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	<title>Chinese Medicine &#124; Herbal</title>
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		<title>Vegetarian diets are associated with reduced cancer risk</title>
		<link>http://www.mmvbs.com/uncategorized/vegetarian-diets-are-associated-with-reduced-cancer-risk</link>
		<comments>http://www.mmvbs.com/uncategorized/vegetarian-diets-are-associated-with-reduced-cancer-risk#comments</comments>
		<pubDate>Thu, 17 May 2012 21:30:50 +0000</pubDate>
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		<description><![CDATA[The most convincing recent direct evidence that vegetarian diets are associated with reduced cancer risk comes from a report on prospective data collected from the Oxford Vegetarian Study and the European Prospective Investigation into Cancer and Nutrition–Oxford (EPIC-Oxford) cohort.33 In &#8230; <a href="http://www.mmvbs.com/uncategorized/vegetarian-diets-are-associated-with-reduced-cancer-risk">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>The most convincing recent direct evidence that vegetarian diets are associated with reduced cancer risk comes from a report on prospective data collected from the Oxford Vegetarian Study and the European Prospective Investigation into Cancer and Nutrition–Oxford (EPIC-Oxford) cohort.<a id="yiv1741568955__tag_213050229" href="http://www.ncbi.nlm.nih.gov/pubmed/19536095" rel="nofollow" target="_blank">33</a> In this analysis, 61,566 British men and women were separated into three dietary pattern groups on the basis of 4 questions on an intake questionnaire. The resultant groups were meat eaters (32,403), fish eaters (nonmeat eaters who did eat fish; 8562), and vegetarians (20,601). After an average of 12.2 years follow-up, 3350 had been diagnosed with cancer (2204 in meat eaters, 317 in fish eaters, and 829 in vegetarians). Interestingly, there are vegans in this cohort, but according to the authors “there are currently too few cancers [among vegans] to be informative”. Overall relative risk (RR) for all cancers (at 20 sites or groups of sites) was 0.88 (0.81–0.96) in vegetarians and 0.82 (0.73–0.93) in fish eaters compared to meat eaters after adjustment for age, smoking, alcohol use, body mass index, physical activity level and in women, parity, and oral contraceptive use.<a id="yiv1741568955__tag_213050181" href="http://www.ncbi.nlm.nih.gov/pubmed/19536095" rel="nofollow" target="_blank">33</a></p>
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		<title>Eggs, meat, milk, mate and prostate cancer</title>
		<link>http://www.mmvbs.com/uncategorized/eggs-meat-milk-mate-and-prostate-cancer</link>
		<comments>http://www.mmvbs.com/uncategorized/eggs-meat-milk-mate-and-prostate-cancer#comments</comments>
		<pubDate>Thu, 10 May 2012 18:57:10 +0000</pubDate>
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		<guid isPermaLink="false">http://www.mmvbs.com/?p=573</guid>
		<description><![CDATA[Cancer Causes Control. 2012 Apr 28. [Epub ahead of print] Food groups and risk of prostate cancer: a case-control study in Uruguay. Deneo-Pellegrini H, Ronco AL, De Stefani E, Boffetta P, Correa P, Mendilaharsu M, Acosta G. Grupo de Epidemiología, &#8230; <a href="http://www.mmvbs.com/uncategorized/eggs-meat-milk-mate-and-prostate-cancer">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>Cancer Causes Control. 2012 Apr 28. [Epub ahead of print]</p>
<p>Food groups and risk of prostate cancer: a case-control study in Uruguay.</p>
<p>Deneo-Pellegrini H, Ronco AL, De Stefani E, Boffetta P, Correa P, Mendilaharsu M, Acosta G.</p>
<p>Grupo de Epidemiología, Departamento de Anatomía Patológica, Hospital de Clínicas, Universidad de la República, Avenida Brasil 3080 department 402, 11300, Montevideo, Uruguay.</p>
<p>&nbsp;</p>
<p>OBJECTIVE: The role of foods and beverages has been studied in detail in order to establish probable risk factors for prostate cancer.</p>
<p>&nbsp;</p>
<p>METHODS: Data were derived from 326 cases with incident and microscopically confirmed adenocarcinomas of the prostate and 652 controls. Odds ratios and 95 % confidence intervals of prostate cancer were estimated by unconditional multiple logistic regression.</p>
