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• W2073591360 abstract "Hypertension is one of the leading risk factors for mortality. The renin–angiotensin–aldosterone system (RAAS) is a potent and powerful mediator in the homeostasis of hypertension. Here, the association between six candidate genes, renin, adrenoceptor β3, angiotensinogen, aldosterone synthase, angiotensin II receptor type 1 and angiotensin II receptor type 2, that are related to RAAS and essential hypertension (EH) was evaluated and explored in northern Chinese Han individuals. A case–control study including 1090 EH cases and 700 controls was performed. Eight single-nucleotide polymorphisms (SNPs), rs699, rs4762, rs5707, rs5186, rs4994, rs1799998, rs5193 and rs5194, located in the six genes were genotyped with TaqMan real-time PCR method. Statistical analysis software (SPSS 17.0) was used for descriptive statistics and association analyses. Among the six genes related to RAAS, the frequencies of rs4994 (ADRB3) and rs5194 (AGTR2) were found to be significantly different between the EH cases and controls (P<0.05). Logistic regression analyses adjusted for covariates showed rs4994 to be closely associated with EH under the recessive (P=0.019, odds ratio (OR)=0.373, 95% confidence interval (CI) 0.163–0.851) and homozygous (P=0.028, OR=0.394, 95% CI 0.172–0.903) models. The association was also significantly close in the male subset (P<0.05). Significant association was also observed between rs1799998 (CYP11B2) and EH (P<0.05) in the dominant, additive and allelic models. These data demonstrated that ADRB3 rs4994 and CYP11B2 rs1799998 were significantly closely associated with EH in northern Han Chinese individuals. The CC of rs4994 and CC or C allele of rs1799998 might be protective genetic factors of hypertension." @default.
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• W2073591360 date "2014-08-07" @default.
• W2073591360 modified "2023-10-11" @default.
• W2073591360 title "Association between single-nucleotide polymorphisms in six hypertensive candidate genes and hypertension among northern Han Chinese individuals" @default.
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• W2073591360 doi "https://doi.org/10.1038/hr.2014.124" @default.
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