure, should be approved across Europe for the treatment of an extremely rare disorder that leaves people unable to digest fat. The treatment consists of a gene that makes a protein to break down fat.

Gene therapy is an experimental technique that tries to cure diseases by replacing genes that don't work. It has never been approved in the U.S. and most trials over the past two decades have failed. China was the first country to approve a gene therapy treatment in 2003 for cancer.

Scientists have struggled to find ways to deliver the genes safely, often by using a harmless virus. There are also concerns that inserting a gene at the wrong spot could cause cancer or that the body's immune system might attack the new gene and the virus used to deliver it.

The EMA previously rejected Glybera three times but it was reconsidered at the request of the European Commission. The agency recommended approval under tough restrictions and will require the company to set up a registry to closely track patients. Previous trials of the treatment only tested it in 27 patients.

"It is only meant for patients with the greatest need," said Monika Benstetter, an EMA spokeswoman, explaining the gene therapy is intended for people with no other treatment options. She said only a handful of gene therapy treatments had been considered before

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How to protect kids from whooping cough outbreaks

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Bounty mutiny descendants have low rates of myopia: study

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In Washington, free HIV-AIDS testing while you wait

"Faced with the highest HIV-AIDS rates in the United States, community health activists in the nation's capital have come up with a novel way for people to save their own lives while killing time. (AFP Photo/Jim Watson)" title

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Nobel laureate, discoverer of HIV, sees 'hope' for cure

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