Glutathione S-transferase M1 polymorphisms and Parkinson's disease risk: a meta-analysis

Dan Wang1,2, Jun-Xia Zhai3, Dian-Wu Liu1

  • 1a Department of Epidemiology and Biostatistics, School of Public Health , Hebei Medical University , Shijiazhuang , China.

Neurological Research
|April 15, 2016
PubMed
Abstract

Insights

This meta-analysis found no significant link between the glutathione S-transferase M1 (GSTM1) null genotype and Parkinson's disease (PD) risk. The study analyzed 23 publications, concluding that GSTM1 polymorphisms do not appear to influence PD development.

Area of Science:

  • Neuroscience
  • Genetics
  • Epidemiology

Background:

  • Parkinson's disease (PD) is a neurodegenerative disorder with complex etiology.
  • Glutathione S-transferase M1 (GSTM1) gene polymorphisms have been investigated as potential risk factors for PD.
  • Previous studies on the association between GSTM1 polymorphisms and PD risk have yielded inconsistent findings.

Purpose of the Study:

  • To clarify the association between glutathione S-transferase M1 (GSTM1) polymorphisms and the risk of developing Parkinson's disease (PD).
  • To conduct a meta-analysis of existing studies to provide a more definitive conclusion on this genetic association.

Main Methods:

  • A comprehensive search of electronic databases was conducted to identify relevant publications.
  • Studies were included based on predefined eligibility criteria.
  • The association was assessed using odds ratios (ORs) and 95% confidence intervals (CIs) within a recessive genetic model (GSTM1 null genotype vs. present genotype).
  • Subgroup analyses were performed based on ethnicity and OR type.

Main Results:

  • A total of 22 publications, comprising 23 studies, were included in the meta-analysis.
  • The overall analysis revealed no significant association between the GSTM1 null genotype and PD risk (ORrandom-effects = 1.06, 95% CI = 0.95-1.19).
  • Subgroup analyses by ethnicity (Caucasians, Asians, Latinos) and OR type (crude vs. adjusted) also showed no significant associations. No publication bias was detected.

Conclusions:

  • The findings from this meta-analysis indicate that the GSTM1 null genotype is not significantly associated with an increased risk of Parkinson's disease.
  • This study contributes to resolving inconsistencies in previous research regarding the role of GSTM1 polymorphisms in PD pathogenesis.

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