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Genetic risk factors for pediatric-onset multiple sclerosis.

Research paper by Milena A MA Gianfrancesco, Pernilla P Stridh, Xiaorong X Shao, Brooke B Rhead, Jennifer S JS Graves, Tanuja T Chitnis, Amy A Waldman, Timothy T Lotze, Teri T Schreiner, Anita A Belman, Benjamin B Greenberg, Bianca B Weinstock-Guttman, Gregory G Aaen, Jan M JM Tillema, Janace J Hart, et al.

Indexed on: 06 Oct '17Published on: 06 Oct '17Published in: Multiple sclerosis (Houndmills, Basingstoke, England)



Abstract

Strong evidence supports the role of both genetic and environmental factors in pediatric-onset multiple sclerosis (POMS) etiology.We comprehensively investigated the association between established major histocompatibility complex (MHC) and non-MHC adult multiple sclerosis (MS)-associated variants and susceptibility to POMS.Cases with onset <18 years ( n = 569) and controls ( n = 16,251) were included from the United States and Sweden. Adjusted logistic regression and meta-analyses were performed for individual risk variants and a weighted genetic risk score (wGRS) for non-MHC variants. Results were compared to adult MS cases ( n = 7588).HLA-DRB1*15:01 was strongly associated with POMS (odds ratio (OR)meta = 2.95, p < 2.0 × 10(-16)). Furthermore, 28 of 104 non-MHC variants studied (23%) were associated ( p < 0.05); POMS cases carried, on average, a higher burden of these 28 variants compared to adults (ORavg = 1.24 vs 1.13, respectively), though the difference was not significant. The wGRS was strongly associated with POMS (ORmeta = 2.77, 95% confidence interval: 2.33, 3.32, p < 2.0 × 10(-16)) and higher, on average, when compared to adult cases. Additional class III risk variants in the MHC region associated with POMS were revealed after accounting for HLA-DRB1*15:01 and HLA-A*02.Pediatric and adult MS share many genetic variants suggesting similar biological processes are present. MHC variants beyond HLA-DRB1*15:01 and HLA-A*02 are also associated with POMS.

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