<p>&nbsp;</p>
<p>RESULTS: We identified the following food items as risk factors: lamb meat, salted meat, whole milk, total eggs, and maté consumption. The highest OR was associated with total eggs (OR, 2.43; 95 % CI, 1.70-3.48), followed by salted meat (OR, 2.65; 95 % CI, 1.36-3.76), maté consumption (OR, 1.96; 95 % CI, 1.17-3.31), and whole milk (OR, 2.01; 95 % CI, 1.26-2.51).</p>
<p>&nbsp;</p>
<p>CONCLUSIONS: The final model, fitted by stepwise forward method, included total eggs, salted meat, whole milk, and maté consumption, whereas fruits were protective.</p>
<p>PMID: 22544454  [PubMed - as supplied by publisher]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/22544454">http://www.ncbi.nlm.nih.gov/pubmed/22544454</a></p>
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		<title>Soy protects the heart after myocardial infarction</title>
		<link>http://www.mmvbs.com/uncategorized/soy-protects-the-heart-after-myocardial-infarction</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-protects-the-heart-after-myocardial-infarction#comments</comments>
		<pubDate>Tue, 01 May 2012 18:47:22 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<guid isPermaLink="false">http://www.mmvbs.com/?p=566</guid>
		<description><![CDATA[Nutr Metab Cardiovasc Dis. 2009 Feb;19(2):91-7. Epub 2008 Jun 19.   Diet with isolated soy protein reduces oxidative stress and preserves ventricular function in rats with myocardial infarction. &#160; Hagen MK, Lehenbauer-Lüdke AR, Paludo AC, Schenkel P, Gonçalves L, Fernandes &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-protects-the-heart-after-myocardial-infarction">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv280360634">
<div id="yui_3_2_0_9_1335897151828429">
<p id="yui_3_2_0_9_1335897151828550">Nutr Metab Cardiovasc Dis. 2009 Feb;19(2):91-7. Epub 2008 Jun 19.</p>
<p id="yui_3_2_0_9_1335897151828428"> </p>
<p>Diet with isolated soy protein reduces oxidative stress and preserves ventricular function in rats with myocardial infarction.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335897151828531">Hagen MK, Lehenbauer-Lüdke AR, Paludo AC, Schenkel P, Gonçalves L, Fernandes TG, Caron R, Llesuy S, Mill JG, Belló-Klein A.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335897151828558">Cardiovascular Physiology Laboratory, Federal University of Rio Grande do Sul, Av. Sarmento Leite 500, CEP 90050170, Porto Alegre, Brazil.</p>
<p>&nbsp;</p>
<p>We investigated the effects of an isolated soy protein (ISP) diet offered over a 9-week period to rats in whom myocardial infarction (MI) had been induced, and a casein diet given as a control. Male Wistar rats were assigned to six groups after infarct size determination (n=8/group): Sham Casein (SC); Infarct Casein &lt;25% (IC&lt;25%); Infarct Casein &gt;25% (IC&gt;25%); Sham Soy (SS); Infarct Soy &lt;25% (IS&lt;25%); and Infarct Soy &gt;25% (IS&gt;25%). MI surgery was performed at the fifth week, and one month later, the animals were hemodynamically assessed to evaluate left ventricular systolic pressure (LVSP), left ventricular end diastolic pressure (LVEDP), contractility and relaxation indexes (+/-dP/dt). Lung and liver specimens were also collected for the estimation of organ congestion. Oxidative stress was evaluated in heart homogenates through chemiluminescence (CL), carbonyl groups, and antioxidant enzyme activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx). Infarcted groups treated with casein showed cardiac hypertrophy, lung and liver congestion, increased LVEDP and decreased LVSP and +/-dP/dt, all typical signals of heart failure. Ventricular dysfunction was correlated with increased myocardial oxidative damage as seen by CL and carbonyl groups data in the groups IC&lt;25% and IC&gt;25% (3 and 10-fold increase, respectively). The ISP diet was able to improve ventricular systolic and diastolic function in the groups IS&lt;25% and IS&gt;25% (LVEDP was reduced by 44% and 24%, respectively) and to decrease myocardial oxidative stress. The overall results confirm the preventive role of soy-derived products in terms of post-MI myocardial dysfunction probably by an antioxidant action.</p>
<p id="yui_3_2_0_9_1335897151828570"> </p>
