Abstract 4361155: Serum Iron Predicts Long-Term Cardiovascular Outcomes in Diabetic Patients with Coronary Artery Disease, Independent of Iron Status

J Jiaxi Cheng (Fuwai Hospital, Peking Union Medical College, Beijing, China) K Kefei Dou (FuWai Hospital, Beijing, China) C Chao Wu

Abstract

Background: Iron status is crucial in the pathophysiology of coronary artery disease (CAD) and diabetes, with both iron deficiency and overload linked to adverse outcomes. However, the role of serum iron in diabetic CAD patients remains unclear. Objective: To evaluate the prognostic value of iron markers in predicting major adverse cardiac and cerebrovascular events (MACCEs) in diabetic CAD patients. Research Design and Methods: Serum iron, ferritin, transferrin, transferrin saturation, and soluble transferrin receptor were measured in 416 prospectively enrolled diabetic CAD patients. The primary endpoint was 1-year MACCEs, including cardiovascular death, myocardial infarction, stroke, revascularization, and heart failure. Results: During a median follow-up of 1.13 years, 38 MACCEs were observed (9.1%). Serum iron was an independent predictor of 1-year MACCEs (hazard ratio [HR]: 0.92; 95% CI: 0.88–0.97; P = 0.003), remaining significant after adjusting for baseline variables, hemoglobin, inflammation, lipid profiles, and iron storage markers (HR: 0.88; 95% CI: 0.81–0.96; P = 0.001). A decreasing exponential relationship was observed, identifying a clinically relevant threshold of 19 μmol/L. Patients with serum iron ≥19 μmol/L had significantly lower MACCEs compared to those with <19 μmol/L ( P < 0.05). Mediation analysis suggested that the protective effect of serum iron was partially mediated through reduced erythrocyte sedimentation rate (15.5%) and increased bilirubin (19.4%). Conclusions: Serum iron predicts long-term outcomes in diabetic CAD patients irrespective of iron storage status. A clinically significant threshold of 19 μmol/L was identified for risk stratification, with its protective effects potentially mediated through anti-inflammatory mechanisms.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (3)

J

Jiaxi Cheng

Fuwai Hospital, Peking Union Medical College, Beijing, China

K

Kefei Dou

FuWai Hospital, Beijing, China

C

Chao Wu