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Updated: Mar 22, 2026

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease
Published on: January 7, 2014
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.
Objectives:
Studies examining whether glutathione S-transferase M1 (GSTM1) polymorphisms are associated with Parkinson's disease (PD) have reported inconsistent results. To clarify those inconsistencies, a meta-analysis was performed.
Methods:
The electronic databases were searched for all publications regarding the association. Studies were included if they met the eligibility criteria. The strength of the association between GSTM1 polymorphisms and PD risk was measured by odds ratios (ORs) and 95% confidence intervals (CIs) in the recessive genetic model (null genotype vs. present genotype). Subgroup analyses by ethnicity and OR type were performed.
Results:
A total of 22 publications (23 studies) were included. There were 14, 7 and 2 studies with Caucasians, Asians and Latinos, respectively. OR types were 15 and 8 studies with crude and adjusted ORs, respectively. The combined results of the overall analysis showed that the GSTM1 null genotype was not significantly associated with PD risk (ORrandom-effects = 1.06, 95% CI = 0.95-1.19). In subgroup analyses by ethnicity, no significant associations were found in Caucasians, Asians or Latinos individually. Similarly, there were no associations in the subgroup analyses by OR type. There were no obvious publication biases in any of the comparisons.
Discussion:
The results of this meta-analysis suggest that the GSTM1 null genotype is not significantly associated with PD risk.
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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