<p id="yui_3_2_0_9_1335897151828568">PMID: 18571392  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/18571392">http://www.ncbi.nlm.nih.gov/pubmed/18571392</a></p>
</div>
</div>
<div> </div>
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		<title>Beans and myocardial infarction</title>
		<link>http://www.mmvbs.com/uncategorized/beans-and-myocardial-infarction</link>
		<comments>http://www.mmvbs.com/uncategorized/beans-and-myocardial-infarction#comments</comments>
		<pubDate>Tue, 01 May 2012 18:41:45 +0000</pubDate>
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		<guid isPermaLink="false">http://www.mmvbs.com/?p=556</guid>
		<description><![CDATA[J Nutr. 2005 Jul;135(7):1770-5. &#160; Decreased consumption of dried mature beans is positively associated with urbanization and nonfatal acute myocardial infarction. &#160; Kabagambe EK, Baylin A, Ruiz-Narvarez E, Siles X, Campos H. &#160; Department of Nutrition, Harvard School of Public &#8230; <a href="http://www.mmvbs.com/uncategorized/beans-and-myocardial-infarction">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv740166282">
<div id="yui_3_2_0_9_1335295595765437">
<p id="yui_3_2_0_9_1335295595765528">J Nutr. 2005 Jul;135(7):1770-5.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335295595765436">Decreased consumption of dried mature beans is positively associated with urbanization and nonfatal acute myocardial infarction.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335295595765544">Kabagambe EK, Baylin A, Ruiz-Narvarez E, Siles X, Campos H.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335295595765547">Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_9_1335295595765550">Legumes may protect against myocardial infarction (MI). The objective of this study was to determine whether consumption of dried mature beans (referred to as beans), the main legume in Latin America, is associated with MI. The cases (n = 2119) were survivors of a first acute MI and were matched by age, sex, and area of residence to randomly selected population controls (n = 2119) in Costa Rica. Dietary intake was assessed with a validated FFQ. Of the population, 69% consumed &gt; or = 1 serving of beans/d (1 serving = one-third cup of cooked beans, approximately 86 g). Consumption of &gt; or = 1 serving/d was significantly higher (P &lt; 0.001) in rural (81%) than in urban (65%) areas. Individuals who never eat dried beans or whose consumption was &lt; 1 time/mo were classified as nonconsumers. Compared with nonconsumers, intake of 1 serving of beans/d was inversely associated with MI in analyses adjusted for smoking, history of diabetes, history of hypertension, abdominal obesity, physical activity, income, intake of alcohol, total energy, saturated fat, trans fat, polyunsaturated fat, and cholesterol [odds ratio (OR) = 0.62; 95% CI: 0.45-0.88]. No further protection was observed with increased number of servings/d (OR = 0.73; 95% CI: 0.52-1.03 for &gt; 1 serving/d). In summary, we found that consumption of 1 serving of beans/d is associated with a 38% lower risk of MI. No additional protection was observed at intakes &gt; 1 serving/d. These findings are timely given the trend toward increased obesity, cardiovascular disease, and a reduction in the intake of beans in Latin American countries.</p>
<p id="yui_3_2_0_9_1335295595765678"> </p>
<p id="yui_3_2_0_9_1335295595765676">PMID: 15987863  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/15987863">http://www.ncbi.nlm.nih.gov/pubmed/15987863</a></p>
</div>
</div>
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		<title>Soy Enhances Tamoxifen</title>
		<link>http://www.mmvbs.com/uncategorized/soy-enhances-tamoxifen</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-enhances-tamoxifen#comments</comments>
		<pubDate>Tue, 01 May 2012 18:39:11 +0000</pubDate>
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		<description><![CDATA[Food Chem Toxicol. 2011 Feb;49(2):434-40. Epub 2010 Nov 17. &#160; Glycine soya diet synergistically enhances the suppressive effect of tamoxifen and inhibits tamoxifen-promoted hepatocarcinogenesis in 7,12-dimethylbenz[α]anthracene-induced rat mammary tumor model. &#160; Mishra R, Bhadauria S, Murthy PK, Murthy PS. &#160; &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-enhances-tamoxifen">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv1134720459">
