Affiliation:
1. 1 Department of Cardiology, Nazilli State Hospital, Aydin, Turkey
2. 2 Department of Endocrinology and Metabolism, Medinova Hospital, Aydin, Turkey
Abstract
Abstract
Background
This study investigated the relationship between coronary collateral circulation (CCC) and non–high-density lipoprotein cholesterol (non–HDL-C) in patients with stable coronary artery disease (CAD). Coronary collateral circulation plays a critical role in supporting blood flow, particularly in the ischemic myocardium. Previous studies show that non–HDL-C plays a more important role in the formation and progression of atherosclerosis than do standard lipid parameters.
Methods
A total of 226 patients with stable CAD and stenosis of more than 95% in at least 1 epicardial coronary artery were included in the study. Rentrop classification was used to assign patients into group 1 (n = 85; poor collateral) or 2 (n = 141; good collateral). To adjust for the observed imbalance in baseline covariates between study groups, propensity-score matching was used. Covariates were diabetes, Gensini score, and angiotensin-converting enzyme inhibitor use.
Results
In the propensity-matched population, the plasma non–HDL-C level (mean [SD], 177.86 [44.0] mg/dL vs 155.6 [46.21] mg/dL; P = .001) was statistically higher in the poor-collateral group. LDL-C (odds ratio [OR], 1.23; 95% CI, 1.11–1.30; P = .01), non–HDL-C (OR, 1.34; 95% CI, 1.20–1.51; P = .01), C-reactive protein (OR, 1.21; 95% CI, 1.11–1.32; P = .03), systemic immune-inflammation index (OR, 1.14; 95% CI, 1.05–1.21; P = .01), and C-reactive protein to albumin ratio (OR, 1.11; 95% CI, 1.06–1.17; P = .01) remained independent predictors of CCC in multivariate logistic regression analysis.
Conclusion
Non–HDL-C was an independent risk factor for developing poor CCC in stable CAD.
Publisher
Texas Heart Institute Journal
Subject
Cardiology and Cardiovascular Medicine
Cited by
1 articles.
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