Positive association between ALDH2 rs671 polymorphism and essential hypertension: A case-control study and meta-analysis

PLoS One. 2017 May 4;12(5):e0177023. doi: 10.1371/journal.pone.0177023. eCollection 2017.

Abstract

Background and objective: Several studies have been conducted to examine the association between aldehyde dehydrogenase 2 family (ALDH2) rs671 polymorphism and essential hypertension (EH). However, the results remain inconsistent. This study aimed to clarify the association between ALDH2 rs671 polymorphism and EH susceptibility.

Methods: One thousand and ninety-four cases and 1236 controls who were ethnic Han Chinese were collected for this population-based case-control study. A meta-analysis was performed to calculate the pooled odds ratio and 95% confidence interval, using allele contrast, dominant, recessive, and co-dominant models using fixed or random-effect models.

Results: Significant differences were observed between EH cases and controls at the level of both genotype (χ2 = 6.656, P<0.05) and alleles (χ2 = 6.314, P<0.05). An additional meta-analysis using 4204 cases and 5435 controls established that rs671 was significantly associated with EH (P<0.00001).

Conclusion: The results of our case-control study and meta-analysis showed that there is a significant association between ALDH2 rs671 polymorphism and EH susceptibility. In addition, the results of the breakdown analysis by gender suggest a male-specific association between the ALDH2 rs671 polymorphism and EH.

Publication types

  • Meta-Analysis

MeSH terms

  • Aldehyde Dehydrogenase, Mitochondrial / genetics*
  • Case-Control Studies
  • China
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Hypertension / genetics*
  • Male
  • Polymorphism, Single Nucleotide*

Substances

  • ALDH2 protein, human
  • Aldehyde Dehydrogenase, Mitochondrial

Grants and funding

This work was supported by the Program for Zhejiang Leading Team of Science and Technology Innovation (No. 2011R50021) and the Zhejiang Provincial Natural Science Foundation of China (No. LQ16H260002). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.