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	<title>US Tele-Medicine Blog &#187; biopsies</title>
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	<link>http://www.epatienthealthcare.com/blog</link>
	<description>A Global Leader in Telemedicine</description>
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		<title>7 Ingredients to Ban from Your Bathroom</title>
		<link>http://www.epatienthealthcare.com/blog/2012/01/17/7-ingredients-to-ban-from-your-bathroom/</link>
		<comments>http://www.epatienthealthcare.com/blog/2012/01/17/7-ingredients-to-ban-from-your-bathroom/#comments</comments>
		<pubDate>Tue, 17 Jan 2012 21:19:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Alternative Medicine]]></category>
		<category><![CDATA[Human Behavior]]></category>
		<category><![CDATA[Lifestyle Health]]></category>
		<category><![CDATA[Medical Studies]]></category>
		<category><![CDATA[7 ingredients]]></category>
		<category><![CDATA[alternative medicine]]></category>
		<category><![CDATA[BAN]]></category>
		<category><![CDATA[bathroom]]></category>
		<category><![CDATA[biopsies]]></category>
		<category><![CDATA[chipping]]></category>
		<category><![CDATA[consumer trust]]></category>
		<category><![CDATA[cosmetics]]></category>
		<category><![CDATA[daily products]]></category>
		<category><![CDATA[DEA]]></category>
		<category><![CDATA[diazolidinyl]]></category>
		<category><![CDATA[grooming]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[imidazolidinyl urea]]></category>
		<category><![CDATA[nanoparticles]]></category>
		<category><![CDATA[nitrosamines]]></category>
		<category><![CDATA[parabens]]></category>
		<category><![CDATA[perfume]]></category>
		<category><![CDATA[personal care]]></category>
		<category><![CDATA[phthalates]]></category>
		<category><![CDATA[plasticizers]]></category>
		<category><![CDATA[polish]]></category>
		<category><![CDATA[shampoo]]></category>
		<category><![CDATA[SLS]]></category>
		<category><![CDATA[sunscreen]]></category>
		<category><![CDATA[synthetic fragrances]]></category>
		<category><![CDATA[tea]]></category>
		<category><![CDATA[telemedicine]]></category>
		<category><![CDATA[US Tele-Medicine]]></category>

		<guid isPermaLink="false">http://www.epatienthealthcare.com/blog/?p=14751</guid>
		<description><![CDATA[The following ingredients usually appear in the products we use daily — shampoo, sunscreen and the like — and general scientific consensus concludes that they’re best avoided: Parabens are a synthetic preservative and antimicrobial agent commonly found in personal-care products with high water content: shampoo, conditioner, lotion, cleansers and body wash. They also turn up [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-14752" href="http://www.epatienthealthcare.com/blog/2012/01/17/7-ingredients-to-ban-from-your-bathroom/np/"><img class="alignleft size-full wp-image-14752" title="np" src="http://www.epatienthealthcare.com/blog/wp-content/np.jpg" alt="" width="201" height="251" /></a>The following ingredients usually appear in the products we use daily — shampoo, sunscreen and the like — and general scientific consensus concludes that <a rel="nofollow" href="http://www.care2.com/greenliving/beauty-beware.html" target="_blank">they’re best avoided</a>:</p>
<p><strong>Parabens</strong> are a synthetic preservative and antimicrobial agent commonly found in personal-care products with high water content: shampoo, conditioner, lotion, cleansers and body wash. They also turn up in solid products like deodorant. They appear as methyl-, ethyl-, butyl- or propylparaben. Studies have found that parabens mimic estrogen in the body and disrupt normal hormone function, and they have been found in breast-tumor biopsies.</p>
<p>Growing awareness about parabens has inspired a number of manufacturers to banish them in favor of safer preservatives, while some have simply accepted a shorter shelf life as the price of doing healthy business. You can often find personal-care products labeled “paraben free,” which will save you a little squinting in the product aisle. Signers of the Compact for Safe Cosmetics have committed to avoiding their use; you can find the list of these companies at <a rel="nofollow" href="http://www.safecosmetics.org/" target="_blank">www.safecosmetics.org</a>.<div class="toggle"></p>
<p><strong>Phthalates</strong> are plasticizers that stabilize scent in perfume and color in cosmetics; they also keep nail polish from chipping. You won’t find them listed on most labels, though they can be present in almost every conceivable personal-care item hidden in the ingredient “fragrance.” (Company formulas are legally protected as proprietary information.) Multiple studies have linked phthalates to depression of normal thyroid function and birth defects, mostly affecting the genital development of young boys and sperm counts in adult men.</p>
<p>Two kinds of phthalates commonly found in cosmetics were banned in the EU with its recent cosmetic safety directive, forcing international companies to reformulate their products for the European market. A number of nail polish manufacturers have removed the “toxic trio” — dibutyl phthalate, toluene (a solvent and neurotoxin) and formaldehyde — from their nail polish formulas. Still, it’s smart to view nail polish and products with caution, especially if you’re pregnant. Water-based polishes are the most benign option.</p>
<p><strong>Nanoparticles</strong> consist of ultra-tiny particles of common ingredients and are used in everything from sports clothing to car tires. They’re often found in sunscreen, to make it transparent instead of white, and in anti-aging products to help them penetrate deeper skin layers; they can be listed on labels as “microfine particles.” These “penetration enhancers” are worrisome in the company of phthalates and parabens. And, because they’re a new and quite powerful technology, environmental-health experts are also concerned about their impact on the environment once they’re washed into rivers and lakes. While the particles alone have not been implicated in health issues, many experts recommend waiting to use them until more studies have been completed.</p>
