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靶向释放布地奈德治疗肾移植后复发性IgA肾病——一例报告

Treatment of recurrent IgA nephropathy after kidney transplantation with targeted-release budesonide - a case report.

作者信息

Packbiers Maximilian, Hahm Annika, Riebeling Theresa, Bräsen Jan Hinrich, Schmitt Roland, Schulte Kevin

机构信息

Department of Nephrology and Hypertension, University Hospital Schleswig-Holstein, Christian-Albrechts-University, Arnold-Heller-Str. 3 Haus C, 24105, Kiel, Germany.

Hannover Med Sch, Inst Pathol, Nephropathol Unit, 30625, Hannover, Germany.

出版信息

J Nephrol. 2025 Sep 12. doi: 10.1007/s40620-025-02405-3.

Abstract

Immunoglobulin A nephropathy (IgAN) is one of the most common forms of primary glomerulonephritis which can lead to kidney failure requiring kidney replacement therapy via dialysis or transplantation. Unfortunately, IgAN can recur within the allograft. For treatment of primary IgAN, a targeted-release formulation of budesonide that acts specifically within the ileum can be used to prevent disease progression. The use of targeted-release budesonide in the setting of recurrent IgAN after transplantation has not yet been studied in detail. We here report a 28-year-old female with IgAN recurrence after transplantation, treated by targeted release budesonide for 9 months. Prior to treatment initiation in April 2023, estimated glomerular filtration rate (eGFR) drastically decreased, reaching  24 ml/min/1.73 m within 10 months. With treatment, the eGFR decrease slowed down considerably (- 6 ml/min/1.73 m within 12 months). The urine protein-to-creatinine-ratio (UPCR) likewise decreased from 4.55 g/g creatinine before therapy start to 1.30 g/g 12 months after therapy start. Despite episodes of poorly controlled hypertension and edema during treatment that were related to interruption of medications, blood pressure was stable at 122/77 mmHg after 9 months and 133/83 mmHg after 12 months. Compared to the beginning of the therapy, the patient lost 3 kg of body weight. There were no serious infections, nor was an increased susceptibility to infections observed. No other serious adverse events occurred. Although the patient experienced corticosteroid-related side effects, treatment was not interrupted. After therapy, the side effects subsided and the patient reports general wellbeing.

摘要

免疫球蛋白A肾病(IgAN)是原发性肾小球肾炎最常见的形式之一,可导致肾衰竭,需要通过透析或移植进行肾脏替代治疗。不幸的是,IgAN可在同种异体移植肾内复发。对于原发性IgAN的治疗,可使用一种在回肠内特异性起作用的布地奈德靶向释放制剂来预防疾病进展。移植后复发性IgAN患者使用靶向释放布地奈德的情况尚未得到详细研究。我们在此报告一名28岁女性,移植后出现IgAN复发,接受靶向释放布地奈德治疗9个月。在2023年4月开始治疗前,估计肾小球滤过率(eGFR)急剧下降,在10个月内降至24 ml/min/1.73m²。经过治疗,eGFR下降速度大幅减缓(12个月内下降6 ml/min/1.73m²)。尿蛋白肌酐比(UPCR)同样从治疗开始前的4.55 g/g肌酐降至治疗开始后12个月的1.30 g/g肌酐。尽管治疗期间出现了与药物中断相关的血压控制不佳和水肿发作,但9个月后血压稳定在122/77 mmHg,12个月后稳定在133/83 mmHg。与治疗开始时相比,患者体重减轻了3 kg。没有发生严重感染,也未观察到感染易感性增加。未发生其他严重不良事件。尽管患者出现了与皮质类固醇相关的副作用,但治疗未中断。治疗后,副作用消退,患者报告总体健康状况良好。

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