Bioinformatic Platform, Instituto de Investigación Biomédica de Málaga - IBIMA, Málaga, Spain.
Division of Gastroenterology, Duke University, Durham, NC, USA.
Arch Toxicol. 2021 May;95(5):1793-1803. doi: 10.1007/s00204-021-03013-3. Epub 2021 Mar 5.
Drug-induced liver injury (DILI) presentation varies biochemically and histologically. Certain drugs present quite consistent injury patterns, i.e., DILI signatures. In contrast, others are manifested as broader types of liver injury. The variety of DILI presentations by a single drug suggests that both drugs and host factors may contribute to the phenotype. However, factors determining the DILI types have not been yet elucidated. Identifying such factors may help to accurately predict the injury types based on drugs and host information and assist the clinical diagnosis of DILI. Using prospective DILI registry datasets, we sought to explore and validate the associations of biochemical injury types at the time of DILI recognition with comprehensive information on drug properties and host factors. Random forest models identified a set of drug properties and host factors that differentiate hepatocellular from cholestatic damage with reasonable accuracy (69-84%). A simplified logistic regression model developed for practical use, consisting of patient's age, drug's lipoaffinity, and hybridization ratio, achieved a fair prediction (68-74%), but suggested potential clinical usability, computing the likelihood of liver injury type based on two properties of drugs taken by a patient and patient's age. In summary, considering both drug and host factors in evaluating DILI risk and phenotypes open an avenue for future DILI research and aid in the refinement of causality assessment.
药物性肝损伤(DILI)的表现从生化和组织学上有所不同。某些药物具有非常一致的损伤模式,即 DILI 特征。相比之下,其他药物则表现为更广泛的肝损伤类型。同一种药物的 DILI 表现多种多样,这表明药物和宿主因素都可能导致表型。然而,决定 DILI 类型的因素尚未阐明。确定这些因素可能有助于根据药物和宿主信息准确预测损伤类型,并协助 DILI 的临床诊断。我们使用前瞻性 DILI 登记数据集,旨在探索和验证 DILI 识别时生化损伤类型与药物特性和宿主因素的综合信息之间的关联。随机森林模型以合理的准确度(69-84%)确定了一组能够区分肝细胞性和胆汁淤积性损伤的药物特性和宿主因素。为实际应用开发的简化逻辑回归模型,由患者年龄、药物脂溶性和亲水性以及杂交比组成,能够实现公平的预测(68-74%),但提示了潜在的临床可用性,即根据患者服用的两种药物的特性和患者年龄计算肝损伤类型的可能性。总之,在评估 DILI 风险和表型时同时考虑药物和宿主因素为未来的 DILI 研究开辟了道路,并有助于因果关系评估的精细化。