<p><strong>Sodium Lauryl/Laureth Sulfate (SLS)</strong> is a synthetic detergent and foaming agent connected to skin and eye irritation. It’s also linked to the byproduct 1-4 dioxane, a suspected carcinogenic contaminant produced by the ethoxylation process, used to make some ingredients less harsh. (Sodium lauryl sulfate is converted to sodium laureth sulfate, for example.) Ethoxylation is one reason why so many “gentler” products — those with a natural slant or made especially for kids — have turned up surprisingly high levels of toxins.</p>
<p>According to researchers at the Organic Consumers Association, who conducted tests for 1-4 dioxane on hundreds of products from 16 major brands in 2008, only 23 products were found to be free of 1-4 dioxane contamination. Many companies have quit using ethoxylated ingredients like sodium lauryl sulfate to avoid 1-4 dioxane contamination as well as allergic reactions, and the standard for the Whole Foods Premium Body Care Seal doesn’t allow it. Look for “-eth” at the end of other ingredient names to detect this process.</p>
<p><strong>Synthetic fragrances</strong> can contain as many as 200 ingredients that manufacturers are not required to disclose. A common allergen, “fragrance” on an ingredient label is a reliable indicator that the product contains phthalates, unless it’s clearly indicated that the fragrance contains no synthetics. Higher-potency fragrances are the likeliest suspects for high concentrations of phthalates. Sophie Uliano, natural-beauty expert and author of Gorgeously Green: 8 Simple Steps to an Earth-Friendly Life (HarperCollins, 2008), points out that “fragrance-free” or “unscented” products aren’t always a dependable alternative, since manufacturers sometimes use masking fragrances in place of identifiable scents. Look for products that explicitly say “no synthetic fragrances” or “natural essential oil fragrance only,” or try to buy from companies that have signed the Compact for Safe Cosmetics.</p>
<p><strong>Diethanolamine (DEA) and Triethanolamine (TEA)</strong> are emulsifiers and foaming agents typically found in shampoo and body wash. They can produce allergic reaction as well as, ironically enough, hair and skin dryness. They belong to the category of “nitrosamines” that Uliano cautions against, which studies have shown can be carcinogenic.</p>
<p><strong>Diazolidinyl and Imidazolidinyl Urea</strong> are frequently used synthetic preservatives that can cause contact dermatitis and are suspected formaldehyde releasers. They appear in sunscreen, lotion, shampoo — the same places you’ll find parabens.</p>
<p>The number of personal-care ingredients with unknown or suspected health effects is quite long; you can find a comprehensive list at <a rel="nofollow" href="http://www.cosmeticsdatabase.com/" target="_blank">www.cosmeticsdatabase.com</a>.</p>
<p><strong>Source for Story:</strong></p>
<p><a rel="nofollow" href="http://www.care2.com/greenliving/7-ingredients-to-ban-from-your-bathroom.html#ixzz1jkd3mUyw">http://www.care2.com/greenliving/7-ingredients-to-ban-from-your-bathroom.html#ixzz1jkd3mUyw</a></p>
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		</item>
		<item>
		<title>Researchers Find Disease-Causing Fat Cells</title>
		<link>http://www.epatienthealthcare.com/blog/2011/09/02/researchers-find-disease-causing-fat-cells/</link>
		<comments>http://www.epatienthealthcare.com/blog/2011/09/02/researchers-find-disease-causing-fat-cells/#comments</comments>
		<pubDate>Fri, 02 Sep 2011 19:12:13 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Medical Studies]]></category>
		<category><![CDATA[Weight Management]]></category>
		<category><![CDATA[BIOLOGICAL INDICATORS]]></category>
		<category><![CDATA[biopsies]]></category>
		<category><![CDATA[blood]]></category>
		<category><![CDATA[cardiovascular disease]]></category>
		<category><![CDATA[chronic disease]]></category>
		<category><![CDATA[diabetes]]></category>
		<category><![CDATA[discovery]]></category>
		<category><![CDATA[disease]]></category>
		<category><![CDATA[endocrinology]]></category>
		<category><![CDATA[EPCs]]></category>
		<category><![CDATA[fat cells]]></category>
		<category><![CDATA[fat tissue]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[heart disease]]></category>
		<category><![CDATA[macrophages]]></category>
		<category><![CDATA[metabolic syndrome]]></category>
		<category><![CDATA[metabolism]]></category>
		<category><![CDATA[obese]]></category>
		<category><![CDATA[researchers]]></category>
		<category><![CDATA[telemedicine]]></category>
		<category><![CDATA[toxic]]></category>
		<category><![CDATA[US Tele-Medicine]]></category>

		<guid isPermaLink="false">http://www.epatienthealthcare.com/blog/?p=11509</guid>
		<description><![CDATA[UC Davis Health System researchers have discovered biological indicators that help explain why some obese people develop chronic diseases such as diabetes and heart disease, and others do not. The researchers took a novel approach of looking specifically at the body fat of people with metabolic syndrome &#8212; a condition characterized by increased blood pressure, [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-11510" href="http://www.epatienthealthcare.com/blog/2011/09/02/researchers-find-disease-causing-fat-cells/obese-2/"><img class="alignleft size-full wp-image-11510" title="obese" src="http://www.epatienthealthcare.com/blog/wp-content/obese1.jpg" alt="" width="269" height="188" /></a>UC Davis Health System researchers have discovered biological indicators that help explain why some obese people develop chronic diseases such as diabetes and heart disease, and others do not. <br /> The researchers took a novel approach of looking specifically at the body fat of people with metabolic syndrome &#8212; a condition characterized by increased blood pressure, high-fasting blood-sugar levels, excess abdominal fat and abnormal cholesterol levels. They found the fat cells released biomarkers associated with insulin resistance and chronic inflammation, conditions often leading to diabetes and cardiovascular disease. </p>
