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Dissecting the genetics of complex traits: lessons from hypertension.

机译:剖析复杂性状的遗传学:高血压课程。

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摘要

Summary of key findings:Newton-Cheh et al. (doi: 10.1038g.328) tested the hypothesis that the common variants in the candidate genes coding for the atrial natriuretic peptides (ANP) and brain natriuretic peptides (BNP) (NNPA and NPPB) are associated with blood pressure [1]. Firstly, in 1705 subjects from a general population cohort, 13 variants (single-nucleotide polymorphisms, SNPs) in this genetic locus were selected for association with higher ANP and BNP levels. Subsequently, a meta-analysis involving 14 743 Caucasian subjects confirmed the association for three SNPs. Next, in 29 717 subjects, these SNPs were found to be associated with lower blood pressure and lower risk for hypertension. The strongest effects were found for the SNPs coded rs5068 (minor allele frequency 6%) and rsl98358 (19%) with reductions per allele of 0.9-1.5 mmHg systolic blood pressure (SBP) and 0.3-0.8 mmHg diastolic blood pressure (DBP), and odds ratios for hypertension of 0.85 and 0.90, respectively.
机译:主要发现摘要:Newton-Cheh等。 (doi:10.1038 / ng.328)检验了以下假设:编码心房利钠肽(ANP)和脑利钠肽(BNP)(NNPA和NPPB)的候选基因中的常见变异与血压有关[1]。首先,在1705名来自一般人群的受试者中,选择了该基因座中的13个变异(单核苷酸多态性,SNP)与更高的ANP和BNP水平相关联。随后,一项涉及14 743名白人受试者的荟萃分析证实了三个SNP的关联。接下来,在29 717名受试者中,发现这些SNP与降低血压和降低高血压风险有关。发现对编码rs5068(次等位基因频率为6%)和rsl98358(19%)的SNP的作用最强,每个等位基因减少了0.9-1.5 mmHg收缩压(SBP)和0.3-0.8 mmHg舒张压(DBP),和高血压的比值比分别为0.85和0.90。

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