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The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease

Both genetic and metabolic factors influence the pathology of nonalcoholic fatty liver disease (NAFLD). The aim of this retrospective study was to evaluate the impact of these factors at each stage of disease. We analysed the impact of obesity, diabetes mellitus and genetic risk factors (alleles of...

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Autores principales: Seko, Yuya, Yamaguchi, Kanji, Yano, Kota, Takahashi, Yusuke, Takeuchi, Kento, Kataoka, Seita, Moriguchi, Michihisa, Itoh, Yoshito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584936/
https://www.ncbi.nlm.nih.gov/pubmed/36266438
http://dx.doi.org/10.1038/s41598-022-22729-5
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author Seko, Yuya
Yamaguchi, Kanji
Yano, Kota
Takahashi, Yusuke
Takeuchi, Kento
Kataoka, Seita
Moriguchi, Michihisa
Itoh, Yoshito
author_facet Seko, Yuya
Yamaguchi, Kanji
Yano, Kota
Takahashi, Yusuke
Takeuchi, Kento
Kataoka, Seita
Moriguchi, Michihisa
Itoh, Yoshito
author_sort Seko, Yuya
collection PubMed
description Both genetic and metabolic factors influence the pathology of nonalcoholic fatty liver disease (NAFLD). The aim of this retrospective study was to evaluate the impact of these factors at each stage of disease. We analysed the impact of obesity, diabetes mellitus and genetic risk factors (alleles of PNPLA3 or HSD17B13) on nonalcoholic steatohepatitis (NASH), significant fibrosis (stage ≥ 2) and advanced fibrosis (stage ≥ 3) in 346 patients. Genetic high risk was defined as having at least 2 risk alleles. The median age was 59 years, median body mass index was 27.1 kg/m(2), and 46.8% had diabetes mellitus. Obesity was a risk factor for NASH, significant fibrosis, and advanced fibrosis. Diabetes mellitus increased the risk of NASH. Genetic risk increased the risk of significant and advanced fibrosis. Odds ratios for NASH, significant fibrosis and advanced fibrosis increased with the number of genetic and metabolic risk factors. The patients with both metabolic and genetic risks had an odds ratio of 12.30 for NASH, 5.50 for significant fibrosis, and 6.25 for advanced fibrosis. Factors strongly impact on the pathology of NAFLD differed according to the fibrosis stages. Synergistic effects were observed between genetic and metabolic factors at all stages.
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spelling pubmed-95849362022-10-22 The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease Seko, Yuya Yamaguchi, Kanji Yano, Kota Takahashi, Yusuke Takeuchi, Kento Kataoka, Seita Moriguchi, Michihisa Itoh, Yoshito Sci Rep Article Both genetic and metabolic factors influence the pathology of nonalcoholic fatty liver disease (NAFLD). The aim of this retrospective study was to evaluate the impact of these factors at each stage of disease. We analysed the impact of obesity, diabetes mellitus and genetic risk factors (alleles of PNPLA3 or HSD17B13) on nonalcoholic steatohepatitis (NASH), significant fibrosis (stage ≥ 2) and advanced fibrosis (stage ≥ 3) in 346 patients. Genetic high risk was defined as having at least 2 risk alleles. The median age was 59 years, median body mass index was 27.1 kg/m(2), and 46.8% had diabetes mellitus. Obesity was a risk factor for NASH, significant fibrosis, and advanced fibrosis. Diabetes mellitus increased the risk of NASH. Genetic risk increased the risk of significant and advanced fibrosis. Odds ratios for NASH, significant fibrosis and advanced fibrosis increased with the number of genetic and metabolic risk factors. The patients with both metabolic and genetic risks had an odds ratio of 12.30 for NASH, 5.50 for significant fibrosis, and 6.25 for advanced fibrosis. Factors strongly impact on the pathology of NAFLD differed according to the fibrosis stages. Synergistic effects were observed between genetic and metabolic factors at all stages. Nature Publishing Group UK 2022-10-20 /pmc/articles/PMC9584936/ /pubmed/36266438 http://dx.doi.org/10.1038/s41598-022-22729-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Seko, Yuya
Yamaguchi, Kanji
Yano, Kota
Takahashi, Yusuke
Takeuchi, Kento
Kataoka, Seita
Moriguchi, Michihisa
Itoh, Yoshito
The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title_full The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title_fullStr The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title_full_unstemmed The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title_short The additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
title_sort additive effect of genetic and metabolic factors in the pathogenesis of nonalcoholic fatty liver disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584936/
https://www.ncbi.nlm.nih.gov/pubmed/36266438
http://dx.doi.org/10.1038/s41598-022-22729-5
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