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Prognostic value of high‐sensitivity cardiac troponin I in patients with non‐ischaemic heart failure: insights from China

AIMS: Evidence of the prognostic value of high‐sensitivity troponin in patients with non‐ischaemic heart failure (NIHF) is scarce. This study aimed to assess the predictive value of high‐sensitivity cardiac troponin I (hs‐cTnI) in NIHF patients. METHODS: Hs‐cTnI was measured at baseline in 650 NIHF...

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Detalles Bibliográficos
Autores principales: Tian, Pengchao, Zhao, Xuemei, Huang, Liyan, Feng, Jiayu, Zhao, Lang, Liang, Lin, Huang, Boping, Zhang, Yuhui, Zhang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715791/
https://www.ncbi.nlm.nih.gov/pubmed/35831235
http://dx.doi.org/10.1002/ehf2.14065
Descripción
Sumario:AIMS: Evidence of the prognostic value of high‐sensitivity troponin in patients with non‐ischaemic heart failure (NIHF) is scarce. This study aimed to assess the predictive value of high‐sensitivity cardiac troponin I (hs‐cTnI) in NIHF patients. METHODS: Hs‐cTnI was measured at baseline in 650 NIHF patients admitted to the Heart Failure Center. The prognostic value of hs‐cTnI was assessed based on a well‐established model (including age, sex, New York Heart Association class, left ventricular ejection fraction, haemoglobin, sodium, estimated glomerular filtration rate, diabetes mellitus, treatment with angiotensin‐converting enzyme inhibitors or angiotensin II receptor blockers, treatment with β‐blockers, and NT‐proBNP). RESULTS: During a median follow‐up of 1036 days, 163 patients died of various causes. In total, 46.92% of patients had high hs‐cTnI (hs‐cTnI >0.011 ng/ml). Over a 3‐year follow‐up, patients with high hs‐cTnI (>0.011 ng/ml) had a 1.54 [95% confidence interval (95% CI) 1.11–2.15] fold higher all‐cause mortality risk than those without. Increasing concertation of hs‐cTnI was also associated with a 23.0% (95% CI 13–33%, per log(2) increase) increment risk of all‐cause mortality. The inclusion of hs‐cTnI significantly improved the risk prediction and stratification of all‐cause mortality (integrated discrimination improvement 1.58%, 95% CI 0.38–2.79%, absolute net reclassification improvement 23.41% 95% CI 4.52–44.49%, additive net reclassification improvement 27.8%, 95% CI 9.29–46.3%) of the well‐established model. CONCLUSIONS: Hs‐cTnI provides significant prognostic value and could further remarkably improve risk stratification and prediction capabilities in NIHF patients.