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CA‐125 variation in acute heart failure: a single‐centre analysis

AIMS: A decrease in carbohydrate antigen 125 (CA‐125) predicts survival advantage in chronic heart failure (HF); the impact of its variation in acute HF is unknown. We studied the association of CA‐125 decrease with prognosis in acute HF. METHODS AND RESULTS: We studied acute hospitalized HF patient...

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Autores principales: Lourenço, Patrícia, Cunha, Filipe M., Elias, Catarina, Fernandes, Catarina, Barroso, Isaac, Guimarães, João T., Bettencourt, Paulo
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/PMC8934914/
https://www.ncbi.nlm.nih.gov/pubmed/34989167
http://dx.doi.org/10.1002/ehf2.13758
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author Lourenço, Patrícia
Cunha, Filipe M.
Elias, Catarina
Fernandes, Catarina
Barroso, Isaac
Guimarães, João T.
Bettencourt, Paulo
author_facet Lourenço, Patrícia
Cunha, Filipe M.
Elias, Catarina
Fernandes, Catarina
Barroso, Isaac
Guimarães, João T.
Bettencourt, Paulo
author_sort Lourenço, Patrícia
collection PubMed
description AIMS: A decrease in carbohydrate antigen 125 (CA‐125) predicts survival advantage in chronic heart failure (HF); the impact of its variation in acute HF is unknown. We studied the association of CA‐125 decrease with prognosis in acute HF. METHODS AND RESULTS: We studied acute hospitalized HF patients. Predictors of admission and discharge CA‐125 were determined by linear regression. Follow‐up was 1 year; endpoint was all‐cause death. The association of admission and discharge CA‐125 with mortality was assessed using a Cox‐regression analysis. A Cox‐regression analysis was also used to assess the prognostic impact of CA‐125 decrease during hospitalization. Analysis was stratified by length of hospital stay (LOS). We studied 363 patients, 51.5% male, mean age 75 ± 12 years, 51.5% ischaemic, 30.0% with preserved ejection fraction, and 57.3% with reduced ejection fraction; patients presented elevated comorbidity burden. Median LOS was 7 (5–11) days. In the subgroup of 262 patients with CA‐125 measured both at admission and at discharge, we reported a significant increase in its levels: 56.0 (26.0–160.7) U/mL to 74.0 (32.3–195.0) U/mL. Independent predictors of admission CA‐125 were higher BNP and lower creatinine. Predictors of discharge CA‐125 were higher discharge BNP, lower discharge albumin, and younger age. Both admission and discharge CA‐125 predicted mortality. During follow‐up, 75 (31.8%) patients died. A decrease in CA‐125 predicted a 68% reduction in the 1 year death risk only in patients with LOS > 10 days. CONCLUSIONS: Our results suggest that an early re‐evaluation (>10 days) with CA‐125 measurement after an acute HF hospitalization may be of interest in patient management.
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spelling pubmed-89349142022-03-24 CA‐125 variation in acute heart failure: a single‐centre analysis Lourenço, Patrícia Cunha, Filipe M. Elias, Catarina Fernandes, Catarina Barroso, Isaac Guimarães, João T. Bettencourt, Paulo ESC Heart Fail Original Articles AIMS: A decrease in carbohydrate antigen 125 (CA‐125) predicts survival advantage in chronic heart failure (HF); the impact of its variation in acute HF is unknown. We studied the association of CA‐125 decrease with prognosis in acute HF. METHODS AND RESULTS: We studied acute hospitalized HF patients. Predictors of admission and discharge CA‐125 were determined by linear regression. Follow‐up was 1 year; endpoint was all‐cause death. The association of admission and discharge CA‐125 with mortality was assessed using a Cox‐regression analysis. A Cox‐regression analysis was also used to assess the prognostic impact of CA‐125 decrease during hospitalization. Analysis was stratified by length of hospital stay (LOS). We studied 363 patients, 51.5% male, mean age 75 ± 12 years, 51.5% ischaemic, 30.0% with preserved ejection fraction, and 57.3% with reduced ejection fraction; patients presented elevated comorbidity burden. Median LOS was 7 (5–11) days. In the subgroup of 262 patients with CA‐125 measured both at admission and at discharge, we reported a significant increase in its levels: 56.0 (26.0–160.7) U/mL to 74.0 (32.3–195.0) U/mL. Independent predictors of admission CA‐125 were higher BNP and lower creatinine. Predictors of discharge CA‐125 were higher discharge BNP, lower discharge albumin, and younger age. Both admission and discharge CA‐125 predicted mortality. During follow‐up, 75 (31.8%) patients died. A decrease in CA‐125 predicted a 68% reduction in the 1 year death risk only in patients with LOS > 10 days. CONCLUSIONS: Our results suggest that an early re‐evaluation (>10 days) with CA‐125 measurement after an acute HF hospitalization may be of interest in patient management. John Wiley and Sons Inc. 2022-01-05 /pmc/articles/PMC8934914/ /pubmed/34989167 http://dx.doi.org/10.1002/ehf2.13758 Text en © 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. 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 Articles
Lourenço, Patrícia
Cunha, Filipe M.
Elias, Catarina
Fernandes, Catarina
Barroso, Isaac
Guimarães, João T.
Bettencourt, Paulo
CA‐125 variation in acute heart failure: a single‐centre analysis
title CA‐125 variation in acute heart failure: a single‐centre analysis
title_full CA‐125 variation in acute heart failure: a single‐centre analysis
title_fullStr CA‐125 variation in acute heart failure: a single‐centre analysis
title_full_unstemmed CA‐125 variation in acute heart failure: a single‐centre analysis
title_short CA‐125 variation in acute heart failure: a single‐centre analysis
title_sort ca‐125 variation in acute heart failure: a single‐centre analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934914/
https://www.ncbi.nlm.nih.gov/pubmed/34989167
http://dx.doi.org/10.1002/ehf2.13758
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