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Genetic Mapping of Vascular Calcified Plaque Loci on Chromosome 16p in European Americans from the Diabetes Heart Study

Authors :
Carl D. Langefeld
Allison B. Lehtinen
Amanda J. Cox
Julie T. Ziegler
Anthony G. Comuzzie
Barry I. Freedman
J. Jeffrey Carr
V. Saroja Voruganti
Jianzhao Xu
Donald W. Bowden
Source :
Annals of Human Genetics. 75:222-235
Publication Year :
2011
Publisher :
Wiley, 2011.

Abstract

A linkage peak for carotid artery calcified plaque (CarCP) on chromosome 16p (LOD 4.39 at 8.4 cM) in families with type 2 diabetes mellitus (T2DM) from the Diabetes Heart Study (DHS) has been refined. Fine mapping encompassed 104 single-nucleotide polymorphisms (SNPs) in 937 subjects from 315 families; including 45 SNPs in six candidate genes (CACNA1H, SEPX1, ABCA3, IL32, SOCS1, CLEC16A). Linkage and association analyses using variance components analysis adjusting for age, gender, body mass index (BMI), and diabetes status refined the CarCP linkage into two distinct peaks (LODs: 3.89 at 6.9 cM and 4.86 at 16.0 cM). Evidence of linkage for coronary calcified plaque (LOD: 2.27 at 19 cM) and a vascular calcification principle component (LOD: 3.71 at 16.0 cM) was also observed. The strongest evidence for association with CarCP was observed with SNPs in the A2BP1 gene region (rs4337300 P= 0.005) with modest evidence of association with SNPs in CACNA1H (P= 0.010-0.033). Bayesian quantitative trait nucleotide (BQTN) analysis identified a SNP, rs1358489, with either a functional effect on CarCP or in linkage disequilibrium (LD) with a functional SNP. This study refined the 16p region contributing to vascular calcification. The causal variants remain to be identified, but results are consistent with a linkage peak that is due to multiple common variants, though rare variants cannot be excluded.

Details

ISSN :
00034800
Volume :
75
Database :
OpenAIRE
Journal :
Annals of Human Genetics
Accession number :
edsair.doi...........8a2138cd08f9cdce818a6a21a89aae71
Full Text :
https://doi.org/10.1111/j.1469-1809.2010.00632.x