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Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis

BACKGROUND AND AIM: Nonalcoholic fatty liver disease (NAFLD) has gradually become one of the most common chronic liver diseases in the world. More and more evidence shows that low skeletal muscle mass index (SMI) may play a role in the development of NAFLD. Our aim was to quantify the association be...

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Autores principales: Cai, Changzhou, Song, Xin, Chen, Yishu, Chen, Xueyang, Yu, Chaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994447/
https://www.ncbi.nlm.nih.gov/pubmed/31290072
http://dx.doi.org/10.1007/s12072-019-09964-1
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author Cai, Changzhou
Song, Xin
Chen, Yishu
Chen, Xueyang
Yu, Chaohui
author_facet Cai, Changzhou
Song, Xin
Chen, Yishu
Chen, Xueyang
Yu, Chaohui
author_sort Cai, Changzhou
collection PubMed
description BACKGROUND AND AIM: Nonalcoholic fatty liver disease (NAFLD) has gradually become one of the most common chronic liver diseases in the world. More and more evidence shows that low skeletal muscle mass index (SMI) may play a role in the development of NAFLD. Our aim was to quantify the association between SMI, sarcopenia and the presence and severity of NAFLD. METHODS: We systematically searched English relevant studies from PubMed, Embase, the Web of Science and the Cochrane Library updated to December 20th, 2018. Studies in which SMI was compared between NAFLD cases and controls were included. So were studies concerning the odds ratio (OR) of NAFLD, non-alcoholic steatohepatitis (NASH) and significant fibrosis in sarcopenia patients. Pooled weighted mean differences and ORs were calculated. RESULTS: Of the 1331 retrieved studies, 19 articles were included. SMI level in NAFLD patients was 1.77 (95% CI 1.15, 2.39) lower than that in normal controls. We also found a significantly higher occurrence risk of NAFLD (OR = 1.33, 95% CI 1.20 to 1.48), NASH (OR = 2.42, 95% CI 1.27 to 3.57) and NAFLD-related significant fibrosis (OR = 1.56, 95% CI 1.34, 1.78) in sarcopenia subjects. CONCLUSIONS: SMI level in patients with NAFLD was lower than healthy people, and patients with sarcopenia have higher occurrence risk of NAFLD, as well as its advanced stages including NASH or NAFLD-related significant fibrosis. Further well-designed prospective studies are required to strengthen the arguments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-019-09964-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-69944472020-02-14 Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis Cai, Changzhou Song, Xin Chen, Yishu Chen, Xueyang Yu, Chaohui Hepatol Int Original Article BACKGROUND AND AIM: Nonalcoholic fatty liver disease (NAFLD) has gradually become one of the most common chronic liver diseases in the world. More and more evidence shows that low skeletal muscle mass index (SMI) may play a role in the development of NAFLD. Our aim was to quantify the association between SMI, sarcopenia and the presence and severity of NAFLD. METHODS: We systematically searched English relevant studies from PubMed, Embase, the Web of Science and the Cochrane Library updated to December 20th, 2018. Studies in which SMI was compared between NAFLD cases and controls were included. So were studies concerning the odds ratio (OR) of NAFLD, non-alcoholic steatohepatitis (NASH) and significant fibrosis in sarcopenia patients. Pooled weighted mean differences and ORs were calculated. RESULTS: Of the 1331 retrieved studies, 19 articles were included. SMI level in NAFLD patients was 1.77 (95% CI 1.15, 2.39) lower than that in normal controls. We also found a significantly higher occurrence risk of NAFLD (OR = 1.33, 95% CI 1.20 to 1.48), NASH (OR = 2.42, 95% CI 1.27 to 3.57) and NAFLD-related significant fibrosis (OR = 1.56, 95% CI 1.34, 1.78) in sarcopenia subjects. CONCLUSIONS: SMI level in patients with NAFLD was lower than healthy people, and patients with sarcopenia have higher occurrence risk of NAFLD, as well as its advanced stages including NASH or NAFLD-related significant fibrosis. Further well-designed prospective studies are required to strengthen the arguments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-019-09964-1) contains supplementary material, which is available to authorized users. Springer India 2019-07-09 /pmc/articles/PMC6994447/ /pubmed/31290072 http://dx.doi.org/10.1007/s12072-019-09964-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Cai, Changzhou
Song, Xin
Chen, Yishu
Chen, Xueyang
Yu, Chaohui
Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title_full Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title_fullStr Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title_full_unstemmed Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title_short Relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
title_sort relationship between relative skeletal muscle mass and nonalcoholic fatty liver disease: a systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994447/
https://www.ncbi.nlm.nih.gov/pubmed/31290072
http://dx.doi.org/10.1007/s12072-019-09964-1
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