Related Experiment Video
Updated: May 31, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
HLA-DRB1 gene polymorphism is associated with idiopathic dilated cardiomyopathy: a meta-analysis
Jinlong Deng1, Rong Luo, Xiaoping Li
1Department of Cardiology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, PR China.
Insights
The HLA-DRB1*1401 allele may increase the risk of idiopathic dilated cardiomyopathy, while HLA-DRB1*0901 and HLA-DRB1*0301 alleles may offer protection against this condition.
Area of Science:
- Immunogenetics
- Cardiology
- Human Genetics
Background:
- The human leukocyte antigen (HLA) system plays a crucial role in immune response.
- Idiopathic dilated cardiomyopathy (IDCM) is a complex heart condition with potential genetic underpinnings.
- Previous studies suggest a link between specific HLA-DRB1 alleles and IDCM, but findings are inconsistent.
Purpose of the Study:
- To conduct a meta-analysis of case-control studies.
- To clarify the association between HLA-DRB1 alleles and idiopathic dilated cardiomyopathy.
- To investigate specific alleles: HLA-DRB1*1401, HLA-DRB1*0901, and HLA-DRB1*0301.
Main Methods:
- Comprehensive literature search across multiple databases (PubMed, SCI, Cochrane, CNKI, CBM, Wanfang, VIP).
- Inclusion of five case-control studies.
- Meta-analysis to pool odds ratios (OR) and confidence intervals (CI) for specific HLA-DRB1 alleles.
Main Results:
- Four studies analyzed for HLA-DRB1*1401 and HLA-DRB1*0901.
- HLA-DRB1*1401 showed a significantly higher frequency in IDCM patients (OR=2.6, P<0.05).
- HLA-DRB1*0901 (OR=0.70, P=0.05) and HLA-DRB1*0301 (OR=0.49, P<0.05) were more frequent in healthy individuals, suggesting a protective effect.
Conclusions:
- The HLA-DRB1*1401 allele may serve as a risk factor for developing idiopathic dilated cardiomyopathy.
- Conversely, HLA-DRB1*0901 and HLA-DRB1*0301 alleles appear to have a protective effect against IDCM.
- These findings contribute to understanding the immunogenetic basis of IDCM.
Objective:
Some studies have reported that the HLA-DRB1 allele was associated with idiopathic dilated cardiomyopathy. However, there have been inconsistent results among different studies. To clarify the association of HLA-DRB1 and idiopathic dilated cardiomyopathy, a meta-analysis of case-control studies was performed.
Methods:
PubMed database, Science Citation Index database, The Cochrane Central Register of Controlled Trials database, China National Knowledge Information database, Chinese Biomedical Literature database, Wanfang database, and VIP database in China were searched. Search terms included dilated cardiomyopathy and DRB1. Five case-control studies were included in the present meta-analysis to assess the association between HLA-DRB1*1401, HLA-DRB1*0901, HLA-DRB1*0301, and idiopathic dilated cardiomyopathy.
Results:
A total of four studies were included in our meta-analysis for HLA-DRB1*1401 and HLA-DRB1*0901. The pooled odds ratio (OR) was 2.6 [95% confidence interval (CI) 1.11-6.11, P<0.05] and 0.70 (95% CI 0.48-1.00, P=0.05), respectively. For the HLA-DRB1*0301 allele, just three studies were included in our meta-analysis. The pooled OR was 0.49 (95% CI 0.27-0.91, P<0.05). The present meta-analysis indicated that the frequency of HLA-DRB1*1401 was higher in idiopathic dilated cardiomyopathy patients than in healthy people, whereas HLA-DRB1*0901 and HLA-DRB1*0301 were higher in healthy people than in idiopathic dilated cardiomyopathy patients.
Conclusion:
The HLA-DRB1*1401 allele might be a risk factor for idiopathic dilated cardiomyopathy and HLA-DRB1*0901 and HLA-DRB1*0301 might protect humans from idiopathic dilated cardiomyopathy.
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Cardiomyopathy V: Interprofessional Care
