Abstract
Myocardial infarction (MI) results from complex interactions of multiple genetic and environmental factors. To disclose genetic backgrounds of MI, we performed a large-scale, case-control association study using 52,608 gene-based single-nucleotide polymorphism (SNP) markers, and identified a candidate SNP located on chromosome 3p21.2-p21.1. Subsequent linkage-disequilibrium mapping indicated very significant association between MI and a SNP in exon 2 of the inter-alpha (globulin) inhibitor 3 gene (ITIH3; χ 2 = 24.88, P = 6.1 × 10-7, 3,353 affected individuals versus 3,807 controls). In vitro functional analyses showed that this SNP enhanced the transcriptional level of the ITIH3 gene. Furthermore, we found expression of the ITIH3 protein in the vascular smooth muscle cells and macrophages in the human atherosclerotic lesions, suggesting ITIH3 SNP to be a novel genetic risk factor of MI. © 2006 The Japan Society of Human Genetics and Springer.
Author supplied keywords
Cite
CITATION STYLE
Ebana, Y., Ozaki, K., Inoue, K., Sato, H., Iida, A., Lwin, H., … Tanaka, T. (2007). A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction. Journal of Human Genetics, 52(3), 220–229. https://doi.org/10.1007/s10038-006-0102-5
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.