- Nasr, Zahra;
- Schoeps, Vinicius Andreoli;
- Ziaei, Amin;
- Virupakshaiah, Akash;
- Adams, Cameron;
- Casper, T Charles;
- Waltz, Michael;
- Rose, John;
- Rodriguez, Moses;
- Tillema, Jan-Mendelt;
- Chitnis, Tanuja;
- Graves, Jennifer S;
- Benson, Leslie;
- Rensel, Mary;
- Krupp, Lauren;
- Waldman, Amy T;
- Weinstock-Guttman, Bianca;
- Lotze, Tim;
- Greenberg, Benjamin;
- Aaen, Gregory;
- Mar, Soe;
- Schreiner, Teri;
- Hart, Janace;
- Simpson-Yap, Steve;
- Mesaros, Clementina;
- Barcellos, Lisa F;
- Waubant, Emmanuelle
Background
We previously reported an association between household chemical exposures and an increased risk of paediatric-onset multiple sclerosis.Methods
Using a case-control paediatric multiple sclerosis study, gene-environment interaction between exposure to household chemicals and genotypes for risk of paediatric-onset multiple sclerosis was estimated.Genetic risk factors of interest included the two major HLA multiple sclerosis risk factors, the presence of DRB1*15 and the absence of A*02, and multiple sclerosis risk variants within the metabolic pathways of common household toxic chemicals, including IL-6 (rs2069852), BCL-2 (rs2187163) and NFKB1 (rs7665090).Results
490 paediatric-onset multiple sclerosis cases and 716 controls were included in the analyses. Exposures to insect repellent for ticks or mosquitos (OR 1.47, 95% CI 1.06 to 2.04, p=0.019), weed control products (OR 2.15, 95% CI 1.51 to 3.07, p<0.001) and plant/tree insect or disease control products (OR 3.25, 95% CI 1.92 to 5.49, p<0.001) were associated with increased odds of paediatric-onset multiple sclerosis. There was significant additive interaction between exposure to weed control products and NFKB1 SNP GG (attributable proportions (AP) 0.48, 95% CI 0.10 to 0.87), and exposure to plant or disease control products and absence of HLA-A*02 (AP 0.56; 95% CI 0.03 to 1.08). There was a multiplicative interaction between exposure to weed control products and NFKB1 SNP GG genotype (OR 2.30, 95% CI 1.00 to 5.30) but not for other exposures and risk variants. No interactions were found with IL-6 and BCL-2 SNP GG genotypes.Conclusions
The presence of gene-environment interactions with household toxins supports their possible causal role in paediatric-onset multiple sclerosis.