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Association of Common Variants in NPPA and NPPB with Circulating Natriuretic Peptides and Blood Pressure

机译:NPPA和NPPB常见变异与循环利钠肽和血压的关系

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摘要

Blood pressure is a heritable trait, but no common genetic variants contributing to blood pressure in humans have been definitively established. Natriuretic peptides (NP) have blood pressure-lowering properties. Genotyping SNPs at the NPPA/NPPB locus in 14,743 individuals of European ancestry identified associations of plasma atrial natriuretic peptide with rs5068 (P=8×10−70), rs198358 (P=8×10−30), and rs632793 (P=2×10−10), and of plasma B-type natriuretic peptide with rs5068 (P=3×10−12), rs198358 (P=1×10−25), and rs632793 (P=2×10−68). In 29,717 individuals, the alleles of rs5068 and rs198358 related to increased circulating NP concentrations were associated with lower systolic (P=2×10−6 and 6×10−5, respectively) and diastolic blood pressure (P=1×10−6 and 5×10−5), and reduced odds of hypertension (odds ratio 0.85, 95% confidence interval, 0.79–0.92, P=4×10−5; odds ratio 0.90, 95% confidence interval, 0.85–0.95, P=2×10−4, respectively). Common genetic variants related to circulating NP concentrations contribute to inter-individual variation in blood pressure and hypertension.
机译:血压是可遗传的特征,但尚未明确确定导致人类血压升高的常见遗传变异。利钠肽(NP)具有降低血压的特性。在欧洲血统的14,743个个体的NPPA / NPPB位点进行基因分型SNPs鉴定血浆心钠素与rs5068(P = 8×10 -70 ),rs198358(P = 8×10 −30 )和rs632793(P = 2×10 −10 ),以及血浆B型利尿钠肽与rs5068(P = 3×10 −12 ),rs198358(P = 1×10 −25 )和rs632793(P = 2×10 −68 )。在29,717个个体中,与循环NP浓度增加相关的rs5068和rs198358等位基因与较低的收缩期相关(P = 2×10 -6 和6×10 -5 ,和舒张压(P = 1×10 −6 和5×10 −5 ),降低高血压的几率(赔率0.85,置信区间为95%) ,0.79–0.92,P = 4×10 −5 ;优势比0.90、95%置信区间,0.85-0.95,P = 2×10 −4 ) 。与循环NP浓度有关的常见遗传变异导致血压和高血压的个体间差异。

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