Clinical Spectrum of Myelin Oligodendrocyte Glycoprotein-Immunoglobulin G-Associated Disease in Korean Children
10.3988/jcn.2020.16.3.461
- Author:
Il Han YOO
1
;
WooJoong KIM
;
Youngkyu SHIM
;
Sun Ah CHOI
;
Soo Yeon KIM
;
Hunmin KIM
;
Byung Chan LIM
;
Hee HWANG
;
Jieun CHOI
;
Ki Joong KIM
;
Yeseul KIM
;
Jae-Won HYUN
;
Su-Hyun KIM
;
Kyungho CHOI
;
Ho Jin KIM
;
Jong-Hee CHAE
Author Information
1. Department of Pediatrics, College of Medicine, The Catholic University of Korea, St. Vincent's Hospital, Suwon, Korea.
- Publication Type:ORIGINAL ARTICLE
- From:Journal of Clinical Neurology
2020;16(3):461-469
- CountryRepublic of Korea
- Language:0
-
Abstract:
Background:and Purpose: The myelin oligodendrocyte glycoprotein (MOG) antibody is detected at a high rate in childhood acquired demyelinating syndrome (ADS). This study aimed to determine the diagnostic value of the MOG antibody in ADS and the spectrum of MOGantibody-positive demyelinating diseases in children.
Methods:This study included 128 patients diagnosed with ADS (n=94) or unexplained encephalitis (n=34). The MOG antibody in serum was tested using an in-house live-cell-based immunofluorescence assay.
Results:The MOG antibody was detected in 48 patients (46 ADS patients and 2 encephalitis patients, comprising 23 males and 25 females). Acute disseminated encephalomyelitis (ADEM) (35.4%) was the most-common diagnosis, followed by the unclassified form (17.4%), isolated optic neuritis (ON) (15.2%), neuromyelitis optica spectrum disorder (13.0%), multiple sclerosis (MS) (10.8%), other clinically isolated syndromes [monophasic event except ADEM, isolated ON, or transverse myelitis (TM)] (8.7%), and unexplained encephalitis (4.3%). At the initial presentation, 35 out of the 46 patients with ADS had brain lesions detected in magnetic resonance imaging, and 54% of these 35 patients had encephalopathy. Nine of the 11 patients without brain lesions exhibited only ON. Thirty-nine percent of the patients experienced a multiphasic event during the mean follow-up period of 34.9 months (range 1.4–169.0 months). Encephalopathy at the initial presentation was frequently confirmed in the monophasic group (p= 0.011).
Conclusions:MOG antibodies were identified in all pediatric ADS phenotypes except for monophasic TM. Therefore, the MOG antibody test is recommended for all pediatric patients with ADS, especially before a diagnosis of MS and for patients without a clear diagnosis.
