Journal
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 87, Issue 11, Pages 1204-1211Publisher
BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2016-313722
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- National Health and Medical Research Council of Australia [54922]
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Background The genetic drivers of multiple sclerosis (MS) clinical course are essentially unknown with limited data arising from severity and clinical phenotype analyses in genome-wide association studies. Methods Prospective cohort study of 127 first demyelinating events with genotype data, where 116 MS risk-associated single nucleotide polymorphisms (SNPs) were assessed as predictors of conversion to MS, relapse and annualised disability progression (Expanded Disability Status Scale, EDSS) up to 5-year review (Delta EDSS). Survival analysis was used to test for predictors of MS and relapse, and linear regression for disability progression. The top 7 SNPs predicting MS/relapse and disability progression were evaluated as a cumulative genetic risk score (CGRS). Results We identified 2 non-human leucocyte antigen (HLA; rs12599600 and rs1021156) and 1 HLA (rs9266773) SNP predicting both MS and relapse risk. Additionally, 3 non-HLA SNPs predicted only conversion to MS; 1 HLA and 2 non-HLA SNPs predicted only relapse; and 7 non-HLA SNPs predicted Delta EDSS. The CGRS significantly predicted MS and relapse in a significant, dose-dependent manner: those having >= 5 risk genotypes had a 6-fold greater risk of converting to MS and relapse compared with those with <= 2. The CGRS for Delta EDSS was also significant: those carrying >= 6 risk genotypes progressed at 0.48 EDSS points per year faster compared with those with <= 2, and the CGRS model explained 32% of the variance in disability in this study cohort. Conclusions These data strongly suggest that MS genetic risk variants significantly influence MS clinical course and that this effect is polygenic.
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