Department of Gastroenterology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Institute of Liver Diseases, Beijing University of Chinese Medicine, Beijing, China.
Front Public Health. 2023 Apr 5;11:1137738. doi: 10.3389/fpubh.2023.1137738. eCollection 2023.
Patients with chronic hepatitis B (CHB) in the immune tolerant (IT) phase were previously thought to have no or slight inflammation or fibrosis in the liver. In fact, some CHB patients with normal ALT levels still experience liver fibrosis. This study aimed to develop and validate a non-invasive model for identifying pseudo-immune tolerance (pseudo-IT) of CHB by predicting significant liver fibrosis.
This multi-center study enrolled a total of 445 IT-phase patients who had undergone liver biopsy for the training cohort ( = 289) and validation cohort ( = 156) during different time periods. A risk model (IT-3) for predicting significant liver fibrosis (Ishak score ≥ 3) was developed using high-risk factors which were identified using multivariate stepwise logistic regression. Next, an online dynamic nomogram was created for the clinical usage. The receiver operating characteristic (ROC) curve, net reclassification improvement and integrated discrimination improvement were used to assess the discrimination of the IT-3 model. Calibration curves were used to evaluate the models' calibration. The clinical practicability of the model was evaluated using decision curve analysis and clinical impact curves.
8.8% (39 of 445) patients presented with significant liver fibrosis in this study. Aspartate aminotransferase (AST), hepatitis B e-antigen (HBeAg), and platelet (PLT) were included in the prediction model (IT-3). The IT-3 model showed good calibration and discrimination both in the training and validation cohorts (AUC = 0.888 and 0.833, respectively). The continuous NRI and IDI showed that the IT-3 model had better predictive accuracy than GPR, APRI, and FIB-4 ( < 0.001). Decision curve analysis and clinical impact curves were used to demonstrate the clinical usefulness. At a cut-off value of 106 points, the sensitivity and specificity were 91.7 and 70.2%, respectively.
The IT-3 model proved an accurate non-invasive method in identifying pseudo-IT of CHB, which can help to formulate more appropriate treatment strategies.
既往认为慢性乙型肝炎(CHB)免疫耐受(IT)期患者肝脏无或仅有轻微炎症或纤维化。实际上,部分 ALT 正常的 CHB 患者仍存在肝纤维化。本研究旨在建立并验证一种通过预测显著肝纤维化来识别 CHB 假 IT 的非侵入性模型。
这项多中心研究纳入了总共 445 例处于 IT 期并在不同时期接受肝活检的患者,其中训练队列( = 289)和验证队列( = 156)。使用多变量逐步逻辑回归确定高风险因素,并建立预测显著肝纤维化(Ishak 评分 ≥ 3)的风险模型(IT-3)。然后,创建了一个在线动态列线图以用于临床应用。使用受试者工作特征(ROC)曲线、净重新分类改善和综合判别改善来评估 IT-3 模型的判别能力。使用校准曲线来评估模型的校准。通过决策曲线分析和临床影响曲线来评估模型的临床实用性。
本研究中,8.8%(445 例中的 39 例)患者存在显著肝纤维化。天门冬氨酸氨基转移酶(AST)、乙型肝炎 e 抗原(HBeAg)和血小板(PLT)被纳入预测模型(IT-3)。IT-3 模型在训练和验证队列中均具有良好的校准和判别能力(AUC 分别为 0.888 和 0.833)。连续 NRI 和 IDI 表明,与 GPR、APRI 和 FIB-4 相比,IT-3 模型具有更好的预测准确性( < 0.001)。决策曲线分析和临床影响曲线用于证明其临床实用性。在截断值为 106 分时,其敏感性和特异性分别为 91.7%和 70.2%。
IT-3 模型是一种识别 CHB 假 IT 的准确非侵入性方法,有助于制定更合适的治疗策略。