Rossi Roberta Elisa, Parisi Ioanna, Despott Edward John, Burroughs Andrew Kenneth, O'Beirne James, Conte Dario, Hamilton Mark Ian, Murray Charles Daniel
Roberta Elisa Rossi, Edward John Despott, Mark Ian Hamilton, Charles Daniel Murray, Centre for Gastroenterology, Royal Free Hospital, London NW3 2QG, United Kingdom.
World J Gastroenterol. 2014 Dec 14;20(46):17352-9. doi: 10.3748/wjg.v20.i46.17352.
Abnormalities in liver function tests, including transient and self-limiting hypertransaminasemia, cholestatic disease and hepatitis, can develop during treatment with anti-tumour-necrosis-factor (TNF) therapy. The optimal management of liver injury related to anti-TNF therapy is still a matter of debate. Although some authors recommend discontinuing treatment in case of both a rise of alanine aminotransferase more than 5 times the upper limit of normal, or the occurrence of jaundice, there are no standard guidelines for the management of anti-TNF-related liver injury. Bibliographical searches were performed in PubMed, using the following key words: inflammatory bowel disease (IBD); TNF inhibitors; hypertransaminasemia; drug-related liver injury; infliximab. According to published data, elevation of transaminases in patients with IBD treated with anti-TNF is a common finding, but resolution appears to be the usual outcome. Anti-TNF agents seem to be safe with a low risk of causing severe drug-related liver injury. According to our centre experience, we found that hypertransaminasemia was a common, mainly self-limiting finding in our IBD cohort and was not correlated to infliximab treatment on both univariate and multivariate analyses. An algorithm for the management of liver impairment occurring during anti-TNF treatment is also proposed and this highlights the need of a multidisciplinary approach and suggests liver biopsy as a key-point in the management decision in case of severe rise of transaminases. However, hepatic injury is generally self-limiting and drug withdrawal seems to be an exception.
在使用抗肿瘤坏死因子(TNF)治疗期间,肝功能检查可能会出现异常,包括短暂性和自限性高转氨酶血症、胆汁淤积性疾病和肝炎。与抗TNF治疗相关的肝损伤的最佳管理仍存在争议。尽管一些作者建议在丙氨酸转氨酶升高超过正常上限5倍或出现黄疸时停止治疗,但对于抗TNF相关肝损伤的管理尚无标准指南。在PubMed上进行了文献检索,使用了以下关键词:炎症性肠病(IBD);TNF抑制剂;高转氨酶血症;药物性肝损伤;英夫利昔单抗。根据已发表的数据,接受抗TNF治疗的IBD患者转氨酶升高是常见现象,但通常会自行缓解。抗TNF药物似乎是安全的,导致严重药物性肝损伤的风险较低。根据我们中心的经验,我们发现高转氨酶血症在我们的IBD队列中是常见的,主要是自限性的,并且在单变量和多变量分析中均与英夫利昔单抗治疗无关。还提出了一种抗TNF治疗期间发生肝功能损害的管理算法,这突出了多学科方法的必要性,并建议在转氨酶严重升高的情况下,肝活检是管理决策的关键点。然而,肝损伤通常是自限性的,停药似乎是个例外。