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Impact of diabetes on the predictive value of heart failure biomarkers

BACKGROUND: Patients with diabetes mellitus (DM) have an increased risk of developing heart failure (HF). Further, DM is associated with poor prognosis in patients with HF. Our aim was to determine whether DM has any impact on the predictive value of a multi-biomarker panel in patients with HF. METH...

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Autores principales: Alonso, Nuria, Lupón, Josep, Barallat, Jaume, de Antonio, Marta, Domingo, Mar, Zamora, Elisabet, Moliner, Pedro, Galán, Amparo, Santesmases, Javier, Pastor, Cruz, Mauricio, Dídac, Bayes-Genis, Antoni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093972/
https://www.ncbi.nlm.nih.gov/pubmed/27809845
http://dx.doi.org/10.1186/s12933-016-0470-x
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author Alonso, Nuria
Lupón, Josep
Barallat, Jaume
de Antonio, Marta
Domingo, Mar
Zamora, Elisabet
Moliner, Pedro
Galán, Amparo
Santesmases, Javier
Pastor, Cruz
Mauricio, Dídac
Bayes-Genis, Antoni
author_facet Alonso, Nuria
Lupón, Josep
Barallat, Jaume
de Antonio, Marta
Domingo, Mar
Zamora, Elisabet
Moliner, Pedro
Galán, Amparo
Santesmases, Javier
Pastor, Cruz
Mauricio, Dídac
Bayes-Genis, Antoni
author_sort Alonso, Nuria
collection PubMed
description BACKGROUND: Patients with diabetes mellitus (DM) have an increased risk of developing heart failure (HF). Further, DM is associated with poor prognosis in patients with HF. Our aim was to determine whether DM has any impact on the predictive value of a multi-biomarker panel in patients with HF. METHODS: We included 1069 consecutive ambulatory HF patients in the study: age 66.2 ± 12.8 years, 33.5 ± 13.3 left ventricular ejection fraction, 36% diabetic patients. We measured serum concentrations of N-terminal pro-brain natriuretic peptide (NT-proBNP), high-sensitivity troponin T (hs-TnT), ST2, galectin-3, high-sensitivity C reactive protein (hs-CRP), cystatin-C, soluble transferrin receptor (sTfR), and neprilysin and followed patients for 4.9 ± 2.8 years. Primary endpoints were all-cause and cardiovascular death. RESULTS: During follow-up, 534 patients died; 283 died of cardiovascular causes. Diabetic subjects had higher mortality (57.7 vs. 45.6%, p < 0.001). NTproBNP (p = 0.07), hs-TnT (p < 0.001), galectin-3 (p < 0.001), and cystatin-C (p = 0.001) concentrations were higher in diabetic patients, whereas sTfR levels were lower (p = 0.005). There were no interactions between DM and NTproBNP, hs-TnT, galectin-3, hs-CRP, cystatin-C, sTfR, and neprilysin relative to risk prediction for all-cause or cardiovascular death. By contrast, ST2 significantly interacted with DM for all-cause (p = 0.02) and cardiovascular (p = 0.03) death. In diabetic patients, HRs for ST2 were 1.27 (95% CI 1.16–1.40, p < 0.001) and 1.23 (95% CI 1.09–1.39, p = 0.001) for all-cause and cardiovascular death, respectively. In nondiabetic patients, HRs for ST2 were 1.53 (95% CI 1.35–1.73, p < 0.001) and 1.64 (95% CI 1.31–2.05, p < 0.001) for all-cause and cardiovascular death, respectively. The multivariable Cox regression analysis showed that hs-TnT and ST2 were the only markers that were independently associated with both all-cause and cardiovascular mortality in patients with HF and diabetes. Moreover, in these patients, the combination of these two markers significantly increased discrimination as assessed by the area under the curve. CONCLUSIONS: Biomarkers used in the general population to predict the clinical course of heart failure are also useful in patients with diabetes. In these patients, among all the biomarkers analysed only hs-TnT and ST2 were independently associated with both all-cause and cardiovascular mortality.
