Kooperberg Charles, Cushman Mary, Hsia Judith, Robinson Jennifer G, Aragaki Aaron K, Lynch John K, Baird Alison E, Johnson Karen C, Kuller Lewis H, Beresford Shirley A A, Rodriguez Beatriz
Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
PLoS Clin Trials. 2007 Jun 15;2(6):e28. doi: 10.1371/journal.pctr.0020028.
The Women's Health Initiative hormone trials identified a 44% increase in ischemic stroke risk with combination estrogen plus progestin and a 39% increase with estrogen alone. We undertook a case-control biomarker study to elucidate underlying mechanisms, and to potentially identify women who would be at lower or higher risk for stroke with postmenopausal hormone therapy (HT).
The hormone trials were randomized, double-blind, and placebo controlled.
The Women's Health Initiative trials were conducted at 40 clinical centers in the United States.
The trials enrolled 27,347 postmenopausal women, aged 50-79 y.
We randomized 16,608 women with intact uterus to conjugated estrogens 0.625 mg with medroxyprogesterone acetate 2.5 mg daily or placebo, and 10,739 women with prior hysterectomy to conjugated estrogens 0.625 mg daily or placebo.
Stroke was ascertained during 5.6 y of follow-up in the estrogen plus progestin trial and 6.8 y of follow-up in the estrogen alone trial.
No baseline clinical characteristics, including gene polymorphisms, identified women for whom the stroke risk from HT was higher. Paradoxically, women with higher baseline levels of some stroke-associated biomarkers had a lower risk of stroke when assigned to estrogen plus progestin compared to placebo. For example, those with higher IL-6 were not at increased stroke risk when assigned to estrogen plus progestin (odds ratio 1.28) but were when assigned to placebo (odds ratio 3.47; p for difference = 0.02). Similar findings occurred for high baseline PAP, leukocyte count, and D-dimer. However, only an interaction of D-dimer during follow-up interaction with HT and stroke was marginally significant (p = 0.03).
Biomarkers did not identify women at higher stroke risk with postmenopausal HT. Some biomarkers appeared to identify women at lower stroke risk with estrogen plus progestin, but these findings may be due to chance.
妇女健康倡议激素试验发现,联合使用雌激素加孕激素会使缺血性中风风险增加44%,单独使用雌激素则会使其增加39%。我们开展了一项病例对照生物标志物研究,以阐明潜在机制,并有可能识别出接受绝经后激素治疗(HT)时中风风险较低或较高的女性。
激素试验为随机、双盲且安慰剂对照试验。
妇女健康倡议试验在美国的40个临床中心进行。
试验招募了27347名年龄在50 - 79岁的绝经后女性。
我们将16608名子宫完好的女性随机分为两组,一组每日服用0.625毫克结合雌激素与2.5毫克醋酸甲羟孕酮,另一组服用安慰剂;将10739名曾做过子宫切除术的女性随机分为两组,一组每日服用0.625毫克结合雌激素,另一组服用安慰剂。
在雌激素加孕激素试验的5.6年随访期以及单独使用雌激素试验的6.8年随访期内确定中风情况。
没有任何基线临床特征,包括基因多态性,能够识别出接受HT时中风风险较高的女性。矛盾的是,与安慰剂相比,一些中风相关生物标志物基线水平较高的女性在被分配接受雌激素加孕激素治疗时中风风险较低。例如,白细胞介素 - 6水平较高的女性在被分配接受雌激素加孕激素治疗时中风风险并未增加(比值比为1.28),但在被分配接受安慰剂治疗时中风风险增加(比值比为3.47;差异p值 = 0.02)。高基线PAP、白细胞计数和D - 二聚体也出现了类似的结果。然而,仅随访期间D - 二聚体与HT及中风的相互作用具有微弱的显著性(p = 0.03)。
生物标志物无法识别出接受绝经后HT时中风风险较高的女性。一些生物标志物似乎能识别出接受雌激素加孕激素治疗时中风风险较低的女性,但这些发现可能是偶然的。