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Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis

BACKGROUND AND AIM: Sarcopenia frequently develops in patient with liver cirrhosis (LC). Ethanol reduces muscle protein synthesis and accelerates proteolysis. However, the relationship between heavy alcohol consumption and sarcopenia remains controversial. This study aimed to investigate the charact...

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Autores principales: Saeki, Chisato, Kanai, Tomoya, Nakano, Masanori, Oikawa, Tsunekazu, Torisu, Yuichi, Saruta, Masayuki, Tsubota, Akihito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264247/
https://www.ncbi.nlm.nih.gov/pubmed/34263070
http://dx.doi.org/10.1002/jgh3.12582
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author Saeki, Chisato
Kanai, Tomoya
Nakano, Masanori
Oikawa, Tsunekazu
Torisu, Yuichi
Saruta, Masayuki
Tsubota, Akihito
author_facet Saeki, Chisato
Kanai, Tomoya
Nakano, Masanori
Oikawa, Tsunekazu
Torisu, Yuichi
Saruta, Masayuki
Tsubota, Akihito
author_sort Saeki, Chisato
collection PubMed
description BACKGROUND AND AIM: Sarcopenia frequently develops in patient with liver cirrhosis (LC). Ethanol reduces muscle protein synthesis and accelerates proteolysis. However, the relationship between heavy alcohol consumption and sarcopenia remains controversial. This study aimed to investigate the characteristics and prevalence of sarcopenia among patients with alcoholic LC (ALC) in real‐world clinical settings. METHODS: This cross‐sectional study included 181 patients with LC. Heavy alcohol consumption was defined as >60 g/day. Sarcopenia was diagnosed according to the Japan Society of Hepatology criteria. RESULTS: Among the 181 patients, 64 (35.4%) were diagnosed with ALC. Patients with ALC were younger (median, 61.5 vs 72.0 years; P < 0.001) and had a lower prevalence of sarcopenia (18.8 vs 32.5%; P = 0.048) than those with non‐ALC. Conversely, the former had a higher prevalence of Child–Pugh class B/C (P = 0.015), higher total bilirubin (P = 0.017), and lower prothrombin time (P < 0.001) than the latter. The prevalence of sarcopenia increased alongside advancing age in patients with ALC (P = 0.007). Multivariate analysis identified older age (but not disease stage/liver function reserve and alcohol consumption) as an independent factor associated with sarcopenia (P = 0.002) in patients with ALC. CONCLUSION: Patients with ALC were younger and had a lower prevalence of sarcopenia, despite advanced disease stage/impaired liver function reserve, compared to those with non‐ALC in real‐world clinical settings. However, older age was strongly associated with sarcopenia, even in patients with ALC. There was no significant influence of heavy alcohol consumption on the development of sarcopenia.
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spelling pubmed-82642472021-07-13 Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis Saeki, Chisato Kanai, Tomoya Nakano, Masanori Oikawa, Tsunekazu Torisu, Yuichi Saruta, Masayuki Tsubota, Akihito JGH Open Original Articles BACKGROUND AND AIM: Sarcopenia frequently develops in patient with liver cirrhosis (LC). Ethanol reduces muscle protein synthesis and accelerates proteolysis. However, the relationship between heavy alcohol consumption and sarcopenia remains controversial. This study aimed to investigate the characteristics and prevalence of sarcopenia among patients with alcoholic LC (ALC) in real‐world clinical settings. METHODS: This cross‐sectional study included 181 patients with LC. Heavy alcohol consumption was defined as >60 g/day. Sarcopenia was diagnosed according to the Japan Society of Hepatology criteria. RESULTS: Among the 181 patients, 64 (35.4%) were diagnosed with ALC. Patients with ALC were younger (median, 61.5 vs 72.0 years; P < 0.001) and had a lower prevalence of sarcopenia (18.8 vs 32.5%; P = 0.048) than those with non‐ALC. Conversely, the former had a higher prevalence of Child–Pugh class B/C (P = 0.015), higher total bilirubin (P = 0.017), and lower prothrombin time (P < 0.001) than the latter. The prevalence of sarcopenia increased alongside advancing age in patients with ALC (P = 0.007). Multivariate analysis identified older age (but not disease stage/liver function reserve and alcohol consumption) as an independent factor associated with sarcopenia (P = 0.002) in patients with ALC. CONCLUSION: Patients with ALC were younger and had a lower prevalence of sarcopenia, despite advanced disease stage/impaired liver function reserve, compared to those with non‐ALC in real‐world clinical settings. However, older age was strongly associated with sarcopenia, even in patients with ALC. There was no significant influence of heavy alcohol consumption on the development of sarcopenia. Wiley Publishing Asia Pty Ltd 2021-05-29 /pmc/articles/PMC8264247/ /pubmed/34263070 http://dx.doi.org/10.1002/jgh3.12582 Text en © 2021 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. 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
Saeki, Chisato
Kanai, Tomoya
Nakano, Masanori
Oikawa, Tsunekazu
Torisu, Yuichi
Saruta, Masayuki
Tsubota, Akihito
Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title_full Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title_fullStr Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title_full_unstemmed Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title_short Clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
title_sort clinical characteristics of sarcopenia in patients with alcoholic liver cirrhosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264247/
https://www.ncbi.nlm.nih.gov/pubmed/34263070
http://dx.doi.org/10.1002/jgh3.12582
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