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Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis
BACKGROUND: Previous studies have highlighted changes in the cerebral cortical structure and cognitive function among nonalcoholic fatty liver disease (NAFLD) patients. However, the impact of NAFLD on cerebral cortical structure and specific affected brain regions remains unclear. Therefore, we aime...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646496/ https://www.ncbi.nlm.nih.gov/pubmed/38027213 http://dx.doi.org/10.3389/fendo.2023.1276576 |
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author | Mai, Zhiliang Mao, Hua |
author_facet | Mai, Zhiliang Mao, Hua |
author_sort | Mai, Zhiliang |
collection | PubMed |
description | BACKGROUND: Previous studies have highlighted changes in the cerebral cortical structure and cognitive function among nonalcoholic fatty liver disease (NAFLD) patients. However, the impact of NAFLD on cerebral cortical structure and specific affected brain regions remains unclear. Therefore, we aimed to explore the potential causal relationship between NAFLD and cerebral cortical structure. METHODS: We conducted a Mendelian randomization (MR) study using genetic predictors of alanine aminotransferase (ALT), NAFLD, and percent liver fat (PLF) and combined them with genome-wide association study (GWAS) summary statistics from the ENIGMA Consortium. Several methods were used to assess the effect of NAFLD on full cortex and specific brain regions, along with sensitivity analyses. RESULTS: At the global level, PLF nominally decreased SA of full cortex; at the functional level, ALT presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of pars orbitalis, and TH of pericalcarine cortex. Besides, NAFLD presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of pars triangularis and TH of pericalcarine cortex, but increased TH of entorhinal cortex, lateral orbitofrontal cortex and temporal pole. Furthermore, PLF presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of cuneus and lingual gyrus, but increased TH of entorhinal cortex. CONCLUSION: NAFLD is suggestively associated with atrophy in specific functional regions of the human brain. |
format | Online Article Text |
id | pubmed-10646496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106464962023-01-01 Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis Mai, Zhiliang Mao, Hua Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Previous studies have highlighted changes in the cerebral cortical structure and cognitive function among nonalcoholic fatty liver disease (NAFLD) patients. However, the impact of NAFLD on cerebral cortical structure and specific affected brain regions remains unclear. Therefore, we aimed to explore the potential causal relationship between NAFLD and cerebral cortical structure. METHODS: We conducted a Mendelian randomization (MR) study using genetic predictors of alanine aminotransferase (ALT), NAFLD, and percent liver fat (PLF) and combined them with genome-wide association study (GWAS) summary statistics from the ENIGMA Consortium. Several methods were used to assess the effect of NAFLD on full cortex and specific brain regions, along with sensitivity analyses. RESULTS: At the global level, PLF nominally decreased SA of full cortex; at the functional level, ALT presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of pars orbitalis, and TH of pericalcarine cortex. Besides, NAFLD presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of pars triangularis and TH of pericalcarine cortex, but increased TH of entorhinal cortex, lateral orbitofrontal cortex and temporal pole. Furthermore, PLF presented a nominal association with reduced SA of parahippocampal gyrus, TH of pars opercularis, TH of cuneus and lingual gyrus, but increased TH of entorhinal cortex. CONCLUSION: NAFLD is suggestively associated with atrophy in specific functional regions of the human brain. Frontiers Media S.A. 2023-11-01 /pmc/articles/PMC10646496/ /pubmed/38027213 http://dx.doi.org/10.3389/fendo.2023.1276576 Text en Copyright © 2023 Mai and Mao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Mai, Zhiliang Mao, Hua Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title | Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title_full | Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title_fullStr | Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title_full_unstemmed | Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title_short | Causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a Mendelian randomization analysis |
title_sort | causal effects of nonalcoholic fatty liver disease on cerebral cortical structure: a mendelian randomization analysis |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646496/ https://www.ncbi.nlm.nih.gov/pubmed/38027213 http://dx.doi.org/10.3389/fendo.2023.1276576 |
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