止血变量与心血管疾病和总死亡率的关系:格拉斯哥莫妮卡研究

G. Lowe, S. Peters, A. Rumley, H. Tunstall-Pedoe, M. Woodward
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引用次数: 1

摘要

血浆中除纤维蛋白原外的止血因子水平与心血管疾病(CVD)和全因死亡率的关系尚不明确。在格拉斯哥MONICA研究的两个阶段,我们检测了凝血因子(VII, VIII, IX和血管性血友病因子),凝血抑制剂(抗凝血酶,蛋白C,蛋白S),凝血激活标志物(凝血酶原片段1 + 2,凝血酶-抗凝血酶复合物,d -二聚体),以及纤维蛋白溶解因子,组织纤溶酶原激活物(t-PA)抗原和纤溶酶原激活物抑制剂1型。在15至20年的时间里,我们随访了382至1123名年龄在30至74岁之间的男性和女性,没有基线CVD, CVD风险和死亡率。年龄和性别调整后的心血管疾病风险比(hr)(前三分之一vs后三分之一)仅在因子VIII (1.30;95%置信区间[CI], 1.06-1.58)和因子IX (1.18;95% ci, 1.01-1.39);进一步校正心血管疾病危险因素后,这些hr分别为1.17 (95% CI, 0.94-1.46)和1.07 (95% CI, 0.92-1.25)。相比之下,因子VIII (HR, 1.63;95% CI, 1.35-1.96), d -二聚体(HR, 2.34;95% CI, 1.26-4.35), t-PA (HR, 2.81;95% CI, 1.43-5.54)与完全危险因素调整后的死亡率密切相关。需要进一步的研究,包括荟萃分析,来评估这些止血因子与中风和心脏病风险以及死亡原因的关系。
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Associations of Hemostatic Variables with Cardiovascular Disease and Total Mortality: The Glasgow MONICA Study
The associations of plasma levels of hemostatic factors, other than fibrinogen, with risks of cardiovascular disease (CVD) and all-cause mortality are not well defined. In two phases of the Glasgow MONICA study, we assayed coagulation factors (VII, VIII, IX, and von Willebrand factor), coagulation inhibitors (antithrombin, protein C, protein S), coagulation activation markers (prothrombin fragment 1 + 2, thrombin–antithrombin complexes, D-dimer), and the fibrinolytic factors, tissue plasminogen activator (t-PA) antigen and plasminogen activator inhibitor type 1. Over 15 to 20 years, we followed up between 382 and 1,123 men and women aged 30 to 74 years, without baseline CVD, for risks of CVD and mortality. Age- and sex-adjusted hazard ratios (HRs) for CVD (top third vs bottom third) were significant only for factor VIII (1.30; 95% confidence interval [CI], 1.06–1.58) and factor IX (1.18; 95% CI, 1.01–1.39); these HRs were attenuated by further adjustment for CVD risk factors: 1.17 (95% CI, 0.94–1.46) and 1.07 (95% CI, 0.92–1.25), respectively. In contrast, factor VIII (HR, 1.63; 95% CI, 1.35–1.96), D-dimer (HR, 2.34; 95% CI, 1.26–4.35), and t-PA (HR, 2.81; 95% CI, 1.43–5.54) were strongly associated with mortality after full risk factor adjustment. Further studies, including meta-analyses, are required to assess the associations of these hemostatic factors with the risks of stroke and heart disease and causes of mortality.
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