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The effect of liver enzymes on adiposity: a Mendelian randomization study
Poorer liver function is positively associated with diabetes in Mendelian randomization (MR) studies. Observationally, adiposity is associated with poorer liver function. To clarify the etiology, we assessed the association of liver enzymes with adiposity observationally and using two-sample MR for...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856156/ https://www.ncbi.nlm.nih.gov/pubmed/31727910 http://dx.doi.org/10.1038/s41598-019-52489-8 |
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author | Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Lin, Shi Lin Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary |
author_facet | Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Lin, Shi Lin Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary |
author_sort | Liu, Junxi |
collection | PubMed |
description | Poorer liver function is positively associated with diabetes in Mendelian randomization (MR) studies. Observationally, adiposity is associated with poorer liver function. To clarify the etiology, we assessed the association of liver enzymes with adiposity observationally and using two-sample MR for validation. In the “Children of 1997” birth cohort, we used multivariable linear regression to assess the associations of alanine transaminase (ALT) and alkaline phosphatase (ALP) at ~17.5 years with body mass index (BMI) (n = 3,458). Using MR, genetic predictors of ALT, ALP and gamma glutamyltransferase (GGT), were applied to genome-wide association studies of BMI (n = 681,275), waist circumference (WC) (n = 224,459) and waist-hip ratio (WHR) (n = 224,459) to obtain unconfounded estimates. Observationally, ALT was positively associated with BMI (0.10 kg/m(2) per IU/L, 95% confidence interval (CI) 0.09 to 0.11). ALP was inversely associated with BMI (−0.018 kg/m(2) per IU/L, 95% CI −0.024 to −0.012). Using MR, ALT was inversely associated with BMI (−0.14 standard deviation per 100% change in concentration, 95% CI −0.20 to −0.07), but not WC or WHR. ALP and GGT were unrelated to adiposity. Poorer liver function might not cause adiposity; instead higher ALT might reduce BMI, raising the question as to the role of ALT in body composition. |
format | Online Article Text |
id | pubmed-6856156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68561562019-11-19 The effect of liver enzymes on adiposity: a Mendelian randomization study Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Lin, Shi Lin Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary Sci Rep Article Poorer liver function is positively associated with diabetes in Mendelian randomization (MR) studies. Observationally, adiposity is associated with poorer liver function. To clarify the etiology, we assessed the association of liver enzymes with adiposity observationally and using two-sample MR for validation. In the “Children of 1997” birth cohort, we used multivariable linear regression to assess the associations of alanine transaminase (ALT) and alkaline phosphatase (ALP) at ~17.5 years with body mass index (BMI) (n = 3,458). Using MR, genetic predictors of ALT, ALP and gamma glutamyltransferase (GGT), were applied to genome-wide association studies of BMI (n = 681,275), waist circumference (WC) (n = 224,459) and waist-hip ratio (WHR) (n = 224,459) to obtain unconfounded estimates. Observationally, ALT was positively associated with BMI (0.10 kg/m(2) per IU/L, 95% confidence interval (CI) 0.09 to 0.11). ALP was inversely associated with BMI (−0.018 kg/m(2) per IU/L, 95% CI −0.024 to −0.012). Using MR, ALT was inversely associated with BMI (−0.14 standard deviation per 100% change in concentration, 95% CI −0.20 to −0.07), but not WC or WHR. ALP and GGT were unrelated to adiposity. Poorer liver function might not cause adiposity; instead higher ALT might reduce BMI, raising the question as to the role of ALT in body composition. Nature Publishing Group UK 2019-11-14 /pmc/articles/PMC6856156/ /pubmed/31727910 http://dx.doi.org/10.1038/s41598-019-52489-8 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Junxi Au Yeung, Shiu Lun Kwok, Man Ki Leung, June Yue Yan Lin, Shi Lin Hui, Lai Ling Leung, Gabriel Matthew Schooling, C. Mary The effect of liver enzymes on adiposity: a Mendelian randomization study |
title | The effect of liver enzymes on adiposity: a Mendelian randomization study |
title_full | The effect of liver enzymes on adiposity: a Mendelian randomization study |
title_fullStr | The effect of liver enzymes on adiposity: a Mendelian randomization study |
title_full_unstemmed | The effect of liver enzymes on adiposity: a Mendelian randomization study |
title_short | The effect of liver enzymes on adiposity: a Mendelian randomization study |
title_sort | effect of liver enzymes on adiposity: a mendelian randomization study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856156/ https://www.ncbi.nlm.nih.gov/pubmed/31727910 http://dx.doi.org/10.1038/s41598-019-52489-8 |
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