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 >1.5mm. 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.
| Original language | English |
|---|---|
| Pages (from-to) | 304-310 |
| Number of pages | 7 |
| Journal | Atherosclerosis |
| Volume | 239 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Apr 1 2015 |
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Keywords
- Atherogenic plaque
- Atherosclerosis
- Carotid artery
- Genome-wide association
- Intima-media thickness
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
- Medicine(all)
Cite this
GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. / 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.
In: Atherosclerosis, Vol. 239, No. 2, 01.04.2015, p. 304-310.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb
AU - Den Hoed, Marcel
AU - Strawbridge, Rona J.
AU - Almgren, Peter
AU - Gustafsson, Stefan
AU - Axelsson, Tomas
AU - Engström, Gunnar
AU - de Faire, Ulf
AU - Hedblad, Bo
AU - Humphries, Steve E.
AU - Lindgren, Cecilia M.
AU - Morris, Andrew P.
AU - Östling, Gerd
AU - Syvänen, Ann Christine
AU - Tremoli, Elena
AU - Hamsten, Anders
AU - Ingelsson, Erik
AU - Melander, Olle
AU - Lind, Lars
PY - 2015/4/1
Y1 - 2015/4/1
N2 - 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 >1.5mm. 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.
AB - 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 >1.5mm. 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.
KW - Atherogenic plaque
KW - Atherosclerosis
KW - Carotid artery
KW - Genome-wide association
KW - Intima-media thickness
UR - http://www.scopus.com/inward/record.url?scp=84922537514&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84922537514&partnerID=8YFLogxK
U2 - 10.1016/j.atherosclerosis.2015.01.032
DO - 10.1016/j.atherosclerosis.2015.01.032
M3 - Article
C2 - 25682028
AN - SCOPUS:84922537514
VL - 239
SP - 304
EP - 310
JO - Atherosclerosis
JF - Atherosclerosis
SN - 0021-9150
IS - 2
ER -