Department of Women's and Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Institute in the Park, National Institute for Health Research Alder Hey Clinical Research Facility, Alder Hey Children's Hospital, East Prescot Road, Liverpool, UK.
Eur J Med Res. 2022 Apr 29;27(1):61. doi: 10.1186/s40001-022-00687-y.
Acute interstitial nephritis (AIN) is an important cause of kidney injury accounting for up to 27% of unexplained renal impairment. In up to 70% of cases, drugs, including aminosalicylates, are reported as the underlying cause. Following two recent paediatric cases of suspected mesalazine induced AIN within our own department, we performed a systematic review of the literature to address the following question: In patients with inflammatory bowel disease (IBD), is interstitial nephritis associated with 5-aminosalicylate (5-ASA) treatment? Our primary objective was to identify the number of cases reported in the literature of biopsy-proven 5-ASA induced interstitial nephritis, in children and adults with IBD. We also aimed to identify which variables influence the onset, severity and recovery of 5-ASA interstitial nephritis.
Embase and PubMed databases were searched from inception to 07/10/20. Search terms had three main themes: "inflammatory bowel disease", "interstitial nephritis" and "aminosalicylates". Studies were included if they reported an outcome of AIN, confirmed on biopsy, suspected to be secondary to a 5-ASA drug in those with IBD. A narrative synthesis was performed.
Forty-one case reports were identified. Mesalazine was the most frequently reported aminosalicylate associated with AIN (95%). The median duration of treatment before AIN was diagnosed was 2.3 years (Interquartile Range (IQR) 12-48 months). The median rise in creatinine was 3.3 times the baseline measurement (IQR 2.5-5.5). Aminosalicylate withdrawal and steroids were the most frequently used treatments. Despite treatment, 15% of patients developed end-stage renal failure.
AIN is a serious adverse drug reaction associated with aminosalicylates, with mesalazine accounting for most reports. The current guidance of annual monitoring of renal function may not be sufficient to identify cases early. Given the severity of AIN and reports in the literature that early treatment with steroids may be beneficial, we would recommend at least 6 monthly monitoring of renal function. PROSPERO registration number CRD42020205387.
急性间质性肾炎(AIN)是导致肾脏损伤的重要原因,占不明原因肾功能损害的 27%。在多达 70%的病例中,药物(包括氨基水杨酸盐)被报告为潜在原因。在我们自己的部门中,最近出现了两例疑似美沙拉嗪引起的AIN 儿科病例后,我们对文献进行了系统回顾,以解决以下问题:在炎症性肠病(IBD)患者中,间质性肾炎是否与 5-氨基水杨酸(5-ASA)治疗有关?我们的主要目标是确定文献中报告的活检证实的 5-ASA 诱导间质性肾炎的病例数量,这些病例发生在患有 IBD 的儿童和成人中。我们还旨在确定哪些变量会影响 5-ASA 间质性肾炎的发病、严重程度和恢复。
从开始到 2020 年 10 月 7 日,在 Embase 和 PubMed 数据库中进行了搜索。搜索词有三个主题:“炎症性肠病”、“间质性肾炎”和“氨基水杨酸盐”。如果报告了AIN 结果,并且在活检中证实,在患有 IBD 的患者中怀疑是 5-ASA 药物引起的,那么研究就包括在内。进行了叙述性综述。
确定了 41 例病例报告。美沙拉嗪是与 AIN 最常相关的氨基水杨酸盐(95%)。AIN 诊断前治疗的中位持续时间为 2.3 年(中位数 12-48 个月)。肌酐中位数升高 3.3 倍基线测量值(中位数 2.5-5.5)。氨基水杨酸的停用和类固醇是最常使用的治疗方法。尽管进行了治疗,但仍有 15%的患者发展为终末期肾衰竭。
AIN 是一种与氨基水杨酸盐相关的严重药物不良反应,其中美沙拉嗪占大多数报告。目前关于每年监测肾功能的指南可能不足以早期发现病例。鉴于 AIN 的严重性和文献中的报道,早期使用类固醇可能有益,我们建议至少每 6 个月监测一次肾功能。PROSPERO 注册号 CRD42020205387。