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凝血因子VIII、ABO血型与缺血性心脏病的发病率

Factor VIII, ABO blood group and the incidence of ischaemic heart disease.

作者信息

Meade T W, Cooper J A, Stirling Y, Howarth D J, Ruddock V, Miller G J

机构信息

MRC Epidemiology and Medical Care Unit, Wolfson Institute of Preventive Medicine, Medical College of St Bartholomew's Hospital, London.

出版信息

Br J Haematol. 1994 Nov;88(3):601-7. doi: 10.1111/j.1365-2141.1994.tb05079.x.

Abstract

Relations of factor VIII activity, FVIIIC, and von Willebrand factor antigen (vWFAg), with ischaemic heart disease (IHD) were examined in 1393 men aged between 40 and 64 years at entry to the Northwick Park Heart Study (NPHS) who experienced 178 first major episodes of IHD during an average follow-up period of 16.1 years. After allowing for the large factor VIII differences between the main ABO blood groups, FVIIIC was probably associated with IHD incidence, possibly more strongly with fatal than non-fatal episodes. Thus, an increase of 1 standard deviation in FVIIIC raised the risk of fatal IHD by about 28%. vWFAg was also significantly associated with fatal events. The observed relation of FVIIIC with IHD incidence probably underestimates the true strength of the association because of the considerable within-person and laboratory variability in factor VIII measurements. FVIIIC and vWFAg were strongly correlated (r = 0.57) and in statistical terms there may be little to choose between them in long-term studies of IHD. Taking account of evidence that haemophiliacs seem to experience less IHD than expected, high factor VIII levels may contribute to the incidence of IHD by increasing thrombogenic potential. The incidence of IHD was significantly higher in those of blood group AB than in those of groups O, A or B, particularly for fatal events. There was no evidence that the FVIIIC and vWFAg associations with IHD are determined by ABO group. The factor VIII and ABO blood group effects therefore appeared to be independent. Group AB may be a genetic marker of characteristics influencing other indices of IHD risk such as short stature, NPHS men (though not women) of group AB being about 2 cm shorter than those of other groups.

摘要

在进入诺斯威克公园心脏研究(NPHS)的1393名年龄在40至64岁之间的男性中,研究了凝血因子VIII活性(FVIIIC)和血管性血友病因子抗原(vWFAg)与缺血性心脏病(IHD)的关系。在平均16.1年的随访期内,这些男性经历了178次首次IHD主要发作。在考虑了主要ABO血型之间凝血因子VIII的巨大差异后,FVIIIC可能与IHD发病率相关,可能与致命性发作的关联比非致命性发作更强。因此,FVIIIC增加1个标准差会使致命性IHD的风险增加约28%。vWFAg也与致命事件显著相关。由于凝血因子VIII测量中存在相当大的个体内和实验室变异性,观察到的FVIIIC与IHD发病率的关系可能低估了关联的真实强度。FVIIIC和vWFAg高度相关(r = 0.57),从统计学角度来看,在IHD的长期研究中,它们之间可能没有太大差别。考虑到有证据表明血友病患者似乎经历的IHD比预期少,高凝血因子VIII水平可能通过增加血栓形成潜力而导致IHD的发生。AB血型者的IHD发病率显著高于O型、A型或B型者,尤其是致命性事件。没有证据表明FVIIIC和vWFAg与IHD的关联由ABO血型决定。因此,凝血因子VIII和ABO血型的影响似乎是独立的。AB血型可能是影响IHD风险其他指标的特征的遗传标记,NPHS中AB血型的男性(女性则不然)比其他组的男性矮约2厘米。

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