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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Angiotensinogen gene polymorphism as a risk factor for ischemic stroke.
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Angiotensinogen gene polymorphism as a risk factor for ischemic stroke.

机译:血管紧张素原基因多态性是缺血性中风的危险因素。

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While gene polymorphism for angiotensinogen (AGT) is reported to contribute to the regulation of blood pressure and salt sensitivity, its effect on the risk of ischemic stroke remains controversial. We hypothesized that polymorphism of the AGT gene could be a risk factor for ischemic stroke. Major clinical risk factors and the AGT gene M235T polymorphism were examined in 147 consecutive stroke patients and 133 healthy age-matched controls. All patients were categorized into four stroke types (single lacuna, multiple lacunae, large-artery atherosclerosis and branch atheromatous disease in brainstem) and two vascular groups (large and perforating arterial lesions). The AGT gene M allele significantly increased the risk of single lacuna, multiple lacunae and small arterial lesions, in male patients (p=0.029, 0.031 and 0.026, respectively). Synergistic effects of the AGT gene polymorphism and clinical risks were not observed. In conclusion, AGT M allele may present a risk of lacunar infarctions in Japanesemen, independent of hypertension.
机译:虽然据报道血管紧张素原(AGT)基因多态性有助于血压和盐敏感性的调节,但其对缺血性中风风险的影响仍存在争议。我们假设AGT基因的多态性可能是缺血性中风的危险因素。在147名连续卒中患者和133名年龄匹配的健康对照者中检查了主要的临床危险因素和AGT基因M235T多态性。所有患者均分为四种中风类型(单腔,多腔,大动脉粥样硬化和脑干分支动脉粥样硬化疾病)和两个血管组(大动脉和穿孔动脉病变)。在男性患者中,AGT基因M等位基因显着增加了单个腔隙,多个腔隙和小动脉病变的风险(分别为p = 0.029、0.031和0.026)。没有观察到AGT基因多态性与临床风险的协同作用。总之,AGT M等位基因可能存在日本人腔隙性梗塞的危险,而与高血压无关。

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