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Age-Associated Risk of Liver-Related Adverse Drug Reactions
OBJECTIVE: Aging population is generally considered more sensitive to adverse drug reactions (ADRs). Yet, big data-based quantitative evidence currently does not exist to support this concept. This study aims to investigate age-associated risks of liver-related ADR (L-ADR). METHODS: Spontaneous repo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968752/ https://www.ncbi.nlm.nih.gov/pubmed/35372391 http://dx.doi.org/10.3389/fmed.2022.832557 |
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author | Han, Yan-zhong Guo, Yu-ming Xiong, Peng Ge, Fei-lin Jing, Jing Niu, Ming Zhao, Xu Bai, Zhao-fang Song, Hai-bo Xiao, Xiao-he Wang, Jia-bo |
author_facet | Han, Yan-zhong Guo, Yu-ming Xiong, Peng Ge, Fei-lin Jing, Jing Niu, Ming Zhao, Xu Bai, Zhao-fang Song, Hai-bo Xiao, Xiao-he Wang, Jia-bo |
author_sort | Han, Yan-zhong |
collection | PubMed |
description | OBJECTIVE: Aging population is generally considered more sensitive to adverse drug reactions (ADRs). Yet, big data-based quantitative evidence currently does not exist to support this concept. This study aims to investigate age-associated risks of liver-related ADR (L-ADR). METHODS: Spontaneous reporting data from 2012 to 2016 were retrieved from the China National ADR Monitoring System. The risk ratio (RR) was used to quantify the relative risk of L-ADR of each age group. The reporting odds ratio (ROR) was used to quantify the correlation with the risk of L-ADR of each drug category or drug in older adults. RESULTS: Totally, 64,702 L-ADR reports were retrieved, covering ages from 1 to 116, with a median age of 49. The RR values increased exponentially with the increase of age, which indicates that the relative risk of L-ADR increased by 33% for every 10-year increase in age. The age cutoff point for relative high risk of L-ADR was estimated at 52.0 years old (RR = 1). In 17 categories composed of 270 drugs, the top 3 drug categories with a high correlation to the risk of L-ADR in older adults were antiarrhythmic (ROR, 5.75; 95% CI: 4.45–7.42), antilipemic (ROR, 4.77; 95% CI: 4.53–5.02), and antihypertensive (ROR, 2.97; 95% CI: 2.59–3.41). CONCLUSIONS: This research illustrates quantitatively that aging is a potential risk factor for L-ADR, with a 33% increase in relative risk for every 10-year increase in age. Risk management should be addressed for older adults when those drugs with a high correlation to the risk of L-ADR are used. |
format | Online Article Text |
id | pubmed-8968752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89687522022-04-01 Age-Associated Risk of Liver-Related Adverse Drug Reactions Han, Yan-zhong Guo, Yu-ming Xiong, Peng Ge, Fei-lin Jing, Jing Niu, Ming Zhao, Xu Bai, Zhao-fang Song, Hai-bo Xiao, Xiao-he Wang, Jia-bo Front Med (Lausanne) Medicine OBJECTIVE: Aging population is generally considered more sensitive to adverse drug reactions (ADRs). Yet, big data-based quantitative evidence currently does not exist to support this concept. This study aims to investigate age-associated risks of liver-related ADR (L-ADR). METHODS: Spontaneous reporting data from 2012 to 2016 were retrieved from the China National ADR Monitoring System. The risk ratio (RR) was used to quantify the relative risk of L-ADR of each age group. The reporting odds ratio (ROR) was used to quantify the correlation with the risk of L-ADR of each drug category or drug in older adults. RESULTS: Totally, 64,702 L-ADR reports were retrieved, covering ages from 1 to 116, with a median age of 49. The RR values increased exponentially with the increase of age, which indicates that the relative risk of L-ADR increased by 33% for every 10-year increase in age. The age cutoff point for relative high risk of L-ADR was estimated at 52.0 years old (RR = 1). In 17 categories composed of 270 drugs, the top 3 drug categories with a high correlation to the risk of L-ADR in older adults were antiarrhythmic (ROR, 5.75; 95% CI: 4.45–7.42), antilipemic (ROR, 4.77; 95% CI: 4.53–5.02), and antihypertensive (ROR, 2.97; 95% CI: 2.59–3.41). CONCLUSIONS: This research illustrates quantitatively that aging is a potential risk factor for L-ADR, with a 33% increase in relative risk for every 10-year increase in age. Risk management should be addressed for older adults when those drugs with a high correlation to the risk of L-ADR are used. Frontiers Media S.A. 2022-03-17 /pmc/articles/PMC8968752/ /pubmed/35372391 http://dx.doi.org/10.3389/fmed.2022.832557 Text en Copyright © 2022 Han, Guo, Xiong, Ge, Jing, Niu, Zhao, Bai, Song, Xiao and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Han, Yan-zhong Guo, Yu-ming Xiong, Peng Ge, Fei-lin Jing, Jing Niu, Ming Zhao, Xu Bai, Zhao-fang Song, Hai-bo Xiao, Xiao-he Wang, Jia-bo Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title | Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title_full | Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title_fullStr | Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title_full_unstemmed | Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title_short | Age-Associated Risk of Liver-Related Adverse Drug Reactions |
title_sort | age-associated risk of liver-related adverse drug reactions |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968752/ https://www.ncbi.nlm.nih.gov/pubmed/35372391 http://dx.doi.org/10.3389/fmed.2022.832557 |
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