Association Between Plasma ADAMTS-9 Levels and Severity of Coronary Artery Disease

Author:

Wei Mengqiu1,Pan Hailin2,Guo Kai34ORCID

Affiliation:

1. Intensive Care Unit, Zhongshan People’s Hospital, Zhongshan City, Guangdong, China

2. Department of Cardiology, Huizhou Municipal Central People’s Hospital, Huizhou City, Guangdong, China

3. Cardiovascular Medicine Department, Guangdong Second Provincial General Hospital, Guangzhou City, Guangdong, China

4. Department of Cardiology, Zhongshan People’s Hospital, Zhongshan City, Guangdong, China

Abstract

Genome-wide association studies have shown that a disintegrin and metalloproteinase with thrombospondin motifs 9 (ADAMTS-9) is associated with the development of atherosclerosis. We assessed the level of ADAMTS-9 in patients with coronary artery disease (CAD) and its severity and prognosis. We selected 666 participants who underwent coronary angiography in our hospital and met the inclusion and exclusion criteria; participants included non-CAD patients, patients with stable angina pectoris (SAP), unstable angina, non-ST-segment elevation myocardial infarction, or ST-segment elevation myocardial infarction. The serum level of ADAMTS-9 was higher in patients with CAD than in non-CAD patients (37.53 ± 8.55 ng/mL vs 12.04 ± 7.02 ng/mL, P < .001) and was an independent predictor for CAD (odds ratio = 1.871, 95% CI: 1.533-2.283, P < .001). Subgroup analysis showed that compared with the SAP group, the acute coronary syndrome groups had higher serum levels of ADAMTS-9. In addition, the level of ADAMTS-9 was related to the SYNTAX score (r = 0.523, P < .001). Patients with acute myocardial infarction (AMI) with elevated levels of ADAMTS-9 had a higher risk of major adverse cardiovascular events (MACE) within 12 months than those with lower levels (log-rank = 4.490, P = .034). Plasma ADAMTS-9 levels may be useful for the diagnosis of CAD and as predictors of MACE in AMI patients.

Funder

Zhongshan Public Welfare Science and Technology Research Project

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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