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Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality
BACKGROUND AND AIM: As the clinical course of metabolic‐associated fatty liver disease (MAFLD) is unclear, we compared the clinical courses of MAFLD and non‐alcoholic FLD (NAFLD). METHODS: Asian FLD patients (n = 987) from 1991 to 2021 (biopsy‐proven in 939) were enrolled. The patients were divided...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290268/ https://www.ncbi.nlm.nih.gov/pubmed/37359113 http://dx.doi.org/10.1002/jgh3.12898 |
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author | Ogasawara, Yuri Kogiso, Tomomi Horiuchi, Kentaro Taniai, Makiko Tokushige, Katsutoshi |
author_facet | Ogasawara, Yuri Kogiso, Tomomi Horiuchi, Kentaro Taniai, Makiko Tokushige, Katsutoshi |
author_sort | Ogasawara, Yuri |
collection | PubMed |
description | BACKGROUND AND AIM: As the clinical course of metabolic‐associated fatty liver disease (MAFLD) is unclear, we compared the clinical courses of MAFLD and non‐alcoholic FLD (NAFLD). METHODS: Asian FLD patients (n = 987) from 1991 to 2021 (biopsy‐proven in 939) were enrolled. The patients were divided into NAFLD (N‐alone, n = 92), both MAFLD and N (M&N, n = 785), and M‐alone (n = 90) groups. Clinical features, complications, and survival rates were compared among the three groups. Risk factors of mortality were subjected to Cox regression analysis. RESULTS: The N‐alone group patients were significantly younger (N alone, M&N, and M alone: 50, 53, and 57 years, respectively), more frequently male (54.3%, 52.6%, and 37.8%), and had a low body mass index (BMI, 23.1, 27.1, and 26.7 kg/m(2)) and FIB‐4 index (1.20, 1.46, and 2.10). Hypopituitarism (5.4%) and hypothyroidism (7.6%) were significantly observed in the N‐alone group. Hepatocellular carcinoma (HCC) developed in 0.0%, 4.2%, and 3.5% of the cases, and extrahepatic malignancies in 6.8%, 8.4%, and 4.7% of the cases, respectively, with no significant differences. The cardiovascular event rate was significantly higher in the M‐alone group (1, 37, and 11 cases, P < 0.01). Survival rates were similar among the three groups. Risk factors for mortality were age and BMI in the N‐alone group; age, HCC, alanine transaminase, and FIB‐4 in the M&N group; and FIB‐4 in the M‐alone group. CONCLUSION: Different risk factors for mortality may exist among the FLD groups. |
format | Online Article Text |
id | pubmed-10290268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-102902682023-06-25 Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality Ogasawara, Yuri Kogiso, Tomomi Horiuchi, Kentaro Taniai, Makiko Tokushige, Katsutoshi JGH Open Original Articles BACKGROUND AND AIM: As the clinical course of metabolic‐associated fatty liver disease (MAFLD) is unclear, we compared the clinical courses of MAFLD and non‐alcoholic FLD (NAFLD). METHODS: Asian FLD patients (n = 987) from 1991 to 2021 (biopsy‐proven in 939) were enrolled. The patients were divided into NAFLD (N‐alone, n = 92), both MAFLD and N (M&N, n = 785), and M‐alone (n = 90) groups. Clinical features, complications, and survival rates were compared among the three groups. Risk factors of mortality were subjected to Cox regression analysis. RESULTS: The N‐alone group patients were significantly younger (N alone, M&N, and M alone: 50, 53, and 57 years, respectively), more frequently male (54.3%, 52.6%, and 37.8%), and had a low body mass index (BMI, 23.1, 27.1, and 26.7 kg/m(2)) and FIB‐4 index (1.20, 1.46, and 2.10). Hypopituitarism (5.4%) and hypothyroidism (7.6%) were significantly observed in the N‐alone group. Hepatocellular carcinoma (HCC) developed in 0.0%, 4.2%, and 3.5% of the cases, and extrahepatic malignancies in 6.8%, 8.4%, and 4.7% of the cases, respectively, with no significant differences. The cardiovascular event rate was significantly higher in the M‐alone group (1, 37, and 11 cases, P < 0.01). Survival rates were similar among the three groups. Risk factors for mortality were age and BMI in the N‐alone group; age, HCC, alanine transaminase, and FIB‐4 in the M&N group; and FIB‐4 in the M‐alone group. CONCLUSION: Different risk factors for mortality may exist among the FLD groups. Wiley Publishing Asia Pty Ltd 2023-05-22 /pmc/articles/PMC10290268/ /pubmed/37359113 http://dx.doi.org/10.1002/jgh3.12898 Text en © 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Ogasawara, Yuri Kogiso, Tomomi Horiuchi, Kentaro Taniai, Makiko Tokushige, Katsutoshi Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title | Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title_full | Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title_fullStr | Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title_full_unstemmed | Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title_short | Outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
title_sort | outcomes of fatty liver disease with and without metabolic comorbidities and risk factors for mortality |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290268/ https://www.ncbi.nlm.nih.gov/pubmed/37359113 http://dx.doi.org/10.1002/jgh3.12898 |
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