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固定剂量华法林降低缺血性心脏病风险因素——凝血因子VII凝血活性(VIIc):一项双盲交叉研究

Reduction of factor VII coagulant activity (VIIC), a risk factor for ischaemic heart disease, by fixed dose warfarin: a double blind crossover study.

作者信息

Poller L, MacCallum P K, Thomson J M, Kerns W

机构信息

UK Reference Laboratory for Anticoagulant Reagents and Control, Withington Hospital, Manchester.

出版信息

Br Heart J. 1990 Apr;63(4):231-3. doi: 10.1136/hrt.63.4.231.

Abstract

An increase in factor VII coagulant activity is known to be an important risk factor for ischaemic heart disease. Four hundred and eight healthy male Post Office workers were screened in an occupational survey. Sixty eight (16.5%) of these had values of factor VII coagulant activity greater than 1.0 SD above the age related mean. A randomised double-blind crossover study was undertaken to investigate the effect of a fixed daily minidose of warfarin (1 mg) on the high activities of factor VII in these men. Forty two agreed to enter the study and 40 completed it. Their mean factor VII coagulant activity before warfarin treatment was 135.9%. Treatment with a fixed minidose of warfarin significantly reduced factor VII coagulant activity to 124.6%; there was no change on placebo. The prothrombin time was also significantly prolonged on active treatment although all the results remained within the normal range. These findings suggested a fixed minidose warfarin regime might be useful in the primary prevention of ischaemic heart disease by reducing high activities of factor VII.

摘要

已知凝血因子VII促凝活性增加是缺血性心脏病的重要危险因素。在一项职业调查中,对408名健康男性邮政工作人员进行了筛查。其中68人(16.5%)的凝血因子VII促凝活性值高于年龄相关平均值1.0个标准差。进行了一项随机双盲交叉研究,以调查每日固定小剂量华法林(1毫克)对这些男性中凝血因子VII高活性的影响。42人同意参加研究,40人完成了研究。他们在华法林治疗前的平均凝血因子VII促凝活性为135.9%。固定小剂量华法林治疗使凝血因子VII促凝活性显著降低至124.6%;安慰剂治疗则无变化。尽管所有结果仍在正常范围内,但在积极治疗时凝血酶原时间也显著延长。这些发现表明,固定小剂量华法林疗法可能通过降低凝血因子VII的高活性而有助于缺血性心脏病的一级预防。

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本文引用的文献

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