Serum ST2 and hospitalization rates in Caucasian and African American outpatients with heart failure.
Autor: | Savvoulidis P; Royal Brompton & Harefield NHS Foundation Trust, London, UK., Snider JV; Critical Diagnostics, San Diego, CA, United States of America., Rawal S; Department of Medicine, Stony Brook University, Stony Brook, NY, United States of America., Morris AA; Department of Medicine, Emory University, Atlanta, GA, United States of America., Butler J; Department of Medicine, University of Mississippi, Jackson, MS, United States of America., Georgiopoulou VV; Department of Medicine, Emory University, Atlanta, GA, United States of America., Kalogeropoulos AP; Department of Medicine, Stony Brook University, Stony Brook, NY, United States of America. Electronic address: andreas.kalogeropoulos@stonybrook.edu. |
---|---|
Jazyk: | angličtina |
Zdroj: | International journal of cardiology [Int J Cardiol] 2020 Apr 01; Vol. 304, pp. 116-121. Date of Electronic Publication: 2019 Nov 06. |
DOI: | 10.1016/j.ijcard.2019.11.002 |
Abstrakt: | Background: Limited data exist on the association between circulating suppression of tumorigenicity 2 (ST2) and recurrent hospitalizations and emergency department (ED) encounters in outpatients with heart failure (HF). In addition, data on ST2 in African American patients with HF are scarce. Methods: We evaluated 307 outpatients with HF (age, 57 ± 12 years; 64.2% men; 51.5% Caucasian, 45.6% African American; median ejection fraction, 35%; ischemic etiology, 41.4%). Median ST2 was 37.8 ng/mL (29.6-51.4). Results: After a median of 3.1 years, there were 584 hospitalizations (224 for HF) and 335 ED visits (80 for HF). Patients (N = 176; 57.3%) with elevated (>35 ng/mL) ST2 had 2-fold higher hospitalization rates in adjusted models (rate ratio [RR] 1.97; 95% CI 1.38-2.82; P < 0.001), driven by 3.5-fold higher HF hospitalization rates (adjusted RR 3.56; 95% CI 1.69-7.49; P < 0.001). These associations persisted after adjusting for baseline B-type natriuretic peptide levels. Findings were similar for elevated ST2 and ED visit rates. Elevated ST2 was associated with the composite of death or HF hospitalization (109 patients; 3-year estimate: 35.4%); risk was 5-fold higher in the first 6 months but declined gradually. The higher hospitalization rates and composite endpoint risk associated with elevated ST2 was similar in African Americans and Caucasians. In landmark analyses in a subset of patients, 6-month (N = 112) and 12-month (N = 149) changes in ST2 levels from baseline added prognostic information. Conclusions: Elevated ST2 in outpatients with HF portends higher healthcare resources utilization and higher risk for accelerated disease progression, regardless of race, especially in the first 6 months. Competing Interests: Declaration of competing interest The authors report no relationships that could be construed as a conflict of interest. (Copyright © 2019 Elsevier B.V. All rights reserved.) |
Databáze: | MEDLINE |
Externí odkaz: |