The Relationship between Circulating APOA-1 and Atherosclerosis Initiation and Progression in Psoriasis

医学 内科学 胰岛素抵抗 四分位数 胆固醇 冠状动脉疾病 流出 稳态模型评估 内分泌学 心脏病学 胰岛素 胃肠病学 置信区间 生物 遗传学
作者
Heather Teague,Haiou Li,Alexander Berg,Christin G. Hong,Rylee F. Petrole,Ross O’Hagan,Elizabeth M. Florida,Andrew Keel,Justin Rodante,Promita Kapoor,Álvaro González-Cantero,Alexander V. Sorokin,Aditya Joshi,Nidhi Patel,Joel M. Gelfand,Martin P. Playford,Nehal N. Mehta
出处
期刊:Journal of Investigative Dermatology [Elsevier]
卷期号:143 (10): 1947-1954.e4 被引量:3
标识
DOI:10.1016/j.jid.2023.01.044
摘要

APOA-1 is central to the high-density lipoprotein function of reverse cholesterol transport measured by cholesterol efflux capacity. Psoriasis is a systemic inflammatory disease associated with poor cholesterol efflux capacity and accelerated noncalcified coronary burden (NCB) as measured by coronary computed tomographic angiography. In this study, we characterized the relationship between APOA-1, cholesterol efflux capacity, and progression of NCB over 4 years. Consecutively recruited participants with psoriasis underwent coronary computed tomographic angiography for NCB quantification (Medis QAngio, Leiden, The Netherlands) at baseline (n = 310) and at four years (n = 124). Blood was assessed for cardiometabolic biomarkers. The lowest quartile of APOA-1 was associated with cardiometabolic blood markers (insulin, homeostatic model assessment for insulin resistance, and cholesterol efflux capacity) and higher NCB (P < 0.001). The low APOA-1 quartile had higher NCB at 4 years (β = -0.36, P = 0.02) in fully adjusted models. Finally, a 10-unit decrease of APOA-1 was associated with a 16% increase in NCB progression over 4 years (OR = 0.83, 95% confidence interval = 0.70-0.99, P = 0.04). In addition to being associated with cardiometabolic disease, low APOA-1 was associated with more NCB over time. These findings show that low APOA-1 is correlated with initiation and progression of coronary artery disease and may have clinical utility in identifying high-risk populations for development of cardiovascular disease.
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