GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb

• Published in: Atherosclerosis 2015-04, Vol.239 (2), p.304-310
• Main Authors: den Hoed, Marcel, Strawbridge, Rona J, Almgren, Peter, Gustafsson, Stefan, Axelsson, Tomas, Engström, Gunnar, de Faire, Ulf, Hedblad, Bo, Humphries, Steve E, Lindgren, Cecilia M, Morris, Andrew P, Östling, Gerd, Syvänen, Ann-Christine, Tremoli, Elena, Hamsten, Anders, Ingelsson, Erik, Melander, Olle, Lind, Lars
• Format: Article
• Language: English
• Subjects: Aged; Alleles; Atherogenic plaque; Atherosclerosis; Cardiac and Cardiovascular Systems; Cardiovascular; Carotid artery; Carotid Artery, Common - pathology; Carotid Intima-Media Thickness; Clinical Medicine; Coronary Disease - genetics; Europe; Female; Genetic Predisposition to Disease; Genome-wide association; Genome-Wide Association Study; Genotype; Humans; Intima-media thickness; Kardiologi; Klinisk medicin; Male; Medical and Health Sciences; Medicin och hälsovetenskap; Middle Aged; Odds Ratio; Plaque, Atherosclerotic - genetics; Polymorphism, Single Nucleotide; Risk Factors
• ISSN: 0021-9150; 1879-1484; 1879-1484
• DOI: 10.1016/j.atherosclerosis.2015.01.032

Abstract Background Large-scale genome-wide association studies (GWAS) have so far identified 45 loci that are robustly associated with coronary heart disease (CHD) in data from adult men and women of European descent. Objectives To examine whether the CHD-associated loci are associated with measures of atherosclerosis in data from up to 9582 individuals of European ancestry. Methods Forty-five SNPs representing the CHD-associated loci were genotyped in middle-aged to elderly individuals of European descent from four independent population-based studies (IMPROVE, MDC-CC, ULSAM and PIVUS). Intima-media thickness (IMT) was measured by external B-mode ultrasonography at the far wall of the bulb (sinus) and common carotid artery. Plaque presence was defined as a maximal IMT of the bulb >1.5 mm. We meta-analysed single-SNP associations across the four studies, and combined them in a genetic predisposition score. We subsequently examined the association of the genetic predisposition score with prevalent CHD and the three indices of atherosclerosis, adjusting for sex, age and Framingham risk factors. Results As anticipated, the genetic predisposition score was associated with prevalent CHD, with each additional risk allele increasing the odds of disease by 5.5% (p = 4.1 × 10−6 ). Moreover, each additional CHD-risk allele across the 45 loci was associated with a 0.24% increase in IMT (p = 4.0 × 10−3 ), and with a 2.8% increased odds of plaque presence (p = 7.4 × 10−6 ) at the far wall of the bulb. The genetic predisposition score was not associated with IMT of the common carotid artery (p = 0.47). Conclusions Our results suggest that the association between the 45 previously identified loci and CHD at least partly acts through atherosclerosis.