Villa Andrés M, Analisa Manin, Guerrero Diego Alarcon, Seimandi Carla, Simison Conrado, Saffe Valentina, Aguirre Florencia
Sección de Neuroinmunología. División Neurología. Hospital Gral. de Agudos Dr. José María Ramos Mejía, Buenos Aires, Argentina; Centro Argentino de Neuroinmunología (CADENI). Facultad de Medicina, Universidad de Buenos Aires. Argentina.
Sección de Neuroinmunología. División Neurología. Hospital Gral. de Agudos Dr. José María Ramos Mejía, Buenos Aires, Argentina; Centro Argentino de Neuroinmunología (CADENI). Facultad de Medicina, Universidad de Buenos Aires. Argentina.
Mult Scler Relat Disord. 2025 Sep 3;103:106719. doi: 10.1016/j.msard.2025.106719.
The incidence of neuromyelitis optica spectrum disorder (NMOSD) in association with other autoimmune diseases is frequent. The coexistence of myasthenia gravis (MG) and NMOSD has been reported, showing a higher-than-expected likelihood of co-occurrence. The aim of this study is to describe the overlap between NMOSD and MG and to analyze these cases within two large real-world cohorts of patients with AQP4 antibody-positive NMOSD and AChR antibody-positive MG in Argentina.
A cross-sectional, retrospective study was conducted at a referral center in Buenos Aires, Argentina, including patients with AQP4-Ab-positive NMOSD and AChR-Ab-positive MG.
A total of 389 medical records were reviewed: 108 NMOSD and 281 MG cases. Among them, 77 patients were AQP4-IgG positive, and 207 were AChR-Ab positive. Three out of 77 AQP4-IgG-positive patients had MG with AChR-Ab positivity, accounting for 3.89% of NMOSD cases. Conversely, three out of 207 AChR-Ab-positive MG patients (1.45 %) had AQP4-IgG-positive antibodies. Patients with concurrent MG and NMOSD were female, had a late onset of NMOSD, and experienced MG onset before NMOSD. They also showed a good response to NMOSD treatment with immunosuppressive therapy. Two patients had undergone thymectomy before NMOSD onset. No patient was receiving immunosuppressive treatment at the time of NMOSD onset.
A total of 3.89 % of AQP4-Ab-positive NMOSD patients had overlapping AChR-Ab-positive MG. This is the first report assessing the association between NMOSD and MG in Argentinian and Latin American (LATAM) patients.
视神经脊髓炎谱系障碍(NMOSD)与其他自身免疫性疾病并存的情况很常见。重症肌无力(MG)与NMOSD并存的情况已有报道,显示其共现可能性高于预期。本研究的目的是描述NMOSD与MG之间的重叠情况,并在阿根廷两个大型真实世界队列中分析这些病例,这两个队列分别为水通道蛋白4(AQP4)抗体阳性的NMOSD患者和乙酰胆碱受体(AChR)抗体阳性的MG患者。
在阿根廷布宜诺斯艾利斯的一家转诊中心进行了一项横断面回顾性研究,纳入了AQP4抗体阳性的NMOSD患者和AChR抗体阳性的MG患者。
共审查了389份病历:108例NMOSD病例和281例MG病例。其中,77例患者AQP4-IgG阳性,207例患者AChR抗体阳性。77例AQP4-IgG阳性患者中有3例同时患有AChR抗体阳性的MG,占NMOSD病例的3.89%。相反,207例AChR抗体阳性的MG患者中有3例(1.45%)具有AQP4-IgG阳性抗体。同时患有MG和NMOSD的患者为女性,NMOSD发病较晚,且MG发病早于NMOSD。他们对免疫抑制治疗的NMOSD治疗反应良好。两名患者在NMOSD发病前接受了胸腺切除术。在NMOSD发病时,没有患者正在接受免疫抑制治疗。
共有3.89%的AQP4抗体阳性的NMOSD患者同时患有AChR抗体阳性的MG。这是第一份评估阿根廷和拉丁美洲(LATAM)患者中NMOSD与MG之间关联的报告。