Arai Yasuhiro, Mano Chihiro
Juntendo Med J. 2025 Mar 12;71(2):115-120. doi: 10.14789/ejmj.JMJ24-0042-R. eCollection 2025.
Down syndrome (DS) is often associated with autoimmune diseases; however, its association with multiple sclerosis (MS) has rarely been reported. In a previous report, the coincidence of DS and MS showed a negative association. Here, we searched for the coincidence of DS and MS, and attempted to resolve this negative association, focusing on the gene dosage effect, by utilizing available reports.
A 44-year-old woman with DS experienced a progressively worsening gait at onset. Auto-immuno-antibodies including aquaporin-4 antibody were negative. On the basis of brain magnetic resonance image (MRI) findings, the patient was diagnosed with possible MS. After three years, the patient demonstrated additional signs and regression symptoms. Re-examined brain MRI showed multiple new focal lesions. Based on the McDonald criteria, the patient was diagnosed with laboratory-supported defined MS.
To date, we have found only one case report in the literature describing the development of MS in a 49-year-old man with DS. The protective effect of DS against the development of MS might be mediated by a gain of function due to a gene dosage effect, and the effect of candidate antigens could be interferon alpha and beta receptors, S100B, and amyloid precursor protein (APP).
In patients with DS, S100B and APP overexpression could protect against MS, but both correlate with the progression of Alzheimer's neuropathological changes. S100B and APP can be seemed to be multiple pathogenesis and co-occurrence of MS with DS and Alzheimer's dementia may advance more severely than MS without DS.
唐氏综合征(DS)常与自身免疫性疾病相关;然而,其与多发性硬化症(MS)的关联鲜有报道。在之前的一份报告中,DS与MS的巧合显示出负相关。在此,我们通过利用现有报告,探寻DS与MS的巧合情况,并试图从基因剂量效应的角度解决这种负相关。
一名44岁的DS女性患者起病时步态逐渐恶化。包括水通道蛋白4抗体在内的自身免疫抗体均为阴性。根据脑部磁共振成像(MRI)结果,该患者被诊断为可能患有MS。三年后,患者出现了更多体征及病情反复。再次检查脑部MRI显示有多个新的局灶性病变。根据麦克唐纳标准,该患者被诊断为实验室支持确诊的MS。
迄今为止,我们在文献中仅发现一例关于一名49岁DS男性患MS的病例报告。DS对MS发病的保护作用可能是由基因剂量效应导致的功能获得介导的,候选抗原可能是干扰素α和β受体、S100B以及淀粉样前体蛋白(APP)。
在DS患者中,S100B和APP的过度表达可能对MS起到保护作用,但两者均与阿尔茨海默病神经病理变化的进展相关。S100B和APP似乎涉及多种发病机制,且MS与DS及阿尔茨海默病痴呆同时发生时可能比无DS的MS进展更为严重。