Central nervous system inflammatory demyelinating disorders among Hong Kong Chinese

被引:19
|
作者
Chan, K. H. [1 ,2 ,3 ]
Lee, R. [4 ]
Lee, J. C. Y. [1 ]
Tse, A. C. T. [1 ]
Pang, S. Y. Y. [1 ]
Lau, G. K. K. [1 ]
Teo, K. C. [1 ]
Ho, P. W. L. [1 ,3 ]
机构
[1] Univ Hong Kong, LKS Fac Med, Queen Mary Hosp, Univ Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, LKS Fac Med, Neuroimmunol & Neuroinflammat Res Lab, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, LKS Fac Med, Res Ctr Heart Brain Hormone & Hlth Aging, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, LKS Fac Med, Queen Mary Hosp, Dept Diagnost Radiol, Hong Kong, Hong Kong, Peoples R China
关键词
Inflammatory demyelinating disorders; Classical multiple sclerosis; Neuromyelitis optica spectrum disorders; Aquaporin-4; autoantibodies; RESONANCE-IMAGING ABNORMALITIES; DEVICS-NEUROMYELITIS-OPTICA; MULTIPLE-SCLEROSIS; DIAGNOSTIC-CRITERIA; BRAIN ABNORMALITIES; AQUAPORIN-4; SPECTRUM; MULTICENTER; THERAPY; LESIONS;
D O I
10.1016/j.jneuroim.2013.06.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Classical multiple sclerosis (CMS) and neuromyelitis optica spectrum disorders (NMOSD) are distinct central nervous system inflammatory demyelinating disorders (CNS IDD). Early diagnosis of CNS IDD is important as appropriate immunotherapies to optimize prognosis. We studied the diagnoses of CNS IDD among Hong Kong Chinese in a hospital-based setting. Consecutive Chinese patients who presented to our hospital with clinically isolated syndrome and subsequently diagnosed to have CNS IDD from 1980 to 2010 were reviewed. Patients with known diagnosis of CNS IDD referred for further care were excluded. Serial sera were assayed for aquaporin-4 autoantibodies (AQP4 Ab), at least 3 assays within 2-5 years. A total of 210 patients diagnosed to have CNS IDD with disease duration of at least 2 years were studied. Among 198 patients with serial sera available, 40 (20.2%, 20 had NMO and 20 other NMOSD) were AQP4 Ab-positive. Four patients who were AQP4 Ab-negative on the initial assay converted to AQP4 Ab-positive on repeated assays. The diagnoses of 210 patients were CMS in 88 (41.9%), NMOSD 47 (22.4%, 27 NMO, 20 other NMOSD), single attack of myelitis 23 (11.0%), single attack of optic neuritis 21(10.0%), relapsing myelitis 10 (4.8%), acute disseminated encephalomyelitis (ADEM) 9 (4.3%), relapsing optic neuritis in 6 (2.9%), opticospinal multiple sclerosis 3 (1.4%) and single attack of brainstem encephalitis 3 (1.4%). Compared to CMS, NMOSD patients had older onset age, lower frequencies of brain MRI abnormalities and CSF OCB, higher frequency of LETM, higher CNS inflammation attack frequency in the first 2 years, worse clinical outcome with higher EDSS score and mortality rate. This hospital-based study suggests that CMS (41.9%) and NMOSD (22.4%) are the most common CNS IDD among Hong Kong Chinese. NMOSD has worse clinical outcome than CMS. Detection of AQP4 Ab facilitates early diagnosis and prompts immunotherapies of NMOSD. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 105
页数:6
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