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本文引用的文献

1
Characteristics and risk factors for recurrence of nonalcoholic steatohepatitis following liver transplantation.肝移植后非酒精性脂肪性肝炎复发的特征及危险因素
Scand J Gastroenterol. 2019 Feb;54(2):233-239. doi: 10.1080/00365521.2019.1577484. Epub 2019 Apr 18.
2
Incidence of Recurrent NASH-Related Allograft Cirrhosis.复发性非酒精性脂肪性肝炎相关移植肝肝硬化的发生率。
Dig Dis Sci. 2019 May;64(5):1356-1363. doi: 10.1007/s10620-018-5413-9. Epub 2018 Dec 17.
3
Management of Recurrent and De Novo NAFLD/NASH After Liver Transplantation.移植肝后复发性和新发非酒精性脂肪性肝病/非酒精性脂肪性肝炎的管理。
Transplantation. 2019 Jan;103(1):57-67. doi: 10.1097/TP.0000000000002485.
4
High incidence of hepatocellular carcinoma and postoperative complications in patients with nonalcoholic steatohepatitis as a primary indication for deceased liver transplantation.非酒精性脂肪性肝炎患者作为尸体肝移植的主要适应证时,肝细胞癌和术后并发症的发生率较高。
Eur J Gastroenterol Hepatol. 2019 Feb;31(2):205-210. doi: 10.1097/MEG.0000000000001270.
5
Recurrent or De Novo Allograft Steatosis and Long-term Outcomes After Liver Transplantation.肝移植后复发性或新发移植物脂肪变性与长期结局。
Transplantation. 2019 Jan;103(1):e14-e21. doi: 10.1097/TP.0000000000002317.
6
Poor Survival After Retransplantation in NASH Cirrhosis.非酒精性脂肪性肝炎肝硬化患者再次肝移植后生存率较差。
Transplantation. 2019 Jan;103(1):101-108. doi: 10.1097/TP.0000000000002135.
7
Systematic review with meta-analysis: de novo non-alcoholic fatty liver disease in liver-transplanted patients.系统评价与荟萃分析:肝移植患者新发非酒精性脂肪性肝病。
Aliment Pharmacol Ther. 2018 Mar;47(6):704-714. doi: 10.1111/apt.14521. Epub 2018 Jan 22.
8
Performance of transient elastography and serum fibrosis biomarkers for non-invasive evaluation of recurrent fibrosis after liver transplantation: A meta-analysis.瞬时弹性成像和血清纤维化生物标志物用于肝移植后复发性纤维化无创评估的性能:一项荟萃分析。
PLoS One. 2017 Sep 27;12(9):e0185192. doi: 10.1371/journal.pone.0185192. eCollection 2017.
9
Everolimus Is Associated With Less Weight Gain Than Tacrolimus 2 Years After Liver Transplantation: Results of a Randomized Multicenter Study.肝移植术后2年,依维莫司比他克莫司导致的体重增加更少:一项随机多中心研究的结果
Transplantation. 2017 Dec;101(12):2873-2882. doi: 10.1097/TP.0000000000001913.
10
The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases.非酒精性脂肪性肝病的诊断与管理:美国肝病研究协会的实践指南
Hepatology. 2018 Jan;67(1):328-357. doi: 10.1002/hep.29367. Epub 2017 Sep 29.

肝移植后非酒精性脂肪性肝炎复发

Nonalcoholic steatohepatitis recurrence after liver transplant.

作者信息

Taneja Sunil, Roy Akash

机构信息

Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Transl Gastroenterol Hepatol. 2020 Apr 5;5:24. doi: 10.21037/tgh.2019.10.12. eCollection 2020.

DOI:10.21037/tgh.2019.10.12
PMID:32258528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7063497/
Abstract

Nonalcoholic steatohepatitis (NASH) is the fastest growing indication for liver transplant (LT)worldwide and is deemed to be the foremost indication in the near future. Recurrence of NASH can occur post LT and has been observed to be a common phenomenon. Baseline metabolic co-morbidities and worsening of metabolic profile post LT are the principal drivers of NASH recurrence. Liver biopsy remains the gold standard for establishing the diagnosis. However, noninvasive methods including transient elastography (TE) and magnetic resonance imaging (MRI) seem to be promising. The implications of recurrent NASH on post LT outcomes, graft steatosis, progression to fibrosis, overall survival, and cardiovascular associations warrant careful evaluation. Control of metabolic parameters and weight gain along with tailored immunosuppression remain the cornerstone of management. Extrapolation of the ever-increasing armamentarium of NASH pharmacotherapy specifically in this population of recurrent NAFLD remains a challenge for the future.

摘要

非酒精性脂肪性肝炎(NASH)是全球范围内肝脏移植(LT)增长最快的适应证,并且被认为在不久的将来会成为首要适应证。NASH可在LT后复发,并且已被观察到是一种常见现象。LT前的基线代谢合并症以及LT后代谢状况的恶化是NASH复发的主要驱动因素。肝活检仍然是确立诊断的金标准。然而,包括瞬时弹性成像(TE)和磁共振成像(MRI)在内的非侵入性方法似乎很有前景。复发性NASH对LT后结局、移植物脂肪变性、纤维化进展、总体生存以及心血管关联的影响值得仔细评估。控制代谢参数和体重增加以及量身定制的免疫抑制仍然是管理的基石。将不断增加的NASH药物治疗手段专门应用于这一复发性非酒精性脂肪性肝病群体仍然是未来的一项挑战。