Key result
Elevated Lp(a) and diabetes act synergistically to heighten cardiovascular and all-cause mortality in CAD.
Why the study?
The joint association of elevated lipoprotein(a) and diabetes mellitus with survival outcomes in coronary artery disease patients was limited and needed investigation.
Does the combination of elevated Lipoprotein(a) and diabetes mellitus increase mortality risk in patients with coronary artery disease?
Cohort (n=65,547)
Yes
Does the combination of elevated Lipoprotein(a) and diabetes mellitus increase mortality risk in patients with coronary artery disease?
Elevated Lipoprotein(a) and diabetes mellitus act synergistically to increase the risk of cardiovascular and all-cause mortality in patients with coronary artery disease.
AIMS: Lipoprotein(a) [Lp(a)] and diabetes mellitus (DM) are independent risk factors for worse outcomes in coronary artery disease (CAD) patients. Evidence of their joint association is limited. We aimed to investigate the combined effect of elevated Lp(a) and DM on survival outcomes in CAD patients. METHODS AND MATERIALS: This study included 65 547 CAD patients (62.6 ± 10.7 years, 27.7% female) from CIN-II and RED-CARPET cohorts. Patients were stratified into four groups by Lp(a) levels (< or ≥ 30 mg/dL) and DM status. Multivariable Cox regression models estimated associations with cardiovascular and all-cause mortality, examining additive and multiplicative interactions. RESULTS: During a median follow-up of 5.5 years, 10 686 (16.3%) patients died from all causes and 5106 (7.8%) died from cardiovascular causes. Patients with Lp(a) ≥ 30 mg/dL and DM were independently associated with cardiovascular mortality (adjusted hazard ratio [aHR]: 1.28, 95% CI: 1.20-1.35; aHR: 1.53, 95% CI: 1.44-1.62, all p < 0.001, respectively). Compared to patients with Lp(a) < 30 mg/dL without DM, the aHRs were 1.26 (95% CI: 1.16-1.36, p < 0.001), 1.51 (95% CI: 1.40-1.62, p < 0.001) and 2.00 (95% CI: 1.83-2.18, p < 0.001) for those with Lp(a) ≥ 30 mg/dL without DM, Lp(a) < 30 mg/dL with DM and Lp(a) ≥ 30 mg/dL with DM, respectively. Significant additive interaction between elevated Lp(a) and DM on cardiovascular mortality was observed, with 12% of the excess risk attributed. Similar associations were observed in all-cause mortality. CONCLUSIONS: In patients with CAD, elevated Lp(a) and DM act synergistically to increase the risk of cardiovascular and all-cause mortality, suggesting that both risks should be considered to integrate management.
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Zhou et al. (2026) conducted a cohort in Coronary artery disease (n=65,547). Elevated Lipoprotein(a) (≥ 30 mg/dL) and Diabetes Mellitus vs. Lipoprotein(a) < 30 mg/dL without Diabetes Mellitus was evaluated on Cardiovascular mortality (HR 2.00, 95% CI 1.83-2.18, p=<0.001). Elevated Lipoprotein(a) ≥30 mg/dL and diabetes mellitus synergistically increased cardiovascular mortality risk in CAD patients compared to neither condition (aHR 2.00; 95% CI 1.83-2.18; p<0.001).
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