Li Zhong-Bin, Chen Dan-Dan, He Qing-Juan, Li Le, Zhou Guangde, Fu Yi-Ming, Deng Ya, Niu Xiao-Xia, Chu Fang, Gao Xiao-Pan, Zou Zhengsheng, Chen Guofeng, Ji Dong
Senior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Department II of Hepatology, The Second People's Hospital of Jingzhou City, Jingzhou, China.
Front Pharmacol. 2021 Aug 18;12:734090. doi: 10.3389/fphar.2021.734090. eCollection 2021.
Currently, there are no satisfactory noninvasive methods for the diagnosis of fibrosis in patients with chronic drug-induced liver injury (DILI). Our goal was to develop an algorithm to improve the diagnostic accuracy of significant fibrosis in this population. In the present study, we retrospectively investigated the biochemical and pathological characteristics of consecutive patients with biopsy-proven chronic DILI, who presented at our hospital from January 2013 to December 2017. A noninvasive algorithm was developed by using multivariate logistic regression, receiver operating characteristic (ROC) curves, and decision curve analysis (DCA) to diagnose significant fibrosis in the training cohort, and the algorithm was subsequently validated in the validation cohort. Totally, 1,130 patients were enrolled and randomly assigned into a training cohort (n = 848) and a validation cohort (n = 282). Based on the multivariate analysis, LSM, CHE, and APRI were independently associated with significant fibrosis. A novel algorithm, LAC, was identified with the AUROC of 0.81, which was significantly higher than LSM (AUROC 0.78), CHE (AUROC 0.73), and APRI (AUROC 0.68), alone. The best cutoff value of LAC in the training cohort was 5.4. When the LAC score was used to diagnose advanced fibrosis and cirrhosis stages, the optimal cutoff values were 6.2 and 6.7, respectively, and the AUROC values were 0.84 and 0.90 in the training cohort and 0.81 and 0.83 in the validation cohort. This study proved that the LAC score can contribute to the accurate assessment of high-risk disease progression and the establishment of optimal treatment strategies for patients with chronic DILI.
目前,对于慢性药物性肝损伤(DILI)患者,尚无令人满意的非侵入性纤维化诊断方法。我们的目标是开发一种算法,以提高该人群显著纤维化的诊断准确性。在本研究中,我们回顾性调查了2013年1月至2017年12月在我院就诊的经活检证实为慢性DILI的连续患者的生化和病理特征。通过多变量逻辑回归、受试者操作特征(ROC)曲线和决策曲线分析(DCA)开发了一种非侵入性算法,用于诊断训练队列中的显著纤维化,随后在验证队列中对该算法进行了验证。总共纳入了1130例患者,并随机分为训练队列(n = 848)和验证队列(n = 282)。基于多变量分析,LSM、CHE和APRI与显著纤维化独立相关。一种新的算法LAC被确定,其曲线下面积(AUROC)为0.81,显著高于单独的LSM(AUROC 0.78)、CHE(AUROC 0.73)和APRI(AUROC 0.68)。训练队列中LAC的最佳截断值为5.4。当使用LAC评分诊断晚期纤维化和肝硬化阶段时,最佳截断值分别为6.2和6.7,训练队列中的AUROC值分别为0.84和0.90,验证队列中的AUROC值分别为0.81和0.83。本研究证明,LAC评分有助于准确评估慢性DILI患者的高危疾病进展,并为其制定最佳治疗策略。