<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Han YZ</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>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).&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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).&lt;h4>Conclusions&lt;/h4>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.</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>832557</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8968752</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Age-Associated Risk of Liver-Related Adverse Drug Reactions.</pubmed_title><pmcid>PMC8968752</pmcid><pubmed_authors>Jing J</pubmed_authors><pubmed_authors>Bai ZF</pubmed_authors><pubmed_authors>Wang JB</pubmed_authors><pubmed_authors>Xiong P</pubmed_authors><pubmed_authors>Guo YM</pubmed_authors><pubmed_authors>Song HB</pubmed_authors><pubmed_authors>Han YZ</pubmed_authors><pubmed_authors>Xiao XH</pubmed_authors><pubmed_authors>Niu M</pubmed_authors><pubmed_authors>Ge FL</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Age-Associated Risk of Liver-Related Adverse Drug Reactions.</name><description>&lt;h4>Objective&lt;/h4>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).&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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).&lt;h4>Conclusions&lt;/h4>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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T21:48:44.685Z</modification><creation>2025-04-19T21:48:44.685Z</creation></dates><accession>S-EPMC8968752</accession><cross_references><pubmed>35372391</pubmed><doi>10.3389/fmed.2022.832557</doi></cross_references></HashMap>