Division of Gastroenterology, Department of Internal Medicine, Taitung Mackay Memorial Hospital, Taiwan; Mackay Medical College, New Taipei, Taiwan.
Department of Pathology, Taitung Mackay Memorial Hospital, Taiwan.
J Formos Med Assoc. 2021 May;120(5):1259-1268. doi: 10.1016/j.jfma.2020.11.018. Epub 2020 Dec 16.
BACKGROUND/PURPOSE: Direct-acting antiviral agents achieve sustained virological response in most chronic hepatitis C patients. However, histological responses are not consistent among all patients. We conducted an observational study to analyze the histological changes after direct-acting antiviral agent therapy.
We recruited 220 patients who achieved sustained virological response after direct-acting antiviral agent. Histology was assessed by liver biopsy and laboratory indices including fibrosis-4 and aspartate aminotransferase to platelet ratio index. Primary outcomes were change in the dynamic laboratory results. Secondary outcomes were histological changes on liver biopsy. We analyzed the factors predictive of histological regression.
The mean fibrosis-4 index decreased from 4.78 at baseline to 3.30, 3.31, 3.65, and 3.66 at week 4, 8, end of treatment, and 12 weeks after treatment, respectively (all p < 0.01). Mean aspartate aminotransferase to platelet ratio index decreased from 1.62 at baseline to 0.61, 0.66, 0.64, and 0.82 at week 4, 8, end of treatment, and 12 weeks after treatment, respectively (all p < 0.01). Mean Histological Activity Index at baseline and post-treatment was 6.9 ± 1.9 and 5.0 ± 2.3. The METAVIR fibrosis scores improved in 61.9% of the patients. We compared patients who achieved fibrosis-regression with the non-regression group. There was no significant difference in the baseline host/virological factors between the groups.
Reversal of liver inflammation and fibrosis was achieved in a significant number of patients who received direct-acting antiviral agent. No baseline host or virological factor was predictive of histological regression after antiviral treatment.
背景/目的:直接作用抗病毒药物可使大多数慢性丙型肝炎患者获得持续病毒学应答。然而,并非所有患者的组织学应答都一致。我们进行了一项观察性研究,以分析直接作用抗病毒药物治疗后的组织学变化。
我们招募了 220 名在直接作用抗病毒药物治疗后获得持续病毒学应答的患者。通过肝活检和包括纤维化-4 和天冬氨酸氨基转移酶与血小板比值指数在内的实验室指标评估组织学。主要结局是动态实验室结果的变化。次要结局是肝活检的组织学变化。我们分析了预测组织学消退的因素。
纤维化-4 指数从基线的 4.78 降至治疗后 4、8、结束和 12 周的 3.30、3.31、3.65 和 3.66(均 p < 0.01)。天冬氨酸氨基转移酶与血小板比值指数从基线的 1.62 降至治疗后 4、8、结束和 12 周的 0.61、0.66、0.64 和 0.82(均 p < 0.01)。基线和治疗后平均组织学活动指数分别为 6.9 ± 1.9 和 5.0 ± 2.3。61.9%的患者 METAVIR 纤维化评分得到改善。我们比较了获得纤维化消退与未消退的患者。两组间基线宿主/病毒学因素无显著差异。
在接受直接作用抗病毒药物治疗的患者中,相当数量的患者实现了肝炎症和纤维化的逆转。抗病毒治疗后组织学消退与基线宿主或病毒学因素无关。