Prognostic value of troponin I in atrial fibrillation.


Por: Quesada, A, Lopez-Valero, L, Marcaida-Benito, G, Bello, J, Quesada-Ocete, J, Rubini-Costa, R, Quesada-Ocete, B, Rubini-Puig, R, Ferez-Marti, A, del Moral-Ronda, V, Palanca-Gil, V, de la Guia-Galipienso, F, Lavie, C, Lippi, G and Sanchis-Gomar, F

Publicada: 1 jul 2021 Ahead of Print: 25 feb 2021
Categoría: Cardiology and cardiovascular medicine

Resumen:
OBJECTIVE: To evaluate whether circulating cardiac troponin I (cTnI) levels are associated with worst outcomes in patients with atrial fibrillation (AF). METHODS: Consecutive patients visiting the emergency room (ER) with a new episode of a previously diagnosed AF or a new diagnosis of AF during ER admission between January 1st, 2010 and December 31st, 2015, were enrolled in the study (n = 2617). After applying exclusion criteria and eliminating repeated episodes, 2013 patients were finally included. Of these, 1080 patients with at least one cTnI measurement in the ER were selected and classified into 4 groups according to cTnI quartiles: Q1 (n = 147) cTnI <10 ng/L (Group 1); Q2 (n = 254): 10-19 ng/L (Group 2); Q3 (n = 409): 20-40 ng/L (Group 3); and Q4 (n = 270): cTnI >40 ng/L (Group 4). The median follow-up period was 47.8 ± 32.8 months. The primary endpoint was all-cause death during the follow-up. RESULTS: A higher mortality was found in group 4 compared with the other groups (58.9% vs. 28.5%, respectively, p < 0.001), along with, hospitalizations (40.4% vs. 30.7%, p = 0.004), and readmissions due to decompensated heart failure (26.7% vs. 2.5%, p = 0.002). The probability of survival without AF recurrences was lower in the Q4 (p = 0.045). Moreover, cTnI levels >40 ng/L (Q4) were an independent risk factor of death (HR, 2.03; 95% CI, 1.64-2.51; p < 0.001). CONCLUSION: The assessment of cTnI at ER admission could be a useful strategy for risk stratification of patients diagnosed with AF by identifying a subgroup with medium-term to long-term increased risk of adverse events and mortality.

Filiaciones:
Quesada, A:
 Gen Univ Hosp Consortium Valencia, Arrhythmia Unit, Cardiol Serv, Av Tres Creus 2, Valencia 46014, Spain

 Catholic Univ Valencia San Vicente Martir, Sch Med, Valencia, Spain

Lopez-Valero, L:
 Catholic Univ Valencia San Vicente Martir, Sch Med, Valencia, Spain

Marcaida-Benito, G:
 Gen Univ Hosp Consortium Valencia, Lab Med Serv, Valencia, Spain

Bello, J:
 Gen Univ Hosp Consortium Valencia, Arrhythmia Unit, Cardiol Serv, Av Tres Creus 2, Valencia 46014, Spain

Quesada-Ocete, J:
 Gen Univ Hosp Consortium Valencia, Arrhythmia Unit, Cardiol Serv, Av Tres Creus 2, Valencia 46014, Spain

Rubini-Costa, R:
 Hosp Virgen de las Nieves, Dept Cardiol, Granada, Spain

Quesada-Ocete, B:
 Johannes Gutenberg Univ Mainz, Univ Med Ctr, Ctr Cardiol, Dept Cardiol II Electroplaysiol, Mainz, Germany

Rubini-Puig, R:
 Gen Univ Hosp Consortium Valencia, Emergency Room Dept, Valencia, Spain

Ferez-Marti, A:
 Gen Univ Hosp Consortium Valencia, Lab Med Serv, Valencia, Spain

del Moral-Ronda, V:
 Hosp Univ Tarragona Joan XXVM, Dept Cardiol, Tarragona, Spain

Palanca-Gil, V:
 Gen Univ Hosp Consortium Valencia, Arrhythmia Unit, Cardiol Serv, Av Tres Creus 2, Valencia 46014, Spain

:
 Cardiol Serv Marina Baixa Hosp, Alicante, Spain

Lavie, C:
 Univ Queensland, Sch Med, John Ochsner Heart & Vasc Inst, Ochsner Clin Sch, New Orleans, LA USA

Lippi, G:
 Univ Verona, Sect Clin Biochem, Verona, Italy

Sanchis-Gomar, F:
 Univ Valencia, Dept Physiol, Fac Med, Av Blasco Ibanez 15, Valencia 46010, Spain

 INCLIVA Biomed Res Inst, Valencia, Spain
ISSN: 00330620





PROGRESS IN CARDIOVASCULAR DISEASES
Editorial
W. B. Saunders Co., Ltd., United States, Estados Unidos America
Tipo de documento: Article
Volumen: 67 Número:
Páginas: 80-88
WOS Id: 000686978200012
ID de PubMed: 33639172

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