Chen Lynna, Srinivasan Ashish, Choy Suet-Wan, Van Jeffrey, Habeeb Habeeb, Nguyen Andrew, Vasudevan Abhinav
Department of Gastroenterology, Eastern Health, Melbourne, Victoria, Australia.
Eastern Health Clinical School, Monash University, Melbourne, Victoria, Australia.
Aliment Pharmacol Ther. 2025 Aug;62(4):400-418. doi: 10.1111/apt.70262. Epub 2025 Jul 2.
The prevalence of chronic kidney disease (CKD) in patients with inflammatory bowel disease (IBD) is increasing. The pharmacokinetic profiles of IBD medications in patients with advanced-stage CKD are not well studied.
To provide evidence-based guidance on the use of medical therapies in patients with IBD and CKD.
We conducted a narrative review of literature up to 31 March 2025 on studies of therapies currently used for the treatment of IBD in the setting of CKD, with a focus on advanced kidney disease and use in renal replacement therapy.
Mesalazine can cause acute interstitial nephritis. Calcineurin inhibitors have been associated with nephrotoxicity. Methotrexate is contraindicated in advanced renal disease, including while on renal replacement therapy, due to higher risks of toxicity and myelosuppression. Dose adjustment of thiopurines should be considered in advanced renal disease due to metabolite accumulation. Monoclonal antibodies, including anti-tumour necrosis factor therapy, anti-integrin therapy and anti-interleukin 12/23 therapies, appear to be safe in renal insufficiency, including haemodialysis. There is limited data available for small molecule therapies; drug metabolism profiles suggest they are safe in CKD, although, for Janus kinase (JAK) inhibitors, including tofacitinib and upadacitinib, dose reduction should be considered in advanced renal disease.
Most therapies used in IBD, particularly biologic therapies, appear safe and effective when used in patients with CKD, including those on renal replacement therapy. Caution should be considered when using conventional therapies and JAK inhibitors.
炎症性肠病(IBD)患者中慢性肾脏病(CKD)的患病率正在上升。晚期CKD患者中IBD药物的药代动力学特征尚未得到充分研究。
为IBD和CKD患者的药物治疗提供循证指导。
我们对截至2025年3月31日的文献进行了叙述性综述,内容涉及目前用于治疗CKD背景下IBD的疗法研究,重点是晚期肾病以及在肾脏替代治疗中的应用。
美沙拉嗪可导致急性间质性肾炎。钙调神经磷酸酶抑制剂与肾毒性有关。甲氨蝶呤在晚期肾病中禁用,包括在肾脏替代治疗期间,因为其毒性和骨髓抑制风险较高。由于代谢产物蓄积,晚期肾病患者应考虑调整硫唑嘌呤的剂量。单克隆抗体,包括抗肿瘤坏死因子疗法、抗整合素疗法和抗白细胞介素12/23疗法,在肾功能不全患者(包括血液透析患者)中似乎是安全的。小分子疗法的数据有限;药物代谢情况表明它们在CKD中是安全的,不过,对于包括托法替布和乌帕替尼在内的Janus激酶(JAK)抑制剂,晚期肾病患者应考虑减量。
IBD中使用的大多数疗法,尤其是生物疗法,在CKD患者(包括接受肾脏替代治疗的患者)中使用时似乎是安全有效的。使用传统疗法和JAK抑制剂时应谨慎。