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Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study

BACKGROUND: Cachexia substantially impacts the prognosis of patients with heart failure (HF); however, there is no standard method for cachexia diagnosis. This study aimed to investigate the association of Evans's criteria, consisting of multiple assessments, with the prognosis of HF in older a...

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Autores principales: Maekawa, Emi, Noda, Takumi, Maeda, Daichi, Yamashita, Masashi, Uchida, Shota, Hamazaki, Nobuaki, Nozaki, Kohei, Saito, Hiroshi, Saito, Kazuya, Ogasahara, Yuki, Konishi, Masaaki, Kitai, Takeshi, Iwata, Kentaro, Jujo, Kentaro, Wada, Hiroshi, Kasai, Takatoshi, Nagamatsu, Hirofumi, Ozawa, Tetsuya, Izawa, Katsuya, Yamamoto, Shuhei, Aizawa, Naoki, Yonezawa, Ryusuke, Oka, Kazuhiro, Ako, Junya, Momomura, Shin‐ichi, Kagiyama, Nobuyuki, Matsue, Yuya, Kamiya, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570094/
https://www.ncbi.nlm.nih.gov/pubmed/37434419
http://dx.doi.org/10.1002/jcsm.13291
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author Maekawa, Emi
Noda, Takumi
Maeda, Daichi
Yamashita, Masashi
Uchida, Shota
Hamazaki, Nobuaki
Nozaki, Kohei
Saito, Hiroshi
Saito, Kazuya
Ogasahara, Yuki
Konishi, Masaaki
Kitai, Takeshi
Iwata, Kentaro
Jujo, Kentaro
Wada, Hiroshi
Kasai, Takatoshi
Nagamatsu, Hirofumi
Ozawa, Tetsuya
Izawa, Katsuya
Yamamoto, Shuhei
Aizawa, Naoki
Yonezawa, Ryusuke
Oka, Kazuhiro
Ako, Junya
Momomura, Shin‐ichi
Kagiyama, Nobuyuki
Matsue, Yuya
Kamiya, Kentaro
author_facet Maekawa, Emi
Noda, Takumi
Maeda, Daichi
Yamashita, Masashi
Uchida, Shota
Hamazaki, Nobuaki
Nozaki, Kohei
Saito, Hiroshi
Saito, Kazuya
Ogasahara, Yuki
Konishi, Masaaki
Kitai, Takeshi
Iwata, Kentaro
Jujo, Kentaro
Wada, Hiroshi
Kasai, Takatoshi
Nagamatsu, Hirofumi
Ozawa, Tetsuya
Izawa, Katsuya
Yamamoto, Shuhei
Aizawa, Naoki
Yonezawa, Ryusuke
Oka, Kazuhiro
Ako, Junya
Momomura, Shin‐ichi
Kagiyama, Nobuyuki
Matsue, Yuya
Kamiya, Kentaro
author_sort Maekawa, Emi
collection PubMed
description BACKGROUND: Cachexia substantially impacts the prognosis of patients with heart failure (HF); however, there is no standard method for cachexia diagnosis. This study aimed to investigate the association of Evans's criteria, consisting of multiple assessments, with the prognosis of HF in older adults. METHODS: This study is a secondary analysis of the data from the FRAGILE‐HF study, a prospective multicentre cohort study that enrolled consecutive hospitalized patients aged ≥65 years with HF. Patients were divided into two groups: the cachexia and non‐cachexia groups. Cachexia was defined according to Evans's criteria by assessing weight loss, muscle weakness, fatigue, anorexia, a decreased fat‐free mass index and an abnormal biochemical profile. The primary outcome was all‐cause mortality, as assessed in the survival analysis. RESULTS: Cachexia was present in 35.5% of the 1306 enrolled patients (median age [inter‐quartile range], 81 [74–86] years; 57.0% male); 59.6%, 73.2%, 15.6%, 71.0%, 44.9% and 64.6% had weight loss, decreased muscle strength, a low fat‐free mass index, abnormal biochemistry, anorexia and fatigue, respectively. All‐cause mortality occurred in 270 patients (21.0%) over 2 years. The cachexia group (hazard ratio [HR], 1.494; 95% confidence interval [CI], 1.173–1.903; P = 0.001) had a higher mortality risk than the non‐cachexia group after adjusting for the severity of HF. Cardiovascular and non‐cardiovascular deaths occurred in 148 (11.3%) and 122 patients (9.3%), respectively. The adjusted HRs for cachexia in cardiovascular mortality and non‐cardiovascular mortality were 1.456 (95% CI, 1.048–2.023; P = 0.025) and 1.561 (95% CI, 1.086–2.243; P = 0.017), respectively. Among the cachexia diagnostic criteria, decreased muscle strength (HR, 1.514; 95% CI, 1.095–2.093; P = 0.012) and low fat‐free mass index (HR, 1.424; 95% CI, 1.052–1.926; P = 0.022) were significantly associated with high all‐cause mortality, but there was no significant association between weight loss alone (HR, 1.147; 95% CI, 0.895–1.471; P = 0.277) and all‐cause mortality. CONCLUSIONS: Cachexia evaluated by multi‐assessment was present in one third of older adults with HF and was associated with a worse prognosis. A multimodal assessment of cachexia may be helpful for risk stratification in older patients with HF.
