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Polymorphisms of CD247 gene is associated with dilated cardiomyopathy in Chinese Han population.

Authors :
Li C
Xie X
Li K
Rao L
Source :
BMC cardiovascular disorders [BMC Cardiovasc Disord] 2024 Sep 12; Vol. 24 (1), pp. 487. Date of Electronic Publication: 2024 Sep 12.
Publication Year :
2024

Abstract

Background: Dilated cardiomyopathy (DCM) is a major cause of heart failure and heart transplantation. Recently, some studies have reported that the autoimmune response in myocardial cells might be related to the pathogenesis of DCM. The CD247 gene has been previously found to be involved in autoimmune disease. Therefore, our study aimed to clarify the hypothesis that there is a certain linkage between polymorphisms of the CD247 gene and the triggering of DCM risk.<br />Methods: In the present study, two single nucleotide polymorphisms (SNPs) of the CD247 gene, rs12141731 and rs858543, were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 355 DCM patients and 404 age- and sex-matched controls.<br />Results: Pearson's chi-squared test for the CD247 gene revealed that SNP rs858543 (p = 0.001, OR = 0.72, 95% CI = (0.588-0.882), but not SNP rs12141731, was associated with DCM in the Chinese Han population. Haplotype analysis revealed that the CC haplotype was associated with increased DCM susceptibility, while CT was a protective haplotype. Cox multivariate survival analysis indicated that the rs858543 TT genotype (HR: 0.608, 95% CI = 0.402-0.921, p = 0.019) was an independent multivariate predictor for longer overall survival in DCM patients. CD247 mRNA expression levels were significantly decreased in DCM patients (p = 0.02).<br />Conclusions: Our study suggested that a polymorphism in the CD247 gene may be a risk factor for DCM in the Chinese Han population.<br />Trial Registration: ChiCTR2000029701.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1471-2261
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
BMC cardiovascular disorders
Publication Type :
Academic Journal
Accession number :
39261809
Full Text :
https://doi.org/10.1186/s12872-024-04160-y