<p> &#8220;Our study shows that not all obesity is the same and some body fat may actually be toxic,&#8221;<div class="toggle"> said Ishwarlal Jialal, UC Davis professor of endocrinology, diabetes and metabolism and senior author of the article, &#8220;Adipose Tissue Dysregulation in Patients with Metabolic Syndrome,&#8221; published online today in the Journal of Clinical Endocrinology &amp; Metabolism. &#8220;We have shown that the dysfunction in the fat of people with metabolic syndrome is more than can be explained by obesity. It tells us that metabolic syndrome is a high-risk condition for people who are obese.&#8221; </p>
<p> While previous studies using circulating blood have found some of these biomarkers in people with metabolic syndrome, the current study is the first to pinpoint fat as a contributing source of these markers. The study is also unique in that it involved patients newly diagnosed with metabolic syndrome who had not yet developed diabetes or cardiovascular disease. Researchers compared fat from study subjects to fat from people who were also obese, but did not have metabolic syndrome. </p>
<p> &#8220;This drives home the point that clearly metabolic syndrome is high-risk for obesity and needs to be treated seriously,&#8221; said Jialal, who directs the UC Davis Laboratory for Atherosclerosis and Metabolic Research. </p>
<p> The Centers for Disease Control and Prevention estimates that 35 percent of American adults have metabolic syndrome, and its prevalence is increasing even in children and young adults globally. It doubles a person&#8217;s chances of developing cardiovascular disease &#8212; which can lead to heart attack or stroke &#8212; and is at least five times the risk for developing diabetes. </p>
<p> &#8220;This is the plague of our time,&#8221; said Jialal, who is also the editor-in-chief of the peer-reviewed journal Metabolic Syndrome and Related Disorders. </p>
<p> In the current study, biopsies were performed to remove subcutaneous adipose tissue, which accounts for about 80 percent of body fat, from the buttocks of 70 patients: 39 newly diagnosed with metabolic syndrome and 26 who were obese. Researchers also took standard measurements, such as fasting glucose and blood pressure, waist circumference and body mass index (BMI). Glucose measurements were used to estimate insulin resistance, and both waist size and BMI were used in the statistical analysis to match test subjects with their control counterparts. </p>
<p> Jialal and his collaborators then measured 11 biomarkers for diabetes and cardiovascular disease, as well as counting the number of macrophages in the fat tissue. These macrophages form crown-like structures around fat cells that have outgrown their blood supply and died. The presence of macrophages &#8212; immune system cells that engulf and destroy cellular waste &#8212; indicates the kind of inflammatory response implicated in cardiovascular disease.</p>
<p>Last year, Jialal published a study on these same 65 patients showing that they have both dysfunctional and fewer endothelial progenitor cells (EPCs) than control subjects. These cells eventually form the lining of blood vessels and are used as a measure of cardiovascular health. As in the current study, this abnormality cannot be explained simply by obesity. Jialal&#8217;s team now is looking at differences in monocytes between the two study groups. The new data suggests intrinsic defects in the critical adipose tissue cells and EPCs that are relevant to increased risk for diabetes and cardiovascular disease. </p>
<p> While metabolic syndrome can be reversed through diet and exercise resulting in weight loss, other kinds of treatment may be needed, Jialal said. <br /> &#8220;I have done this for 34 years. It is hard to get people to stick to therapeutic lifestyle changes,&#8221; he said, adding that researchers need to address the dysfunction of fat cells, using existing or novel drug therapies to block the production of damaging biomarkers. </p>
<p> &#8220;Once people have cardiovascular disease or diabetes, it&#8217;s too late and far more expensive given the complications that ensue. Metabolic syndrome is the antecedent. This is where we need to intervene,&#8221; said Jialal.</p>
<p><strong>Source for Story:</strong></p>
<p>http://www.jpost.com/Health/Article.aspx?id=236350</p>
</div>]]></content:encoded>
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		<title>Today hybrid Versions of Grains Contain significantly more Gluten than Traditional Varieties</title>
		<link>http://www.epatienthealthcare.com/blog/2011/06/27/today-hybrid-versions-of-grains-contain-significantly-more-gluten-than-traditional-varieties/</link>
		<comments>http://www.epatienthealthcare.com/blog/2011/06/27/today-hybrid-versions-of-grains-contain-significantly-more-gluten-than-traditional-varieties/#comments</comments>
		<pubDate>Mon, 27 Jun 2011 21:22:35 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Alternative Medicine]]></category>
		<category><![CDATA[Human Behavior]]></category>
		<category><![CDATA[Lifestyle Health]]></category>
		<category><![CDATA[biopsies]]></category>
		<category><![CDATA[blood]]></category>
		<category><![CDATA[celiac]]></category>
		<category><![CDATA[diagnostic tools]]></category>
		<category><![CDATA[diet]]></category>
		<category><![CDATA[digest]]></category>
		<category><![CDATA[genetics]]></category>
		<category><![CDATA[gliadin]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[gluten]]></category>
		<category><![CDATA[gluten intolerance]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[healthy food]]></category>
		<category><![CDATA[Hybrid grains]]></category>
		<category><![CDATA[immune system]]></category>
		<category><![CDATA[intestine]]></category>
		<category><![CDATA[lifestyle health]]></category>
		<category><![CDATA[saliva]]></category>
		<category><![CDATA[snacks]]></category>
