Cargando…
Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease
BACKGROUND: Sarcopenia is a significant indicator of the severity of non‐alcoholic fatty liver disease. We investigated whether sarcopenia could identify subgroups with different risk of liver fibrosis and atherosclerotic cardiovascular disease (ASCVD) among subjects with metabolic dysfunction‐assoc...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517359/ https://www.ncbi.nlm.nih.gov/pubmed/34337887 http://dx.doi.org/10.1002/jcsm.12754 |
_version_ | 1784583999410143232 |
---|---|
author | Chun, Ho Soo Kim, Mi Na Lee, Jae Seung Lee, Hye Won Kim, Beom Kyung Park, Jun Yong Kim, Do Young Ahn, Sang Hoon Kim, Seung Up |
author_facet | Chun, Ho Soo Kim, Mi Na Lee, Jae Seung Lee, Hye Won Kim, Beom Kyung Park, Jun Yong Kim, Do Young Ahn, Sang Hoon Kim, Seung Up |
author_sort | Chun, Ho Soo |
collection | PubMed |
description | BACKGROUND: Sarcopenia is a significant indicator of the severity of non‐alcoholic fatty liver disease. We investigated whether sarcopenia could identify subgroups with different risk of liver fibrosis and atherosclerotic cardiovascular disease (ASCVD) among subjects with metabolic dysfunction‐associated fatty liver disease (MAFLD). METHODS: Subjects from the Korea National Health and Nutrition Examination Survey 2008–2011 were selected (n = 8361). Sarcopenia was defined using the sarcopenia index. Hepatic steatosis was defined as a fatty liver index ≥30. Significant liver fibrosis was defined as a fibrosis‐4 index (FIB‐4) ≥2.67 or the highest quartile of non‐alcoholic fatty liver disease fibrosis score (NFS). High probability of ASCVD was defined as ASCVD risk score >10%. RESULTS: The mean age was 48.5 ± 15.6 years, and 42.6% of subjects were male. The prevalence of MAFLD was 37.3% (n = 3116 of 8361), and the proportion of sarcopenic subjects was 9.9% among those with MAFLD. After adjusting for confounders, the risk of significant liver fibrosis significantly increased from non‐sarcopenic subjects with MAFLD [odds ratio (OR) = 1.57 by FIB‐4 and 2.13 by NFS] to sarcopenic subjects with MAFLD (OR = 4.51 by FIB‐4 and 5.72 by NFS), compared with subjects without MAFLD (all P < 0.001). The risk for high probability of ASCVD significantly increased from non‐sarcopenic subjects with MAFLD (OR = 1.47) to sarcopenic subjects with MAFLD (OR = 4.08), compared with subjects without MAFLD (all P < 0.001). CONCLUSIONS: The risks of significant liver fibrosis and ASCVD differed significantly according to sarcopenic status among subjects with MAFLD. An assessment of sarcopenia might be helpful in risk stratification among subjects with MAFLD. |
format | Online Article Text |
id | pubmed-8517359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85173592021-10-21 Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease Chun, Ho Soo Kim, Mi Na Lee, Jae Seung Lee, Hye Won Kim, Beom Kyung Park, Jun Yong Kim, Do Young Ahn, Sang Hoon Kim, Seung Up J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Sarcopenia is a significant indicator of the severity of non‐alcoholic fatty liver disease. We investigated whether sarcopenia could identify subgroups with different risk of liver fibrosis and atherosclerotic cardiovascular disease (ASCVD) among subjects with metabolic dysfunction‐associated fatty liver disease (MAFLD). METHODS: Subjects from the Korea National Health and Nutrition Examination Survey 2008–2011 were selected (n = 8361). Sarcopenia was defined using the sarcopenia index. Hepatic steatosis was defined as a fatty liver index ≥30. Significant liver fibrosis was defined as a fibrosis‐4 index (FIB‐4) ≥2.67 or the highest quartile of non‐alcoholic fatty liver disease fibrosis score (NFS). High probability of ASCVD was defined as ASCVD risk score >10%. RESULTS: The mean age was 48.5 ± 15.6 years, and 42.6% of subjects were male. The prevalence of MAFLD was 37.3% (n = 3116 of 8361), and the proportion of sarcopenic subjects was 9.9% among those with MAFLD. After adjusting for confounders, the risk of significant liver fibrosis significantly increased from non‐sarcopenic subjects with MAFLD [odds ratio (OR) = 1.57 by FIB‐4 and 2.13 by NFS] to sarcopenic subjects with MAFLD (OR = 4.51 by FIB‐4 and 5.72 by NFS), compared with subjects without MAFLD (all P < 0.001). The risk for high probability of ASCVD significantly increased from non‐sarcopenic subjects with MAFLD (OR = 1.47) to sarcopenic subjects with MAFLD (OR = 4.08), compared with subjects without MAFLD (all P < 0.001). CONCLUSIONS: The risks of significant liver fibrosis and ASCVD differed significantly according to sarcopenic status among subjects with MAFLD. An assessment of sarcopenia might be helpful in risk stratification among subjects with MAFLD. John Wiley and Sons Inc. 2021-08-01 2021-10 /pmc/articles/PMC8517359/ /pubmed/34337887 http://dx.doi.org/10.1002/jcsm.12754 Text en © 2021 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-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Chun, Ho Soo Kim, Mi Na Lee, Jae Seung Lee, Hye Won Kim, Beom Kyung Park, Jun Yong Kim, Do Young Ahn, Sang Hoon Kim, Seung Up Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title | Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title_full | Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title_fullStr | Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title_full_unstemmed | Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title_short | Risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
title_sort | risk stratification using sarcopenia status among subjects with metabolic dysfunction‐associated fatty liver disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517359/ https://www.ncbi.nlm.nih.gov/pubmed/34337887 http://dx.doi.org/10.1002/jcsm.12754 |
work_keys_str_mv | AT chunhosoo riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT kimmina riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT leejaeseung riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT leehyewon riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT kimbeomkyung riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT parkjunyong riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT kimdoyoung riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT ahnsanghoon riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease AT kimseungup riskstratificationusingsarcopeniastatusamongsubjectswithmetabolicdysfunctionassociatedfattyliverdisease |