14 bp deletion polymorphism in the HLA-G gene is a risk factor for idiopathic dilated cardiomyopathy in a Chinese Han population

40Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Human leukocyte antigen (HLA) has been reported to be associated with the pathogenesis of autoimmune-associated idiopathic dilated cardiomyopathy (IDC). However, the HLA-G in this context is limited. In the current study, a total of 117 IDC patients and age and sex matched 401 unrelated healthy controls in a Chinese Han population were HLA-G genotyped for the 14 bp insertion and deletion polymorphism. IDC patients showed markedly increased frequencies of -14 bp/-14 bp genotype [Pc = 0.00049, odds ratio (OR) = 2.17] and -14 bp alleles (Pc = 4.1 × 10-5, OR = 1.97) when compared with healthy controls. Whereas the frequencies of +14 bp/+14 bp genotype (P c = 0.0036, OR = 0.35) and +14 bp alleles (Pc = 4.1 × 10-5, OR = 0.51) were significantly lower in IDC. These data, for the first time, indicated that 14 bp insertion/deletion polymorphism in HLA-G gene could be a genetic risk factor for the susceptibility to IDC. © 2007 The Authors.

Cite

CITATION STYLE

APA

Lin, A., Yan, W. H., Xu, H. H., Tang, L. J., Chen, X. F., Zhu, M., & Zhou, M. Y. (2007). 14 bp deletion polymorphism in the HLA-G gene is a risk factor for idiopathic dilated cardiomyopathy in a Chinese Han population. Tissue Antigens, 70(5), 427–431. https://doi.org/10.1111/j.1399-0039.2007.00926.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free