Istanbul Universitygrid.9601.e-Cerrahpasa, Cerrahpasa Medical School, Department of Internal Medicine, Section of Gastroenterology, Istanbul, Turkey.
Diyarbakir State Hospital, Diyarbakir, Turkey.
Antimicrob Agents Chemother. 2022 Jan 18;66(1):e0158621. doi: 10.1128/AAC.01586-21. Epub 2021 Oct 25.
Chronic delta hepatitis (CDH) has a worse outcome than other types of viral hepatitis. High-dose, long-term alpha interferon (IFN-α) is the approved treatment and may ameliorate the course of infection. We evaluated long-term histological outcomes of CDH patients treated with IFN-α. Patients with histologically proved noncirrhotic CDH who were treated with high-dose IFN-α for at least 1 year were classified as cirrhotic or noncirrhotic at the end of treatment. Noncirrhotic patients also had posttreatment liver biopsies. Patients were designated histologically responsive or nonresponsive on the basis of fibrosis status. Histological, virological, and biochemical courses were analyzed. Forty-eight patients were treated with IFN-α (conventional and/or pegylated) for a median of 24 months with a posttreatment follow-up of 5 years. During the follow-up, cirrhosis developed in 24 patients, 5 of whom were decompensated. There was no difference between pre- and posttreatment fibrosis scores for 24 noncirrhotic patients at the end of follow-up. Among patients, 13% ( = 6) had decreased, 21% ( = 10) had steady, and 16% ( = 8) had increased fibrosis scores. Persistent viral response (PVR) was achieved in 16 patients (33%). Twenty percent of the entire group was histologically responsive (decreasing or steady fibrosis scores with improved necroinflammatory scores), while nearly 80% had histological progression/cirrhosis. PVR was significantly associated with histological response. The long-term natural course of patients who were treated with high dose IFN-α for at least 1 year was evaluated clinically and histologically. Despite the association of PVR with histological response, IFN-α treatment did not change the natural course of CDH; clinical and histological progression continued in two-thirds of the cases despite treatment.
慢性 delta 肝炎 (CDH) 的预后比其他类型的病毒性肝炎更差。高剂量、长期的α干扰素 (IFN-α) 是批准的治疗方法,可能改善感染过程。我们评估了接受 IFN-α治疗的 CDH 患者的长期组织学结果。经组织学证实为非肝硬化 CDH 的患者,接受高剂量 IFN-α治疗至少 1 年,在治疗结束时分为肝硬化或非肝硬化。非肝硬化患者还进行了治疗后肝活检。根据纤维化状态将患者指定为组织学反应或无反应。分析了组织学、病毒学和生化过程。48 例患者接受 IFN-α(常规和/或聚乙二醇化)治疗,中位数为 24 个月,治疗后随访 5 年。在随访期间,24 例患者发展为肝硬化,其中 5 例失代偿。在随访结束时,24 例非肝硬化患者的治疗前后纤维化评分无差异。在患者中,13%(=6)的纤维化评分降低,21%(=10)的纤维化评分稳定,16%(=8)的纤维化评分增加。16 例患者(33%)获得持续病毒应答(PVR)。整个组中有 20%的患者具有组织学反应(纤维化评分降低或稳定,坏死性炎症评分改善),而近 80%的患者具有组织学进展/肝硬化。PVR 与组织学反应显著相关。用高剂量 IFN-α治疗至少 1 年的患者的长期自然病程进行了临床和组织学评估。尽管 PVR 与组织学反应相关,但 IFN-α治疗并未改变 CDH 的自然病程;尽管治疗,但三分之二的病例仍出现临床和组织学进展。