ADRB2 polymorphisms and dyslipidemia risk in Chinese hypertensive patients

ABSTRACT

Single nucleotide polymorphisms (SNPs) within a β-adrenergic receptor (ADRB2) were shown to be related to lipid traits or hyperlipidemia in different ethnicities, but not in a Chinese population. We performed the present study to investigate the possible relationship between them in a Chinese hypertensive population. Seven hundred and eighty-three hypertensive subjects were enrolled in the hospital-based retrospective research. Using the TaqMan PCR method, three polymorphisms (C-47T, A46G, and C79G) of ADRB2 were detected. For the whole population, no significant statistical difference was found for all serum lipids. Similar findings were seen in men and women subgroups. Subsequently, in the case-control study, we observed that the A46G polymorphism was significantly associated with the elevated risk of hypertriglyceridemia in the dominant model (OR: 1.47, 95%CI: 1.05–2.06, P = 0.025). There are no significant differences in the other four models. With regard to C79G and C-47T, no significant association was seen in this population. In addition, haplotype analysis showed that the TAC haplotype carrying frequent alleles of the three SNPs played a reduced role in hypertriglyceridemia risk and the TGC haplotype carrying rare allele of A46G expressed a significant risk effect. In conclusion, these findings indicated that the ADRB2 SNPs might be a genetic risk factor for dyslipidemia in the Chinese hypertensive patients.

KEYWORDS:

• β2 adrenergic receptor or ADRB2
• Chinese
• lipid
• polymorphism

Acknowledgments

We are very grateful to all the participants in this study.

Declaration of interest

The authors reported no conflicts of interest.

Funding

This study was financially supported by the Beijing Natural Science Foundation of China (Grant No. 7120001).

Additional information

Funding

This study was financially supported by the Beijing Natural Science Foundation of China (Grant No. 7120001).