Duan P, Wang Z-M, Liu J, Wang L-N, Yang Z, Tu P
Department of Endocrinology and Metabolism, Nanchang Key Laboratory of Diabetes, The Third Hospital of Nanchang, Nanchang city, People's Republic of China.
J Hum Hypertens. 2015 Dec;29(12):749-53. doi: 10.1038/jhh.2015.13. Epub 2015 Mar 26.
Recent studies have revealed that the receptor activator of nuclear factor-kappa B ligand/RANK/osteoprotegerin (RANKL/RANK/OPG) system has an important role in vascular calcification, which is contributory to various cardiovascular diseases and intimately linked to the regulation of blood pressure. Therefore, we performed a case-control study to investigate the associations of 21 single-nucleotide polymorphisms (SNPs) in the TNFSF11, TNFRSF11A and TNFRSF11B genes in the RANKL/RANK/OPG system with hypertension and blood pressure in post-menopausal Chinese women. In this study, 503 hypertensive patients and 509 normal controls were recruited. Genotyping was performed using the high-throughput Sequenom genotyping platform. The results showed that two SNPs (rs6567270 and rs4603673) in the TNFRSF11A were associated with hypertension (P=0.010 and P=0.013, respectively) and systolic blood pressure (P=0.024 and P=0.023, respectively). One SNP (rs9646629) in the TNFRSF11A showed significant association with diastolic blood pressure (P=0.031). The results of this study suggest that TNFRSF11A but not TNFSF11 and TNFRSF11B genetic variation is associated with hypertension and blood pressure in Chinese women. The findings provide additional support for the genetic role of RANKL/RANK/OPG system in hypertension and blood pressure regulation.
近期研究表明,核因子-κB受体活化因子配体/核因子-κB受体活化因子/骨保护素(RANKL/RANK/OPG)系统在血管钙化中起重要作用,而血管钙化会导致各种心血管疾病,且与血压调节密切相关。因此,我们开展了一项病例对照研究,以调查RANKL/RANK/OPG系统中TNFSF11、TNFRSF11A和TNFRSF11B基因的21个单核苷酸多态性(SNP)与绝经后中国女性高血压及血压的关联。本研究招募了503例高血压患者和509例正常对照。采用高通量Sequenom基因分型平台进行基因分型。结果显示,TNFRSF11A中的两个SNP(rs6567270和rs4603673)与高血压相关(分别为P=0.010和P=0.013)以及收缩压相关(分别为P=0.024和P=0.023)。TNFRSF11A中的一个SNP(rs9646629)与舒张压显著相关(P=0.031)。本研究结果表明,在中国女性中,与高血压及血压相关的是TNFRSF11A基因变异,而非TNFSF11和TNFRSF11B基因变异。这些发现为RANKL/RANK/OPG系统在高血压及血压调节中的遗传作用提供了更多支持。