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凝血因子XIII - A基因中的常见突变(VAL34Leu):原发性脑出血的危险因素对动脉粥样硬化血栓形成性疾病具有保护作用。

A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.

作者信息

Gemmati D, Serino M L, Ongaro A, Tognazzo S, Moratelli S, Resca R, Moretti M, Scapoli G L

机构信息

Department of Biomedical Sciences and Advanced Therapies, Centre for the Study of Haemostasis and Thrombosis, University of Ferrara, Ferrara, Italy.

出版信息

Am J Hematol. 2001 Jul;67(3):183-8. doi: 10.1002/ajh.1104.

Abstract

The role of a common polymorphism in the factor XIII A-subunit gene (FXIII Val34Leu) has been recently investigated as a protective genetic factor against arterial and venous thrombosis. In addition, the less frequent Leu34 allele has been described as a risk factor for intracerebral hemorrhage. We evaluated the prevalence of this polymorphism by PCR in three case-control studies of patients diagnosed as having primary intracerebral hemorrhage (PCH, n = 130), coronary heart diseases (CHD, n = 240; myocardial infarction/no myocardial infarction, 120/120), and cerebrovascular diseases (CVD, n = 240; cerebral infarction/transient ischaemic attack, 120/120). The matched control groups consisted of patients admitted to the hospital without history of vascular disease. In addition, 200 healthy subjects were investigated. The frequency of the mutated allele (Leu34) was higher in patients with PCH than in controls (33.8% vs. 23.1%, P = 0.009) and lower in CHD and CVD patients compared to controls (18.1% vs. 25.2%, P = 0.010 and 17.3% vs. 24.2%, P = 0.011, respectively). Moreover, among the patients with CHD, the Leu34 allele was underrepresented in cases with myocardial infarction than without (12.9% vs. 23.3%, P = 0.004) and than in controls (12.9% vs. 25.2%, P < 0.001). Similar findings were obtained in patients with CVD comparing the cases with cerebral infarction versus cases with transient ischaemic attack (12.5% vs. 22.1%, P = 0.008) and versus controls (12.5% vs. 24.2%, P < 0.001). Finally, considering altogether the groups of ischaemic patients (CHD and CVD, n = 480), it was noted a trend towards a higher mean age of the clinical onset in homozygotes for the Leu allele than in the wild types (P = 0.078). This study indicates that in our population possession of the FXIII Val34Leu mutation predisposes to the occurrence of primary intracerebral hemorrhage and protects against cerebral and myocardial infarction. A wider modulatory role in the progression and onset of atherothrombotic diseases could be ascribed to FXIII Val34Leu.

摘要

最近,凝血因子 XIII A 亚基基因中的一种常见多态性(FXIII Val34Leu)作为抗动脉和静脉血栓形成的保护性遗传因素受到了研究。此外,较罕见的 Leu34 等位基因被描述为脑出血的危险因素。我们通过聚合酶链反应(PCR)在三项病例对照研究中评估了这种多态性的患病率,这些研究的对象分别为被诊断患有原发性脑出血(PCH,n = 130)、冠心病(CHD,n = 240;心肌梗死/无心肌梗死,120/120)和脑血管疾病(CVD,n = 240;脑梗死/短暂性脑缺血发作,120/120)的患者。匹配的对照组由无血管疾病病史的住院患者组成。此外,还对 200 名健康受试者进行了调查。PCH 患者中突变等位基因(Leu34)的频率高于对照组(33.8% 对 23.1%,P = 0.009),而 CHD 和 CVD 患者中的该频率低于对照组(分别为 18.1% 对 25.2%,P = 0.010;17.3% 对 24.2%,P = 0.011)。此外,在 CHD 患者中,与无心肌梗死的患者相比,Leu34 等位基因在心肌梗死患者中所占比例较低(12.9% 对 23.3%,P = 0.004),且低于对照组(12.9% 对 25.2%,P < 0.001)。在 CVD 患者中,比较脑梗死患者与短暂性脑缺血发作患者以及与对照组时也获得了类似的结果(分别为 12.5% 对 22.1%,P = 0.008;12.5% 对 24.2%)。最后,综合考虑缺血性疾病患者组(CHD 和 CVD,n = 480),发现 Leu 等位基因纯合子的临床发病平均年龄有高于野生型的趋势(P = 0.078)。这项研究表明,在我们研究的人群中,拥有 FXIII Val34Leu 突变易引发原发性脑出血,但可预防脑梗死和心肌梗死。FXIII Val34Leu 可能在动脉粥样硬化血栓形成疾病的进展和发病中发挥更广泛的调节作用。

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