Department of Infectious Diseases, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, People's Republic of China.
Department of Infectious Diseases, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, People's Republic of China.
Biomed Pharmacother. 2021 Feb;134:111150. doi: 10.1016/j.biopha.2020.111150. Epub 2021 Jan 1.
Risk factors related to the development of acetaminophen (APAP)-induced adverse reactions and liver injury remain uncertain. Sleep disorders have been linked to some health outcomes. This study examined the associations of sleep disorders with APAP-induced adverse reactions or liver injury and the possible mechanisms. From NIS database, adverse reactions, liver injury and sleep disorders were identified. Factors associated with the risk of the total adverse effects or liver injury were examined with logistic regression. From Gene Expression Omnibus database, datasets GSE111828, containing transcriptome data based on RNA-seq analysis from liver samples extracted from mice post APAP administration, and GSE92913, containing transcriptome data based on microarray analysis from liver samples extracted from mice with sleep deprivation, were analyzed. A total of 4372754 patients without and 91314 patients with sleep disorders were eligible for analyses. Both before and after propensity score matching, APAP-induced adverse reactions were higher in patients with sleep disorders than in patients without. In multivariate regression, sleep disorders were associated with higher odds of APAP-induced adverse reactions (adjusted OR [aOR] 2.005, 95 % CI 1.343-2.995) and liver injury (aOR 2.788, 95 % CI 1.310-5.932). Genes that were enriched in bile secretion and retinol metabolism and PPAR signaling pathways were basically down-regulated in livers of mice after APAP administration and livers of mice with sleep deprivation. This study shows that sleep disorders may be novel independent risk factors for APAP-associated adverse reactions and liver injury and provides bioinformation linking sleep disorders to increased risk of APAP-induced liver injury.
与乙酰氨基酚 (APAP) 诱导的不良反应和肝损伤相关的风险因素仍不确定。睡眠障碍与一些健康结果有关。本研究探讨了睡眠障碍与 APAP 诱导的不良反应或肝损伤的关系及其可能的机制。从 NIS 数据库中确定了不良反应、肝损伤和睡眠障碍。使用逻辑回归检查与总不良反应或肝损伤风险相关的因素。从基因表达综合数据库中,分析了数据集 GSE111828,其中包含了基于 RNA-seq 分析从 APAP 给药后提取的小鼠肝脏样本的转录组数据,以及 GSE92913,其中包含了基于微阵列分析从睡眠剥夺的小鼠肝脏样本的转录组数据。共有 4372754 名无睡眠障碍和 91314 名有睡眠障碍的患者适合进行分析。在倾向评分匹配前后,有睡眠障碍的患者发生 APAP 诱导的不良反应的几率均高于无睡眠障碍的患者。在多变量回归中,睡眠障碍与 APAP 诱导的不良反应的发生几率较高相关 (调整后的 OR [aOR] 2.005,95 % CI 1.343-2.995) 和肝损伤 (aOR 2.788,95 % CI 1.310-5.932)。在 APAP 给药后和睡眠剥夺的小鼠肝脏中,参与胆汁分泌和视黄醇代谢以及 PPAR 信号通路的基因基本下调。本研究表明,睡眠障碍可能是 APAP 相关不良反应和肝损伤的新的独立危险因素,并提供了将睡眠障碍与增加的 APAP 诱导的肝损伤风险联系起来的生物信息。