Association between angiotensin converting enzyme gene polymorphism and essential hypertension: A systematic review and meta-analysis

J Renin Angiotensin Aldosterone Syst. 2021 Jan-Dec;22(1):1470320321995074. doi: 10.1177/1470320321995074.

Abstract

Background: The current meta-analytic study explored the relation between ACE gene insertion/deletion (I/D), and the risk of EH by reviewing relevant trials so as to determine the association between Angiotensin Converting Enzyme (ACE) gene polymorphism and essential hypertension (EH) susceptibility.

Methods: Relevant studies published before May 2019 were collected from the PubMed, Cochrane, Embase, CNKI, VANFUN, and VIP databases.

Results: Fifty-seven studies involving a total of 32,862 patients were included. These studies found that ACE gene D allele was associated with higher EH susceptibility in allelic model, homozygote model, dominant model, and regressive model, and that Asian population with ACE gene D allele showed a higher EH susceptibility in all these models. Moreover, ACE gene D allele was found closely related to a higher EH susceptibility in the subgroups of HWE, NO HWE, Caucasian population, and Mixed population, with the majority being males in allelic model, homozygote model, and regressive model and the majority being females in allelic model.

Conclusion: ACE gene D allele is associated with an overall higher EH susceptibility, which is confirmed in the subgroup analysis of Asian population, HWE, NO HWE, Caucasian population, and Mixed population.

Keywords: Angiotensin converting enzyme; essential hypertension; gene polymorphism; meta-analysis.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Adult
  • Aged
  • Essential Hypertension / enzymology*
  • Essential Hypertension / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • INDEL Mutation / genetics
  • Male
  • Middle Aged
  • Models, Genetic
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Risk Factors

Substances

  • Peptidyl-Dipeptidase A