Faculty of Medicine, University of Iceland, Iceland; Department of Gastroenterology, Landspitali University Hospital Reykjavik, Iceland.
Unidad de Gestión Clínica de Enfermedades Digestivas, Instituto de Investigación Biomédica de Málaga-IBIMA, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
J Hepatol. 2022 Feb;76(2):435-445. doi: 10.1016/j.jhep.2021.10.011. Epub 2021 Oct 22.
Drug-induced liver injury (DILI) has a very variable clinical and biochemical phenotype and differs widely in severity, from mild injury to life-threatening liver failure. Chronic injury has also been reported to occur at a variable frequency, ranging from 3.4% to 39%, 6-12 months after discontinuing the implicated agent. This wide range is probably related to various definitions of chronic liver injury and variable selection of patients. The long-term sequalae of this chronic injury in terms of morbidity and mortality are unclear, although rare vanishing bile duct syndrome is associated with an unfavourable prognosis, with increased risk of chronic liver failure and need for liver transplantation. Other forms of long-term sequalae associated with DILI are progressive fibrosis, autoimmune-like hepatitis, secondary sclerosing cholangitis, sinusoidal obstruction syndrome and, as a common final stage, the development of cirrhosis, portal hypertension and its complications. Immune checkpoint inhibitors, which can cause an autoimmune-like phenotype have also recently been shown to cause sclerosing cholangitis with cytotoxic T CD8+ cell infiltration in biliary tracts. DILI has been shown to have a significant impact on health-related quality of life but very little is known about its psychological consequences in the long-term. Further investigations with structured long-term follow-up and periodic quality of life surveys are needed to assess the impact of DILI on psychological outcomes, particularly in those with chronic sequelae.
药物性肝损伤(DILI)具有非常多变的临床和生化表型,严重程度差异很大,从轻度损伤到危及生命的肝衰竭不等。据报道,在停用可疑药物后 6-12 个月,也会以不同的频率发生慢性损伤,范围从 3.4%到 39%。这种广泛的范围可能与慢性肝损伤的各种定义以及患者的不同选择有关。尽管罕见的消失胆管综合征与不良预后相关,增加了慢性肝衰竭和需要肝移植的风险,但这种慢性损伤的长期后果(包括发病率和死亡率)尚不清楚。其他与 DILI 相关的长期后果包括进行性纤维化、自身免疫样肝炎、继发性硬化性胆管炎、窦状隙阻塞综合征,以及作为共同的终末期,发展为肝硬化、门静脉高压及其并发症。最近还发现,免疫检查点抑制剂可引起自身免疫样表型,也可引起胆管内细胞毒性 T 细胞 CD8+浸润的硬化性胆管炎。DILI 已被证明对健康相关生活质量有重大影响,但对其长期心理后果知之甚少。需要进一步进行有结构的长期随访和定期生活质量调查,以评估 DILI 对心理结果的影响,特别是在那些有慢性后遗症的患者中。