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脑梗死急性期患者血小板膜糖蛋白Ia C807T基因多态性和血小板功能
引用本文:沈明强,石冬敏,程庆璋,戴兰.脑梗死急性期患者血小板膜糖蛋白Ia C807T基因多态性和血小板功能[J].微循环学杂志,2013,23(1):28-30,5,1.
作者姓名:沈明强  石冬敏  程庆璋  戴兰
作者单位:1. 南京医科大学附属苏州医院神经内科,苏州,215002
2. 南京医科大学附属苏州医院检验科,苏州,215002
3. 苏州大学附属第一医院,江苏省血液研究所,苏州,215006
摘    要:目的:探讨血小板膜糖蛋白(GP)Ia C807T基因多态性及与脑梗死急性期患者血小板功能的关系。方法:应用聚合酶链反应限制性片段长度多态性(PCR-RELP)方法检测97例急性期脑梗死患者(脑梗死组)及99例正常对照者(对照组)的GPIa C807T基因型,采用全血流式细胞术检测血小板P选择素(CD62P)表达率,采用比浊法检测花生四烯酸、二磷酸腺苷诱导的血小板最大聚集率(MARAA、MARADP)。结果:脑梗死组GPIa T等位基因频率高于对照组,差异有统计学意义(χ2=5.369,P<0.05);脑梗死组CD62P表达率、血小板MARAA、MARADP高于对照组(P<0.05)。对照组TT+CT基因型CD62P表达率和MARADP高于CC基因型(P<0.05);脑梗死组TT+CT基因型CD62P表达率和MARAA、MARADP与CC基因型差异无统计学意义(P>0.05)。结论:GPIaC807T可能是脑梗死发病的遗传危险因素。血小板活化和聚集功能增强可能是T等位基因促进脑梗死发病的机制之一。

关 键 词:脑梗死  血小板  活化  聚集  血小板膜蛋白Ia  基因多态性

Research of Platelet Glycoprotein Ia C807T Gene Golymorphism and the Function of Platelet in Acute Cerebral Infarction
Shen Mingqiang,Shi Dongmin,Cheng Qingzhang,Dai Lan.Research of Platelet Glycoprotein Ia C807T Gene Golymorphism and the Function of Platelet in Acute Cerebral Infarction[J].Chinese Journal of Microcirculation,2013,23(1):28-30,5,1.
Authors:Shen Mingqiang  Shi Dongmin  Cheng Qingzhang  Dai Lan
Institution:1Department of Neurology; 2Department of Clinical Laboratory; Suzhou Hospital Affiliated Nanjing Medical University, Suzhou 215002,China; 3The First Affiliated Hospital of Suzhou University, Jiangsu Institute of Hematology, Suzhou 215006,China;
Abstract:Objective: To investigate the platelet glycoprotein Ia(GPIa) C807T gene polymorphism and the association of function of platelet in acute cerebral infarction. Method: By PCR-restriction fragment length polymorphism technique, GPIa C807T genotypes were detected in 97 patients with cerebral infarction(cerebral infarction group) and 99 healthy controls(control group). P-selectin(CD62P) was measured by flow cytometry, arachidonic acid-induced platelet maximal aggregation rate (MARAA),adenosine diphosphate-induced platelet maximal aggregation rate(MARADP ) were performed by turbidimetry. Results: The frequencies of GPIa T allele were significantly higher in the infarction group than in the control (χ2=5.369,P<0.05). The expression of CD62P and platelet MAR were significantly higher in the infarction group than in the control (P<0.05). The expression of CD62P and platelet MARADP in the control group with T allele were significantly higher than in those with CC genotype (P<0.05). The expression of CD62P and platelet MAR in the cerebral infarction group with T allele were not significantly higher than in those with CC genotype (P>0.05). Conclusion: GP Ia C807T allele might be an independent risk factor in the development of cerebral infarction. Enhanced platelet function might be one of the mechanisms of T allele in the pathogenesis of cerebral infarction.
Keywords:Cerebral infarction  Platelet  Activation  Aggregation  Platelet glycoprotein Ia  Gene polymorphism
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