Abstract 4371516: Hemoglobin and suPAR Predict 5 Year MACE in Men but Not Women with HFpEF and Coronary Artery Disease

B Bernard Evenhuis (Emory University School of Medicine, Morrow, Georgia, United States) A Austin Rim (Emory University, Atlanta, Georgia, United States) T Taha Ahmed (Emory University School of Medicine, Morrow, Georgia, United States) K Kristen Harris (Emory University, Duluth, Georgia, United States) P Puja Mehta (EMORY UNIVERSITY, Atlanta, Georgia, United States) A Arshed Quyyumi (EMORY UNIVERSITY, Atlanta, Georgia, United States)

Abstract

Introduction: Heart failure with preserved ejection fraction (HFpEF) shows clear sex differences in pathophysiology and outcomes, but it is unknown circulating biomarkers major adverse cardiovascular events (MACE) risk differently between men and women. Hypothesis Circulating biomarkers predict MACE differently in female and male HFpEF patients with coronary artery disease (CAD). Methods: We retrospectively analyzed patients with HFpEF and CAD from the Emory Cardiovascular Biobank. After imputing missing data, we screened a broad panel of clinical variables and biomarkers (ejection fraction, eGFR, lipid profile, renal function tests, blood counts, CRP, BNP/NTproBNP, suPAR, troponin, C-peptide, B12, lipoprotein(a), Gal3, vitamin D, ApoA1, ApoB, insulin, homocysteine, testosterone, and DHEAS). We used ElasticNet to select pertinent predictors for 5-year MACE and CV death. Selected features were entered into a non-penalized Cox model, adjusting for race, age, BMI, ACE/ARB use, statin/beta-blocker use, smoking history, hypertension, hyperlipidemia, diabetes, prior myocardial infarction, ejection fraction, and eGFR. Results: We included 760 patients with HFpEF and CAD (315 women, 445 men). Men were younger (median 67 vs. 73 years; p < 0.001), with more CKD (40.0% vs. 29.2%; p = 0.003) and prior MI (26.9% vs. 20.1%; p = 0.039). In men , ElasticNet selected hemoglobin and suPAR as key variables associated with 5-year MACE. In adjusted Cox models, hemoglobin (HR 0.62; 95% CI 0.47-0.82; p = 0.001) and suPAR (HR 1.37; 95% CI 1.13-1.64; p = 0.001) independently predicted MACE (Table 1); hemoglobin also predicted CV death. In women , ElasticNet did not identify any biomarker as a predictor of MACE or CV death. Instead, adjusted Cox models identified age ≥75 years (HR 3.59; 95% CI 1.23-10.49; p = 0.020), BMI <18.5 kg/m2 (HR 4.66; 95% CI 1.30-16.73; p = 0.018), obesity (BMI ≥30 kg/m2; HR 3.02; 95% CI 1.33-6.85; p = 0.008), and smoking (HR 1.98; 95% CI 1.18-3.31; p = 0.009) as independent predictors of 5-year MACE, while age, underweight BMI, obesity, and smoking increased CV death risk, with ACEI/ARB use and higher hemoglobin protective (Table 2). Adjusted Kaplan-Meier curves demonstrate clear separation by suPAR level for men but not for women (Figure 1). Conclusions: In HFpEF and CAD, lower hemoglobin and higher suPAR predict 5 year MACE in men only. In women, MACE risk was predicted by age, underweight or obese BMI, and smoking rather than circulating biomarkers.

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 (6)

B

Bernard Evenhuis

Emory University School of Medicine, Morrow, Georgia, United States

A

Austin Rim

Emory University, Atlanta, Georgia, United States

T

Taha Ahmed

Emory University School of Medicine, Morrow, Georgia, United States

K

Kristen Harris

Emory University, Duluth, Georgia, United States

P

Puja Mehta

EMORY UNIVERSITY, Atlanta, Georgia, United States

A

Arshed Quyyumi

EMORY UNIVERSITY, Atlanta, Georgia, United States