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Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males
Alanine aminotransferase (ALT) levels reflect skeletal muscle volume and general performance, which are associated with chronic obstructive pulmonary disease (COPD) development and prognosis. This study aimed to investigate ALT levels as a risk factor for COPD development. This 13-year population-ba...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295341/ https://www.ncbi.nlm.nih.gov/pubmed/34290312 http://dx.doi.org/10.1038/s41598-021-94385-0 |
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author | Choi, Yong Jun Kwon, Do Sun Kim, Taehee Cho, Jae Hwa Kim, Hyung Jung Byun, Min Kwang Park, Hye Jung |
author_facet | Choi, Yong Jun Kwon, Do Sun Kim, Taehee Cho, Jae Hwa Kim, Hyung Jung Byun, Min Kwang Park, Hye Jung |
author_sort | Choi, Yong Jun |
collection | PubMed |
description | Alanine aminotransferase (ALT) levels reflect skeletal muscle volume and general performance, which are associated with chronic obstructive pulmonary disease (COPD) development and prognosis. This study aimed to investigate ALT levels as a risk factor for COPD development. This 13-year population-based retrospective observational cohort study included 422,452 participants for analysis. We classified groups according to the baseline ALT levels (groups 1–5: ALT (IU/L) < 10; 10–19; 20–29; 30–39; and ≥ 40, respectively). The incidence of COPD was the highest in group 1, decreasing as the group number increased in males, but not in females. The Cox regression analysis in males revealed that a lower ALT level, as a continuous variable, was a significant risk factor for COPD development [univariable, hazard ratio (HR): 0.992, 95% confidence interval (CI): 0.991–0.994; multivariable, HR: 0.998, 95% CI: 0.996–0.999]. In addition, COPD was more likely to develop in the lower ALT level groups (groups 1–4; < 40 IU/L), than in the highest ALT level group (group 5; ≥ 40 IU/L) (univariable, HR: 1.341, 95% CI: 1.263–1.424; multivariable, HR: 1.097, 95% CI: 1.030–1.168). Our findings suggest that males with low ALT levels should be carefully monitored for COPD development. |
format | Online Article Text |
id | pubmed-8295341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82953412021-07-23 Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males Choi, Yong Jun Kwon, Do Sun Kim, Taehee Cho, Jae Hwa Kim, Hyung Jung Byun, Min Kwang Park, Hye Jung Sci Rep Article Alanine aminotransferase (ALT) levels reflect skeletal muscle volume and general performance, which are associated with chronic obstructive pulmonary disease (COPD) development and prognosis. This study aimed to investigate ALT levels as a risk factor for COPD development. This 13-year population-based retrospective observational cohort study included 422,452 participants for analysis. We classified groups according to the baseline ALT levels (groups 1–5: ALT (IU/L) < 10; 10–19; 20–29; 30–39; and ≥ 40, respectively). The incidence of COPD was the highest in group 1, decreasing as the group number increased in males, but not in females. The Cox regression analysis in males revealed that a lower ALT level, as a continuous variable, was a significant risk factor for COPD development [univariable, hazard ratio (HR): 0.992, 95% confidence interval (CI): 0.991–0.994; multivariable, HR: 0.998, 95% CI: 0.996–0.999]. In addition, COPD was more likely to develop in the lower ALT level groups (groups 1–4; < 40 IU/L), than in the highest ALT level group (group 5; ≥ 40 IU/L) (univariable, HR: 1.341, 95% CI: 1.263–1.424; multivariable, HR: 1.097, 95% CI: 1.030–1.168). Our findings suggest that males with low ALT levels should be carefully monitored for COPD development. Nature Publishing Group UK 2021-07-21 /pmc/articles/PMC8295341/ /pubmed/34290312 http://dx.doi.org/10.1038/s41598-021-94385-0 Text en © The Author(s) 2021 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 Choi, Yong Jun Kwon, Do Sun Kim, Taehee Cho, Jae Hwa Kim, Hyung Jung Byun, Min Kwang Park, Hye Jung Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title | Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title_full | Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title_fullStr | Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title_full_unstemmed | Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title_short | Low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
title_sort | low alanine aminotransferase as a risk factor for chronic obstructive pulmonary disease in males |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295341/ https://www.ncbi.nlm.nih.gov/pubmed/34290312 http://dx.doi.org/10.1038/s41598-021-94385-0 |
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