Literature DB >> 9198254

Postmenopausal hormone replacement therapy and cardiovascular disease.

C U Chae1, P M Ridker, J E Manson.   

Abstract

Cardiovascular disease is the leading cause of mortality in postmenopausal women in developed countries. A possible cardioprotective role of hormone replacement therapy (HRT) is suggested by epidemiologic studies of HRT and reduced risk of coronary heart disease, as well as by randomized trials of HRT and lipid subfractions. Estrogen has beneficial effects on the lipid profile, raising high-density lipoprotein cholesterol levels and reducing low-density lipoprotein cholesterol levels each by approximately 10%. Other possible biologic mechanisms include beneficial effects on vascular function, oxidative status, endothelial-dependent vasodilation, intimal hyperplasia and insulin sensitivity. Estrogen's net effects on coagulation and fibrinolysis are less clear. Estrogen replacement therapy is associated with decreased atherosclerosis in several animal models. However, most of the available data on HRT derive from observational studies or small randomized trials assessing biologic intermediates rather than clinical events. Further research, including large-scale randomized clinical trials, are required to evaluate definitively the role of estrogen replacement therapy, especially given uncertainties about the effects of combined estrogen-progestin therapy and the balance of benefits and risk of this common intervention in postmenopausal women.

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Year:  1997        PMID: 9198254

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  5 in total

1.  Phytoestrogen alpha-zearalanol inhibits atherogenesis and improves lipid profile in ovariectomized cholesterol-fed rabbits.

Authors:  Shunling Dai; Jinhong Duan; Yuan Lu; Yihua Zhang; Jinxuan Cheng; Jun Ren; Xiaoyuan Zhao; Yunqing Wu; Yue Yu; Pingping Zuo; Yiyong Wu; Qinsheng Ge
Journal:  Endocrine       Date:  2004-11       Impact factor: 3.633

2.  Estrogen receptor-alpha mediates gender differences in atherosclerosis induced by HIV protease inhibitors.

Authors:  Kimberly F Allred; Eric J Smart; Melinda E Wilson
Journal:  J Biol Chem       Date:  2005-11-18       Impact factor: 5.157

3.  Estrogen receptor alpha is a major mediator of 17beta-estradiol's atheroprotective effects on lesion size in Apoe-/- mice.

Authors:  J B Hodgin; J H Krege; R L Reddick; K S Korach; O Smithies; N Maeda
Journal:  J Clin Invest       Date:  2001-02       Impact factor: 14.808

4.  Interactions between endothelial nitric oxide synthase and sex hormones in vascular protection in mice.

Authors:  Jeffrey B Hodgin; Joshua W Knowles; Hyung-Suk Kim; Oliver Smithies; Nobuyo Maeda
Journal:  J Clin Invest       Date:  2002-02       Impact factor: 14.808

5.  Endothelial dysfunction of resistance vessels in female apolipoprotein E-deficient mice.

Authors:  Maine S Cola; Agata L Gava; Silvana S Meyrelles; Elisardo C Vasquez
Journal:  Lipids Health Dis       Date:  2010-05-19       Impact factor: 3.876

  5 in total

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