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MOG-IgG Frequency in Multiple Sclerosis: Diagnostic Challenges With Low-Titer Results
Jae-Won Hyun1, Jieun Chung1, Rosah May Palermo Payumo1
1Department of Neurology, Research Institute and Hospital of National Cancer Center, Goyang, Republic of Korea.
European Journal of Neurology
|September 5, 2025
Summary
Myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG) positivity is rare in people with multiple sclerosis (pwMS), even in Asian cohorts. Low-titer results may challenge diagnosis, emphasizing clinical assessment.
Area of Science:
- Neuroimmunology
- Autoimmunity
- Neurological Disorders
Background:
- Myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG) positivity presents diagnostic challenges in people with multiple sclerosis (pwMS).
- Previous studies on MOG-IgG prevalence in pwMS are primarily from Caucasian populations.
- Understanding MOG-IgG frequency in diverse ethnic groups, like Asian populations, is crucial for accurate diagnosis.
Purpose of the Study:
- To determine the prevalence of MOG-IgG in a large, predominantly Asian cohort of people with multiple sclerosis (pwMS).
- To assess the diagnostic utility of MOG-IgG testing in a non-Caucasian MS population.
- To investigate the frequency of low-titer MOG-IgG positivity and its implications for MS diagnosis.
Main Methods:
- Serum samples from 405 pwMS diagnosed by 2017 McDonald criteria were analyzed.
- An in-house live cell-based assay was used to detect MOG-IgG at 1:20 dilution.
- Positive or borderline samples underwent retesting at 1:100 dilution by blinded investigators.
Main Results:
- The study included 405 pwMS, with 98% being of Asian ethnicity.
- Overall MOG-IgG positive or borderline results were found in 1.5% of the cohort.
- Clear MOG-IgG positivity was rare (0.3%), with 1.2% showing low-titer positive or borderline results.
Conclusions:
- True MOG-IgG positivity is uncommon in people with multiple sclerosis across different populations.
- Low-titer MOG-IgG positive or borderline results can complicate the diagnosis of MS.
- Comprehensive clinical evaluation and repeat testing at higher dilutions are essential to avoid misdiagnosis.