		<category><![CDATA[spelt]]></category>
		<category><![CDATA[telemedicine]]></category>
		<category><![CDATA[traditional varieties]]></category>
		<category><![CDATA[US Tele-Medicine]]></category>

		<guid isPermaLink="false">http://www.epatienthealthcare.com/blog/?p=9513</guid>
		<description><![CDATA[Over the past decade, the frequency of conversations about gluten intolerance (GI) and celiac disease (CD) in the United States has gone from almost unheard of to commonplace. Chances are your local supermarket sells dozens of items labeled &#8220;gluten free&#8221; where none existed five years ago. Restaurants and school lunch programs frequently offer gluten-free alternatives. [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-9514" href="http://www.epatienthealthcare.com/blog/2011/06/27/today-hybrid-versions-of-grains-contain-significantly-more-gluten-than-traditional-varieties/seeds/"><img class="alignleft size-full wp-image-9514" title="seeds" src="http://www.epatienthealthcare.com/blog/wp-content/seeds.jpg" alt="" width="278" height="181" /></a>Over the past decade, the frequency of conversations about gluten intolerance (GI) and celiac disease (CD) in the United States has gone from almost unheard of to commonplace. Chances are your local supermarket sells dozens of items labeled &#8220;gluten free&#8221; where none existed five years ago. Restaurants and school lunch programs frequently offer gluten-free alternatives. What happened?</p>
<p>&#8220;Gluten&#8221; is the general term for a mixture of tiny protein fragments (called polypeptides), which are found in cereal grains such as wheat, rye, barley, spelt, faro, and kamut. Gluten is classified in two groups: prolamines and glutelins. The most troublesome component of gluten is the prolamine gliadin. Gliadin is the cause of the painful inflammation in gluten intolerance and instigates <div class="toggle">the immune response and intestinal damage found in celiac disease. Although both conditions have similar symptoms (pain, gas, bloating, diarrhea), or sometimes no gastrointestinal symptoms at all, celiac disease is an autoimmune reaction to gluten that can cause severe degradation of the small intestine; whereas, gluten intolerance/sensitivity is an inability to digest gliadin with no damage to the intestines.</p>
<p>The medical community&#8217;s use of improved diagnostic tools (saliva, blood, and stool tests; and bowel biopsies) as well as self-diagnosis by aware individuals has certainly contributed to the swelling ranks of people afflicted with these maladies; however, that&#8217;s not the whole story. A combination of hybridized grains, America&#8217;s growing appetite for snacks and fast food, and the genetics of gluten intolerance and celiac disease have brought discussions of these once uncommon conditions front and center.</p>
<p>New evidence indicates that the hybrid versions of grains we eat today contain significantly more gluten than traditional varieties of the same grains. Experts such as Dr. Alessio Fasano, medical director of the Center for Celiac Research at the University of Maryland School of Medicine, believe this recent increase in the amount of gluten in our diet has given rise to the number of people suffering from gluten intolerance and celiac disease.</p>
<p>According to Fasano, &#8220;The prevalence of celiac disease in this country is soaring partly because changes in agricultural practices have increased gluten levels in crops.&#8221; He further states, &#8220;We are in the midst of an epidemic.&#8221;</p>
<p>For example, the ancient wheat that Moses ate was probably very different from our wheat today. Moses lived about 3,500 years ago, when wheat, spelt, and barley were all popular grains. Modern wheat varieties, however, have been bred to grow faster, produce bigger yields, harvest more efficiently, and bake better bread. The downside to today&#8217;s hybridized cereal grains is that they contain more gluten.</p>
<p>Celiac disease was once considered a rare malady and was estimated to have afflicted approximately 1 in 2,000 people in the United States. According to research done by the Mayo Clinic, CD is four times more common today that it was five decades ago. This increase is due to increased awareness and diagnostics, and the estimate today is that 1 out of every 133 people in the United States has celiac disease. To read more facts and figures please read The University of Chicago Celiac Disease center at http://www.uchospitals.edu/pdf/uch_&#8230;</p>
<p><strong>Here are estimates for other parts of the world:</strong></p>
<p>· 3 in 100: United Kingdom</p>
<p>· 1 in 370: Italy</p>
<p>· 1 in 122: Northern Ireland</p>
<p>· 1 in 99: Finland</p>
<p>· 1 in 133: United States</p>
<p>· Once thought rare for African-, Hispanic- and Asian-Americans, current estimates in these populations: 1 in 236</p>
<p>· 1 in 30 are estimated to have gluten intolerance in the United States.</p>
<p>More than 6,000 years before Moses was born, an agricultural revolution took place in the Middle East that allowed humans to embrace farming (sewing and harvesting wild seeds), herding, and other forms of agriculture and move away from our hunter-fisher-gatherer ancestors. This was the first major introduction of gluten into the human diet.</p>
<p>According to Dr. Loren Cordain, PhD, author of The Paleo Diet, &#8220;The foods that agriculture brought us &#8212; cereals, dairy products, fatty meats, salted foods, and refined sugars and oils- proved disastrous for our Paleolithic bodies&#8230;. studies of the bones and teeth early farmers revealed that they had more infectious diseases, more childhood mortality, shorter life spans, more osteoporosis, rickets, and other bone mineral density disorders than their ancestors thanks to the cereal-based diet. They were plagued with vitamin and mineral deficiencies and developed cavities in their teeth.&#8221;</p>
<p>In other words, people traded their health for sustainable food sources and a less nomadic way of life.</p>
