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Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease

机译:体重指数全基因组关联研究的路径分析凸显了心血管疾病的风险路径

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摘要

Cardiovascular disease (CVD) is a class of diseases that involve the heart or blood vessels. It is reported that body mass index (BMI) is risk factor for CVD. Genome-wide association studies (GWAS) have recently provided rapid insights into genetics of CVD and its risk factors. However, the specific mechanisms how BMI influences CVD risk are largely unknown. We think that BMI may influences CVD risk by shared genetic pathways. In order to confirm this view, we conducted a pathway analysis of BMI GWAS, which examined approximately 329,091 single nucleotide polymorphisms from 4763 samples. We identified 31 significant KEGG pathways. There is literature evidence supporting the involvement of GnRH signaling, vascular smooth muscle contraction, dilated cardiomyopathy, Gap junction, Wnt signaling, Calcium signaling and Chemokine signaling in CVD. Collectively, our study supports the potential role of the CVD risk pathways in BMI. BMI may influence CVD risk by the shared genetic pathways. We believe that our results may advance our understanding of BMI mechanisms in CVD.
机译:心血管疾病(CVD)是一类涉及心脏或血管的疾病。据报道,体重指数(BMI)是CVD的危险因素。全基因组关联研究(GWAS)最近提供了对CVD遗传学及其危险因素的快速见解。但是,BMI如何影响CVD风险的具体机制尚不清楚。我们认为BMI可能通过共享的遗传途径影响CVD风险。为了证实这种观点,我们进行了BMI GWAS的途径分析,该分析检查了来自4763个样品的大约329,091个单核苷酸多态性。我们确定了31条重要的KEGG途径。有文献证据支持CVD涉及GnRH信号传导,血管平滑肌收缩,扩张型心肌病,Gap连接,Wnt信号传导,钙信号传导和趋化因子信号传导。总体而言,我们的研究支持CVD风险通路在BMI中的潜在作用。 BMI可能通过共享的遗传途径影响CVD风险。我们相信我们的结果可能会加深我们对CVD中BMI机制的理解。

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