<div id="yui_3_2_0_1_1335897151828123">
<p>Food Chem Toxicol. 2011 Feb;49(2):434-40. Epub 2010 Nov 17.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_1_1335897151828132">Glycine soya diet synergistically enhances the suppressive effect of tamoxifen and inhibits tamoxifen-promoted hepatocarcinogenesis in 7,12-dimethylbenz[α]anthracene-induced rat mammary tumor model.</p>
<p>&nbsp;</p>
<p>Mishra R, Bhadauria S, Murthy PK, Murthy PS.</p>
<p>&nbsp;</p>
<p>Division of Toxicology, Central Drug Research Institute, Council of Scientific and Industrial Research (CSIR), Lucknow, India. <a href="mailto:rajeevcdri@gmail.com" rel="nofollow" target="_blank">rajeevcdri@gmail.com</a></p>
<p>&nbsp;</p>
<p>There is increasing interest in phytoestrogens as potential alternatives to synthetic selective estrogen receptor modulators (SERMs) in the prevention and therapy of breast cancer. The present study is aimed at determining whether dietary glycine soya (Glycine max seeds; GS), which is rich in phytoestrogens, can enhance the anti breast cancer efficacy of the SERM tamoxifen (TAM) and the effect of TAM and GS, either alone or in combination, on DMBA-initiated hepatocarcinogenesis in rat. For determination of enhancing effect, rats bearing palpable 7, 12-dimethylbenz[α] anthracene (DMBA)-induced mammary tumors were treated with TAM (10 mg kg(-1)/day) while being fed AIN-93G diet with or without added GS (3×10(4) mg kg(-1)), and the tumor growth was monitored up to 5 weeks of treatment. For determining the effect on hepatocarcinogenesis, DMBA-initiated rats were exposed to TAM and dietary GS as above for 6 weeks during promotion stage in a medium-term bioassay, and the development of placental form of glutathione-S-transferase (GST-P)-expressing preneoplastic liver lesions was quantified. Exposure to both TAM and dietary GS enhanced the anti tumor efficacy of TAM via a combination of tumor cell apoptosis (determined by TUNEL) and inhibition of tumor cell proliferation (determined by PCNA immunostaining) and suppressed the growth of GST-P-positive liver lesions. The findings show that dietary GS enhances the therapeutic efficacy of TAM against mammary tumors and minimizes TAM&#8217;s hepatocarcinogenesis promotion potential.</p>
<p>&nbsp;</p>
<p>Copyright © 2010 Elsevier Ltd. All rights reserved.</p>
</div>
</div>
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		<title>Soy and Breast Cancer Survival</title>
		<link>http://www.mmvbs.com/uncategorized/soy-and-breast-cancer-survival</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-and-breast-cancer-survival#comments</comments>
		<pubDate>Thu, 26 Apr 2012 21:00:58 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[JAMA. 2009 Dec 9;302(22):2437-43. &#160; Soy food intake and breast cancer survival. &#160; Shu XO, Zheng Y, Cai H, Gu K, Chen Z, Zheng W, Lu W. &#160; Department of Medicine, Vanderbilt Epidemiology Center, 2525 West End Ave, Ste 600, &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-and-breast-cancer-survival">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv2032830096">
<div id="yui_3_2_0_1_1335473803765104">
<p id="yui_3_2_0_1_1335473803765123">JAMA. 2009 Dec 9;302(22):2437-43.</p>
<p>&nbsp;</p>
<p>Soy food intake and breast cancer survival.</p>
<p>&nbsp;</p>
<p>Shu XO, Zheng Y, Cai H, Gu K, Chen Z, Zheng W, Lu W.</p>
<p>&nbsp;</p>
<p>Department of Medicine, Vanderbilt Epidemiology Center, 2525 West End Ave, Ste 600, Nashville, TN 37203-1738, USA. <a href="mailto:xiao-ou.shu@vanderbilt.edu" rel="nofollow" target="_blank">xiao-ou.shu@vanderbilt.edu</a></p>
<p>&nbsp;</p>
<p>Comment in</p>
<p>    JAMA. 2009 Dec 9;302(22):2483-4.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_1_1335473803765125">CONTEXT: Soy foods are rich in isoflavones, a major group of phytoestrogens that have been hypothesized to reduce the risk of breast cancer. However, the estrogen-like effect of isoflavones and the potential interaction between isoflavones and tamoxifen have led to concern about soy food consumption among breast cancer patients.</p>
