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Plasminogen activator inhibitor-1 4G/5G polymorphism is associated with metabolic syndrome parameters in Malaysian subjects

机译:纤溶酶原激活物抑制剂1 4G / 5G多态性与马来西亚受试者的代谢综合征参数有关

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摘要

The plasminogen activator inhibitor-1 4G/5G and tissue plasminogen activator Alu-repeat insertion/deletion polymorphisms might be genetic determinations of increased or decreased of their plasma activities. The aim of this study was to investigate the association of plasminogen activator inhibitor-1 4G/5G and tissue plasminogen activator Alu-repeat I/D polymorphisms with metabolic syndrome parameters in normal Malaysian subjects and to assess the impact of these polymorphisms on their plasma activities and antigens. The genetic polymorphisms were genotyped in 130 normal subjects. In addition, the plasma activities and antigens of plasminogen activator inhibitor-1 and tissue plasminogen activator as well as levels of insulin, glucose, and lipid profile at fasting state were investigated. The subjects with homozygous 4G/4G showed association with an increased triglyceride (p = 0.007), body mass index (p = 0.01) and diastolic blood pressure (p = 0.03). In addition, the plasminogen activator inhibitor-1 4G/5G polymorphism modulates plasma plasminogen activator inhibitor-1 activity and antigen and tissue plasminogen activator activity (p = 0.002, 0.014, 0.003) respectively. These results showed that, the plasminogen activator inhibitor-1 4G/5G polymorphism is associated with metabolic syndrome parameters, plasminogen activator inhibitor-1 and tissue plasminogen activator activities in Malaysian subjects, and may serve to increase the risk of type 2 diabetes and cardiovascular disease in Malaysian subjects.
机译:纤溶酶原激活物抑制剂1 4G / 5G和组织纤溶酶原激活物Alu-repeat插入/缺失多态性可能是其血浆活性升高或降低的遗传学决定。这项研究的目的是调查正常马来西亚受试者中纤溶酶原激活物抑制剂1 4G / 5G和组织纤溶酶原激活物Alu-repeat I / D多态性与代谢综合征参数的关系,并评估这些多态性对其血浆活性的影响。和抗原。遗传多态性在130名正常受试者中进行了基因分型。此外,研究了空腹状态下纤溶酶原激活物抑制剂-1和组织纤溶酶原激活物的血浆活性和抗原,以及胰岛素,葡萄糖和脂质的水平。具有纯合子4G / 4G的受试者表现出甘油三酸酯增加(p = 0.007),体重指数(p = 0.01)和舒张压(p = 0.03)。此外,纤溶酶原激活物抑制剂1 4G / 5G多态性分别调节血浆纤溶酶原激活物抑制剂1的活性以及抗原和组织纤溶酶原激活物的活性(p = 0.002、0.014、0.003)。这些结果表明,纤溶酶原激活物抑制剂1 4G / 5G多态性与马来西亚受试者的代谢综合征参数,纤溶酶原激活物抑制剂-1和组织纤溶酶原激活物活性有关,可能有助于增加2型糖尿病和心血管疾病的风险在马来西亚科目中。

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