Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study

被引:17
作者
Durda, Peter [1 ]
Raffield, Laura M. [2 ]
Lange, Ethan M. [3 ]
Olson, Nels C. [1 ]
Jenny, Nancy Swords [1 ]
Cushman, Mary [1 ,4 ]
Deichgraeber, Pia [5 ,6 ]
Grarup, Niels [7 ]
Jonsson, Anna [7 ]
Hansen, Torben [7 ]
Mychaleckyj, Josyf C. [8 ]
Psaty, Bruce M. [9 ]
Reiner, Alex P. [10 ]
Tracy, Russell P. [1 ,11 ]
Lange, Leslie A. [3 ]
机构
[1] Univ Vermont, Dept Pathol & Lab Med, Larner Coll Med, 89 Beaumont Ave, Burlington, VT 05405 USA
[2] Univ N Carolina, Dept Genet, Chapel Hill, NC 27515 USA
[3] Univ Colorado, Dept Med, Div Biomed Informat & Personalized Med, Anschutz Med Campus, Aurora, CO USA
[4] Univ Vermont, Dept Med, Larner Coll Med, Burlington, VT 05405 USA
[5] Aarhus Univ Hosp, Steno Diabet Ctr, Aarhus, Denmark
[6] Aarhus Univ Hosp, Dept Endocrinol & Internal Med, Aarhus, Denmark
[7] Novo Nordisk Fdn, Ctr Basic Metab Res, Copenhagen, Denmark
[8] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA USA
[9] Univ Washington, Dept Med Epidemiol & Hlth Serv, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
[10] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[11] Univ Vermont, Dept Biochem, Larner Coll Med, 89 Beaumont Ave, Burlington, VT 05405 USA
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2022年 / 11卷 / 21期
基金
美国国家卫生研究院;
关键词
cardiovascular diseases; CD163; antigen; genome-wide association study; humans; monocytes; risk factors; SCAVENGER RECEPTOR CD163; T-CELL-ACTIVATION; DIFFERENTIATION ANTIGEN; HEART-FAILURE; IN-VITRO; MACROPHAGES; ATHEROSCLEROSIS; LOCI; MECHANISMS; MARKERS;
D O I
10.1161/JAHA.121.024374
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Monocytes/macrophages participate in cardiovascular disease. CD163 (cluster of differentiation 163) is a monocyte/macrophage receptor, and the shed sCD163 (soluble CD163) reflects monocyte/macrophage activation. We examined the association of sCD163 with incident cardiovascular disease events and performed a genome-wide association study to identify sCD163-associated variants. Methods and Results We measured plasma sCD163 in 5214 adults (aged >= 65 years, 58.7% women, 16.2% Black) of the CHS (Cardiovascular Health Study). We used Cox regression models (associations of sCD163 with incident events and mortality); median follow-up was 26 years. Genome-wide association study analyses were stratified on race. Adjusted for age, sex, and race and ethnicity, sCD163 levels were associated with all-cause mortality (hazard ratio [HR], 1.08 [95% CI, 1.04-1.12] per SD increase), cardiovascular disease mortality (HR, 1.15 [95% CI, 1.09-1.21]), incident coronary heart disease (HR, 1.10 [95% CI, 1.04-1.16]), and incident heart failure (HR, 1.18 [95% CI, 1.12-1.25]). When further adjusted (eg, cardiovascular disease risk factors), only incident coronary heart disease lost significance. In European American individuals, genome-wide association studies identified 38 variants on chromosome 2 near MGAT5 (top result rs62165726, P=3.3x10(-18)),19 variants near chromosome 17 gene ASGR1 (rs55714927, P=1.5x10(-14)), and 18 variants near chromosome 11 gene ST3GAL4. These regions replicated in the European ancestry ADDITION-PRO cohort, a longitudinal cohort study nested in the Danish arm of the Anglo-Danish-Dutch study of Intensive Treatment Intensive Treatment In peOple with screeNdetcted Diabetes in Primary Care. In Black individuals, we identified 9 variants on chromosome 6 (rs3129781 P=7.1x10(-9)) in the HLA region, and 3 variants (rs115391969 P=4.3x10(-8)) near the chromosome 16 gene MYLK3(.) Conclusions Monocyte function, as measured by sCD163, may be predictive of overall and cardiovascular-specific mortality and incident heart failure.
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页数:14
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