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

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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 Parkinsons 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 = 0.8891.102, p = 0.856) or PD (OR = 1.067, 95% CI = 0.9071.255, 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 = 0.5661.419, p = 0.640; OR = 1.057, 95% CI = 0.9031.238, p = 0.492; OR = 1.111, 95% CI = 0.8891.389, 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.

Original languageEnglish
Pages (from-to)434-442
Number of pages9
JournalJRAAS - Journal of the Renin-Angiotensin-Aldosterone System
Volume16
Issue number2
DOIs
Publication statusPublished - 2015 Jan 1

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Peptidyl-Dipeptidase A
Parkinson Disease
Meta-Analysis
Schizophrenia
Alleles
Ethnic Groups

Keywords

  • Angiotensin-converting enzyme
  • meta-analysis
  • Parkinson's disease
  • polymorphism
  • schizophrenia

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology

Cite this

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title = "The insertion/deletion polymorphism in the angiotensin-converting enzyme and susceptibility to schizophrenia or Parkinson's disease: A meta-analysis",
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 Parkinsons 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 = 0.8891.102, p = 0.856) or PD (OR = 1.067, 95{\%} CI = 0.9071.255, 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 = 0.5661.419, p = 0.640; OR = 1.057, 95{\%} CI = 0.9031.238, p = 0.492; OR = 1.111, 95{\%} CI = 0.8891.389, 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, meta-analysis, Parkinson's disease, polymorphism, schizophrenia",
author = "Song, {Gwan Gyu} and Lee, {Young Ho}",
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N2 - 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 Parkinsons 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 = 0.8891.102, p = 0.856) or PD (OR = 1.067, 95% CI = 0.9071.255, 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 = 0.5661.419, p = 0.640; OR = 1.057, 95% CI = 0.9031.238, p = 0.492; OR = 1.111, 95% CI = 0.8891.389, 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.

AB - 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 Parkinsons 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 = 0.8891.102, p = 0.856) or PD (OR = 1.067, 95% CI = 0.9071.255, 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 = 0.5661.419, p = 0.640; OR = 1.057, 95% CI = 0.9031.238, p = 0.492; OR = 1.111, 95% CI = 0.8891.389, 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.

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