The insertion/deletion polymorphism in the angiotensin-converting enzyme and susceptibility to schizophrenia or Parkinson's disease: A meta-analysis

J Renin Angiotensin Aldosterone Syst. 2015 Jun;16(2):434-42. doi: 10.1177/1470320313495909. Epub 2014 Aug 20.

Abstract

Introduction: The purpose of this study was to examine whether the insertion (I) and deletion (D) polymorphism of the angiotensin-converting enzyme (ACE) confers susceptibility to schizophrenia and Parkinson's disease (PD).

Materials and methods: A meta-analysis was performed of the associations between the ACE I/D polymorphism and schizophrenia and PD.

Results: Thirteen studies with 2024 cases and 2230 controls comprising eight studies on schizophrenia and five on PD were included in the meta-analysis. The meta-analysis revealed no association between the ACE D allele and schizophrenia (OR = 0.990, 95% CI = 0.889-1.102, p = 0.856) or PD (OR = 1.067, 95% CI = 0.907-1.255, p = 0.433). Stratification by ethnicity indicated no association between the ACE D allele and schizophrenia in European, Asian, or Turkish ethnic groups (OR = 0.896, 95% CI = 0.566-1.419, p = 0.640; OR = 1.057, 95% CI = 0.903-1.238, p = 0.492; OR = 1.111, 95% CI = 0.889-1.389, p = 0.354, respectively). Ethnicity-specific meta-analysis was not conducted for PD because only one ethnic PD study was available.

Conclusions: This meta-analysis found no association between the ACE I/D polymorphism and schizophrenia or PD.

Keywords: Angiotensin-converting enzyme; Parkinson’s disease; meta-analysis; polymorphism; schizophrenia.

Publication types

  • Meta-Analysis

MeSH terms

  • Alleles
  • Confidence Intervals
  • Ethnicity / genetics
  • Gene Frequency
  • Genetic Heterogeneity
  • Genetic Predisposition to Disease*
  • Humans
  • INDEL Mutation / genetics*
  • Odds Ratio
  • Parkinson Disease / enzymology
  • Parkinson Disease / genetics*
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Publication Bias
  • Schizophrenia / enzymology
  • Schizophrenia / genetics*

Substances

  • ACE protein, human
  • Peptidyl-Dipeptidase A