Author:
Bis Joshua C.,White Charles C.,Franceschini Nora,Brody Jennifer,Zhang Xiaoling,Muzny Donna,Santibanez Jireh,Gibbs Richard,Liu Xiaoming,Lin Honghuang,Boerwinkle Eric,Psaty Bruce M.,North Kari E.,Cupples L. Adrienne,O’Donnell Christopher J.
Abstract
Background—
Atherosclerosis, the precursor to coronary heart disease and stroke, is characterized by an accumulation of fatty cells in the arterial intimal-medial layers. Common carotid intima media thickness (cIMT) and plaque are subclinical atherosclerosis measures that predict cardiovascular disease events. Previously, genome-wide association studies demonstrated evidence for association with cIMT (
SLC17A4
) and plaque (
PIK3CG
).
Methods and Results—
We sequenced 120 kb around
SLC17A4
(6p22.2) and 251 kb around
PIK3CG
(7q22.3) among 3669 European ancestry participants from the Atherosclerosis Risk in Communities (ARIC) study, Cardiovascular Health Study (CHS), and Framingham Heart Study (FHS) in Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Primary analyses focused on 438 common variants (minor allele frequency ≥1%), which were independently meta-analyzed. A 3′ untranslated region
CCDC71L
variant (rs2286149), upstream from
PIK3CG
, was the most significant finding in cIMT (
P
=0.00033) and plaque (
P
=0.0004) analyses. A
SLC17A4
intronic variant was also associated with cIMT (
P
=0.008). Both were in low linkage disequilibrium with the genome-wide association study single nucleotide polymorphisms. Gene-based tests including T1 count and sequence kernel association test for rare variants (minor allele frequency <1%) did not yield statistically significant associations. However, we observed nominal associations for rare variants in
CCDC71L
and
SLC17A3
with cIMT and of the entire
7q22
region with plaque (
P
=0.05).
Conclusions—
Common and rare variants in
PIK3CG
and
SLC17A4
regions demonstrated modest association with subclinical atherosclerosis traits. Although not conclusive, these findings may help to understand the genetic architecture of regions previously implicated by genome-wide association studies and identify variants within these regions for further investigation in larger samples.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),Cardiology and Cardiovascular Medicine,Genetics
Cited by
16 articles.
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