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Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study

Background: Since the association of homocysteine and clinical results of observational studies are controversial on non-alcoholic fatty liver related disease, we compute the two-sample Mendelian Randomization (MR) study. Objective: To evaluate whether the plasma level of homocysteine has an effect...

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Autores principales: Chen, Pengcheng, Yang, Ze, Guo, Lingyun, Huang, Yingfei, Li, Jingjia, Chen, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763576/
https://www.ncbi.nlm.nih.gov/pubmed/36561351
http://dx.doi.org/10.3389/fmolb.2022.1083855
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author Chen, Pengcheng
Yang, Ze
Guo, Lingyun
Huang, Yingfei
Li, Jingjia
Chen, Xin
author_facet Chen, Pengcheng
Yang, Ze
Guo, Lingyun
Huang, Yingfei
Li, Jingjia
Chen, Xin
author_sort Chen, Pengcheng
collection PubMed
description Background: Since the association of homocysteine and clinical results of observational studies are controversial on non-alcoholic fatty liver related disease, we compute the two-sample Mendelian Randomization (MR) study. Objective: To evaluate whether the plasma level of homocysteine has an effect on the risk of Non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), and Cirrhosis after its progress, we investigated the causal relationships between plasma homocysteine and the three non-alcoholic fatty liver related diseases mentioned above. Design and methods: Summary estimates were elicited from the inverse-variance weighted (IVW) method through 12 single nucleotide polymorphisms (SNPs) which related to the plasma homocysteine, the SNPs were obtained from a large genome-wide association studies (GWAS) of 44,147 European participants. And the summary statistics for the latest and largest GWAS datasets for NAFLD (307576 in total and 1,578 cases), NASH (309055 in total and 99 cases) and Cirrhosis (306145 in total and 826 cases) were collected from Ristey FinnGen website where the association of genetic variations with blood metabolite levels was conducted using comprehensive metabolite profiling. The study was performed through two-sample MR method. Results: The result indicated that the plasma homocysteine is not significantly associated with NAFLD, and its progression, NASH and Cirrhosis. Conclusion: The evidence in this study is quite deficient to support the causal association of the individual plasma homocysteine with NAFLD, NASH and Cirrhosis, the putative of associations is not exist.
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spelling pubmed-97635762022-12-21 Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study Chen, Pengcheng Yang, Ze Guo, Lingyun Huang, Yingfei Li, Jingjia Chen, Xin Front Mol Biosci Molecular Biosciences Background: Since the association of homocysteine and clinical results of observational studies are controversial on non-alcoholic fatty liver related disease, we compute the two-sample Mendelian Randomization (MR) study. Objective: To evaluate whether the plasma level of homocysteine has an effect on the risk of Non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), and Cirrhosis after its progress, we investigated the causal relationships between plasma homocysteine and the three non-alcoholic fatty liver related diseases mentioned above. Design and methods: Summary estimates were elicited from the inverse-variance weighted (IVW) method through 12 single nucleotide polymorphisms (SNPs) which related to the plasma homocysteine, the SNPs were obtained from a large genome-wide association studies (GWAS) of 44,147 European participants. And the summary statistics for the latest and largest GWAS datasets for NAFLD (307576 in total and 1,578 cases), NASH (309055 in total and 99 cases) and Cirrhosis (306145 in total and 826 cases) were collected from Ristey FinnGen website where the association of genetic variations with blood metabolite levels was conducted using comprehensive metabolite profiling. The study was performed through two-sample MR method. Results: The result indicated that the plasma homocysteine is not significantly associated with NAFLD, and its progression, NASH and Cirrhosis. Conclusion: The evidence in this study is quite deficient to support the causal association of the individual plasma homocysteine with NAFLD, NASH and Cirrhosis, the putative of associations is not exist. Frontiers Media S.A. 2022-12-06 /pmc/articles/PMC9763576/ /pubmed/36561351 http://dx.doi.org/10.3389/fmolb.2022.1083855 Text en Copyright © 2022 Chen, Yang, Guo, Huang, Li and Chen. 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 Molecular Biosciences
Chen, Pengcheng
Yang, Ze
Guo, Lingyun
Huang, Yingfei
Li, Jingjia
Chen, Xin
Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title_full Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title_fullStr Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title_full_unstemmed Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title_short Effects of homocysteine on nonalcoholic fatty liver related disease: A mendelian randomization study
title_sort effects of homocysteine on nonalcoholic fatty liver related disease: a mendelian randomization study
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763576/
https://www.ncbi.nlm.nih.gov/pubmed/36561351
http://dx.doi.org/10.3389/fmolb.2022.1083855
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