Abstract

BackgroundIn Northern European descended populations, genetic susceptibility for multiple sclerosis (MS) is associated with alleles of the human leukocyte antigen (HLA) Class II gene DRB1. Whether other major histocompatibility complex (MHC) genes contribute to MS susceptibility is controversial.Methodology/Principal FindingsA case control analysis was performed using 958 single nucleotide polymorphisms (SNPs) spanning the MHC assayed in two independent datasets. The discovery dataset consisted of 1,018 cases and 1,795 controls and the replication dataset was composed of 1,343 cases and 1,379 controls. The most significantly MS-associated SNP in the discovery dataset was rs3135391, a Class II SNP known to tag the HLA-DRB1*15:01 allele, the primary MS susceptibility allele in the MHC (O.R. = 3.04, p<1×10−78). To control for the effects of the HLA-DRB1*15:01 haplotype, case control analysis was performed adjusting for this HLA-DRB1*15:01 tagging SNP. After correction for multiple comparisons (false discovery rate = .05) 52 SNPs in the Class I, II and III regions were significantly associated with MS susceptibility in both datasets using the Cochran Armitage trend test. The discovery and replication datasets were merged and subjects carrying the HLA-DRB1*15:01 tagging SNP were excluded. Association tests showed that 48 of the 52 replicated SNPs retained significant associations with MS susceptibility independently of the HLA-DRB1*15:01 as defined by the tagging SNP. 20 Class I SNPs were associated with MS susceptibility with p-values ≤1×10−8. The most significantly associated SNP was rs4959039, a SNP in the downstream un-translated region of the non-classical HLA-G gene (Odds ratio 1.59, 95% CI 1.40, 1.81, p = 8.45×10−13) and is in linkage disequilibrium with several nearby SNPs. Logistic regression modeling showed that this SNP's contribution to MS susceptibility was independent of the Class II and Class III SNPs identified in this screen.ConclusionsA MHC Class I locus contributes to MS susceptibility independently of the HLA-DRB1*15:01 haplotype.

Highlights

  • The autoimmune disease multiple sclerosis (MS) is one of the leading causes of neurological disability in young adults

  • A major histocompatibility complex (MHC) Class I locus contributes to MS susceptibility independently of the human leukocyte antigen (HLA)-DRB1*15:01 haplotype

  • Case control study Following quality control, 958 markers were genotyped in both datasets

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Summary

Introduction

The autoimmune disease multiple sclerosis (MS) is one of the leading causes of neurological disability in young adults. The etiology is not fully understood, MS is a complex genetic disorder and whole genome studies indicate that the major histocompatibility complex (MHC) on chromosome 6p21 represents the strongest genome-wide MS susceptibility locus [1,2] In both Northern European and African descended populations, MS susceptibility is associated with alleles of the HLA Class II gene DRB1 [2,3,4,5] whereas the contribution of other genes within the extended MHC has been controversial [6,7,8]. Whether other major histocompatibility complex (MHC) genes contribute to MS susceptibility is controversial

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