Prediction of biochemical nonresolution in patients with chronic drug‐induced liver injury: A large multicenter study

Background and Aims To clarify high‐risk factors and develop a nomogram model to predict biochemical resolution or biochemical nonresolution (BNR) in patients with chronic DILI. Approach and Results Retrospectively, 3655 of 5326 patients with chronic DILI were enrolled from nine participating hospit...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2022-06, Vol.75 (6), p.1373-1385
Hauptverfasser: Wang, Chun‐Yan, Deng, Ya, Li, Ping, Zheng, Sujun, Chen, Guofeng, Zhou, Guangde, Xu, Jing, Chen, Yan‐Ping, Wang, Zheng, Jin, Xueyuan, Tang, Jin‐Mo, Hu, Kun‐Peng, Bi, Jing‐Feng, Zhang, Ping, Li, Chun‐Xia, Huang, Ang, Lv, Gui‐Ji, Xiao, Xiao‐He, Zou, Zhengsheng, Ji, Dong
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Sprache:eng
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Zusammenfassung:Background and Aims To clarify high‐risk factors and develop a nomogram model to predict biochemical resolution or biochemical nonresolution (BNR) in patients with chronic DILI. Approach and Results Retrospectively, 3655 of 5326 patients with chronic DILI were enrolled from nine participating hospitals, of whom 2866 underwent liver biopsy. All of these patients were followed up for over 1 year and their clinical characteristics were retrieved from electronic medical records. The endpoint was BNR, defined as alanine aminotransferase or aspartate aminotransferase >1.5× upper limit of normal or alkaline phosphatase >1.1× ULN, at 12 months from chronic DILI diagnosis. The noninvasive high‐risk factors for BNR identified by multivariable logistic regression were used to establish a nomogram, which was validated in an independent external cohort. Finally, 19.3% (707 of 3655) patients presented with BNR. Histologically, with the increase in liver inflammation grades and fibrosis stages, the proportion of BNR significantly increased. The risk of BNR was increased by 21.3‐fold in patients with significant inflammation compared to none or mild inflammation (p 
ISSN:0270-9139
1527-3350
DOI:10.1002/hep.32283