<p>Two hundred years ago, the global diet received another big injection of gluten with the birth of the Industrial Revolution and steam-powered mills that were able to produce refined-grain flours that had significantly longer shelf lives, making flour (aka: gluten) more accessible and available to an almost global market. &#8220;We were able to mill and process grains for consumption and eat them in larger quantities than we had ever done in the past,&#8221; writes Cordain.</p>
<p>Jack Challem, &#8220;The Nutrition Reporter,&#8221; offers a different long view of human consumption of gluten: &#8220;Look at in another way, 100,000 generations of people were hunter-gatherers, 500 generations have depended on agriculture, and only 10 generations have lived since the start of the industrial age, and only two generations have grown up with highly processed fast foods. This short period of time in the course of man&#8217;s existence that grains have been around has proven that many of us are not physiologically able to tolerate gluten.&#8221;</p>
<p>Historical evidence of people having trouble digesting gluten was first documented in the 2nd century A.D. when the Greek physician Aretaeus of Cappadocia, diagnosed patients with celiac disease. The symptoms included &#8220;wasting and characteristic stools.&#8221; Since Aretaeus&#8217; time, the disease has gone by a variety of names, including &#8220;non-tropical sprue,&#8221; &#8220;celiac sprue,&#8221; &#8220;non-celiac gluten intolerance,&#8221; &#8220;gluten intolerance enteropathy,&#8221; and &#8220;gluten sensitive enteropathy.&#8221;</p>
<p>Fast forward to 1950, when the Dutch pediatrician Willem-Karel Dicke proposed wheat gluten was the cause of the disease. His theory was based on observations that celiac children improved during World War II when wheat was scarce in Holland.</p>
<p>As Challem points out, today, thanks in large part to the fast food and snack food industries, gluten is in just about every kind of food imaginable.</p>
<p><strong>So Why Can&#8217;t Everyone Handle Gluten?</strong></p>
<p>People who that carry any of the genes for CD and GI (expressed or not) are more susceptible to developing either condition. You can carry two dominate genes for celiac disease and perhaps end up developing CD or you can carry one dominant gene and one recessive gene and develop only GI. Your genes determine the body&#8217;s immune response in the presence of gluten, and many different health problems may result from that response. Some people may have their brain affected and develop cognitive problems such as depression or impaired brain function, while others suffer pancreatic problems and develop diabetes. Research still needs to be done to answer the question as to why these maladies affect different parts of the body in different people.</p>
<p>When populations that are genetically predisposed to CD and GI are exposed to cereal grains with higher gluten content, there&#8217;s little wonder why more people are having these genes &#8220;turned on&#8221; and develop gluten insensitivity on a much larger scale &#8212; especially now that the flour made from these grains are part of the &#8220;hidden ingredients&#8221; in foods from ice cream to lunch meats.</p>
<p><strong>OK, Now What?</strong></p>
<p>So, gluten has changed, and we have changed, and it appears not for the better. Fortunately or unfortunately, depending on how you look at it, identifying and eliminating the foods and ingredients from your life that do not work for your body is the only answer. There is no magic pill to take to make it all go away.</p>
<p>If you, or someone you know, is experiencing major health issues that aren&#8217;t getting better, enlisting a knowledgeable physician who understands the complexities of CD and GI testing is an excellent idea; however, on average, it takes the medical community 10 years to diagnose people who are suffering with severe health problems from undiagnosed CD and GI.?</p>
<p><strong>The Bottom Line</strong></p>
<p>Gluten intolerance is not a fad diet. I have seen countless cases display miraculous improvements in?long standing ailments &#8212; simply by adapting this lifestyle. Even if you have a test for CD and it comes back negative?and medical community clears you to continue?eating gluten, but you feel better without it,?listen to your body. You?know yourself far better than anyone else and you deserve?good health. If you have doubts about your diet, try going gluten-free for two weeks and see how you feel. Those with more advanced illnesses (autoimmune diseases and such) will usually not experience changes until they have been gluten-free for six months to a year.</p>
<p><strong>Source for Story:</strong> http://www.naturalnews.com/032823_gluten_intolerance_celiac_disease.html#ixzz1QVpQ0dqM</p>
</div>]]></content:encoded>
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		<title>Imaging Techniques Can Identify Plaques Likely to Cause Heart Attacks</title>
		<link>http://www.epatienthealthcare.com/blog/2010/01/06/imaging-techniques-can-identify-plaques-likely-to-cause-heart-attacks/</link>
		<comments>http://www.epatienthealthcare.com/blog/2010/01/06/imaging-techniques-can-identify-plaques-likely-to-cause-heart-attacks/#comments</comments>
		<pubDate>Wed, 06 Jan 2010 07:29:57 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[NEW YORK &#8211;  Imaging techniques can help identify the types of vulnerable plaque that are most likely to cause adverse cardiac events before they occur, say researchers. This finding comes from a clinical trial called Providing Regional Observations to Study Predictors of Events in the Coronary Tree (PROSPECT), which is the first prospective natural history [...]]]></description>
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<p class="MsoNormal">NEW YORK &#8211; <span> </span>Imaging techniques can help identify the types of vulnerable plaque that are most likely to cause adverse cardiac events before they occur, say researchers.<o:p></o:p></p>
