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	<title>Dr. Tori Hudson, N.D. &#187; Endometriosis</title>
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		<copyright>Copyright &#xA9; Dr. Tori Hudson, N.D. 2010 </copyright>
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		<itunes:summary>Naturopathic Physician, Author, Educator and Researcher</itunes:summary>
		<itunes:author>Dr. Tori Hudson, N.D.</itunes:author>
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		<title>Tea and risk of endometrial cancer</title>
		<link>http://drtorihudson.com/botanicals/tea-and-risk-of-endometrial-cancer/</link>
		<comments>http://drtorihudson.com/botanicals/tea-and-risk-of-endometrial-cancer/#comments</comments>
		<pubDate>Fri, 06 Aug 2010 18:01:00 +0000</pubDate>
		<dc:creator>Tori Hudson, N.D.</dc:creator>
				<category><![CDATA[Botanicals]]></category>
		<category><![CDATA[Endometriosis]]></category>
		<category><![CDATA[Green Tea]]></category>

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		<description><![CDATA[This meta-analysis was done to assess the association between tea consumption and endometrial cancer. A total of 7 studies with 2 cohort studies and 5 case-control studies met the criteria for inclusion in this meta-analysis. Green teas and black teas were included in the search. A total of 3487 cases and of endometrial cancer and [...]]]></description>
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<p><a href="http://drtorihudson.com/wp-content/uploads/2010/08/clip_image001.jpg"><img style="border-bottom: 0px; border-left: 0px; display: inline; margin-left: 0px; border-top: 0px; margin-right: 0px; border-right: 0px" title="clip_image001" border="0" hspace="12" alt="clip_image001" align="left" src="http://drtorihudson.com/wp-content/uploads/2010/08/clip_image001_thumb.jpg" width="278" height="331" /></a>This meta-analysis was done to assess the association between tea consumption and endometrial cancer. A total of 7 studies with 2 cohort studies and 5 case-control studies met the criteria for inclusion in this meta-analysis. Green teas and black teas were included in the search. A total of 3487 cases and of endometrial cancer and 104,643 non cases appeared in the pooled analysis. The results suggested that tea consumption was statistically significantly associated with reduced risk of endometrial cancer. The combine relative risk for ever drinkers vs. non/lowest drinkers was 0.85. Compared with non/lowest drinkers, the relative risk was 0.88 for low to moderate drinkers and 0.75 for high drinkers. An increase in tea intake of 2 cups per day was associated with a 25% decreased risk of endometrial cancer. In analysis by subgroup, green tea consumption was significantly associated with decreased risk whereas an association with black tea was not observed.</p>
<p><b>Commentary</b>: The mechanisms whereby tea reduces the risk of endometrial cancer are multifactorial. Tea, even green tea, contains caffeine, which lowers free estrogen levels. A number of antioxidants are in green tea, and these “catechins” affect carcinogenesis in numerous ways including inducing apoptosis (cell death), inhibiting estrogen-induced activation of endometrial cells and scavenging free radicals. Tea also contains phytoestrogens and can have an estrogen antagonist effect on endometrial cells. Tea consumption also modifies genetic polymorphisms relevant in the development of endometrial cancer. </p>
<p><b>Reference</b></p>
<p><i>Tang N, Hua L, Qiu Y, Zhou G, Ma J. Tea consumption and risk of endometrial cancer : a metaanalysis. Am J Obstet Gynecol 2009;201:605.e1-8</i></p>
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		<title>Pine bark extract and endometriosis</title>
		<link>http://drtorihudson.com/general/pine-bark-extract-and-endometriosis/</link>
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		<pubDate>Sat, 06 Dec 2008 05:18:23 +0000</pubDate>
		<dc:creator>Tori Hudson, N.D.</dc:creator>
				<category><![CDATA[Endometriosis]]></category>
		<category><![CDATA[General]]></category>

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		<description><![CDATA[Fifty eight women were surgically diagnosed with endometriosis and were then started on Pycnogenol within 6 months of the surgery after confirming regular menstruation and ovulation for three months. Women were randomized to receive either pycnogenol 30 mg twice daily for 48 weeks or a gonadotropin-releasing hormone agonist (Gn-RHa), leuprorelin acetate depot, 3.75 mg IM [...]]]></description>
			<content:encoded><![CDATA[<p><img align="right" alt="Endometriosis" title="Endometriosis" src="http://drtorihudson.com/files/endometriosis.jpg" />Fifty eight women were surgically diagnosed with endometriosis and were then started on Pycnogenol within 6 months of the surgery after confirming regular menstruation and ovulation for three months. Women were randomized to receive either pycnogenol 30 mg twice daily for 48 weeks or a gonadotropin-releasing hormone agonist (Gn-RHa), leuprorelin acetate depot, 3.75 mg IM six times every four weeks for 24 weeks.  Patients were monitored at 4, 12, 24, and 48 weeks after treatment began.</p>
<p>Results:  Both groups had similar symptoms before the treatments began: severe pain, pelvic tenderness and pelvic indurations.  After four weeks on  Pycnogenol, patients slowly but steadily improved reducing symptoms from severe to moderate. Overall, this group experienced a 33% reduction in symptoms of their endometriosis. The leuprorelin group had a greater response within the treatment period, but relapsed after 24 weeks post treatment.  The Pycnogenol group maintained regular menses and normal estrogen levels during treatment and as expected, the leuprorelin group had suppressed menstruation and drastically lowered estrogen levels during treatment.  In addition, five women in the trial taking Pycnogenol became pregnant.</p>
<blockquote><p>Kohama T, Herai K, Inoue M.  <a target="_blank" title="Pine bark extract and endometriosis" href="http://www.ncbi.nlm.nih.gov/pubmed/17879831">Effect of French maritime pine bark extract on endometriosis as compared with leuprorelin acetate</a>.  <em>J Reprod Med</em> 2007; 52(8):703-708.</p></blockquote>
<p><strong>Commentary:</strong> One of the most common causes of pelvic pain and infertility, endometriosis is a challenging problem for women and a complex problem to treat with natural medicine.  New research shows multiple potential factors involved in the etiology and progression of the disease including:</p>
<ul>
<li>Retrograde menstruation</li>
<li>Coelomic metaplasia</li>
<li>Metastasis</li>
<li>Iatrogenic</li>
<li>Genetic</li>
<li>Environmental factors</li>
<li>Altered cellular immunity</li>
<li>Increased inflammatory mediators</li>
</ul>
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