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Journal of Clinical Endocrinology & Metabolism , doi:10.1210/jc.2004-1211
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The Journal of Clinical Endocrinology & Metabolism Vol. 90, No. 2 1041-1046
Copyright © 2005 by The Endocrine Society

Correlating Androgen and Estrogen Steroid Receptor Expression with Coronary Calcification and Atherosclerosis in Men without Known Coronary Artery Disease

Peter Y. Liu, Rose C. Christian, Ming Ruan, Virginia M. Miller and Lorraine A. Fitzpatrick

Division of Endocrinology, Metabolism, Diabetes and Nutrition (P.Y.L., R.C.C., M.R., L.A.F.), Department of Surgery (V.M.M.) and Department of Physiology and Biophysics (V.M.M.), Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905

Address all correspondence and requests for reprints to: Peter Y. Liu, M.B.B.S., Ph.D., Division of Endocrinology, Harbor-UCLA Medial Center, 1000 West Carson Street, Box 446, Torrance, California 90502. E-mail: pliu{at}labiomed.org.

Background: Accumulating data emphasize the gender specificity of key components of the atherosclerotic process and the importance of gonadal steroids on the human vasculature. Steroid receptors, including the androgen receptor (AR) and estrogen receptors (ERs) {alpha} and ß are expressed in key vascular tissues, including endothelial cells and vascular smooth muscle cells. However, the relative abundance and importance of these receptors in the coronary artery are not well defined, particularly in men. We therefore examined AR, ER{alpha}, and ERß expression as a function of key components of atherosclerosis, namely plaque and calcium area, in male human coronary arteries.

Methods: Coronary arteries were obtained at autopsy from 24 men without known coronary artery disease. Coronary calcification was measured by contact microradiography, and atherosclerotic plaque area was quantified histologically. Coronary artery cross-sections were immunostained for AR, ER{alpha}, and ERß and then measured semiquantitatively in each arterial wall layer (intima, adventitia, and media).

Results: AR, ERß, and ER{alpha} were expressed in all artery wall layers but most avidly in the media (P < 0.001). ERß exceeded ER{alpha} expression (P < 0.0005). AR expression in the media correlated negatively with plaque area (P = 0.006, R = –0.55), whereas intimal ERß expression correlated positively with plaque area (P = 0.012, R = 0.50).

Conclusions: We conclude that both AR and ERß are important in relatively early coronary atherosclerosis, but inversely so, because decreasing AR and increasing ERß expression correlate with more extensive atherosclerosis. ERß seems to be the predominate ER in coronary arteries harvested from men without known coronary artery disease. Interventional studies are required to assess the functional significance of these observations.




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