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Growth differentiation factor-15 predicts major adverse cardiac events and all-cause mortality in patients with atrial fibrillation
被引:16
作者:

Nopp, Stephan
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Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria

Koenigsbruegge, Oliver
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Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria

Kraemmer, Daniel
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Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria

Pabinger, Ingrid
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Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria

Ay, Cihan
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Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
机构:
[1] Med Univ Vienna, Dept Med 1, Clin Div Haematol & Haemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
关键词:
Atrial fibrillation;
Biomarkers;
Growth Differentiation Factor 15;
Mortality;
Prognosis;
RISK STRATIFICATION;
CARDIOVASCULAR EVENTS;
HEART-FAILURE;
DISEASE;
MARKER;
BIOMARKER;
STROKE;
ANTICOAGULATION;
APIXABAN;
WARFARIN;
D O I:
10.1016/j.ejim.2021.02.011
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Growth-differentiation factor-15 (GDF-15) has recently been described as a potential biomarker for predicting risk of mortality and cardiovascular events in patients with atrial fibrillation (AF) but requires validation in clinical practice. Methods: The study population consisted of 362 patients (mean age: 71 years, 37% women) with non-valvular AF included in a prospective cohort study. Relationship of GDF-15 with all-cause mortality and major adverse cardiac events (MACE) was analyzed using Cox regression. Survival analysis stratified by GDF-15 was based on national death records, while MACE was recorded at personal follow-up. Further, we evaluated the recently developed GDF-15 based prognostic score towards prediction of all-cause mortality (ABC-death score). Results: Over a median observation period of 4.3 years, 81 (23.3%) patients died, and over a median personal follow-up of 316 days 47 MACE occurred. GDF-15 was independently associated with all-cause mortality (adjusted HR per double increase 2.33, 95%CI 1.74-3.13) and MACE (adjusted HR per double increase 2.33, 95% CI 1.60-3.39). GDF-15 levels, measured at follow-up, were similarly associated with mortality, and longitudinal measurements of GDF-15 did not significantly differ. Six-year survival probability of patients above vs. below the median GDF-15 level was 44% (95%CI 34-57) and 84% (95%CI 76-93), respectively. The ABC-death score revealed a C-statistic of 0.80. Conclusion: GDF-15 predicts risk of all-cause mortality and MACE in patients with non-valvular AF. Further, the ABC-death score showed good predictive accuracy in a "real-world" cohort. Therefore, introduction of GDF15 into clinical practice would enhance risk prediction of morbidity and mortality in AF patients.
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页码:35 / 42
页数:8
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