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血小板糖蛋白IIIa的PIA1/A2多态性与心肌梗死、中风和静脉血栓形成的风险

PIA1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke, and venous thrombosis.

作者信息

Ridker P M, Hennekens C H, Schmitz C, Stampfer M J, Lindpaintner K

机构信息

Division of Preventive Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

Lancet. 1997 Feb 8;349(9049):385-8. doi: 10.1016/S0140-6736(97)80010-4.

Abstract

BACKGROUND

The gene encoding the platelet glycoprotein IIIa receptor (GPIIIa), shows polymorphism (PIA1/A2). In a previous study, men with acute coronary ischaemia were more likely than controls to carry the PIA2 allele. This receptor has an important role in acute thrombus formation; these findings therefore raise the possibility of inherited platelet risk factors for both arterial and venous thrombosis. We investigated whether the PIA2 allele is associated with myocardial infarction, stroke, and venous thrombosis in a large prospective cohort of men in the USA.

METHODS

14916 initially healthy men participating in the Physicians Health Study provided baseline blood specimens for DNA analysis and were followed prospectively for a mean of 8.6 years. 374 men had a first myocardial infarction, 209 stroke, and 121 venous thrombosis during follow-up (704 cases). Distribution of the PIA1/A2 polymorphism was investigated by a PCR based on restriction-fragment length polymorphism in these men and in a sample of 704 matched study participants who remained free of thrombosis during follow-up (controls).

FINDINGS

The frequency of the PIA2 allele was similar to the control frequency (14.8%) among men who had myocardial infarction (13.5%, p = 0.4), stroke (13.4%, p = 0.5), or venous thrombosis (14.5%, p = 0.9). The relative risk of any vascular event among men homozygous or heterozygous for PIA2 compared with men homozygous for PIA1 was 0.96 (95% CI 0.8-1.2). We found no evidence of association between the PIA2 allele and myocardial infarction (relative risk 0.93 [95 0.7-1.2]), stroke (0.93 [0.7-1.3]), or venous thrombosis (1.07 [0.7-1.6]). There was no evidence of association in subgroup analyses by age, smoking status, and presence of family history of premature coronary disease, hypercholesterolaemia, hypertension, or diabetes. Aspirin use had no effect on these findings.

INTERPRETATION

In a large cohort of apparently healthy men, carriage of the GPIIIa PIA2 allele was not associated with any increase in subsequent risk of myocardial infarction, stroke, or venous thrombosis.

摘要

背景

编码血小板糖蛋白IIIa受体(GPIIIa)的基因存在多态性(PIA1/A2)。在先前的一项研究中,急性冠状动脉缺血男性比对照组更有可能携带PIA2等位基因。该受体在急性血栓形成中起重要作用;因此,这些发现增加了动脉和静脉血栓形成存在遗传性血小板危险因素的可能性。我们在美国一大群男性前瞻性队列中研究了PIA2等位基因是否与心肌梗死、中风和静脉血栓形成相关。

方法

14916名最初健康的男性参与了医师健康研究,提供了用于DNA分析的基线血样,并进行了平均8.6年的前瞻性随访。随访期间,374名男性发生首次心肌梗死,209名发生中风,121名发生静脉血栓形成(共704例病例)。通过基于限制性片段长度多态性的聚合酶链反应(PCR)研究了这些男性以及704名在随访期间未发生血栓形成的匹配研究参与者样本(对照组)中PIA1/A2多态性的分布。

研究结果

在发生心肌梗死的男性中(13.5%,p = 0.4)、中风的男性中(13.4%,p = 0.5)或静脉血栓形成的男性中(14.5%,p = 0.9),PIA2等位基因的频率与对照组频率(14.8%)相似。与PIA1纯合子男性相比,PIA2纯合子或杂合子男性发生任何血管事件的相对风险为0.96(95%可信区间0.8 - 1.2)。我们没有发现PIA2等位基因与心肌梗死(相对风险0.93 [95%可信区间0.7 - 1.2])、中风(0.93 [0.7 - 1.3])或静脉血栓形成(1.07 [0.7 - 1.6])之间存在关联的证据。按年龄、吸烟状况以及是否存在早发冠心病、高胆固醇血症、高血压或糖尿病家族史进行亚组分析时,也没有发现关联的证据。阿司匹林的使用对这些结果没有影响。

解读

在一大群看似健康的男性中,携带GPIIIa PIA2等位基因与随后发生心肌梗死、中风或静脉血栓形成的风险增加无关。

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