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Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies

Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease in the world. The complete natural history of NAFLD is unknown because few high‐quality follow‐up studies have been conducted. Our aim was to find variables predicting disease severity through an extended follow‐up...

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Autores principales: Nasr, Patrik, Ignatova, Simone, Kechagias, Stergios, Ekstedt, Mattias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796332/
https://www.ncbi.nlm.nih.gov/pubmed/29404527
http://dx.doi.org/10.1002/hep4.1134
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author Nasr, Patrik
Ignatova, Simone
Kechagias, Stergios
Ekstedt, Mattias
author_facet Nasr, Patrik
Ignatova, Simone
Kechagias, Stergios
Ekstedt, Mattias
author_sort Nasr, Patrik
collection PubMed
description Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease in the world. The complete natural history of NAFLD is unknown because few high‐quality follow‐up studies have been conducted. Our aim was to find variables predicting disease severity through an extended follow‐up with serial biopsies. In a prospective cohort study, 129 patients who enrolled between 1988 and 1993 were asked to participate in a follow‐up study on two occasions; biochemical, clinical, and histologic data were documented. The mean time between biopsies was 13.7 (±1.7) and 9.3 (±1.0) years, respectively. At the end of the study period, 12 patients (9.3%) had developed end‐stage liver disease and 34% had advanced fibrosis. Out of the 113 patients with baseline low fibrosis (<3), 16% developed advanced fibrosis. Fibrosis progression did not differ among the different stages of baseline fibrosis (P = 0.374). Fifty‐six patients (43%) had isolated steatosis, of whom 9% developed advanced fibrosis (3 patients with biopsy‐proven fibrosis stage F3‐F4 and 2 patients with end‐stage liver disease). Fibrosis stage, ballooning, and diabetes were more common in patients who developed end‐stage liver disease; however, there were no baseline clinical, histologic, or biochemical variables that predicted clinical significant disease progression. Conclusion: NAFLD is a highly heterogeneous disease, and it is surprisingly hard to predict fibrosis progression. Given enough time, NAFLD seems to have a more dismal prognosis then previously reported, with 16% of patients with fibrosis stage <3 developing advanced fibrosis and 9.3% showing signs of end‐stage liver disease. (Hepatology Communications 2018;2:199–210)
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spelling pubmed-57963322018-02-05 Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies Nasr, Patrik Ignatova, Simone Kechagias, Stergios Ekstedt, Mattias Hepatol Commun Original Articles Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease in the world. The complete natural history of NAFLD is unknown because few high‐quality follow‐up studies have been conducted. Our aim was to find variables predicting disease severity through an extended follow‐up with serial biopsies. In a prospective cohort study, 129 patients who enrolled between 1988 and 1993 were asked to participate in a follow‐up study on two occasions; biochemical, clinical, and histologic data were documented. The mean time between biopsies was 13.7 (±1.7) and 9.3 (±1.0) years, respectively. At the end of the study period, 12 patients (9.3%) had developed end‐stage liver disease and 34% had advanced fibrosis. Out of the 113 patients with baseline low fibrosis (<3), 16% developed advanced fibrosis. Fibrosis progression did not differ among the different stages of baseline fibrosis (P = 0.374). Fifty‐six patients (43%) had isolated steatosis, of whom 9% developed advanced fibrosis (3 patients with biopsy‐proven fibrosis stage F3‐F4 and 2 patients with end‐stage liver disease). Fibrosis stage, ballooning, and diabetes were more common in patients who developed end‐stage liver disease; however, there were no baseline clinical, histologic, or biochemical variables that predicted clinical significant disease progression. Conclusion: NAFLD is a highly heterogeneous disease, and it is surprisingly hard to predict fibrosis progression. Given enough time, NAFLD seems to have a more dismal prognosis then previously reported, with 16% of patients with fibrosis stage <3 developing advanced fibrosis and 9.3% showing signs of end‐stage liver disease. (Hepatology Communications 2018;2:199–210) John Wiley and Sons Inc. 2017-12-27 /pmc/articles/PMC5796332/ /pubmed/29404527 http://dx.doi.org/10.1002/hep4.1134 Text en © 2017 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://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
Nasr, Patrik
Ignatova, Simone
Kechagias, Stergios
Ekstedt, Mattias
Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title_full Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title_fullStr Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title_full_unstemmed Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title_short Natural history of nonalcoholic fatty liver disease: A prospective follow‐up study with serial biopsies
title_sort natural history of nonalcoholic fatty liver disease: a prospective follow‐up study with serial biopsies
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796332/
https://www.ncbi.nlm.nih.gov/pubmed/29404527
http://dx.doi.org/10.1002/hep4.1134
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