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Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study
Background and aim: Non-alcoholic fatty liver disease (NAFLD) may progress to severe liver fibrosis and cirrhosis. A limited number of studies with a long follow up assessed fibrosis progression and related predictors in untreated patients with a histological diagnosis of NAFLD. This study aims to i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573625/ https://www.ncbi.nlm.nih.gov/pubmed/36233834 http://dx.doi.org/10.3390/jcm11195969 |
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author | Mangia, Alessandra Piazzolla, Annarita Valeria Squillante, Maria Maddalena Cocomazzi, Giovanna Valori, Vanna Maria Copetti, Massimiliano Parente, Paola Attino, Vito Guido, Maria |
author_facet | Mangia, Alessandra Piazzolla, Annarita Valeria Squillante, Maria Maddalena Cocomazzi, Giovanna Valori, Vanna Maria Copetti, Massimiliano Parente, Paola Attino, Vito Guido, Maria |
author_sort | Mangia, Alessandra |
collection | PubMed |
description | Background and aim: Non-alcoholic fatty liver disease (NAFLD) may progress to severe liver fibrosis and cirrhosis. A limited number of studies with a long follow up assessed fibrosis progression and related predictors in untreated patients with a histological diagnosis of NAFLD. This study aims to investigate rate and predictors of NAFLD progression. Methods: For 9 (2–16.7) years, we followed up a cohort of patients histologically diagnosed. Disease progression was defined by a composite endpoint as evidence of cirrhosis in patients without cirrhosis at baseline, evidence of de novo occurrence of cirrhosis complications, histologically established worsening of stage 1 of fibrosis or increase of 20% in liver stiffness by transient elastography in patients rejecting a second liver biopsy. Results: A total of 91 patients were enrolled. Of them, 31 had NAFL and 60 NASH. A second liver biopsy was performed in 22 NASH patients and in 4 NAFL. Disease progression was observed in 38.5% NASH and in 12.0% NAFL (p = 0.034). Patients with portal inflammation had a higher risk of progression (66.7% vs 26%, p = 0.021). High triglycerides levels, advanced fibrosis at baseline and the duration of follow-up predict disease progression (p = 0.021; OR = 6.93, 95% CI 1.33–36.08, p = 0.43; OR 8.37; 95% CI 1.07–65.58 and p = 0.034; OR = 0.88; 95% CI 0.78–0.99, respectively). Conclusions: Our results reinforce the evidence that, in the absence of pharmacologic treatment, NASH progresses in about 40% of patients. Liver biopsy is the only mean to discriminate NAFL from NASH. The prognostic role of portal inflammation needs to be explored in larger series. |
format | Online Article Text |
id | pubmed-9573625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95736252022-10-17 Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study Mangia, Alessandra Piazzolla, Annarita Valeria Squillante, Maria Maddalena Cocomazzi, Giovanna Valori, Vanna Maria Copetti, Massimiliano Parente, Paola Attino, Vito Guido, Maria J Clin Med Article Background and aim: Non-alcoholic fatty liver disease (NAFLD) may progress to severe liver fibrosis and cirrhosis. A limited number of studies with a long follow up assessed fibrosis progression and related predictors in untreated patients with a histological diagnosis of NAFLD. This study aims to investigate rate and predictors of NAFLD progression. Methods: For 9 (2–16.7) years, we followed up a cohort of patients histologically diagnosed. Disease progression was defined by a composite endpoint as evidence of cirrhosis in patients without cirrhosis at baseline, evidence of de novo occurrence of cirrhosis complications, histologically established worsening of stage 1 of fibrosis or increase of 20% in liver stiffness by transient elastography in patients rejecting a second liver biopsy. Results: A total of 91 patients were enrolled. Of them, 31 had NAFL and 60 NASH. A second liver biopsy was performed in 22 NASH patients and in 4 NAFL. Disease progression was observed in 38.5% NASH and in 12.0% NAFL (p = 0.034). Patients with portal inflammation had a higher risk of progression (66.7% vs 26%, p = 0.021). High triglycerides levels, advanced fibrosis at baseline and the duration of follow-up predict disease progression (p = 0.021; OR = 6.93, 95% CI 1.33–36.08, p = 0.43; OR 8.37; 95% CI 1.07–65.58 and p = 0.034; OR = 0.88; 95% CI 0.78–0.99, respectively). Conclusions: Our results reinforce the evidence that, in the absence of pharmacologic treatment, NASH progresses in about 40% of patients. Liver biopsy is the only mean to discriminate NAFL from NASH. The prognostic role of portal inflammation needs to be explored in larger series. MDPI 2022-10-10 /pmc/articles/PMC9573625/ /pubmed/36233834 http://dx.doi.org/10.3390/jcm11195969 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mangia, Alessandra Piazzolla, Annarita Valeria Squillante, Maria Maddalena Cocomazzi, Giovanna Valori, Vanna Maria Copetti, Massimiliano Parente, Paola Attino, Vito Guido, Maria Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title | Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title_full | Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title_fullStr | Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title_full_unstemmed | Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title_short | Nonalcoholic Steatohepatitis: A 9-Year Follow Up Cohort Study |
title_sort | nonalcoholic steatohepatitis: a 9-year follow up cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573625/ https://www.ncbi.nlm.nih.gov/pubmed/36233834 http://dx.doi.org/10.3390/jcm11195969 |
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