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

Mengqiu Wei1, Hailin Pan2, Kai Guo3,4

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

Angiology
|December 14, 2020
PubMed

Insights

Elevated levels of a disintegrin and metalloproteinase with thrombospondin motifs 9 (ADAMTS-9) are linked to coronary artery disease (CAD) and predict worse outcomes in acute myocardial infarction patients.

Area of Science:

  • Cardiovascular Medicine
  • Biomarkers
  • Genetics

Background:

  • Genome-wide association studies suggest a link between ADAMTS-9 and atherosclerosis.
  • Coronary artery disease (CAD) poses a significant global health burden.
  • Understanding novel biomarkers for CAD diagnosis and prognosis is crucial.

Purpose of the Study:

  • To investigate the association of ADAMTS-9 serum levels with the presence, severity, and prognosis of CAD.
  • To evaluate ADAMTS-9 as a potential diagnostic and prognostic biomarker for CAD.

Main Methods:

  • A cohort of 666 participants undergoing coronary angiography was studied.
  • Serum ADAMTS-9 levels were measured and correlated with CAD status, severity (SYNTAX score), and clinical outcomes.
  • Statistical analyses included logistic regression and survival analysis.

Main Results:

  • Serum ADAMTS-9 levels were significantly higher in CAD patients compared to non-CAD controls (37.53 vs 12.04 ng/mL, P < .001).
  • ADAMTS-9 was an independent predictor of CAD (OR = 1.871, P < .001) and correlated with the SYNTAX score (r = 0.523, P < .001).
  • Elevated ADAMTS-9 predicted a higher risk of major adverse cardiovascular events (MACE) in acute myocardial infarction patients within 12 months (P = .034).

Conclusions:

  • Plasma ADAMTS-9 levels are elevated in patients with coronary artery disease.
  • ADAMTS-9 serves as an independent predictor for CAD diagnosis.
  • ADAMTS-9 levels are associated with disease severity and can predict MACE in acute myocardial infarction patients, highlighting its potential clinical utility.

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