<p>&nbsp;</p>
<p>OBJECTIVE: To evaluate the association of soy food intake after diagnosis of breast cancer with total mortality and cancer recurrence.</p>
<p>&nbsp;</p>
<p>DESIGN, SETTING, AND PARTICIPANTS: The Shanghai Breast Cancer Survival Study, a large, population-based cohort study of 5042 female breast cancer survivors in China. Women aged 20 to 75 years with diagnoses between March 2002 and April 2006 were recruited and followed up through June 2009. Information on cancer diagnosis and treatment, lifestyle exposures after cancer diagnosis, and disease progression was collected at approximately 6 months after cancer diagnosis and was reassessed at 3 follow-up interviews conducted at 18, 36, and 60 months after diagnosis. Annual record linkage with the Shanghai Vital Statistics Registry database was carried out to obtain survival information for participants who were lost to follow-up. Medical charts were reviewed to verify disease and treatment information.</p>
<p>&nbsp;</p>
<p>MAIN OUTCOME MEASURES: Total mortality and breast cancer recurrence or breast cancer-related deaths. Cox regression analysis was carried out with adjustment for known clinical predictors and other lifestyle factors. Soy food intake was treated as a time-dependent variable.</p>
<p>&nbsp;</p>
<p>RESULTS: During the median follow-up of 3.9 years (range, 0.5-6.2 years), 444 deaths and 534 recurrences or breast cancer-related deaths were documented in 5033 surgically treated breast cancer patients. Soy food intake, as measured by either soy protein or soy isoflavone intake, was inversely associated with mortality and recurrence. The hazard ratio associated with the highest quartile of soy protein intake was 0.71 (95% confidence interval [CI], 0.54-0.92) for total mortality and 0.68 (95% CI, 0.54-0.87) for recurrence compared with the lowest quartile of intake. The multivariate-adjusted 4-year mortality rates were 10.3% and 7.4%, and the 4-year recurrence rates were 11.2% and 8.0%, respectively, for women in the lowest and highest quartiles of soy protein intake. The inverse association was evident among women with either estrogen receptor-positive or -negative breast cancer and was present in both users and nonusers of tamoxifen.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_1_1335473803765107">CONCLUSION: Among women with breast cancer, soy food consumption was significantly associated with decreased risk of death and recurrence.</p>
<p>&nbsp;</p>
<p>PMCID: PMC2874068</p>
<p>PMID: 19996398  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/19996398">http://www.ncbi.nlm.nih.gov/pubmed/19996398</a></p>
<p>&nbsp;</p>
</div>
</div>
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		<title>Soy Safety</title>
		<link>http://www.mmvbs.com/uncategorized/soy-safety</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-safety#comments</comments>
		<pubDate>Tue, 24 Apr 2012 20:11:19 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[Climacteric. 2010 Aug;13(4):368-75.   Long-term endometrial and breast safety of a specific, standardized soy extract.   Palacios S, Pornel B, Vázquez F, Aubert L, Chantre P, Marès P.   Palacios Institute of Women&#8217;s Health, Antonio Acuña 9, Madrid, Spain.   &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-safety">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv2073327203">
<div id="yui_3_2_0_5_1335295595765445">
<p id="yui_3_2_0_5_1335295595765576">Climacteric. 2010 Aug;13(4):368-75.</p>
<p id="yui_3_2_0_5_1335295595765574"> </p>
<p>Long-term endometrial and breast safety of a specific, standardized soy extract.</p>
<p id="yui_3_2_0_5_1335295595765569"> </p>
<p id="yui_3_2_0_5_1335295595765567">Palacios S, Pornel B, Vázquez F, Aubert L, Chantre P, Marès P.</p>
<p id="yui_3_2_0_5_1335295595765615"> </p>
<p id="yui_3_2_0_5_1335295595765565">Palacios Institute of Women&#8217;s Health, Antonio Acuña 9, Madrid, Spain.</p>
<p id="yui_3_2_0_5_1335295595765562"> </p>
