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The effect of liver enzymes on body composition: A Mendelian randomization study
BACKGROUND: Higher alanine transaminase (ALT), indicating poor liver function, is positively associated with diabetes but inversely associated with body mass index (BMI) in Mendelian randomization (MR) studies, suggesting liver function affects muscle mass. To clarify, we assessed the associations o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012438/ https://www.ncbi.nlm.nih.gov/pubmed/32045441 http://dx.doi.org/10.1371/journal.pone.0228737 |
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author | Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary |
author_facet | Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary |
author_sort | Liu, Junxi |
collection | PubMed |
description | BACKGROUND: Higher alanine transaminase (ALT), indicating poor liver function, is positively associated with diabetes but inversely associated with body mass index (BMI) in Mendelian randomization (MR) studies, suggesting liver function affects muscle mass. To clarify, we assessed the associations of liver enzymes with muscle and fat mass observationally with two-sample MR as a validation. METHODS: In the population-representative “Children of 1997” birth cohort (n = 3,455), we used multivariable linear regression to assess the adjusted associations of ALT and alkaline phosphatase (ALP) at ~17.5 years with muscle mass and body fat percentage observationally. Genetic variants predicting ALT, ALP and gamma glutamyltransferase (GGT) were applied to fat-free and fat mass in the UK Biobank (n = ~331,000) to obtain unconfounded MR estimates. RESULTS: Observationally, ALT was positively associated with muscle mass (0.11 kg per IU/L, 95% confidence interval (CI) 0.10 to 0.12) and fat percentage (0.15% per IU/L, 95% CI 0.13 to 0.17). ALP was inversely associated with muscle mass (-0.03 kg per IU/L, 95% CI -0.04 to -0.02) and fat percentage (-0.02% per IU/L, 95% CI -0.03 to -0.01). Using MR, ALT was inversely associated with fat-free mass (-0.41 kg per 100% in concentration, 95% CI -0.64 to -0.19) and fat mass (-0.58 kg per 100% in concentration, 95% CI -0.85 to -0.30). ALP and GGT were unclearly associated with fat-free mass or fat mass. CONCLUSION: ALT reducing fat-free mass provides a possible pathway for the positive association of ALT with diabetes and suggests a potential target of intervention. |
format | Online Article Text |
id | pubmed-7012438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70124382020-02-21 The effect of liver enzymes on body composition: A Mendelian randomization study Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary PLoS One Research Article BACKGROUND: Higher alanine transaminase (ALT), indicating poor liver function, is positively associated with diabetes but inversely associated with body mass index (BMI) in Mendelian randomization (MR) studies, suggesting liver function affects muscle mass. To clarify, we assessed the associations of liver enzymes with muscle and fat mass observationally with two-sample MR as a validation. METHODS: In the population-representative “Children of 1997” birth cohort (n = 3,455), we used multivariable linear regression to assess the adjusted associations of ALT and alkaline phosphatase (ALP) at ~17.5 years with muscle mass and body fat percentage observationally. Genetic variants predicting ALT, ALP and gamma glutamyltransferase (GGT) were applied to fat-free and fat mass in the UK Biobank (n = ~331,000) to obtain unconfounded MR estimates. RESULTS: Observationally, ALT was positively associated with muscle mass (0.11 kg per IU/L, 95% confidence interval (CI) 0.10 to 0.12) and fat percentage (0.15% per IU/L, 95% CI 0.13 to 0.17). ALP was inversely associated with muscle mass (-0.03 kg per IU/L, 95% CI -0.04 to -0.02) and fat percentage (-0.02% per IU/L, 95% CI -0.03 to -0.01). Using MR, ALT was inversely associated with fat-free mass (-0.41 kg per 100% in concentration, 95% CI -0.64 to -0.19) and fat mass (-0.58 kg per 100% in concentration, 95% CI -0.85 to -0.30). ALP and GGT were unclearly associated with fat-free mass or fat mass. CONCLUSION: ALT reducing fat-free mass provides a possible pathway for the positive association of ALT with diabetes and suggests a potential target of intervention. Public Library of Science 2020-02-11 /pmc/articles/PMC7012438/ /pubmed/32045441 http://dx.doi.org/10.1371/journal.pone.0228737 Text en © 2020 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary The effect of liver enzymes on body composition: A Mendelian randomization study |
title | The effect of liver enzymes on body composition: A Mendelian randomization study |
title_full | The effect of liver enzymes on body composition: A Mendelian randomization study |
title_fullStr | The effect of liver enzymes on body composition: A Mendelian randomization study |
title_full_unstemmed | The effect of liver enzymes on body composition: A Mendelian randomization study |
title_short | The effect of liver enzymes on body composition: A Mendelian randomization study |
title_sort | effect of liver enzymes on body composition: a mendelian randomization study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012438/ https://www.ncbi.nlm.nih.gov/pubmed/32045441 http://dx.doi.org/10.1371/journal.pone.0228737 |
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