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PEAR1 is not a human hypertension-susceptibility gene

机译:PEAR1不是人类高血压易感基因

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摘要

Objective: Platelet endothelial aggregation receptor 1 (PEAR1) is a membrane protein involved in platelet contact-induced activation and sustained platelet aggregation. Experimental studies identified PEAR1, as a candidate gene that may be linked to the blood-pressure driven kidney injury in salt-sensitive Dahl rats. Aim: In a family-based European population study (mean age 39.7 years; 52.2% women), we searched for association of changes in blood pressure or incidence of hypertension with genetic variation in PEAR1. Methods: Among 1973 randomly recruited people, genotyped for PEAR1, we measured blood pressure at baseline and follow-up. Results: Median follow-up was 10.0 years. While accounting for family clusters and blood pressure at baseline and with adjustments applied for sex, age, body mass index, smoking and drinking, total cholesterol, and antihypertensive drug treatment, all associations of systolic and diastolic blood pressure changes with nine single nucleotide polymorphisms (SNPs) in PEAR1 were all non-significant (p ≥ 0.059). With similar adjustments, the incidence of hypertension (397 cases among 1532 participants were normotensive at baseline [25.9%]) was not related to the SNPs in PEAR1 (hazard ratios ≤ 1.09; p ≥ 0.09). Conclusion: Our study suggests that PEAR1 is not a hypertension susceptibility gene in humans.
机译:目的:血小板内皮聚集受体1(PEAR1)是一种参与血小板接触诱导的活化和持续血小板聚集的膜蛋白。实验研究确定,PEAR1是一种候选基因,可能与盐敏感性达尔小鼠的血压驱动的肾损伤有关。目的:在一项基于家庭的欧洲人口研究(平均年龄39.7岁;女性52.2%)中,我们搜索了血压变化或高血压发生率与PEAR1基因变异的关系。方法:在1973年随机入组的PEAR1基因型患者中,我们测量了基线和随访时的血压。结果:中位随访时间为10.0年。在考虑基线时的家庭聚类和血压并针对性别,年龄,体重指数,吸烟和饮酒,总胆固醇和降压药物治疗进行调整后,所有收缩压和舒张压的变化均与9个单核苷酸多态性有关( PEAR1中的SNPs均无统计学意义(p≥0.059)。通过类似的调整,高血压的发生率(1532名参与者中的397例在基线时为血压正常[25.9%])与PEAR1中的SNP无关(危险比≤1.09; p≥0.09)。结论:我们的研究表明PEAR1不是人类的高血压易感基因。

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