No strong HLA association with MOG antibody disease in the UK population

Ann Clin Transl Neurol. 2021 Jul;8(7):1502-1507. doi: 10.1002/acn3.51378. Epub 2021 May 15.

Abstract

Improvements in assays for detecting serum antibodies against myelin oligodendrocyte glycoprotein (MOG) have led to the appreciation of MOG-antibody-associated disease (MOGAD) as a novel disorder. However, much remains unknown about its etiology. We performed human leukocyte antigen (HLA) analysis in 82 MOGAD patients of European ancestry in the UK population. No HLA class II associations were observed, thus questioning the mechanism of anti-MOG antibody generation. A weak protective association of HLA-C*03:04 was observed (OR = 0.26, 95% CI = 0.10-0.71, pc = 0.013), suggesting a need for continued efforts to better understand MOGAD genetics and pathophysiology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Autoantibodies / blood*
  • Biomarkers / blood
  • Cohort Studies
  • Female
  • Genetic Association Studies / methods*
  • HLA Antigens / blood*
  • HLA Antigens / genetics
  • Humans
  • Male
  • Middle Aged
  • Myelin-Oligodendrocyte Glycoprotein / blood*
  • Myelin-Oligodendrocyte Glycoprotein / genetics
  • Neuromyelitis Optica / blood*
  • Neuromyelitis Optica / epidemiology*
  • Neuromyelitis Optica / genetics
  • United Kingdom / epidemiology
  • Young Adult

Substances

  • Autoantibodies
  • Biomarkers
  • HLA Antigens
  • Myelin-Oligodendrocyte Glycoprotein