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家族性地中海热(FMF)中炎症性/脱髓鞘性中枢神经系统受累:巧合还是关联?

Inflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): coincidence or association?

作者信息

Akman-Demir G, Gul A, Gurol E, Ozdogan H, Bahar S, Oge A E, Gurvit H, Saruhan-Direskeneli G, Yazici H, Eraksoy M

机构信息

Istanbul University, Istanbul Faculty of Medicine, Department of Neurology (Nöroloji), Capa 34390, Istanbul, Turkey.

出版信息

J Neurol. 2006 Jul;253(7):928-34. doi: 10.1007/s00415-006-0137-8. Epub 2006 Mar 6.

Abstract

BACKGROUND AND OBJECTIVE

Familial Mediterranean fever (FMF) is an inherited inflammatory disease characterized by recurrent febrile polyserositis. Central nervous system (CNS) involvement in FMF is uncommon, but recently cases with multiple sclerosis (MS) and FMF have been reported. Here we assess patients with both FMF and MS, in order to clarify any relationship between FMF and MS, and to evaluate disease characteristics.

PATIENTS AND METHODS

Our MS database between 1986-2005 was screened retrospectively, and patients with both FMF and inflammatory/demyelinating CNS disease were evaluated among a total of 2800 patients including definite MS (n = 2268) and other demyelinating disorders.

RESULTS

There were 12 patients with FMF, who developed a CNS disorder with multifocal white matter lesions. Median age at onset of FMF was 7 years, and median age at neurological onset was 26.8 years. Nine patients (including two siblings) had definite MS according to clinical and MRI findings, whereas 3 patients had atypical features suggesting other demyelinating disorders. Disease severity varied among the patients between very mild to a fatal course. All 8 patients evaluated for oligoclonal IgG bands in CSF were positive.

CONCLUSION

The rate of FMF among our patients with definite MS is almost 4 times the expected prevalence in Turkey. Our series including a sibling pair concordant for FMF and MS may suggest that similar genetic susceptibility and environmental factors might be responsible, although coincidence still remains a possibility. A prospective study on a larger sample seems to be justified.

摘要

背景与目的

家族性地中海热(FMF)是一种遗传性炎症性疾病,其特征为反复发热性多浆膜炎。FMF累及中枢神经系统(CNS)并不常见,但最近有FMF合并多发性硬化(MS)的病例报道。在此,我们对FMF和MS患者进行评估,以阐明FMF与MS之间的关系,并评估疾病特征。

患者与方法

我们回顾性筛查了1986 - 2005年间的MS数据库,在包括确诊MS(n = 2268)和其他脱髓鞘疾病的2800例患者中,对FMF合并炎症性/脱髓鞘性CNS疾病的患者进行评估。

结果

有12例FMF患者发生了伴有多灶性白质病变的CNS疾病。FMF发病的中位年龄为7岁,神经症状发作的中位年龄为26.8岁。根据临床和MRI表现,9例患者(包括2对兄弟姐妹)确诊为MS,而3例患者具有提示其他脱髓鞘疾病的非典型特征。患者的疾病严重程度差异很大,从非常轻微到致命病程不等。对8例脑脊液寡克隆IgG带进行评估的患者均为阳性。

结论

在我们确诊MS的患者中,FMF的发生率几乎是土耳其预期患病率的4倍。我们的系列研究包括一对FMF和MS均一致的兄弟姐妹,这可能表明相似的遗传易感性和环境因素可能起作用,尽管仍有可能是巧合。对更大样本进行前瞻性研究似乎是合理的。

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