Tang Angela W, Prieto Jimenez Paula M, Miller Ian K T, Madan Juliette C, Nguyen Jaden, Ma Meiqian, Silverman Melissa, Farhadian Bahare, Wilson Jenny, Goyal Alka, Manko Cindy, Davies Yinka, Rabizadeh Shervin, Frankovich Jennifer
Immune Behavioral Health Clinic and Research Program at Stanford Medicine Children's Health, Palo Alto, California, USA.
Pediatric Divisions of Allergy, Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, California, USA.
Dev Neurosci. 2025 Feb 10:1-16. doi: 10.1159/000543969.
Pediatric acute-onset neuropsychiatric syndrome (PANS) is an immune-mediated disease characterized by abrupt onset neurobehavioral changes. Inflammatory bowel disease (IBD) includes ulcerative colitis (UC) and Crohn's disease (CD), chronic conditions characterized by gastrointestinal inflammation. We describe eight individuals with both PANS and IBD.
All individuals with both IBD and PANS were identified from Stanford Immune Behavioral Health Clinic, Cedars-Sinai Medical Center Pediatric Inflammatory Bowel Disease Program, and Dartmouth Neuroimmune Psychiatric Disorders (NIPD) Clinic. Data were collected by chart review.
Eight cases of PANS with IBD were identified. Five were male. The mean age of onset was 9.3 years for PANS and 15.6 years for IBD. PANS preceded development of IBD in 7 of 8 cases by a mean of 8.4 years. Seven patients (88%) had a first-degree relative with an immune-mediated disease, including 5 with psoriasis or psoriatic arthritis. Five patients themselves had arthralgias or arthritis (63%). All 5 cases where PANS preceded IBD treatment sufficiently for analysis were free of major behavioral relapses after IBD was managed.
The triad of PANS, joint complaints, and family history of autoimmunity, including psoriasis, may represent a subset of PANS at heightened risk for IBD and additional immune-mediated disorders. For children with this triad, clinicians should have a low threshold to evaluate for gastrointestinal inflammation with biomarkers like hemoglobin, CRP, fecal calprotectin, and diagnostic endoscopy when indicated. PANS symptoms may improve with effective treatment of IBD. The high prevalence of joint complaints in our cohort and psoriasis in first-degree family members suggests this subset of PANS may share immune mechanisms with psoriasis and arthritis. Treatment strategies used in IBD and arthritis should be studied for potential application in PANS.
儿童急性起病神经精神综合征(PANS)是一种以神经行为突然改变为特征的免疫介导性疾病。炎症性肠病(IBD)包括溃疡性结肠炎(UC)和克罗恩病(CD),是胃肠道炎症的慢性疾病。我们描述了8例同时患有PANS和IBD的个体。
所有同时患有IBD和PANS的个体均来自斯坦福免疫行为健康诊所、雪松西奈医疗中心儿科炎症性肠病项目以及达特茅斯神经免疫精神障碍(NIPD)诊所。通过查阅病历收集数据。
共确定了8例PANS合并IBD的病例。5例为男性。PANS的平均发病年龄为9.3岁,IBD的平均发病年龄为15.6岁。8例中有7例PANS先于IBD发病,平均提前8.4年。7例患者(88%)有免疫介导性疾病的一级亲属,其中5例患有银屑病或银屑病关节炎。5例患者自身有关节痛或关节炎(63%)。在IBD得到充分治疗以便进行分析的所有5例PANS先于IBD发病的病例中,IBD病情得到控制后均未出现严重行为复发。
PANS、关节症状以及包括银屑病在内的自身免疫性疾病家族史这三者可能代表了PANS中患IBD及其他免疫介导性疾病风险较高的一个亚组。对于具有这三者特征的儿童,临床医生在有指征时,应积极利用血红蛋白、CRP、粪便钙卫蛋白等生物标志物以及诊断性内镜检查来评估胃肠道炎症。IBD的有效治疗可能会改善PANS症状。我们队列中关节症状的高发生率以及一级亲属中银屑病的高发生率表明,这一PANS亚组可能与银屑病和关节炎具有共同的免疫机制。应研究IBD和关节炎的治疗策略在PANS中的潜在应用。