<p class="MsoNormal">This finding comes from a clinical trial called Providing Regional Observations to Study Predictors of Events in the Coronary Tree (PROSPECT), which is the first prospective natural history study of atherosclerosis using multi-modality imaging to characterize the coronary tree.<o:p></o:p></p>
<p class="MsoNormal">A presentation on the study was made at the 21st annual Transcatheter Cardiovascular Therapeutics (TCT) scientific symposium, sponsored by the Cardiovascular Research Foundation (CRF).<o:p></o:p></p>
<p class="MsoNormal">“As a result of the PROSPECT trial, we are closer to being able to predict-and therefore prevent &#8211; sudden, unexpected adverse cardiac events,” said principal investigator Dr. Gregg W. Stone, immediate past chairman of CRF, professor of medicine at Columbia University Hospital and Director of Cardiovascular Research and Education at the Center for Interventional Vascular Therapy at NewYork-Presbyterian Hospital/Columbia University Medical Center.<o:p></o:p></p>
<p class="MsoNormal">During the multi-centre trial, 700 patients with acute coronary syndromes (ACS) were studied using three-vessel multimodality intra-coronary imaging-angiography, intravascular ultrasound (IVUS), and virtual histology.<o:p></o:p></p>
<p class="MsoNormal">The purpose was to quantify the clinical event rate due to atherosclerotic progression, and to identify those lesions that place patients at risk for unexpected adverse cardiovascular events-sudden death, cardiac arrest, heart attacks and unstable or progressive angina.<o:p></o:p></p>
<p class="MsoNormal">The study revealed that most untreated plaques that cause unexpected heart attacks are not mild lesions, as previously thought, but actually have a large plaque burden and a small lumen area. These are characteristics that were invisible to the coronary angiogram but easily identifiable by IVUS.<o:p></o:p></p>
<p class="MsoNormal">Only about half of new cardiac events due to non-culprit lesions exemplified the classic notion of vulnerable plaque (rapid lesion progression of non flow limiting lesions), while half were attributable to unrecognized and untreated severe disease with minimal change over time.<o:p></o:p></p>
<p class="MsoNormal">Perhaps most importantly, for the first time it was demonstrated that characterization of the underlying plaque composition (with virtual histology) was able to significantly improve the ability to predict future adverse events beyond other more standard imaging techniques.<o:p></o:p></p>
<p class="MsoNormal">“These results mean that using a combination of imaging modalities, including IVUS to identify lesions with a large plaque burden and/or small lumen area, and virtual histology to identify a large necrotic core without a visible cap (a thin cap fibroatheroma) identifies the lesions that are at especially high risk of causing future adverse cardiovascular events,” Dr. <st1:sn w:st="on">Stone</st1:sn> said.</p>
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		<item>
		<title>Introducing &#8211;  CoQ10</title>
		<link>http://www.epatienthealthcare.com/blog/2009/12/23/introducing-coq10/</link>
		<comments>http://www.epatienthealthcare.com/blog/2009/12/23/introducing-coq10/#comments</comments>
		<pubDate>Thu, 24 Dec 2009 01:48:05 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[Other Names: Coenzyme Q10, Co Q10, Ubiquinone, Vitamin Q CoQ10 is a naturally-occuring compound found in every cell in the body. CoQ10&#8242;s alternate name, ubiquinone, comes from the word ubiquitous, which means &#8220;found everywhere.&#8221; CoQ10 plays a key role in producing energy in the mitochondria, the part of a cell responsible for the production of [...]]]></description>
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<p class="MsoNormal">Other Names: Coenzyme Q10, Co Q10, Ubiquinone, Vitamin Q</p>
<p class="MsoNormal">CoQ10 is a naturally-occuring compound found in every cell in the body. CoQ10&#8242;s alternate name, ubiquinone, comes from the word ubiquitous, which means &#8220;found everywhere.&#8221;</p>
<p class="MsoNormal">CoQ10 plays a key role in producing energy in the mitochondria, the part of a cell responsible for the production of energy in the form of ATP.</p>
<p class="MsoNormal"><strong>Why People Use CoQ10<o:p></o:p></strong></p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">Heart      failure</li>
<li class="MsoNormal">Cardiomyopathy</li>
<li class="MsoNormal">Heart      Attack Prevention and Recovery</li>
<li class="MsoNormal">High      Blood Pressure</li>
<li class="MsoNormal">Diabetes</li>
<li class="MsoNormal">Gum      Disease</li>
<li class="MsoNormal">Kidney      Failure</li>
<li class="MsoNormal">Migraine</li>
<li class="MsoNormal">Counteract      Prescription Drug Effects</li>
<li class="MsoNormal">Parkinson&#8217;s      disease</li>
<li class="MsoNormal">Weight      loss</li>
</ul>
<p class="MsoNormal"><strong>What is the Evidence For CoQ10?<o:p></o:p></strong></p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">Heart      failure<br />
People with heart failure have been found to have lower levels of CoQ10 in      heart muscle cells. Double-blind research suggests that CoQ10 may reduce      symptoms related to heart failure, such as shortness of breath, difficulty      sleeping, and swelling. CoQ10 is thought to increase energy production in      the heart muscle, increasing the strength of the pumping action. Recent      human studies, however, haven&#8217;t supported this.</li>
</ul>
<p class="MsoNormal">In one study, 641 people with congestive heart failure were randomized to receive either CoQ10 (2 mg per kg body weight) or a placebo plus standard treatment. People who took the CoQ10 had a significant reduction in symptom severity and fewer hospitalizations.</p>
<p class="MsoNormal">In another study, 32 patients with end-stage heart failure awaiting heart transplantation received either 60 mg of CoQ10 or a placebo for 3 months. Patients who took the CoQ10 experienced a significant improvement in functional status, clinical symptoms, and quality of life, however there were no changes in echocardiogram (heart ultrasound) or in objective markers.</p>
