Long-term estrogen therapy improves vascular function in male to female transsexuals

被引:151
作者
New, G
Timmins, KL
Duffy, SJ
Tran, BT
OBrien, RC
Harper, RW
Meredith, IT
机构
[1] MONASH MED CTR,CARDIOL UNIT,CARDIOVASC RES CTR,MELBOURNE,VIC 3168,AUSTRALIA
[2] MONASH UNIV,DEPT MED,MELBOURNE,VIC 3004,AUSTRALIA
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0735-1097(97)00080-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study sought to examine the effects of longterm estrogen therapy on vascular function in male to female transsexuals and to compare the findings with those observed in men and premenopausal women. Background. Gender differences in coronary artery disease have largely been attributed to the beneficial effects of estrogen on vascular function and plasma lipids in women. However, the effects of estrogen on the male vasculature have not been widely studied. Methods. We compared the effects of estrogen on vascular function in 14 male to female transsexuals, 14 age-matched men and 15 premenopausal women. Plow-mediated vasodilation and response to nitroglycerin were assessed in the brachial artery using noninvasive ultrasound. Results. Flow-mediated vasodilation was similar in transsexuals and women but greater than that in men ([mean +/- SE] 11.5 +/- 1.3% and 9.4 +/- 1.1% vs, 5.2 +/- 1.0% respectively, p < 0.005). Responses to nitroglycerin were also greater in transsexuals and women than in men (21.6 +/- 1.7% and 21.0 +/- 0.9% vs. 14.5 +/- 1.2%, respectively, p = 0.0005). These differences persisted even after adjusting for vessel size. Despite similar total cholesterol levels, transsexuals had high density lipoprotein cholesterol levels similar to those in women and greater than those observed in men (1.76 +/- 0.12 and 1.82 +/- 0.11 mmol/liter vs. 1.35 +/- 0.07 mmol/liter, respectively, p < 0.005). Moreover, triglyceride levels were greater in transsexuals than in men and women, and low density lipoprotein cholesterol (LDL-C) particle size was smaller (25.7 +/- 0.2 nm vs. 26.2 +/- 0.1 and 26.6 +/- 0.1 nm, respectively, p = 0.0001), Serum testosterone (an index of estrogen therapy in transsexuals) was markedly suppressed in transsexuals and similar to that in women. Univariate analysis revealed that there was a strong inverse correlation between serum testosterone and flow-mediated vasodilation (r(s) = -0.48, p < 0.005). Multivariate analysis revealed that the best combination of predictors of dow-mediated vasodilation was serum testosterone, vessel size and LDL-C (R-2 = 0.3, p < 0.005). Conclusions. Long-term estrogen therapy appears to improve vascular function in male to female transsexuals and occurs despite higher triglyceride levels and the presence of small, dense LDL-C. The beneficial effects of estrogen are not gender specific or solely mediated through endothelium-derived nitric oxide. (C) 1997 by the American College of Cardiology.
引用
收藏
页码:1437 / 1444
页数:8
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