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spelling pubmed-50939722016-11-07 Impact of diabetes on the predictive value of heart failure biomarkers Alonso, Nuria Lupón, Josep Barallat, Jaume de Antonio, Marta Domingo, Mar Zamora, Elisabet Moliner, Pedro Galán, Amparo Santesmases, Javier Pastor, Cruz Mauricio, Dídac Bayes-Genis, Antoni Cardiovasc Diabetol Original Investigation BACKGROUND: Patients with diabetes mellitus (DM) have an increased risk of developing heart failure (HF). Further, DM is associated with poor prognosis in patients with HF. Our aim was to determine whether DM has any impact on the predictive value of a multi-biomarker panel in patients with HF. METHODS: We included 1069 consecutive ambulatory HF patients in the study: age 66.2 ± 12.8 years, 33.5 ± 13.3 left ventricular ejection fraction, 36% diabetic patients. We measured serum concentrations of N-terminal pro-brain natriuretic peptide (NT-proBNP), high-sensitivity troponin T (hs-TnT), ST2, galectin-3, high-sensitivity C reactive protein (hs-CRP), cystatin-C, soluble transferrin receptor (sTfR), and neprilysin and followed patients for 4.9 ± 2.8 years. Primary endpoints were all-cause and cardiovascular death. RESULTS: During follow-up, 534 patients died; 283 died of cardiovascular causes. Diabetic subjects had higher mortality (57.7 vs. 45.6%, p < 0.001). NTproBNP (p = 0.07), hs-TnT (p < 0.001), galectin-3 (p < 0.001), and cystatin-C (p = 0.001) concentrations were higher in diabetic patients, whereas sTfR levels were lower (p = 0.005). There were no interactions between DM and NTproBNP, hs-TnT, galectin-3, hs-CRP, cystatin-C, sTfR, and neprilysin relative to risk prediction for all-cause or cardiovascular death. By contrast, ST2 significantly interacted with DM for all-cause (p = 0.02) and cardiovascular (p = 0.03) death. In diabetic patients, HRs for ST2 were 1.27 (95% CI 1.16–1.40, p < 0.001) and 1.23 (95% CI 1.09–1.39, p = 0.001) for all-cause and cardiovascular death, respectively. In nondiabetic patients, HRs for ST2 were 1.53 (95% CI 1.35–1.73, p < 0.001) and 1.64 (95% CI 1.31–2.05, p < 0.001) for all-cause and cardiovascular death, respectively. The multivariable Cox regression analysis showed that hs-TnT and ST2 were the only markers that were independently associated with both all-cause and cardiovascular mortality in patients with HF and diabetes. Moreover, in these patients, the combination of these two markers significantly increased discrimination as assessed by the area under the curve. CONCLUSIONS: Biomarkers used in the general population to predict the clinical course of heart failure are also useful in patients with diabetes. In these patients, among all the biomarkers analysed only hs-TnT and ST2 were independently associated with both all-cause and cardiovascular mortality. BioMed Central 2016-11-03 /pmc/articles/PMC5093972/ /pubmed/27809845 http://dx.doi.org/10.1186/s12933-016-0470-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Alonso, Nuria
Lupón, Josep
Barallat, Jaume
de Antonio, Marta
Domingo, Mar
Zamora, Elisabet
Moliner, Pedro
Galán, Amparo
Santesmases, Javier
Pastor, Cruz
Mauricio, Dídac
Bayes-Genis, Antoni
Impact of diabetes on the predictive value of heart failure biomarkers
title Impact of diabetes on the predictive value of heart failure biomarkers
title_full Impact of diabetes on the predictive value of heart failure biomarkers
title_fullStr Impact of diabetes on the predictive value of heart failure biomarkers
title_full_unstemmed Impact of diabetes on the predictive value of heart failure biomarkers
title_short Impact of diabetes on the predictive value of heart failure biomarkers
title_sort impact of diabetes on the predictive value of heart failure biomarkers
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093972/
https://www.ncbi.nlm.nih.gov/pubmed/27809845
http://dx.doi.org/10.1186/s12933-016-0470-x
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