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A Systematically Assembled Signature of Genes to be Deep-Sequenced for Their Associations with the Blood Pressure Response to Exercise

机译:系统组装的基因签名其与运动对血压的反应具有很深的关联性

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摘要

Background: Exercise is one of the best nonpharmacologic therapies to treat hypertension. The blood pressure (BP) response to exercise is heritable. Yet, the genetic basis for the antihypertensive effects of exercise remains elusive. Methods: To assemble a prioritized gene signature, we performed a systematic review with a series of Boolean searches in PubMed (including Medline) from earliest coverage. The inclusion criteria were human genes in major BP regulatory pathways reported to be associated with: (1) the BP response to exercise; (2) hypertension in genome-wide association studies (GWAS); (3) the BP response to pharmacotherapy; (4a) physical activity and/or obesity in GWAS; and (4b) BP, physical activity, and/or obesity in non-GWAS. Included GWAS reports disclosed the statistically significant thresholds used for multiple testing. Results: The search yielded 1422 reports. Of these, 57 trials qualified from which we extracted 11 genes under criteria 1, 18 genes under criteria 2, 28 genes under criteria 3, 27 genes under criteria 4a, and 29 genes under criteria 4b. We also included 41 genes identified from our previous work. Conclusions: Deep-sequencing the exons of this systematically assembled signature of genes represents a cost and time efficient approach to investigate the genomic basis for the antihypertensive effects of exercise.
机译:背景:运动是治疗高血压的最佳非药物疗法之一。血压对运动的反应是可遗传的。然而,运动抗高血压作用的遗传基础仍然难以捉摸。方法:为了组装优先的基因签名,我们从最早的报道中对PubMed(包括Medline)中的一系列布尔搜索进行了系统的综述。纳入标准是主要的BP调节途径中的人类基因,据报道与以下方面有关:(1)BP对运动的反应; (2)全基因组关联研究中的高血压(GWAS); (3)血压对药物治疗的反应; (4a)GWAS中的身体活动和/或肥胖; (4b)非GWAS中的血压,身体活动和/或肥胖。随附的GWAS报告披露了用于多次测试的具有统计意义的阈值。结果:搜索获得1422份报告。在这些合格的57项试验中,我们从标准1下提取11个基因,在标准2下提取18个基因,在标准3下提取28个基因,在标准4a下提取27个基因,在标准4b下提取29个基因。我们还包括了从我们以前的工作中鉴定出的41个基因。结论:对该系统组装的基因签名的外显子进行深度测序代表了一种研究运动抗高血压作用的基因组基础的经济高效的方法。

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