Management of comorbid Crohn's disease and alopecia universalis with upadacitinib and oral minoxidil.

IF 3.9
Jasmine Levine, Divija Sharma, Serena Morsia, Benjamin Ungar
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Abstract

Purpose: This study describes the use of upadacitinib, a JAK1 inhibitor, in combination with oral minoxidil for treatment of alopecia universalis (AU) with comorbid Crohn's disease (CD) and atopic dermatitis (AD). AU is the most extensive form of alopecia areata (AA), a chronic autoimmune condition that often requires systemic therapy for hair regrowth. While JAK inhibitors (JAKis) have demonstrated efficacy in each condition, data on upadacitinib's use in patients with coexisting disease are limited.

Materials and methods: We report the case of a 20-year-old male with CD who developed AU one year after initiating adalimumab. Following inadequate CD control and progression of hair loss, he was diagnosed with coexisting AU and AD. An IBD-directed regimen of upadacitinib (45 mg/day induction, 30 mg/day maintenance) was initiated with oral minoxidil, increased from 2.5 to 10 mg/day.

Results: By 7 weeks, he experienced resolution of gastrointestinal symptoms and early hair regrowth; by 11 weeks, he achieved complete regrowth of scalp, eyebrow, eyelash, and beard hair. Colonoscopy confirmed histologic remission.

Conclusions: This case highlights the potential of JAK is to address potentially overlapping immune-mediated disorders and suggests that upadacitinib, in combination with oral minoxidil, may promote rapid AU remission. These findings may inform future treatment approaches for complex autoimmune presentations.

upadacitinib和口服米诺地尔治疗克罗恩病和普遍脱发的合并症。
目的:本研究描述了JAK1抑制剂upadacitinib联合口服米诺地尔治疗伴有克罗恩病(CD)和特应性皮炎(AD)的普遍性脱发(AU)。AU是斑秃(AA)的最广泛形式,AA是一种慢性自身免疫性疾病,通常需要全身治疗才能再生头发。虽然JAK抑制剂(JAKis)已证明对每种疾病都有效,但upadacitinib在共存疾病患者中的使用数据有限。材料和方法:我们报告一例20岁男性CD患者在开始阿达木单抗治疗一年后发生AU。由于乳糜泻控制不足和脱发的进展,他被诊断为AU和AD并存。ibd导向的upadacitinib方案(45 mg/天诱导,30 mg/天维持)开始与口服米诺地尔,从2.5 mg/天增加到10 mg/天。结果:7周时,患者胃肠道症状缓解,毛发早期再生;到11周时,他的头皮、眉毛、睫毛和胡须都完全再生了。结肠镜检查证实组织学缓解。结论:该病例强调了JAK解决潜在重叠免疫介导疾病的潜力,并提示upadacitinib联合口服米诺地尔可能促进AU快速缓解。这些发现可能为未来复杂自身免疫表现的治疗方法提供信息。
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