A NOTCH4 missense mutation confers resistance to multiple sclerosis in Japanese

Mult Scler. 2013 Nov;19(13):1696-703. doi: 10.1177/1352458513482512. Epub 2013 Apr 2.

Abstract

Background: The G allele of NOTCH4 rs422951 is protective against demyelinating disease in Japanese.

Objectives: The purpose of this study was to assess the relation of the G allele to neuromyelitis optica (NMO)/NMO spectrum disorder (NMOSD) and multiple sclerosis (MS) and the interaction between the G allele and HLA-DRB1 alleles, and to clarify any association of the G allele with clinical features.

Methods: DNA sequencing was used to genotype 106 NMO/NMOSD patients, 118 MS patients and 152 healthy controls (HCs) for rs422951.

Results: G allele frequency in MS patients, but not that in NMO/NMOSD patients, was lower than that in HCs (8.9% vs 21.7%, p<0.0001, odds ratio (OR)=0.35). HLA-DRB1*0405 was positively associated with MS (OR=2.22, p(corr) =0.0380) while DRB1*0901 was negatively associated (OR=0.32, p(corr) =0.0114). Logistic regression analyses revealed that, after adjusting for gender and either HLA-DRB1*0405 or DRB1*0901, rs422951 was associated with MS in the dominant model (OR=0.37, 95% confidence interval (CI)= 0.20-0.66, p=0.0012). Haplotype analyses identified two susceptible and three resistant haplotypes formed from rs422951 and either HLA-DRB1*0405 or DRB1*0901. There were no statistically significant differences in clinical features between G allele carriers and non-G allele carriers.

Conclusion: This NOTCH4 missense mutation decreased the risk for developing MS in Japanese, but did not affect clinical features of those who had already developed the disease.

Keywords: NOTCH4; Multiple sclerosis; genetics; human leukocyte antigen; polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Aquaporin 4 / genetics
  • Aquaporin 4 / immunology
  • Confidence Intervals
  • DNA / genetics
  • Disease Resistance / genetics
  • Female
  • Gene Frequency
  • Genotype
  • HLA-DRB1 Chains / genetics
  • Haplotypes
  • Humans
  • Japan / epidemiology
  • Linkage Disequilibrium
  • Logistic Models
  • Male
  • Multiple Sclerosis / epidemiology
  • Multiple Sclerosis / genetics*
  • Mutation, Missense / genetics*
  • Neuromyelitis Optica / epidemiology
  • Neuromyelitis Optica / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide
  • Proto-Oncogene Proteins / genetics*
  • Receptor, Notch4
  • Receptors, Dopamine D1 / genetics
  • Receptors, Notch / genetics*

Substances

  • Aquaporin 4
  • HLA-DRB1 Chains
  • HLA-DRB1*04:05 antigen
  • NOTCH4 protein, human
  • Proto-Oncogene Proteins
  • Receptor, Notch4
  • Receptors, Dopamine D1
  • Receptors, Notch
  • DNA