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Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study
This study aimed to investigate the risk of metabolic syndrome (MS) in participants whose alanine aminotransferase (ALT) levels were within the normal range in the general population. A cross-sectional study was conducted using nationally representative samples from the Korea National Health and Nut...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141677/ https://www.ncbi.nlm.nih.gov/pubmed/32267895 http://dx.doi.org/10.1371/journal.pone.0231485 |
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author | Cho, Ju-Yeon Jeong, Jae Yoon Sohn, Won |
author_facet | Cho, Ju-Yeon Jeong, Jae Yoon Sohn, Won |
author_sort | Cho, Ju-Yeon |
collection | PubMed |
description | This study aimed to investigate the risk of metabolic syndrome (MS) in participants whose alanine aminotransferase (ALT) levels were within the normal range in the general population. A cross-sectional study was conducted using nationally representative samples from the Korea National Health and Nutrition Examination Survey 2007–2015. A total of 43,402 adults (men, 17,535; women, 25,867) with ALT ≤40 U/L without a history of hepatitis B and C, liver cirrhosis, or liver cancer were analyzed. The risk of MS was evaluated according to the ALT level. The prevalence of MS significantly increased as the ALT levels increased. The proportions of MS in men were 12.6%, 25.2%, and 39.7% in the ALT levels of <15, 15~30, and 30~40 U/L, respectively (p < 0.001), and those of women were 7.2%, 23.3%, and 44.7% in the ALT levels of <10, 10~20, and 20~40 U/L, respectively (p < 0.001). There was an ALT-dependent relationship in the risk of MS in participants with normal ALT level after adjustment for age, alcohol intake, and body mass index. The adjusted odds ratio (aOR) of MS in men was 2.48 (95% confidence interval [CI], 2.16–2.85) in an ALT level of 30~40 U/L compared with that in ALT <15 U/L (p < 0.001), and the aOR of MS in women was 2.67 (95% CI, 2.26–3.15) in an ALT level of 20~40 U/L compared with that in ALT <10 U/L (p < 0.001). Although within the normal range of ALT, the risk of MS increases as the ALT levels increase. The ALT level in the general population without a history of chronic liver disease may be a useful marker to evaluate for MS. |
format | Online Article Text |
id | pubmed-7141677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71416772020-04-10 Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study Cho, Ju-Yeon Jeong, Jae Yoon Sohn, Won PLoS One Research Article This study aimed to investigate the risk of metabolic syndrome (MS) in participants whose alanine aminotransferase (ALT) levels were within the normal range in the general population. A cross-sectional study was conducted using nationally representative samples from the Korea National Health and Nutrition Examination Survey 2007–2015. A total of 43,402 adults (men, 17,535; women, 25,867) with ALT ≤40 U/L without a history of hepatitis B and C, liver cirrhosis, or liver cancer were analyzed. The risk of MS was evaluated according to the ALT level. The prevalence of MS significantly increased as the ALT levels increased. The proportions of MS in men were 12.6%, 25.2%, and 39.7% in the ALT levels of <15, 15~30, and 30~40 U/L, respectively (p < 0.001), and those of women were 7.2%, 23.3%, and 44.7% in the ALT levels of <10, 10~20, and 20~40 U/L, respectively (p < 0.001). There was an ALT-dependent relationship in the risk of MS in participants with normal ALT level after adjustment for age, alcohol intake, and body mass index. The adjusted odds ratio (aOR) of MS in men was 2.48 (95% confidence interval [CI], 2.16–2.85) in an ALT level of 30~40 U/L compared with that in ALT <15 U/L (p < 0.001), and the aOR of MS in women was 2.67 (95% CI, 2.26–3.15) in an ALT level of 20~40 U/L compared with that in ALT <10 U/L (p < 0.001). Although within the normal range of ALT, the risk of MS increases as the ALT levels increase. The ALT level in the general population without a history of chronic liver disease may be a useful marker to evaluate for MS. Public Library of Science 2020-04-08 /pmc/articles/PMC7141677/ /pubmed/32267895 http://dx.doi.org/10.1371/journal.pone.0231485 Text en © 2020 Cho 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 Cho, Ju-Yeon Jeong, Jae Yoon Sohn, Won Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title | Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title_full | Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title_fullStr | Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title_full_unstemmed | Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title_short | Risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: A population-based nationwide study |
title_sort | risk of metabolic syndrome in participants within the normal range of alanine aminotransferase: a population-based nationwide study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141677/ https://www.ncbi.nlm.nih.gov/pubmed/32267895 http://dx.doi.org/10.1371/journal.pone.0231485 |
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