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spelling pubmed-105700942023-10-14 Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study Maekawa, Emi Noda, Takumi Maeda, Daichi Yamashita, Masashi Uchida, Shota Hamazaki, Nobuaki Nozaki, Kohei Saito, Hiroshi Saito, Kazuya Ogasahara, Yuki Konishi, Masaaki Kitai, Takeshi Iwata, Kentaro Jujo, Kentaro Wada, Hiroshi Kasai, Takatoshi Nagamatsu, Hirofumi Ozawa, Tetsuya Izawa, Katsuya Yamamoto, Shuhei Aizawa, Naoki Yonezawa, Ryusuke Oka, Kazuhiro Ako, Junya Momomura, Shin‐ichi Kagiyama, Nobuyuki Matsue, Yuya Kamiya, Kentaro J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Cachexia substantially impacts the prognosis of patients with heart failure (HF); however, there is no standard method for cachexia diagnosis. This study aimed to investigate the association of Evans's criteria, consisting of multiple assessments, with the prognosis of HF in older adults. METHODS: This study is a secondary analysis of the data from the FRAGILE‐HF study, a prospective multicentre cohort study that enrolled consecutive hospitalized patients aged ≥65 years with HF. Patients were divided into two groups: the cachexia and non‐cachexia groups. Cachexia was defined according to Evans's criteria by assessing weight loss, muscle weakness, fatigue, anorexia, a decreased fat‐free mass index and an abnormal biochemical profile. The primary outcome was all‐cause mortality, as assessed in the survival analysis. RESULTS: Cachexia was present in 35.5% of the 1306 enrolled patients (median age [inter‐quartile range], 81 [74–86] years; 57.0% male); 59.6%, 73.2%, 15.6%, 71.0%, 44.9% and 64.6% had weight loss, decreased muscle strength, a low fat‐free mass index, abnormal biochemistry, anorexia and fatigue, respectively. All‐cause mortality occurred in 270 patients (21.0%) over 2 years. The cachexia group (hazard ratio [HR], 1.494; 95% confidence interval [CI], 1.173–1.903; P = 0.001) had a higher mortality risk than the non‐cachexia group after adjusting for the severity of HF. Cardiovascular and non‐cardiovascular deaths occurred in 148 (11.3%) and 122 patients (9.3%), respectively. The adjusted HRs for cachexia in cardiovascular mortality and non‐cardiovascular mortality were 1.456 (95% CI, 1.048–2.023; P = 0.025) and 1.561 (95% CI, 1.086–2.243; P = 0.017), respectively. Among the cachexia diagnostic criteria, decreased muscle strength (HR, 1.514; 95% CI, 1.095–2.093; P = 0.012) and low fat‐free mass index (HR, 1.424; 95% CI, 1.052–1.926; P = 0.022) were significantly associated with high all‐cause mortality, but there was no significant association between weight loss alone (HR, 1.147; 95% CI, 0.895–1.471; P = 0.277) and all‐cause mortality. CONCLUSIONS: Cachexia evaluated by multi‐assessment was present in one third of older adults with HF and was associated with a worse prognosis. A multimodal assessment of cachexia may be helpful for risk stratification in older patients with HF. John Wiley and Sons Inc. 2023-07-11 /pmc/articles/PMC10570094/ /pubmed/37434419 http://dx.doi.org/10.1002/jcsm.13291 Text en © 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Maekawa, Emi
Noda, Takumi
Maeda, Daichi
Yamashita, Masashi
Uchida, Shota
Hamazaki, Nobuaki
Nozaki, Kohei
Saito, Hiroshi
Saito, Kazuya
Ogasahara, Yuki
Konishi, Masaaki
Kitai, Takeshi
Iwata, Kentaro
Jujo, Kentaro
Wada, Hiroshi
Kasai, Takatoshi
Nagamatsu, Hirofumi
Ozawa, Tetsuya
Izawa, Katsuya
Yamamoto, Shuhei
Aizawa, Naoki
Yonezawa, Ryusuke
Oka, Kazuhiro
Ako, Junya
Momomura, Shin‐ichi
Kagiyama, Nobuyuki
Matsue, Yuya
Kamiya, Kentaro
Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title_full Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title_fullStr Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title_full_unstemmed Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title_short Prognostic impact of cachexia by multi‐assessment in older adults with heart failure: FRAGILE‐HF cohort study
title_sort prognostic impact of cachexia by multi‐assessment in older adults with heart failure: fragile‐hf cohort study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570094/
https://www.ncbi.nlm.nih.gov/pubmed/37434419
http://dx.doi.org/10.1002/jcsm.13291
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