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Published on: August 1, 2014
HLA-DR3 antigen in the resistance to idiopathic dilated cardiomyopathy
Insights
Individuals with the HLA-DR3 antigen may be protected against idiopathic dilated cardiomyopathy (IDC). This meta-analysis found a decreased frequency of the HLA-DR3 allele in IDC patients, suggesting a protective genetic role.
Area of Science:
- Immunogenetics
- Cardiovascular Disease Epidemiology
Background:
- Idiopathic dilated cardiomyopathy (IDC) is a complex condition potentially triggered by environmental factors in genetically susceptible individuals.
- The role of specific human leukocyte antigen (HLA) alleles, such as HLA-DR3, in IDC risk remains unclear due to conflicting published data.
Purpose of the Study:
- To conduct a meta-analysis to precisely evaluate the association between the HLA-DR3 antigen and the risk of developing IDC.
- To provide a clearer understanding of the genetic susceptibility factors in IDC.
Main Methods:
- A systematic literature search was performed on PUBMED and Embase databases up to June 2015.
- Data from 19 case-control studies, encompassing 1378 IDC cases and 10383 controls, were analyzed.
- Subgroup analyses were conducted based on myocardial biopsy status and ethnicity.
Main Results:
- A significantly decreased frequency of the HLA-DR3 allele was observed in IDC patients compared to controls (OR=0.72, P=0.004).
- This protective association was more pronounced in myocardial biopsy-confirmed IDC cases (OR=0.69, P=0.0003).
- A borderline statistically significant decreased risk was noted among European populations (OR=0.76, P=0.05).
Conclusions:
- The findings suggest that the presence of the HLA-DR3 antigen may confer a protective effect against the development of idiopathic dilated cardiomyopathy.
- HLA-DR3 could be a significant genetic factor influencing susceptibility or resistance to IDC.
Abstract:
Idiopathic dilated cardiomyopathy (IDC) has been hypothesized as a multifactorial disorder initiated by an environment trigger in individuals with predisposing human leukocyte antigen (HLA) alleles. Published data on the association between HLA-DR3 antigen and IDC risk are inconclusive. To derive a more precise estimation of the relationship, a meta-analysis was performed. Studies were identified by searching the PUBMED and Embase database (starting from June 2015). A total of 19 case-control studies including 1378 cases and 10383 controls provided data on the association between HLA-DR3 antigen and genetic susceptibility to IDC. Overall, significantly decreased frequency of HLA-DR3 allele (OR=0.72; 95%CI=0.58-0.90; P=0.004) was found in patients with IDC compared with controls. When stratified by myocardial biopsy or non-biopsy cases, statistically decreased risk was found for IDC in myocardial biopsy cases (OR=0.69; 95%CI=0.57-0.84; P=0.0003). In the subgroup analysis by ethnicity, borderline statistically significantly decreased risk was found among Europeans from 12 case-control studies (OR=0.76; 95%CI=0.58-1.00; P=0.05). In conclusion, our results suggest that individuals with HLA-DR3 antigen may have a protective effect against IDC.
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