<p id="yui_3_2_0_5_1335295595765613">OBJECTIVE: To assess the effects of an oral soy isoflavone extract (Phytosoya) on endometrium and breast in postmenopausal women treated for 3 years.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1335295595765560">METHODS: A total of 395 postmenopausal women were included in this international prospective, open-label study. The number of patients who completed the 3-year study was 197. The women were treated for 3 years with a specific, standardized soy isoflavone extract (total 70 mg/day). Endometrial biopsy, transvaginal ultrasonography and mammography were performed before and after 3 years of treatment.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1335295595765537">RESULTS: No case of hyperplasia/cancer was diagnosed among the 192 interpretable biopsies at 3 years. Only one case of simple hyperplasia was diagnosed among 197 post-baseline interpretable biopsies. The endometrial safety of this extract has been demonstrated (point estimate 0.5%). There was no statistically significant change in endometrial thickness after 3 years (98.4% inactive or atrophic and 0.3% proliferative endometrium at 1 year). Mammography results showed no notable change from baseline. No patient in any set developed an ACR classification of 4 or 5 after 3 years of treatment. The global safety was rated as either &#8216;excellent&#8217; or &#8216;good&#8217; by 99.1% of investigators and 99.0% of patients after 3 years of treatment. The adverse events were as follows: eight patients had metrorrhagia and seven patients had at least one breast adverse event: three patients had &#8216;breast pain&#8217;, two patients reported &#8216;breast tenderness&#8217; and two patients had &#8216;hypertrophic breast&#8217; (most of them were possibly treatment-related).</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1335295595765593">CONCLUSIONS: As no case of hyperplasia was diagnosed among the 301 interpretable biopsies at 1 year and there was only one case of simple hyperplasia in the 197 post-baseline biopsies at 3 years, the endometrial safety of this extract has been demonstrated. Furthermore, as demonstrated by the lack of change in endometrial thickness associated with the histologic results, we suggest that this extract does not exert a mitogenic effect on the endometrium. These results suggest that daily administration of 70 mg of a specific, standardized isoflavone extract for 3 years could be a safe treatment for both endometrium and breast.</p>
<p id="yui_3_2_0_5_1335295595765725"> </p>
<p id="yui_3_2_0_5_1335295595765723">PMID: 20380569  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/20380569">http://www.ncbi.nlm.nih.gov/pubmed/20380569</a></p>
<p id="yui_3_2_0_5_1335295595765720"> </p>
</div>
</div>
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		<title>Soy, nuts and heart attacks, Part 2</title>
		<link>http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks-part-2</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks-part-2#comments</comments>
		<pubDate>Tue, 24 Apr 2012 00:18:34 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[ J Nutr. 2009 Jul;139(7):1333-8. Epub 2009 May 6. &#160; Regular consumption of nuts is associated with a lower risk of cardiovascular disease in women with type 2 diabetes. &#160; Li TY, Brennan AM, Wedick NM, Mantzoros C, Rifai N, Hu &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks-part-2">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p> J Nutr. 2009 Jul;139(7):1333-8. Epub 2009 May 6.</p>
<p>&nbsp;</p>
<p>Regular consumption of nuts is associated with a lower risk of cardiovascular disease in women with type 2 diabetes.</p>
<p>&nbsp;<br />
Li TY, Brennan AM, Wedick NM, Mantzoros C, Rifai N, Hu FB.<br />
Department of Nutrition, and 4Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA.</p>
<p>&nbsp;</p>
