Division of Gastroenterology, Department of Medicine, Western University, London, Ontario, Canada.
Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Aliment Pharmacol Ther. 2019 Aug;50(4):416-424. doi: 10.1111/apt.15408. Epub 2019 Jul 12.
There is conflicting evidence about nephrotoxicity risk associated with 5-aminosalicylates for treatment of IBD.
To determine population-based temporal trends for 5-aminosalicylates and estimated risk of nephrotoxicity associated with 5-aminosalicylate use for ulcerative colitis (UC) and Crohn's disease (CD).
Retrospective cohort and nested case-control study, using the Health Improvement Network primary care database linked to hospital discharge coding for patients in England, 1996-2017. Nephrotoxicity risk analysis was a first recorded renal impairment diagnosis adjusted for key variables and was assessed between 2008 and 2017.
A total of 35 601 patients with prevalent UC or CD were included. The proportion of patients prescribed 5-aminosalicylates fell from 83% in 1996-1999 to 71% in 2012-2015 for UC patients and 64% to 45% for CD patients. Thirty per cent of patients had prolonged 5-aminosalicylate use. Between 2008 and 2017, the incident rate of nephrotoxicity was similar and stable for UC (12.6/1000 person-years) and CD (10.9/1000 person-years) patients. Multivariate analysis showed no evidence for association between current prescription of 5-aminosalicylate and nephrotoxicity in UC or CD patients, comparing ≤ 30 days prescription prior to index vs 31-≤180 days. However, active disease, disease duration, concomitant cardiovascular disease or diabetes and nephrotoxic drug use were independently associated with development of nephrotoxicity in UC and CD.
Despite the paucity of evidence for their benefit, 5-aminosalicylates were prescribed to approximately half of CD patients (30% prolonged therapy). Nephrotoxicity was rare in this patient cohort, and was not associated with 5-aminosalicylate use, but rather with disease status, comorbidity and use of nephrotoxic drugs.
关于 5-氨基水杨酸类药物治疗 IBD 的肾毒性风险存在相互矛盾的证据。
确定基于人群的 5-氨基水杨酸类药物的时间趋势,并评估 5-氨基水杨酸类药物治疗溃疡性结肠炎(UC)和克罗恩病(CD)相关肾毒性的估计风险。
使用英格兰医疗改进网络初级保健数据库进行回顾性队列和嵌套病例对照研究,该数据库与医院出院编码相关联,时间范围为 1996 年至 2017 年。肾毒性风险分析是首次记录的肾功能损害诊断,经过关键变量调整,并在 2008 年至 2017 年进行评估。
共纳入 35601 例 UC 或 CD 患者。UC 患者中,2008-2015 年接受 5-氨基水杨酸治疗的患者比例从 1996-1999 年的 83%下降至 71%,CD 患者从 64%下降至 45%。30%的患者存在长期使用 5-氨基水杨酸。2008 年至 2017 年间,UC(12.6/1000人年)和 CD(10.9/1000人年)患者的肾毒性发生率相似且稳定。多变量分析显示,UC 或 CD 患者当前处方 5-氨基水杨酸与肾毒性之间无关联,与指数前 30 天内处方(≤30 天)相比,31-180 天内处方(31-≤180 天)无关联。然而,活动期疾病、疾病持续时间、合并心血管疾病或糖尿病以及肾毒性药物的使用与 UC 和 CD 患者肾毒性的发生独立相关。
尽管缺乏获益证据,但约一半的 CD 患者(30%为长期治疗)仍开具 5-氨基水杨酸。在该患者队列中,肾毒性罕见,与 5-氨基水杨酸的使用无关,而是与疾病状态、合并症和使用肾毒性药物有关。