Leitão Antônio Miguel Furtado, Thomas Florian P, Souza Marcellus Henrique Loiola Ponte de, Braga Lúcia Libanez Bessa Campelo, Gondim Francisco de Assis Aquino
Universidade Federal do Ceará, Faculdade de Medicina, Departamento de Morfologia, Fortaleza CE, Brazil.
Hackensack University Medical Center, Hackensack Meridian School of Medicine, Department of Neurology, Hackensack NJ, United States.
Arq Neuropsiquiatr. 2025 Apr;83(4):1-9. doi: 10.1055/s-0045-1807717. Epub 2025 May 13.
Comorbid autoimmune disorders affect approximately 0.2% of the population. A second autoimmune disease occurs in up to 15% of myasthenia gravis (MG) patients.To evaluate the association between MG and inflammatory bowel disease (IBD).We conducted a cross-sectional study involving a Brazilian cohort of IBD patients and a literature review.In 2022, we found 1 MG patient with ulcerative colitis and 3 with Crohn's disease out of 606 IBD patients (0.66% prevalence). The patient with UC and MG died in April 2024. The mean IBD onset age was 33.5 ± 2.7; patients were 45.8 ± 7.3-years-old at evaluation. Further, 2 patients were acetylcholine receptor antibody positive, 1 was anti-muscle specific kinase positive, and 1 seronegative. Also, 3 had abnormal repetitive nerve stimulation, all had normal nerve conduction studies, abnormal skin wrinkling test, and mild small fiber neuropathy. None had thymoma and/or underwent thymectomy. According to the MG Foundation's classification, one was class V, one IVb, and two IIa. The MG diagnosis was masked by immunotherapy in all. The prevalence ratio of MG in IBD patients versus the proportion of MG among all patients in our center was 8.56 ( < 0.0001, CI = 3.1-23.5). Considering the lowest and highest prevalence of this condition reported in the literature, the ratio is 44.0 ( < 0.0001, CI: 16.3-118.4) and 26.4 ( < 0.0001, CI: 9.8-70.6), respectively.The prevalence of MG is higher in IBD, may include muscle specific kinase positive disease (first report in the literature) and frequently overlaps with other autoimmune conditions and small fiber neuropathy.
合并自身免疫性疾病影响约0.2%的人群。第二种自身免疫性疾病发生在高达15%的重症肌无力(MG)患者中。为了评估MG与炎症性肠病(IBD)之间的关联。我们进行了一项横断面研究,涉及巴西的一组IBD患者,并进行了文献综述。2022年,在606例IBD患者中,我们发现1例溃疡性结肠炎合并MG患者和3例克罗恩病合并MG患者(患病率为0.66%)。患有溃疡性结肠炎和MG的患者于2024年4月死亡。IBD的平均发病年龄为33.5±2.7岁;评估时患者年龄为45.8±7.3岁。此外,2例患者乙酰胆碱受体抗体阳性,1例抗肌肉特异性激酶阳性,1例血清阴性。另外,3例患者重复神经刺激异常,所有患者神经传导研究正常,皮肤皱纹试验异常以及轻度小纤维神经病变。均无胸腺瘤和/或接受胸腺切除术。根据MG基金会的分类,1例为V级,1例为IVb级,2例为IIa级。所有患者的MG诊断均被免疫治疗掩盖。IBD患者中MG的患病率与我们中心所有患者中MG的比例之比为8.56(<0.0001,CI=3.1-23.5)。考虑到文献中报道的该疾病的最低和最高患病率,该比例分别为44.0(<0.0001,CI:16.3-118.4)和26.4(<0.0001,CI:9.8-70.6)。MG在IBD中的患病率更高,可能包括肌肉特异性激酶阳性疾病(文献中的首次报道),并且经常与其他自身免疫性疾病和小纤维神经病变重叠。