<p>Higher nut consumption has been associated with lower risk of coronary heart disease (CHD) events in several epidemiologic studies. The study examined the association between intake of nuts and incident cardiovascular disease (CVD) in a cohort of women with type 2 diabetes. For the primary analysis, there were 6309 women with type 2 diabetes who completed a validated FFQ every 2-4 y between 1980 and 2002 and were without CVD or cancer at study entry. Major CVD events included incident myocardial infarction (MI), revascularization, and stroke. During 54,656 person-years of follow-up, there were 452 CHD events (including MI and revascularization) and 182 incident stroke cases. Frequent nut and peanut butter consumption was inversely associated with total CVD risk in age-adjusted analyses. After adjustment for conventional CVD risk factors, consumption of at least 5 servings/wk of nuts or peanut butter [serving size, 28 g (1 ounce) for nuts and 16 g (1 tablespoon) for peanut butter] was significantly associated with a lower risk of CVD (relative risk = 0.56; 95% CI: 0.36-0.89). Furthermore, when we evaluated plasma lipid and inflammatory biomarkers, we observed that increasing nut consumption was significantly associated with a more favorable plasma lipid profile, including lower LDL cholesterol, non-HDL cholesterol, total cholesterol, and apolipoprotein-B-100 concentrations. However, we did not observe significant associations for HDL cholesterol or inflammatory markers. These data suggest that frequent nut and peanut butter consumption is associated with a significantly lower CVD risk in women with type 2 diabetes.</p>
<p>&nbsp;</p>
<p>PMCID: PMC2696988</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696988/">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696988/</a></p>
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		<title>Soy, nuts and heart attacks</title>
		<link>http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks</link>
		<comments>http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks#comments</comments>
		<pubDate>Mon, 23 Apr 2012 22:52:20 +0000</pubDate>
		<dc:creator>admin</dc:creator>
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		<description><![CDATA[Singapore Med J. 2010 Oct;51(10):781-9.   Effects of a soybean protein diet on ovariectomised female albino rats subjected to myocardial infarction.   Hamed GM, Bahgat NM, El-Agaty SM, Soliman GZ, Emara MM. Department of Physiology, Faculty of Medicine, Ain Shams &#8230; <a href="http://www.mmvbs.com/uncategorized/soy-nuts-and-heart-attacks">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div id="yiv943700138">
<div id="yui_3_2_0_22_1333494310754414">
<p>Singapore Med J. 2010 Oct;51(10):781-9.</p>
<p> <br />
Effects of a soybean protein diet on ovariectomised female albino rats subjected to myocardial infarction.</p>
<p> <br />
Hamed GM, Bahgat NM, El-Agaty SM, Soliman GZ, Emara MM.<br />
Department of Physiology, Faculty of Medicine, Ain Shams University, Abbassia Square, Cairo 11566, Arab Republic of Egypt.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_22_1333494310754515">INTRODUCTION: Cardiovascular disease is the leading cause of death among menopausal women in developed countries, mostly due to the loss of endogenous oestrogen protection. Soybean protein (SP) is rich in isoflavone phytoestrogens. This study aimed to determine the effect of SP on ovariectomised rats subjected to myocardial infarction and its possible cardio-protection.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_22_1333494310754561">METHODS: The study was conducted on 30 adult female albino rats, which were divided into three groups: Group I comprised the sham-operated rats; Group II, the ovariectomised (OVX) rats fed a standard diet; and Group III, OVX rats fed a standard diet supplemented with SP (OVX plus SP). The rats were anaesthetised, and electrocardiograms were conducted. The rats were then sacrificed, after which their hearts and livers were removed, weighed and subjected to histopathological examination. Blood was collected to determine the lipid profile, and the levels of total triiodothyronine, tetraiodothyronine (T4), thyroid-stimulating hormone (TSH), creatinine phosphokinase (CPK), lactate dehydrogenase, superoxide dismutase (SOD) and malonedialdehyde (MDA).</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_22_1333494310754593">RESULTS: The biochemical studies showed a significant increase in plasma CPK (Group II), MDA and triacylglycerol (Groups II and III) levels compared to Group I. The plasma SOD showed a significant decrease in Group II compared to Group I. Total cholesterol, low and very low density lipoprotein cholesterol levels showed a significant increase in Group II, and a significant decrease compared to Group I. Significant increases in T4 and TSH were found in Group III compared to Group II.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1335221062862594">II. CONCLUSION: SP intake can be valuable in protecting the heart against an attack of acute myocardial infarction.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1335221062862598">PMID: 21103813  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/21103813">http://www.ncbi.nlm.nih.gov/pubmed/21103813</a></p>
