Growth Differentiation Factor 15: A Prognostic Marker in Patients with Acute Chest Pain without Acute Myocardial Infarction

被引:7
作者
Myrmel, Gard M. S. [1 ]
Steiro, Ole-Thomas [1 ]
Tjora, Hilde L. [2 ]
Langorgen, Jorund [1 ]
Bjorneklett, Rune [2 ,3 ]
Skadberg, Oyvind [4 ]
Bonarjee, Vernon V. S. [5 ]
Mjelva, oistein R. [6 ]
Pedersen, Eva K. R. [1 ,7 ]
Vikenes, Kjell [1 ,7 ]
Omland, Torbjorn [8 ,9 ]
Aakre, Kristin M. [1 ,7 ,10 ]
机构
[1] Haukeland Hosp, Dept Heart Dis, Bergen, Norway
[2] Haukeland Hosp, Emergency Care Clin, Bergen, Norway
[3] Univ Bergen, Dept Clin Med, Bergen, Norway
[4] Stavanger Univ Hosp, Lab Med Biochem, Stavanger, Norway
[5] Stavanger Univ Hosp, Dept Cardiol, Stavanger, Norway
[6] Stavanger Univ Hosp, Dept Med, Stavanger, Norway
[7] Univ Bergen, Dept Clin Sci, Bergen, Norway
[8] Univ Oslo, Inst Clin Med, KG Jebsen Ctr Cardiac Biomarkers, Oslo, Norway
[9] Akershus Univ Hosp, Dept Cardiol, Oslo, Norway
[10] Haukeland Hosp, Dept Med Biochem & Pharmacol, Bergen, Norway
关键词
TROPONIN-I; HEART; ASSOCIATION; DIAGNOSIS; EVENTS; GDF-15; MEMBER;
D O I
10.1093/clinchem/hvad015
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Acute chest pain is associated with an increased risk of death and cardiovascular events even when acute myocardial infarction (AMI) has been excluded. Growth differentiation factor-15 (GDF-15) is a strong prognostic marker in patients with acute chest pain and AMI, but the prognostic value in patients without AMI is uncertain. This study sought to investigate the ability of GDF-15 to predict long-term prognosis in patients presenting with acute chest pain without AMI. Methods In total, 1320 patients admitted with acute chest pain without AMI were followed for a median of 1523 days (range: 4 to 2208 days). The primary end point was all-cause mortality. Secondary end points included cardiovascular (CV) death, future AMI, heart failure hospitalization, and new-onset atrial fibrillation (AF). Results Higher concentrations of GDF-15 were associated with increased risk of death from all causes (median concentration in non-survivors vs survivors: 2124 pg/mL vs 852 pg/mL, P < 0.001), and all secondary end points. By multivariable Cox regression, GDF-15 concentration >= 4th quartile (compared to <4th quartile) remained an independent predictor of all-cause death (adjusted hazard ratio (HR): 2.75; 95% CI, 1.69-4.45, P < 0.001), CV death (adjusted HR: 3.74; 95% CI, 1.31-10.63, P = 0.013), and heart failure hospitalization (adjusted HR: 2.60; 95% CI, 1.11-6.06, P = 0.027). Adding GDF-15 to a model consisting of established risk factors and high-sensitivity cardiac troponin T (hs-cTnT) led to a significant increase in C-statistics for prediction of all-cause mortality. Conclusions Higher concentrations of GDF-15 were associated with increased risk of mortality from all causes and risk of future CV events.
引用
收藏
页码:649 / 660
页数:12
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