Natour Randa Taher, Haimi Motti, Hazan Rawi, Saadi Tarek, Baker Fadi Abu
Technion Israel Institute of Technology, Rappaport Faculty of Medicine, Haifa, Israel.
Department of Gastroenterology and Hepatology, Hillel Yaffe Medical Center, Hadera, Israel.
J Viral Hepat. 2025 Oct;32(10):e70071. doi: 10.1111/jvh.70071.
The coexistence of chronic hepatitis B (CHB) and metabolic dysfunction-associated liver disease (MASLD) gained recognition, but the diagnostic performance of non-invasive markers regarding it remains underexplored. This study aimed to evaluate the utility of the FIB-4 index for fibrosis prediction in CHB patients and investigate its performance in the distinct subgroup of CHB-MASLD. A prospective study from 2021 to 2022 included 109 CHB and 64 CHB-MASLD patients. All underwent liver stiffness measurement via elastography and FIB-4 calculation. MASLD criteria were defined, creating CHB-alone and CHB-MASLD groups. FIB-4 values were compared to the liver stiffness measurements. Statistical analyses included t-tests, ROC curves, and correlation assessments. No significant age, gender, or ethnicity differences were observed between the CHB and CHB-MASLD groups. CHB-MASLD patients exhibited higher BMI, dysglycemia, and dyslipidemia. HBeAg negativity and nucleoside/tide treatment rates were comparable. FIB-4 and APRI scores were elevated in CHB-MASLD. ROC analysis revealed an AUC of 0.86 for FIB-4 in the CHB group, with an optimal cutoff of 1.95. Subgroup analysis by BMI showed consistent FIB-4 performance. In the CHB-MASLD group, the ROC curve showed an AUC of 0.61 (p = 0.12), indicating non-significance. Our study affirms FIB-4's robust performance in predicting fibrosis in CHB patients across varied BMI profiles. Yet, challenges surface when applying FIB-4 to those with concurrent CHB and MASLD. These limitations stress the urgency of refined fibrosis prediction tools, essential for navigating the complex interplay of viral and metabolic factors in the CHB-MASLD population.
慢性乙型肝炎(CHB)与代谢功能障碍相关肝病(MASLD)并存已得到认可,但关于其无创标志物的诊断性能仍未得到充分研究。本研究旨在评估FIB-4指数在CHB患者纤维化预测中的效用,并研究其在CHB-MASLD不同亚组中的表现。一项2021年至2022年的前瞻性研究纳入了109例CHB患者和64例CHB-MASLD患者。所有患者均通过弹性成像进行肝脏硬度测量并计算FIB-4。定义了MASLD标准,创建了单纯CHB组和CHB-MASLD组。将FIB-4值与肝脏硬度测量结果进行比较。统计分析包括t检验、ROC曲线和相关性评估。CHB组和CHB-MASLD组之间未观察到显著的年龄、性别或种族差异。CHB-MASLD患者表现出更高的BMI、血糖异常和血脂异常。HBeAg阴性率和核苷/核苷酸治疗率相当。CHB-MASLD患者的FIB-4和APRI评分升高。ROC分析显示,CHB组中FIB-4 的AUC为0.86,最佳截断值为1.95。按BMI进行的亚组分析显示FIB-4表现一致。在CHB-MASLD组中,ROC曲线显示AUC为0.61(p = 0.12),表明无统计学意义。我们的研究证实了FIB-4在预测不同BMI分布的CHB患者纤维化方面的强大性能。然而,将FIB-4应用于同时患有CHB和MASLD的患者时会出现挑战。这些局限性凸显了改进纤维化预测工具的紧迫性,这对于应对CHB-MASLD人群中病毒和代谢因素的复杂相互作用至关重要。