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Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women
We tested whether alanine aminotransferase/aspartate aminotransferase (ALT/AST), a marker of hepatosteatosis, associates with insulin resistance, β-cell function and postglucose glycemia. We studied 311 young and 148 middle-aged Japanese women, whose BMI averaged < 23.0 kg/m(2). Insulinogenic ind...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185667/ https://www.ncbi.nlm.nih.gov/pubmed/37188859 http://dx.doi.org/10.1038/s41598-023-35001-1 |
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author | Minato-Inokawa, Satomi Tsuboi-Kaji, Ayaka Honda, Mari Takeuchi, Mika Kitaoka, Kaori Kurata, Miki Wu, Bin Kazumi, Tsutomu Fukuo, Keisuke |
author_facet | Minato-Inokawa, Satomi Tsuboi-Kaji, Ayaka Honda, Mari Takeuchi, Mika Kitaoka, Kaori Kurata, Miki Wu, Bin Kazumi, Tsutomu Fukuo, Keisuke |
author_sort | Minato-Inokawa, Satomi |
collection | PubMed |
description | We tested whether alanine aminotransferase/aspartate aminotransferase (ALT/AST), a marker of hepatosteatosis, associates with insulin resistance, β-cell function and postglucose glycemia. We studied 311 young and 148 middle-aged Japanese women, whose BMI averaged < 23.0 kg/m(2). Insulinogenic index and Matsuda index were evaluated in 110 young and 65 middle-aged women. In two groups of women, ALT/AST was associated positively with homeostasis model assessment insulin resistance (HOMA-IR) and inversely with Matsuda index. In middle-aged women only, the ratio was also associated positively with fasting and postload glycemia and HbA1c. The ratio showed negative association with disposition index (a product of insulinogenic index and Matsuda index). On multivariate linear regression analysis, HOMA-IR emerged as a single determinant of ALT/AST in young and middle-aged women (standardized β: 0.209, p = 0.003 and 0.372, p = 0.002, respectively). ALT/AST was associated with insulin resistance and β-cell function even in non-obese Japanese women, suggesting a pathophysiologic basis in its prediction of diabetic risk. |
format | Online Article Text |
id | pubmed-10185667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101856672023-05-17 Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women Minato-Inokawa, Satomi Tsuboi-Kaji, Ayaka Honda, Mari Takeuchi, Mika Kitaoka, Kaori Kurata, Miki Wu, Bin Kazumi, Tsutomu Fukuo, Keisuke Sci Rep Article We tested whether alanine aminotransferase/aspartate aminotransferase (ALT/AST), a marker of hepatosteatosis, associates with insulin resistance, β-cell function and postglucose glycemia. We studied 311 young and 148 middle-aged Japanese women, whose BMI averaged < 23.0 kg/m(2). Insulinogenic index and Matsuda index were evaluated in 110 young and 65 middle-aged women. In two groups of women, ALT/AST was associated positively with homeostasis model assessment insulin resistance (HOMA-IR) and inversely with Matsuda index. In middle-aged women only, the ratio was also associated positively with fasting and postload glycemia and HbA1c. The ratio showed negative association with disposition index (a product of insulinogenic index and Matsuda index). On multivariate linear regression analysis, HOMA-IR emerged as a single determinant of ALT/AST in young and middle-aged women (standardized β: 0.209, p = 0.003 and 0.372, p = 0.002, respectively). ALT/AST was associated with insulin resistance and β-cell function even in non-obese Japanese women, suggesting a pathophysiologic basis in its prediction of diabetic risk. Nature Publishing Group UK 2023-05-15 /pmc/articles/PMC10185667/ /pubmed/37188859 http://dx.doi.org/10.1038/s41598-023-35001-1 Text en © The Author(s) 2023 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 Minato-Inokawa, Satomi Tsuboi-Kaji, Ayaka Honda, Mari Takeuchi, Mika Kitaoka, Kaori Kurata, Miki Wu, Bin Kazumi, Tsutomu Fukuo, Keisuke Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title | Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title_full | Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title_fullStr | Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title_full_unstemmed | Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title_short | Associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
title_sort | associations of alanine aminotransferase/aspartate aminotransferase with insulin resistance and β-cell function in women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185667/ https://www.ncbi.nlm.nih.gov/pubmed/37188859 http://dx.doi.org/10.1038/s41598-023-35001-1 |
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