Cargando…
Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation
BACKGROUND: Hospitalization for heart failure (HF) is very common in patients with atrial fibrillation (AF). We hypothesized that biomarkers of inflammation can identify patients with AF at increased risk of this important complication. METHODS AND RESULTS: Patients with established AF were prospect...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174180/ https://www.ncbi.nlm.nih.gov/pubmed/33843247 http://dx.doi.org/10.1161/JAHA.120.019168 |
_version_ | 1783702851490414592 |
---|---|
author | Benz, Alexander P. Aeschbacher, Stefanie Krisai, Philipp Moschovitis, Giorgio Blum, Steffen Meyre, Pascal Blum, Manuel R. Rodondi, Nicolas Di Valentino, Marcello Kobza, Richard De Perna, Maria Luisa Bonati, Leo H. Beer, Jürg H. Kühne, Michael Osswald, Stefan Conen, David |
author_facet | Benz, Alexander P. Aeschbacher, Stefanie Krisai, Philipp Moschovitis, Giorgio Blum, Steffen Meyre, Pascal Blum, Manuel R. Rodondi, Nicolas Di Valentino, Marcello Kobza, Richard De Perna, Maria Luisa Bonati, Leo H. Beer, Jürg H. Kühne, Michael Osswald, Stefan Conen, David |
author_sort | Benz, Alexander P. |
collection | PubMed |
description | BACKGROUND: Hospitalization for heart failure (HF) is very common in patients with atrial fibrillation (AF). We hypothesized that biomarkers of inflammation can identify patients with AF at increased risk of this important complication. METHODS AND RESULTS: Patients with established AF were prospectively enrolled. Levels of hs‐CRP (high‐sensitivity C‐reactive protein) and interleukin‐6 were measured from plasma samples obtained at baseline. We calculated an inflammation score ranging from 0 to 4 (1 point for each biomarker between the 50th and 75th percentile, 2 points for each biomarker above the 75th percentile). Individual associations of biomarkers and the inflammation score with HF hospitalization were obtained from multivariable Cox proportional hazards models. A total of 3784 patients with AF (median age 72 years, 24% prior HF) were followed for a median of 4.0 years. The median (interquartile range) plasma levels of hs‐CRP and interleukin‐6 were 1.64 (0.81–3.69) mg/L and 3.42 (2.14–5.60) pg/mL, respectively. The overall incidence of HF hospitalization was 3.04 per 100 person‐years and increased from 1.34 to 7.31 per 100 person‐years across inflammation score categories. After multivariable adjustment, both biomarkers were significantly associated with the risk of HF hospitalization (per increase in 1 SD, adjusted hazard ratio [HR], 1.22; 95% CI, 1.11–1.34 for log‐transformed hs‐CRP; adjusted HR, 1.48; 95% CI, 1.35–1.62 for log‐transformed interleukin‐6). Similar results were obtained for the inflammation score (highest versus lowest score, adjusted HR, 2.43; 95% CI, 1.80–3.30; P value for trend <0.001). CONCLUSIONS: Biomarkers of inflammation strongly predicted HF hospitalization in a large, contemporary sample of patients with AF. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02105844. |
format | Online Article Text |
id | pubmed-8174180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81741802021-06-11 Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation Benz, Alexander P. Aeschbacher, Stefanie Krisai, Philipp Moschovitis, Giorgio Blum, Steffen Meyre, Pascal Blum, Manuel R. Rodondi, Nicolas Di Valentino, Marcello Kobza, Richard De Perna, Maria Luisa Bonati, Leo H. Beer, Jürg H. Kühne, Michael Osswald, Stefan Conen, David J Am Heart Assoc Original Research BACKGROUND: Hospitalization for heart failure (HF) is very common in patients with atrial fibrillation (AF). We hypothesized that biomarkers of inflammation can identify patients with AF at increased risk of this important complication. METHODS AND RESULTS: Patients with established AF were prospectively enrolled. Levels of hs‐CRP (high‐sensitivity C‐reactive protein) and interleukin‐6 were measured from plasma samples obtained at baseline. We calculated an inflammation score ranging from 0 to 4 (1 point for each biomarker between the 50th and 75th percentile, 2 points for each biomarker above the 75th percentile). Individual associations of biomarkers and the inflammation score with HF hospitalization were obtained from multivariable Cox proportional hazards models. A total of 3784 patients with AF (median age 72 years, 24% prior HF) were followed for a median of 4.0 years. The median (interquartile range) plasma levels of hs‐CRP and interleukin‐6 were 1.64 (0.81–3.69) mg/L and 3.42 (2.14–5.60) pg/mL, respectively. The overall incidence of HF hospitalization was 3.04 per 100 person‐years and increased from 1.34 to 7.31 per 100 person‐years across inflammation score categories. After multivariable adjustment, both biomarkers were significantly associated with the risk of HF hospitalization (per increase in 1 SD, adjusted hazard ratio [HR], 1.22; 95% CI, 1.11–1.34 for log‐transformed hs‐CRP; adjusted HR, 1.48; 95% CI, 1.35–1.62 for log‐transformed interleukin‐6). Similar results were obtained for the inflammation score (highest versus lowest score, adjusted HR, 2.43; 95% CI, 1.80–3.30; P value for trend <0.001). CONCLUSIONS: Biomarkers of inflammation strongly predicted HF hospitalization in a large, contemporary sample of patients with AF. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02105844. John Wiley and Sons Inc. 2021-04-10 /pmc/articles/PMC8174180/ /pubmed/33843247 http://dx.doi.org/10.1161/JAHA.120.019168 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Benz, Alexander P. Aeschbacher, Stefanie Krisai, Philipp Moschovitis, Giorgio Blum, Steffen Meyre, Pascal Blum, Manuel R. Rodondi, Nicolas Di Valentino, Marcello Kobza, Richard De Perna, Maria Luisa Bonati, Leo H. Beer, Jürg H. Kühne, Michael Osswald, Stefan Conen, David Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title | Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title_full | Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title_fullStr | Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title_full_unstemmed | Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title_short | Biomarkers of Inflammation and Risk of Hospitalization for Heart Failure in Patients With Atrial Fibrillation |
title_sort | biomarkers of inflammation and risk of hospitalization for heart failure in patients with atrial fibrillation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174180/ https://www.ncbi.nlm.nih.gov/pubmed/33843247 http://dx.doi.org/10.1161/JAHA.120.019168 |
work_keys_str_mv | AT benzalexanderp biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT aeschbacherstefanie biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT krisaiphilipp biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT moschovitisgiorgio biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT blumsteffen biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT meyrepascal biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT blummanuelr biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT rodondinicolas biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT divalentinomarcello biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT kobzarichard biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT depernamarialuisa biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT bonatileoh biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT beerjurgh biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT kuhnemichael biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT osswaldstefan biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT conendavid biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation AT biomarkersofinflammationandriskofhospitalizationforheartfailureinpatientswithatrialfibrillation |