Lee Jennifer S, Yaffe Kristine, Lui Li-Yung, Cauley Jane, Taylor Brent, Browner Warren, Cummings Steven
Division of Endocrinology, Clinical Nutrition, and Vascular Medicine, Department of Internal Medicine, University of California-Davis, 4150 V Street, Sacramento, CA 95817, USA.
Arch Neurol. 2010 Feb;67(2):195-201. doi: 10.1001/archneurol.2009.322.
To test the hypothesis that circulating endogenous estradiol is associated with stroke risk in older postmenopausal women. Stroke incidence increases after menopause, when endogenous estrogen levels fall, yet exogenous estrogen increases strokes in older postmenopausal women. The relation between endogenous estrogen and stroke is unclear.
Prospective case-control study.
Study of Osteoporotic Fractures.
Women at least age 65 years (99% follow-up) who were not taking estrogen at baseline.
Free estradiol index (FEI) was calculated by dividing total estradiol by sex hormone-binding globulin concentrations measured in banked baseline serum. Using logistic regression, odds ratios were estimated for a first-ever atherothrombotic stroke associated with endogenous FEI in 196 women who had a subsequent validated stroke (median follow-up, 8 years) compared with 219 randomly selected women who did not. Potential mediators were assessed in multivariable models.
The age-adjusted odds of atherothrombotic stroke increased with increasing FEI quartiles (P(trend) = .007). Women in the highest FEI quartile had an age-adjusted 2.31-fold (odds ratio, 2.31; 95% confidence interval, 1.28-4.17) higher odds than women in the lowest quartile. Women with greater central adiposity had a suggestively stronger association (P = .08). Atherogenic dyslipidemia, type 2 diabetes mellitus, and C-reactive protein level were potential mediators of this relation.
Endogenous estradiol level is an indicator of stroke risk in older postmenopausal women, especially in those with greater central adiposity. Potential mediators, including atherogenic dyslipidemia, insulin resistance, and inflammation, might underlie this association. Whether estradiol, independent of atherogenic adiposity, influences such mediators and stroke risk needs to be determined. Estrogen-altering agents might be harmful or beneficial depending on endogenous estradiol levels, especially in women with greater central adiposity.
验证绝经后老年女性循环内源性雌二醇与中风风险相关这一假设。绝经后,随着内源性雌激素水平下降,中风发病率升高,但外源性雌激素却会增加绝经后老年女性的中风风险。内源性雌激素与中风之间的关系尚不清楚。
前瞻性病例对照研究。
骨质疏松性骨折研究。
年龄至少65岁(随访率99%)且基线时未服用雌激素的女性。
游离雌二醇指数(FEI)通过将总雌二醇除以储存的基线血清中测得的性激素结合球蛋白浓度来计算。采用逻辑回归分析,对196名随后发生经证实中风(中位随访时间8年)的女性与219名随机选择未发生中风的女性中,与内源性FEI相关的首次动脉粥样硬化血栓形成性中风的比值比进行估计。在多变量模型中评估潜在的中介因素。
经年龄调整后,动脉粥样硬化血栓形成性中风的比值随着FEI四分位数的增加而升高(P趋势=0.007)。FEI四分位数最高的女性经年龄调整后的比值比是最低四分位数女性的2.31倍(比值比为2.31;95%置信区间为1.28 - 4.17)。中心性肥胖程度较高的女性之间的关联更显著(P = 0.08)。动脉粥样硬化性血脂异常、2型糖尿病和C反应蛋白水平是这种关系的潜在中介因素。
内源性雌二醇水平是绝经后老年女性中风风险的一个指标,尤其是在中心性肥胖程度较高的女性中。包括动脉粥样硬化性血脂异常、胰岛素抵抗和炎症在内的潜在中介因素可能是这种关联的基础。雌二醇是否独立于动脉粥样硬化性肥胖影响这些中介因素和中风风险尚需确定。改变雌激素的药物可能有害或有益,这取决于内源性雌二醇水平,尤其是在中心性肥胖程度较高的女性中。