<p>&nbsp;</p>
</div>
</div>
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		<title>Avocado for Arthritis</title>
		<link>http://www.mmvbs.com/uncategorized/avocado-for-arthritis</link>
		<comments>http://www.mmvbs.com/uncategorized/avocado-for-arthritis#comments</comments>
		<pubDate>Tue, 27 Mar 2012 20:16:17 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://www.mmvbs.com/?p=517</guid>
		<description><![CDATA[Osteoarthritis Cartilage. 2007 Nov;15(11):1249-55. Epub 2007 Sep 12. &#160; Avocado soybean unsaponifiables (ASU) suppress TNF-alpha, IL-1beta, COX-2, iNOS gene expression, and prostaglandin E2 and nitric oxide production in articular chondrocytes and monocyte/macrophages. &#160; Au RY, Al-Talib TK, Au AY, Phan &#8230; <a href="http://www.mmvbs.com/uncategorized/avocado-for-arthritis">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p id="yui_3_2_0_5_1332875776578705">Osteoarthritis Cartilage. 2007 Nov;15(11):1249-55. Epub 2007 Sep 12.</p>
<p>&nbsp;</p>
<p>Avocado soybean unsaponifiables (ASU) suppress TNF-alpha, IL-1beta, COX-2, iNOS gene expression, and prostaglandin E2 and nitric oxide production in articular chondrocytes and monocyte/macrophages.</p>
<p>&nbsp;</p>
<p>Au RY, Al-Talib TK, Au AY, Phan PV, Frondoza CG.<br />
Nutramax Laboratories, Inc., Edgewood, MD 21040, USA.</p>
<p>&nbsp;</p>
<p>Comment in<br />
Osteoarthritis Cartilage. 2008 Oct;16(10):1275-6.Osteoarthritis Cartilage. 2008 Sep;16(9):1118-9; author reply 1120.</p>
<p>&nbsp;</p>
<p>OBJECTIVE: To evaluate the effects of avocado soybean unsaponifiables (ASU) on proinflammatory mediators in chondrocytes and monocyte/macrophage-like cells.</p>
<p>&nbsp;</p>
<p>DESIGN: To determine the dose response of ASU, chondrocytes (5 x 10(5) cells/well) were incubated at 5% CO(2), 37 degrees C for 72 h with (1) control media alone or (2) ASU at concentrations of 0.3, 0.9, 2.7, 8.3, and 25 microg/ml. Cells were activated with 20 ng/ml lipopolysaccharide (LPS) for 24 h and cell supernatants were analyzed for prostaglandin E(2) (PGE(2)) and nitrite content. Chondrocytes and THP-1 monocyte/macrophages (5 x 10(5) cells/well) were incubated at 5% CO(2), 37 degrees C for 72 h with (1) control media alone or (2) ASU (25 mug/ml). One set of cells was activated for 1 h with LPS (20 ng/ml) for both reverse-transcriptase PCR and real-time PCR analysis of tumor necrosis factor-alpha (TNF-alpha), interleukin-1-beta (IL-1beta), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS) expression. One set of cells was activated for 24 h to analyze secreted PGE(2) and nitrite levels in the cellular supernatant.</p>
<p>&nbsp;</p>
<p>RESULTS: ASU reduced TNF-alpha, IL-1beta, COX-2, and iNOS expression in LPS-activated chondrocytes to levels similar to nonactivated control levels. The suppression of COX-2 and iNOS expression was paralleled by a significant reduction in PGE(2) and nitrite, respectively, in the cellular supernatant. ASU also reduced TNF-alpha and IL-1beta expression in LPS-activated monocyte/macrophage-like cells.</p>
<p>&nbsp;</p>
<p>CONCLUSION: The present study demonstrates that the anti-inflammatory activity of ASU is not restricted to chondrocytes, but also affects monocyte/macrophage-like cells that serve as a prototype for macrophages in the synovial membrane. These observations provide a scientific rationale for the pain-reducing and anti-inflammatory effects of ASU observed in osteoarthritis patients.</p>
<p>&nbsp;</p>
<p id="yui_3_2_0_5_1332875776578680">PMID: 17845860  [PubMed - indexed for MEDLINE]</p>
<p>&nbsp;</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/17845860">http://www.ncbi.nlm.nih.gov/pubmed/17845860</a></p>
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