Diagnosis and management of de novo inflammatory bowel disease after solid organ transplantation in the era of biologic therapy: a case series.

Frontiers in transplantation Pub Date : 2025-01-08 eCollection Date: 2024-01-01 DOI:10.3389/frtra.2024.1483943
Willie Mohammed Johnson, Byron P Vaughn, Nicholas Lim
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Abstract

Introduction: The clinical characteristics of de novo inflammatory bowel disease (dnIBD) diagnosed after solid organ transplant (SOT) are not well-described, particularly since the advent of biologic therapy for treatment of IBD.

Methods: We conducted a single-center, retrospective review of SOT recipients between 2010 and 2022 at the University of Minnesota Medical Center who were diagnosed with IBD after transplant.

Results: Of 89 patients at our center with IBD and a history of SOT, five (5.6%) patients were diagnosed with IBD post-transplant (three liver, one kidney, and one simultaneous liver and kidney): three patients were female and four were Caucasian. Mean age at transplant and IBD diagnosis were 46.7 and 49.4 years respectively. Indication for transplant were alcohol-related cirrhosis (n = 2), idiopathic fulminant hepatic failure (n = 1), metabolic dysfunction-associated steatotic liver disease (n = 1), and IgA nephropathy (n = 1). Four patients were diagnosed with ulcerative colitis (UC) and one with Crohn's disease (CD). Three patients (all with UC) required escalation to a biologic therapy. Four patients were in clinical remission from IBD at last follow-up, one patient required IBD surgery, while there was no rejection and no deaths following IBD diagnosis.

Conclusion: dnIBD post-SOT is uncommon, while newer IBD therapies may be safe and effective. Further study is required to better understand the natural history and IBD outcomes of this population relative to non-SOT patients.

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生物治疗时代实体器官移植后新发炎性肠病的诊断和治疗:一个病例系列。
引言:实体器官移植(SOT)后诊断的新发炎症性肠病(dnIBD)的临床特征尚未得到很好的描述,特别是自从IBD的生物治疗出现以来。方法:我们对2010年至2022年间在明尼苏达大学医学中心被诊断为移植后IBD的SOT受者进行了一项单中心回顾性研究。结果:本中心89例IBD合并SOT病史患者中,5例(5.6%)移植后诊断为IBD(3肝、1肾、1肝肾同时发生),其中3例为女性,4例为白人。移植和IBD诊断的平均年龄分别为46.7岁和49.4岁。移植指征为酒精相关性肝硬化(n = 2)、特发性暴发性肝功能衰竭(n = 1)、代谢功能障碍相关脂肪变性肝病(n = 1)和IgA肾病(n = 1)。4例患者被诊断为溃疡性结肠炎(UC), 1例被诊断为克罗恩病(CD)。3例患者(均为UC)需要升级到生物治疗。在最后一次随访中,4例患者的IBD临床缓解,1例患者需要进行IBD手术,而IBD诊断后没有排斥反应和死亡。结论:sot后dnIBD并不常见,而新的IBD治疗方法可能是安全有效的。需要进一步的研究来更好地了解这一人群相对于非sot患者的自然史和IBD结局。
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