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Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis

Sarcopenia has a negative impact on the prognosis of patients with liver cirrhosis (LC). We investigated the significance of skeletal muscle volume and its changes in LC patients taking levocarnitine (L-carnitine). We retrospectively analyzed 51 LC patients taking L-carnitine from December 2012 to M...

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Autores principales: Fujita, Masashi, Abe, Kazumichi, Hayashi, Manabu, Takahashi, Atsushi, Ohira, Hiromasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360248/
https://www.ncbi.nlm.nih.gov/pubmed/32664122
http://dx.doi.org/10.1097/MD.0000000000021061
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author Fujita, Masashi
Abe, Kazumichi
Hayashi, Manabu
Takahashi, Atsushi
Ohira, Hiromasa
author_facet Fujita, Masashi
Abe, Kazumichi
Hayashi, Manabu
Takahashi, Atsushi
Ohira, Hiromasa
author_sort Fujita, Masashi
collection PubMed
description Sarcopenia has a negative impact on the prognosis of patients with liver cirrhosis (LC). We investigated the significance of skeletal muscle volume and its changes in LC patients taking levocarnitine (L-carnitine). We retrospectively analyzed 51 LC patients taking L-carnitine from December 2012 to March 2019. Skeletal mass index was calculated as the left-right sum of the major × minor axis of psoas muscle at the third lumbar vertebra, divided by height squared (psoas muscle index [PMI]). Patients were classified into 2 groups (low and normal PMI) depending on PMI < 6.0 and < 3.4 cm(2)/m(2) for men and women, respectively. Changes in PMI per month during L-carnitine administration (ΔPMI/m) were calculated, and we classified the patients into 2 groups (severe and mild muscle atrophy) depending on ΔPMI/m below the lower quartile. We assessed overall survival (OS). At the start of L-carnitine administration, there were no significant differences in OS between groups with low and normal PMI. Multivariate analysis showed that ΔPMI/m (hazard ratio [HR], 0.007; P = .005) and L-carnitine administration period (HR, 0.956; P = .021) were significantly associated with OS. Patients with severe muscle atrophy had a significantly lower OS than those with mild muscle atrophy. There was the positive correlation relationship between ΔPMI/m and L-carnitine administration period. Among LC patients taking L-carnitine, progressive muscle volume loss was a predictor of poor prognosis. L-carnitine administration for longer may be able to prevent muscle volume loss and lead to a better prognosis in LC patients.
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spelling pubmed-73602482020-08-05 Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis Fujita, Masashi Abe, Kazumichi Hayashi, Manabu Takahashi, Atsushi Ohira, Hiromasa Medicine (Baltimore) 4500 Sarcopenia has a negative impact on the prognosis of patients with liver cirrhosis (LC). We investigated the significance of skeletal muscle volume and its changes in LC patients taking levocarnitine (L-carnitine). We retrospectively analyzed 51 LC patients taking L-carnitine from December 2012 to March 2019. Skeletal mass index was calculated as the left-right sum of the major × minor axis of psoas muscle at the third lumbar vertebra, divided by height squared (psoas muscle index [PMI]). Patients were classified into 2 groups (low and normal PMI) depending on PMI < 6.0 and < 3.4 cm(2)/m(2) for men and women, respectively. Changes in PMI per month during L-carnitine administration (ΔPMI/m) were calculated, and we classified the patients into 2 groups (severe and mild muscle atrophy) depending on ΔPMI/m below the lower quartile. We assessed overall survival (OS). At the start of L-carnitine administration, there were no significant differences in OS between groups with low and normal PMI. Multivariate analysis showed that ΔPMI/m (hazard ratio [HR], 0.007; P = .005) and L-carnitine administration period (HR, 0.956; P = .021) were significantly associated with OS. Patients with severe muscle atrophy had a significantly lower OS than those with mild muscle atrophy. There was the positive correlation relationship between ΔPMI/m and L-carnitine administration period. Among LC patients taking L-carnitine, progressive muscle volume loss was a predictor of poor prognosis. L-carnitine administration for longer may be able to prevent muscle volume loss and lead to a better prognosis in LC patients. Wolters Kluwer Health 2020-07-10 /pmc/articles/PMC7360248/ /pubmed/32664122 http://dx.doi.org/10.1097/MD.0000000000021061 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4500
Fujita, Masashi
Abe, Kazumichi
Hayashi, Manabu
Takahashi, Atsushi
Ohira, Hiromasa
Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title_full Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title_fullStr Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title_full_unstemmed Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title_short Skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
title_sort skeletal muscle volume loss among liver cirrhosis patients receiving levocarnitine predicts poor prognosis
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360248/
https://www.ncbi.nlm.nih.gov/pubmed/32664122
http://dx.doi.org/10.1097/MD.0000000000021061
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