<p class="MsoNormal">A study randomized 55 patients with congestive heart failure to receive either 200 mg per day of CoQ10 or a placebo in addition to standard treatment. Although serum levels of CoQ10 increased in patients receiving CoQ10, CoQ10 didn&#8217;t affect ejection fraction, peak oxygen consumption, or exercise duration.</p>
<p class="MsoNormal">A longer-term study investigated the use of 100 mg of CoQ10 or a placebo in addition to standard treatment in 79 patients with stable chronic congestive heart failure. The results indicated that CoQ10 only slightly improved maximal exercise capacity and quality of life compared with the placebo.</p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">Cardiomyopathy</li>
</ul>
<p class="MsoNormal">Several small trials have found CoQ10 may be helpful for certain types of cardiomyopathy.</p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">Parkinson&#8217;s      disease</li>
</ul>
<p class="MsoNormal">Lower levels of CoQ10 have also been observed in people with Parkinson&#8217;s disease. Preliminary research has found that increasing CoQ10 may increase levels of the neurotransmitter dopamine, which is thought to be lowered in people with Parkinson&#8217;s disease. It has also been suggested that CoQ10 might protect brain cells from damage by free radicals.</p>
<p class="MsoNormal">A small, randomized controlled trial examined the use of 360 mg CoQ10 or a placebo in 28 treated and stable Parkinson&#8217;s disease patients. After 4 weeks, CoQ10 provided a mild but significant significant mild improvement in early <st1:sn w:st="on">Parkinson</st1:sn>&#8216;s symptoms and significantly improved performance in visual function.</p>
<p class="MsoNormal">A larger 16 month trial funded by the National Institutes of Health explored the use of CoQ10 (300, 600 or 1200 mg/day) or a placebo in 80 patients with early stage Parkinson&#8217;s disease. The results suggested that CoQ10, especially at the 1200 mg per day dose, had a significant reduction in disability compared to those who took a placebo.</p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">CoQ10      and Statin Drugs</li>
</ul>
<p class="MsoNormal">Some research suggests that statin drugs, or HMG-CoA reductase inhibitors, a class of drugs used to lower cholesterol, may interfere with the body&#8217;s production of CoQ10. However, research on the use of CoQ10 supplements in people taking statins is still inconclusive, and it is not routinely recommended in combination with statin therapy.</p>
<ul style="margin-top: 0in" type="disc">
<li class="MsoNormal">Diabetes<br />
In a 12-week randomized controlled trial, 74 people with type 2 diabetes      were randomized to receive either 100 mg CoQ10 twice daily, 200 mg per day      of fenofibrate (a lipid regulating drug), both or neither for 12 weeks.      CoQ10 supplementation significantly improved blood pressure and glycemic      control. However, two studies found that CoQ10 supplementation failed to      find any effect on glycemic control.</li>
<li class="MsoNormal">Gum      disease<br />
A small study looked at the topical application of CoQ10 to the      periodontal pocket. Ten male periodontitis patients with 30 periodontal      pockets were selected. During the first 3 weeks, the patients applied      topical CoQ10. There was significant improvement in symptoms.</li>
</ul>
<p class="MsoNormal"><strong>Dosage<o:p></o:p></strong></p>
<p class="MsoNormal">A typical CoQ10 dosage is 30 to 90 mg per day, taken in divided doses, but the recommended amount can be as high as 200 mg per day.</p>
<p class="MsoNormal">CoQ10 is fat-soluble, so it is better absorbed when taken with a meal that contains oil or fat.</p>
<p class="MsoNormal">The clinical effect is not immediate and may take up to eight weeks.</p>
<p class="MsoNormal"><strong>Safety<o:p></o:p></strong></p>
<p class="MsoNormal">Consult your doctor before trying CoQ10, especially if you have heart disease, kidney failure, or cancer.</p>
<p class="MsoNormal">Side effects of CoQ10 may include diarrhea and rash.</p>
<p class="MsoNormal">CoQ10 is used in combination with standard treatment, not to replace it.</p>
<p class="MsoNormal">CoQ10 may lower blood sugar levels, so people with diabetes should not use CoQ10 unless under a doctor&#8217;s supervision. CoQ10 may also lower blood pressure.</p>
<p class="MsoNormal">The safety of Co q10 in pregnant or nursing women or children has not been established.</p>
<p class="MsoNormal"><strong>PLEASE SEE THE POST ON &#8220;POLICOSANOL&#8221; FOR LOWERING CHOLESTEROL </strong></p>
<p class="MsoNormal"><o:p> </o:p></p>
]]></content:encoded>
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		<slash:comments>619</slash:comments>
		</item>
		<item>
		<title>Resynchronization Cuts Down Risk of Heart Failures</title>
		<link>http://www.epatienthealthcare.com/blog/2009/11/28/resynchronization-cuts-down-risk-of-heart-failures/</link>
		<comments>http://www.epatienthealthcare.com/blog/2009/11/28/resynchronization-cuts-down-risk-of-heart-failures/#comments</comments>
		<pubDate>Sat, 28 Nov 2009 20:24:46 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[CHICAGO &#8211;  A therapy called cardiac ‘resynchronization’ reduced risk of heart failures by 41 percent, says an international study. “This shows, for the first time, that the onset of heart failure symptoms and hospitalization for heart failure can be delayed with pacing therapy,” said David Wilber, director of the Cardiovascular Institute at Loyola University (Chicago) [...]]]></description>
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<p class="MsoNormal"><st1:sn w:st="on">CHICAGO</st1:sn> &#8211; <span> </span>A therapy called cardiac ‘resynchronization’ reduced risk of heart failures by 41 percent, says an international study.<o:p></o:p></p>
