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How Weight Gain And Obesity In Men Reduce PSA Velocity And May Interfere With Prostate Cancer Detection
EHE International recently announced the findings of a study indicating that elevated PSA levels, often associated with prostate cancer, are potentially harder to detect in men who are obese or experiencing weight gain. Prostate specific antigens (PSAs) are proteins produced by the cells of the prostate gland and because elevated levels may be indicative of prostate cancer, PSAs are regularly measured in annual physicals. PSA velocity is a measure of how fast PSA levels are changing in a man through time, and a high PSA velocity is an important indicator of prostate cancer risk. The study describes how obesity and increases in Body Mass Index (BMI) make PSA velocity scores appear lower than they really are, thereby potentially obscuring clinically relevant changes in circulating PSA.
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Newsweek Magazine Reporters Win Second Annual Endocrine Society Award For Excellence In Science And Medical Journalism
Today, The Endocrine Society announced Newsweek Reporters Barbara Kantrowitz and Patrice Wingert recipients of the Society"s second annual Award for Excellence in Science and Medical Journalism. The co-authors of the winning article, "Uh, O!" (O for Oprah) were honored last night at the Society"s 91st Annual Meeting in Washington, DC.
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Evidence Challenges Effectiveness Of Embryo Screening For Older Women
There is growing evidence that a procedure for identifying chromosomal abnormalities in embryos prior to in vitro fertilization is ineffective at helping older women become pregnant, the Wall Street Journal reports. The procedure -- known as pre-implantation genetic screening, or PGS -- is performed in dozen of U.S. fertility clinics and sometimes marketed to older women as a way to increase the odds of a healthy live birth. PGS involves extracting a single cell from a six-cell embryo and inspecting it for chromosomal abnormalities known as aneuploidies; unaffected embryos can then be implanted through IVF. Women older than age 35 have a higher risk of aneuploidies, in which embryos have fewer or more than the usual number of 23 pairs of chromosomes. Aneuploidies can trigger early miscarriage or certain genetics conditions, such as Down syndrome. Most medical experts agree that embryo screening is capable of significantly reducing the risk of Down syndrome and other serious chromosome-related illnesses. However, evidence from several studies increasingly suggests that the procedure does not increase older women"s chances of healthy live births. The American Society for Reproductive Medicine released an initial opinion about PGS in 2007, saying that available evidence does not support the use of embryo screening to increase live birth rates in older women. Andrew La Barbera, scientific director of the society, said, "Since that time, there have been several more trials that have reached the same conclusion." Another shortcoming is that most clinics can only test for fewer than half of the 23 chromosomes, meaning that many defects can go undetected. However, medical experts say that the use of PGS has increased in the two years since ASRM issued its recommendations. According to the Journal, PGS can add more than $2,000 to the roughly $10,000 cost of one IVF cycle. Very few health insurers cover PGS, though some pay for IVF. Some experts contend that studies showing a lack of clinical benefit from PGS do not use more efficient biopsy techniques that can prevent damage to the embryo. Santiago Munne, scientific director for Reprogenetics, said that the treatment is "effective." In a 2007 study, Munne and colleagues used PGS to reduce the rate at which patients miscarried. However, the chances of a woman getting pregnant largely were unchanged, which the authors said could be attributed to the small number of study participants (Naik, Wall Street Journal, 6/1).
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Quality And Purity Of Popular Stevia Sweetener Strengthened By New Reference Standards

As the number of food and beverage products sweetened with stevia-based ingredients continues to grow in the United States and worldwide, the U.S. Pharmacopeial (USP) Convention announces that new reference standards for Rebaudioside A and Stevioside are now available. The reference standards for these two ingredients complement the soon to be released written testing standard for high-purity Rebaudioside A in the Food Chemicals Codex (FCC), a collection of documentary standards for food ingredients that allow manufacturers to demonstrate the quality, and thus related aspects of safety, of the products they provide to consumers. The reference standards for Rebaudioside A and Stevioside are authenticated pure chemicals against which both producers and purchasers can compare their ingredients to help ensure and substantiate the identity, quality, purity, strength and consistency of their food ingredient, protecting their products and brands from low-quality, potentially adulterated ingredients, thus helping to maintain food safety. The internationally recognized FCC and its associated reference standards are produced by USP, a nonprofit scientific organization that has set chemical standards for close to 200 years. These standards - for pharmaceuticals, excipients, dietary supplements and food ingredients - are used in more than 130 countries throughout the world. The new stevia standards demonstrate the commitment of USP to continue to support the food industry with quality monographs and reference standards. "These new reference standards, taken together with the written standards in the FCC, provide a powerful tool to help ensure the authenticity of the ingredients manufacturers are using in their new stevia-based product lines," said James Griffiths, Ph.D., vice president of food, dietary supplement and excipient standards for USP. "As these ingredients are produced all over the world in widely disparate facilities, their authenticity, quality and purity cannot be taken for granted. It is thus important for ingredient producers who want to safeguard their products to demonstrate the quality of their ingredients to their customers. USP is well poised and committed to providing useful tools for enabling interested parties to readily verify new stevia-based sweeteners and numerous other food ingredients." The new reference standards have been thoroughly tested and endorsed by USP"s Reference Standards Expert Committee, a group of independent volunteer experts, to ensure their suitability for use. The written FCC testing standard for high-purity Rebaudioside A is expected to be released August 31, 2009. Francine Pierson US Pharmacopeia


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