Literature DB >> 10822123

The estrogen replacement and atherosclerosis (ERA) study: study design and baseline characteristics of the cohort.

D M Herrington1, D M Reboussin, K P Klein, P C Sharp, S A Shumaker, T E Snyder, K R Geisinger.   

Abstract

The Estrogen Replacement and Atherosclerosis (ERA) trial is a three-arm, randomized, placebo-controlled, double-blind trial to evaluate the effects of estrogen replacement therapy (0.625 mg/day oral conjugated estrogen) with or without continuous low-dose progestin (2.5 mg oral medroxyprogesterone acetate/day) versus placebo on progression of atherosclerosis. A total of 309 postmenopausal women at five sites underwent baseline coronary angiography and were randomized. Participants will have repeat coronary angiography after an average of 3.25 years of treatment. The primary outcome of interest will be change in minimum diameter of the major epicardial segments, as assessed by quantitative coronary angiography. The primary aim is to test the hypothesis that either form of hormone therapy will slow the progression or induce regression of coronary atherosclerosis compared to placebo. The secondary aims are to assess the effects of the two treatments versus placebo on endothelial function (measured using flow-mediated vasodilator responses), on several presumed mediators of estrogen's effect on atherosclerosis (i.e., plasma lipids and lipoproteins, blood pressure, glucose metabolism, hemostatic factors, and antioxidant activity), on other factors that influence the development of coronary heart disease (i.e., diet, smoking status, exercise, weight, and health-related quality of life issues), and on clinical cardiovascular events. The ERA trial is the first angiographic endpoint clinical trial to examine the effects of postmenopausal hormone replacement on coronary atherosclerosis in women. It will provide an unparalleled opportunity to determine if either regimen of hormone therapy is effective in slowing the progress of angiographically defined coronary atherosclerosis. This study will complement other estrogen replacement trials, such as the PEPI, HERS, and Women's Health Initiative studies, to provide a more comprehensive examination of the effects of estrogen replacement on cardiovascular risk factors, anatomic and functional manifestations of atherosclerosis, and risk for coronary heart disease in postmenopausal women. Control Clin Trials 2000;21:257-285

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Year:  2000        PMID: 10822123     DOI: 10.1016/s0197-2456(00)00054-4

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN: 0197-2456


  12 in total

Review 1.  Long-term hormone therapy for perimenopausal and postmenopausal women.

Authors:  Jane Marjoribanks; Cindy Farquhar; Helen Roberts; Anne Lethaby; Jasmine Lee
Journal:  Cochrane Database Syst Rev       Date:  2017-01-17

2.  Effect of hormone replacement therapy on plasma lipoprotein levels and coronary atherosclerosis progression in postmenopausal women according to type 2 diabetes mellitus status.

Authors:  Stefania Lamon-Fava; David M Herrington; Katalin V Horvath; Ernst J Schaefer; Bela F Asztalos
Journal:  Metabolism       Date:  2010-06-26       Impact factor: 8.694

Review 3.  Hormone replacement therapy for preventing cardiovascular disease in post-menopausal women.

Authors:  Sánchez R Gabriel; L Carmona; M Roque; Gómez L M Sánchez; X Bonfill
Journal:  Cochrane Database Syst Rev       Date:  2005-04-18

4.  Dietary fats, carbohydrate, and progression of coronary atherosclerosis in postmenopausal women.

Authors:  Dariush Mozaffarian; Eric B Rimm; David M Herrington
Journal:  Am J Clin Nutr       Date:  2004-11       Impact factor: 7.045

5.  Research into Specific Modulators of Vascular Sex Hormone Receptors in the Management of Postmenopausal Cardiovascular Disease.

Authors:  Graciliano R A do Nascimento; Yaskara V R Barros; Amanda K Wells; Raouf A Khalil
Journal:  Curr Hypertens Rev       Date:  2009-11

6.  Novel circulating fatty acid patterns and risk of cardiovascular disease: the Cardiovascular Health Study.

Authors:  Fumiaki Imamura; Rozenn N Lemaitre; Irena B King; Xiaoling Song; Alice H Lichtenstein; Nirupa R Matthan; David M Herrington; David S Siscovick; Dariush Mozaffarian
Journal:  Am J Clin Nutr       Date:  2012-10-24       Impact factor: 7.045

7.  Interleukin-10 concentration and coronary heart disease (CHD) event risk in the estrogen replacement and atherosclerosis (ERA) study.

Authors:  Susan G Lakoski; Yongmei Liu; K Bridget Brosnihan; David M Herrington
Journal:  Atherosclerosis       Date:  2007-08-13       Impact factor: 5.162

8.  Association of polymorphisms in genes involved in lipoprotein metabolism with plasma concentrations of remnant lipoproteins and HDL subpopulations before and after hormone therapy in postmenopausal women.

Authors:  Stefania Lamon-Fava; Bela F Asztalos; Timothy D Howard; David M Reboussin; Katalin V Horvath; Ernst J Schaefer; David M Herrington
Journal:  Clin Endocrinol (Oxf)       Date:  2009-05-29       Impact factor: 3.478

9.  Adherence to 2005 Dietary Guidelines for Americans is associated with a reduced progression of coronary artery atherosclerosis in women with established coronary artery disease.

Authors:  Fumiaki Imamura; Paul F Jacques; David M Herrington; Gerard E Dallal; Alice H Lichtenstein
Journal:  Am J Clin Nutr       Date:  2009-05-13       Impact factor: 7.045

10.  Changes in remnant and high-density lipoproteins associated with hormone therapy and progression of coronary artery disease in postmenopausal women.

Authors:  Stefania Lamon-Fava; David M Herrington; David M Reboussin; Michelle Sherman; Katalin Horvath; Ernst J Schaefer; Bela F Asztalos
Journal:  Atherosclerosis       Date:  2008-12-24       Impact factor: 5.162

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