دورية أكاديمية

Tissue Factor Pathway Inhibitor, Activated Protein C Resistance, and Risk of Ischemic Stroke due to Postmenopausal Hormone Therapy

التفاصيل البيبلوغرافية
العنوان: Tissue Factor Pathway Inhibitor, Activated Protein C Resistance, and Risk of Ischemic Stroke due to Postmenopausal Hormone Therapy
المؤلفون: Rossouw, Jacques E., Johnson, Karen C., Pettinger, Mary, Cushman, Mary, Sandset, Per Morten, Kuller, Lewis, Rosendaal, Frits, Rosing, Jan, Wasserthal-Smoller, Sylvia, Martin, Lisa W., Manson, JoAnn E., Lakshminarayan, Kamakshi, Merino, Jose G., Lynch, John
المصدر: Rossouw , J E , Johnson , K C , Pettinger , M , Cushman , M , Sandset , P M , Kuller , L , Rosendaal , F , Rosing , J , Wasserthal-Smoller , S , Martin , L W , Manson , J E , Lakshminarayan , K , Merino , J G & Lynch , J 2012 , ' Tissue Factor Pathway Inhibitor, Activated Protein C Resistance, and Risk of Ischemic Stroke due to Postmenopausal Hormone Therapy ' , Stroke , vol. 43 , no. 4 , pp. 952-957 . https://doi.org/10.1161/STROKEAHA.111.643072Test
سنة النشر: 2012
المجموعة: Maastricht University Research Publications
مصطلحات موضوعية: cerebrovascular accident, estrogen, hemostasis, menopause, randomized controlled trials
الوصف: Background and Purpose-To test whether changes in plasma tissue factor pathway inhibitor (TFPI) levels or activated protein C resistance (normalized activated protein C resistance ratio [nAPCsr]) modify the increased risk of ischemic stroke due to postmenopausal hormone therapy. Methods-Nested case-control study of 455 cases of ischemic stroke and 565 matched control subjects in the Women's Health Initiative trials of postmenopausal hormone therapy. Results-Baseline free TFPI was associated with ischemic stroke risk (OR per SD increase, 1.17; 95% CI, 1.01-1.37; P=0.039), but baseline nAPCsr was not (OR per SD increase, 0.89; 95% CI, 0.75-1.05; P=0.15). Baseline TFPI levels and nAPCsr did not modify the effect of postmenopausal hormone therapy on ischemic stroke. Treatment-induced mean changes of -28% in free TFPI and +65% in nAPCsr did not change the risk of ischemic stroke (interaction P=0.452 and 0.971, respectively). In subgroup analyses, baseline nAPCsr was inversely associated with lacunar strokes (OR per SD increase, 0.74; 95% CI, 0.57-0.96; P=0.025) and baseline free TFPI interacted with treatment to increase large vessel atherosclerotic strokes (P=0.008). Conclusions-Procoagulant changes in TFPI or nAPCsr do not modify the increased ischemic stroke risk due to postmenopausal hormone therapy.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1161/STROKEAHA.111.643072
الإتاحة: https://doi.org/10.1161/STROKEAHA.111.643072Test
https://cris.maastrichtuniversity.nl/en/publications/02420462-0c4f-438f-901b-bbfd1429fe83Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.43C33F86
قاعدة البيانات: BASE