Key result
Higher total plaque volume on CCTA is independently linked to increased MACE risk.
Why the study?
Chronic kidney disease is associated with an increased risk of cardiovascular events, motivating a comparison of CCTA-assessed coronary plaque characteristics between patients with and without CKD and an evaluation of their associations with MACE.
Does quantitative coronary plaque characterization and perivascular fat attenuation index assessment on CCTA predict major adverse cardiovascular events in patients with chronic kidney disease and suspected coronary artery disease?
Cohort
Does quantitative coronary plaque characterization and perivascular fat attenuation index assessment on CCTA predict major adverse cardiovascular events in patients with chronic kidney disease and suspected coronary artery disease?
In patients with chronic kidney disease and suspected coronary artery disease, CCTA-derived lipid plaque burden and perivascular fat attenuation index independently predict major adverse cardiovascular events, offering enhanced cardiovascular risk stratification.
CCTA plaque volume may aid MACE risk stratification in CKD; leaves open prospective validation before clinical adoption.
Background: Chronic kidney disease (CKD) is associated with an increased risk of cardiovascular events. This study compared coronary plaque characteristics assessed by coronary computed tomography angiography (CCTA) between patients with and without CKD and evaluated their associations with major adverse cardiovascular events (MACE). Methods: This secondary analysis of the multicenter CREATION-CHINA cohort included patients with suspected coronary artery disease who underwent CCTA during 2016–2020. CKD was defined as an estimated glomerular filtration rate <60 mL/min/1.73 m 2 . Propensity score matching (1:3) used age, sex, hypertension, diabetes mellitus, smoking, family history of coronary artery disease, and hyperlipidemia. Quantitative plaque characteristics and perivascular fat attenuation index (FAI) were assessed. MACE comprised all-cause death, non-fatal myocardial infarction, stroke, or revascularization >90 days after CCTA. Cox models estimated hazard ratios (HRs) and 95% confidence intervals (CIs); analyses of CCTA-derived predictors were adjusted for age, body mass index, and hypertension. High plaque burden was defined as total plaque burden in the highest quartile. Results: After matching, 2,267 patients were included (588 with CKD and 1,679 without CKD). During a median follow-up of 3.47 years (interquartile range, 2.36–4.10), MACE occurred in 30 patients with CKD (5.1%) and 52 without CKD (3.1%; P=0.035). Patients with CKD had higher median total plaque volume (39.90 vs. 0 mm 3 ), median total plaque burden (8.83% vs. 0%), and prevalence of high-risk plaque (9.35% vs. 4.35%; all P<0.001). Among patients with CKD, lipid plaque burden (adjusted HR =1.107, 95% CI: 1.006–1.218; P=0.038) and high FAI (adjusted HR =4.027, 95% CI: 2.329–6.960; P<0.001) were independently associated with MACE. Compared with patients without CKD and with low plaque burden, those with CKD and high plaque burden had a higher risk of MACE (adjusted HR =6.153, 95% CI: 2.937–12.890; P<0.001). Conclusions: CKD was associated with greater coronary plaque burden and a higher incidence of MACE. Lipid plaque burden and high FAI were independently associated with MACE after adjustment for age, body mass index, and hypertension, supporting their potential role in cardiovascular risk assessment in patients with CKD.
No takes yet. Share an insight, caveat, or question.
Yuan et al. (2026) conducted a cohort in Chronic kidney disease and coronary artery disease. Total plaque volume on coronary computed tomography angiography vs. Lower plaque volume / Non-CKD cohort was evaluated on Major adverse cardiovascular events (MACE) (HR 1.000080, 95% CI 1.000045–1.000114, p=<0.001). Total plaque volume on CCTA was independently associated with major adverse cardiovascular events in multivariable Cox analysis (HR 1.000080, 95% CI 1.000045–1.000114, P<0.001).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: