Carotid Intima-Media Thickness Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UK Biobank

被引:25
作者
Strawbridge, Rona J. [1 ]
Ward, Joey [1 ]
Bailey, Mark E. S. [2 ]
Cullen, Breda [1 ]
Ferguson, Amy [1 ]
Graham, Nicholas [1 ]
Johnston, Keira J. A. [1 ,2 ,4 ]
Lyall, Laura M. [1 ]
Pearsall, Robert [1 ]
Pell, Jill [1 ]
Shaw, Richard J. [1 ,3 ]
Tank, Rachana [1 ]
Lyall, Donald M. [1 ]
Smith, Daniel J. [1 ]
机构
[1] Univ Glasgow, Inst Hlth & Wellbeing, Glasgow, Lanark, Scotland
[2] Univ Glasgow, Sch Life Sci, Coll Med Vet & Life Sci, Glasgow, Lanark, Scotland
[3] Karolinska Inst, Cardiovasc Med Unit, Dept Med Solna, Hlth Data Res United Kingdom, Stockholm, Sweden
[4] Univ Edinburgh, Div Psychiat, Coll Med, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会; 英国科研创新办公室;
关键词
atherosclerosis; carotid artery; coronary artery disease; diabetes; type; 2; genetics; association studies; intima-media thickness; obesity; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; METAANALYSIS; ATHEROSCLEROSIS; DETERMINANTS; CHOLESTEROL; VARIANTS; RISK; IDENTIFICATION; VISUALIZATION;
D O I
10.1161/ATVBAHA.119.313226
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Atherosclerosis is the underlying cause of most cardiovascular disease, but mechanisms underlying atherosclerosis are incompletely understood. Ultrasound measurement of the carotid intima-media thickness (cIMT) can be used to measure vascular remodeling, which is indicative of atherosclerosis. Genome-wide association studies have identified many genetic loci associated with cIMT, but heterogeneity of measurements collected by many small cohorts have been a major limitation in these efforts. Here, we conducted genome-wide association analyses in UKB (UK Biobank; N=22 179), the largest single study with consistent cIMT measurements. Approach and Results: We used BOLT-LMM software to run linear regression of cIMT in UKB, adjusted for age, sex, and genotyping chip. In white British participants, we identified 5 novel loci associated with cIMT and replicated most previously reported loci. In the first sex-specific analyses of cIMT, we identified a locus on chromosome 5, associated with cIMT in women only and highlight VCAN as a good candidate gene at this locus. Genetic correlations with body mass index and glucometabolic traits were also observed. Two loci influenced risk of ischemic heart disease. ConclusionS: These findings replicate previously reported associations, highlight novel biology, and provide new directions for investigating the sex differences observed in cardiovascular disease presentation and progression.
引用
收藏
页码:446 / 461
页数:16
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