<p class="MsoNormal">“This shows, for the first time, that the onset of heart failure symptoms and hospitalization for heart failure can be delayed with pacing therapy,” said <st2:personname w:st="on"><st1:givenname w:st="on">David</st1:givenname>  <st1:sn w:st="on">Wilber</st1:sn></st2:personname>, director of the Cardiovascular Institute at Loyola University (<st1:sn w:st="on">Chicago</st1:sn>) Stritch School of Medicine.<o:p></o:p></p>
<p class="MsoNormal">Cardiac resynchronization therapy (CRT) is an innovative new therapy that can relieve congestive heart failure (CHF) symptoms, by improving the coordination of its contractions.<o:p></o:p></p>
<p class="MsoNormal">It is done with the help of electrical impulses delivered by a device implanted in the upper chest, that help synchronize contractions of the left ventricle, the heart’s main pumping chamber.<o:p></o:p></p>
<p class="MsoNormal">The study included 1,820 patients from 110 centers in the US, Canada and Europe. All patients in the trial had been diagnosed with early stage, mild heart failure (Class 1 and Class 2 on the New York Heart Association classification system), according to a <st1:sn w:st="on">Loyola</st1:sn> release.<o:p></o:p></p>
<p class="MsoNormal">For instance, <st1:sn w:st="on">Loyola</st1:sn> heart failure patient <st2:personname w:st="on"><st1:givenname w:st="on">Rosemary</st1:givenname>  <st1:sn w:st="on">Jakubowski</st1:sn></st2:personname> of Elmwood Park said before she received cardiac resynchronization, she had experienced significant fatigue. “I always had that dragging feeling,” she said.<o:p></o:p></p>
<p class="MsoNormal">Since receiving resynchronization, Jakubowski has been taking kickboxing and swim aerobics classes, without fatigue. “I’m 100 percent better — complete satisfaction,” she said. “It’s like I’m a new person.”<o:p></o:p></p>
<p class="MsoNormal">The Food and Drug Administration has approved cardiac resynchronization for patients with Class 3 (moderate) and Class 4 (severe) heart failure. Such patients experience marked limitations in physical activity or are unable to do any physical activity at all without discomfort.<o:p></o:p></p>
<p class="MsoNormal">“With this study, we have shown that certain patients with early-stage, mild heart failure also can benefit from cardiac resynchronization,” Wilber said.<o:p></o:p></p>
<p class="MsoNormal">These findings were published in the New England Journal of Medicine.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.epatienthealthcare.com/blog/2009/11/28/resynchronization-cuts-down-risk-of-heart-failures/feed/</wfw:commentRss>
		<slash:comments>4</slash:comments>
		</item>
		<item>
		<title>New Microchip-Based Device Can Put an End to Painful Biopsies</title>
		<link>http://www.epatienthealthcare.com/blog/2009/11/23/new-microchip-based-device-can-put-an-end-to-painful-biopsies/</link>
		<comments>http://www.epatienthealthcare.com/blog/2009/11/23/new-microchip-based-device-can-put-an-end-to-painful-biopsies/#comments</comments>
		<pubDate>Tue, 24 Nov 2009 00:13:09 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<guid isPermaLink="false">http://www.gembpatients.com/blog/2009/11/23/new-microchip-based-device-can-put-an-end-to-painful-biopsies/</guid>
		<description><![CDATA[TORONTO &#8211; Canadian experts at the University of Toronto have come up with a microchip technology that they believe can prove helpful in diagnosing cancer and infectious disease in just half an hour. Just as big in size as a BlackBerry, the novel device is expected to revolutionize the diagnosis and treatment of a wide [...]]]></description>
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<p class="MsoNormal">TORONTO &#8211; Canadian experts at the University of Toronto have come up with a microchip technology that they believe can prove helpful in diagnosing cancer and infectious disease in just half an hour.<o:p></o:p></p>
<p class="MsoNormal">Just as big in size as a BlackBerry, the novel device is expected to revolutionize the diagnosis and treatment of a wide range of cancers and other ailments.<o:p></o:p></p>
<p class="MsoNormal">The researchers say that it is aimed at eliminating the need for painful biopsies by detecting the presence and severity of cancer via a urine sample.<o:p></o:p></p>
<p class="MsoNormal">They hope that their device will also eliminate equally painful wait times that patients undergoing cancer diagnoses routinely endure, as test results computed by it can be completed in just 30 minutes.<o:p></o:p></p>
<p class="MsoNormal">“Today, it takes a room filled with computers to evaluate a clinically relevant sample of cancer biomarkers and the results aren’t quickly available,” the Globe and Mail quoted Shana Kelley, the U of T professor who was a lead investigator on the project, as saying.<o:p></o:p></p>
<p class="MsoNormal">“Our team was able to measure biomolecules on an electronic chip the size of your fingertip and analyze the sample within half an hour,” <st1:givenname w:st="on">Kelley</st1:givenname> added.<o:p></o:p></p>
<p class="MsoNormal">The device, though in the engineering phase, has been tested on prostate cancer and head and neck cancer models.<o:p></o:p></p>
<p class="MsoNormal">The university team believe that it may potentially be used to diagnose and assess other cancers, besides detecting infectious diseases like HIV, MRSA and H1N1 flu.<o:p></o:p></p>
<p class="MsoNormal">“The system…is a revolutionary technology that could allow us to track biomarkers that might have significant relevance to cancer, with a combination of speed, sensitivity, and accuracy not available with any current technology. This type of approach could have a profound impact on the future management for our cancer patients,” says <st2:personname w:st="on"><st1:title w:st="on">Dr.</st1:title> <st1:givenname w:st="on">Fei-Fei</st1:givenname> <st1:sn w:st="on">Liu</st1:sn></st2:personname>, a radiation oncologist at Princess Margaret Hospital and Head of the Applied Molecular Oncology Division at the Ontario Cancer Institute.<o:p></o:p></p>
<p class="MsoNormal">A research paper describing the novel device has been published in the journal Nature Nanotechnology.</p>
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