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Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in chinese children

机译:肥胖对中国儿童全基因组关联研究确定的遗传变异与高血压风险之间关联的影响

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Background Childhood hypertension is a complex disease influenced by both genetic and environmental factors. We aimed to examine how obesity status influences the association of 6 single nucleotide polymorphisms (SNPs) identified by genome-wide association studies (GWASs) with systolic/diastolic blood pressure (SBP/DBP) and hypertension in Chinese children. methods We recruited 619 hypertensive case subjects and 2,458 individuals with normal blood pressure from the Beijing Child and Adolescent Metabolic Syndrome study, a population-based case-control study. We selected 6 SNPs from earlier GWASs of hypertension and genotyped them using TaqMan assay. Results In the normal weight group, we did not observe any significant association of 6 SNPs and the genetic risk score (GRS) with SBP/DBP and hypertension (all P < 0.05). Only STK39 rs3754777 was significantly associated with higher DBP (P = 0.02) in the overweight subjects. In the obese group, 3 SNPs and the GRS were significantly associated with higher SBP (ATP2B1 rs17249754: P = 0.02; CSK rs1378942: P = 0.003; CYP17A1 rs1004467: P = 0.04; GRS: P = 0.0002). We also observed a significant association of 4 SNPs and the GRS with hypertension (ATP2B1 rs17249754: P = 0.02; CSK rs1378942: P = 0.02; CYP17A1 rs1004467: P = 0.02; MTHFR rs1801133: P = 0.03; GRS: P = 0.0004). Correction for multiple testing had no influence on the statistical significance of the association of GRS with SBP/hypertension. Conclusions This study shows a significant association of hypertension susceptibility loci only in obese Chinese children, suggesting a likely influence of childhood obesity on the risk of hypertension.
机译:背景技术儿童高血压是一种复杂的疾病,受遗传和环境因素影响。我们旨在研究肥胖状况如何影响通过全基因组关联研究(GWAS)确定的6个单核苷酸多态性(SNP)与中国儿童的收缩压/舒张压(SBP / DBP)和高血压的关联。方法我们从北京儿童青少年代谢综合征研究(基于人群的病例对照研究)中招募了619名高血压病例和2458名血压正常的人。我们从早期的GWAS中选择​​了6个SNP,并使用TaqMan分析对它们进行基因分型。结果在正常体重组中,我们未发现6个SNP和遗传风险评分(GRS)与SBP / DBP和高血压之间存在显着相关性(所有P <0.05)。在超重受试者中,只有STK39 rs3754777与较高的DBP(P = 0.02)显着相关。在肥胖组中,3个SNP和GRS与较高的SBP显着相关(ATP2B1 rs17249754:P = 0.02; CSK rs1378942:P = 0.003; CYP17A1 rs1004467:P = 0.04; GRS:P = 0.0002)。我们还观察到4个SNP和GRS与高血压之间存在显着关联(ATP2B1 rs17249754:P = 0.02; CSK rs1378942:P = 0.02; CYP17A1 rs1004467:P = 0.02; MTHFR rs1801133:P = 0.03; GRS:P = 0.0004)。多项测试的校正对GRS与SBP /高血压相关性的统计学意义没有影响。结论该研究表明,仅在中国肥胖儿童中高血压易感基因位点显着相关,表明儿童肥胖对高血压风险的可能影响。

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