Department of Medicine, University of Hong Kong, Hong Kong.
Eur J Endocrinol. 2010 Aug;163(2):251-7. doi: 10.1530/EJE-10-0251. Epub 2010 Jun 1.
Low plasma adiponectin level can predict the development of hypertension after 5 years in our population. We therefore investigated whether single-nucleotide polymorphisms (SNPs) in the adiponectin gene influenced plasma adiponectin level and whether they were associated with hypertension.
We genotyped 14 tagging SNPs in 1616 subjects with persistent normotensive or hypertensive status during a 6.4-year follow-up period in the Hong Kong Cardiovascular Risk Factor Prevalence Study-2 (CRISPS-2). Plasma adiponectin level was measured in 1385 subjects using in-house sandwich ELISA.
The minor G allele of the SNP rs266729 was significantly associated with higher odds of hypertension (odds ratio (95% confidence interval)=1.49 (1.13-1.95), P=0.0044) after adjusting for covariates. In stepwise multiple logistic regression, this SNP (P=0.006) was a significant independent factor of hypertension, together with age (P<0.001), body mass index (P<0.001), triglycerides (P=0.021), and insulin resistance index (P<0.001). Among the 14 SNPs, rs266729 (beta=-0.067, P=0.0037), -10677C>T (beta=0.069, P=0.0027), rs182052 (beta=-0.097, P<0.0001), and rs12495941 (beta=0.103, P<0.0001) were significantly associated with adiponectin level after adjusting for covariates. No significant sex interaction was found for the associations of SNPs with hypertension and adiponectin level. Similar results were obtained in haplotype analysis.
In our population, genetic variants in the adiponectin gene influenced plasma adiponectin levels, and one of them was associated with hypertension. This study has provided further evidence for a role of adiponectin in the development of hypertension.
在我们的人群中,低血浆脂联素水平可预测 5 年后高血压的发生。因此,我们研究了脂联素基因中的单核苷酸多态性(SNP)是否影响血浆脂联素水平,以及它们是否与高血压相关。
我们对香港心血管风险因素患病率研究-2(CRISPS-2)中 1616 例持续血压正常或高血压患者在 6.4 年随访期间的 14 个标记 SNP 进行了基因分型。使用内部夹心 ELISA 测量了 1385 例患者的血浆脂联素水平。
SNP rs266729 的次要 G 等位基因与调整协变量后高血压的更高发病几率显著相关(比值比(95%置信区间)=1.49(1.13-1.95),P=0.0044)。在逐步多元逻辑回归中,该 SNP(P=0.006)与年龄(P<0.001)、体重指数(P<0.001)、甘油三酯(P=0.021)和胰岛素抵抗指数(P<0.001)一起是高血压的重要独立因素。在 14 个 SNP 中,rs266729(β=-0.067,P=0.0037)、-10677C>T(β=0.069,P=0.0027)、rs182052(β=-0.097,P<0.0001)和 rs12495941(β=0.103,P<0.0001)在调整协变量后与脂联素水平显著相关。在 SNP 与高血压和脂联素水平的关联中未发现性别交互作用的显著差异。在单体型分析中也得到了类似的结果。
在我们的人群中,脂联素基因中的遗传变异影响血浆脂联素水平,其中一种与高血压相关。本研究进一步证明了脂联素在高血压发展中的作用。