| Literature DB >> 26309447 |
Mohammad H Rahbar1, Maureen Samms-Vaughan2, Jianzhong Ma3, Jan Bressler4, Aisha S Dickerson5, Manouchehr Hessabi5, Katherine A Loveland6, Megan L Grove3, Sydonnie Shakespeare-Pellington2, Compton Beecher7, Wayne McLaughlin8, Eric Boerwinkle4.
Abstract
We used data from 100 age- and sex-matched case-control pairs (age 2-8 years) from Jamaica to investigate whether there is an interaction between glutathione-S-transferase (GST) genes and blood manganese concentrations (BMC) in relation to Autism Spectrum Disorder (ASD). Our findings, indicate that among children who had the Ile/Ile genotype for GST pi 1 (GSTP1), those with BMC ≥ 12µg/L had about 4 times higher odds of ASD than those with BMC < 12µg/L, (P=0.03) under a co-dominant genetic model. After adjusting for potential confounders, among the subgroup of children with genotype Ile/Ile, those with BMC ≥ 12µg/L had about six times higher odds of ASD than those with BMC < 12µg/L, (P=0.04). The results were similar when a recessive genetic model was used. These findings suggest a possible synergic effect of BMC and GSTP1 in ASD. Since our analysis included a variety of genetic models and was not adjusted for multiple testing, replication in other populations is warranted.Entities:
Keywords: Autism Spectrum Disorder (ASD); Glutathione S-transferase (GST) genes; Interactions; Jamaica; Manganese; Oxidative stress
Year: 2015 PMID: 26309447 PMCID: PMC4542005 DOI: 10.1016/j.rasd.2015.08.001
Source DB: PubMed Journal: Res Autism Spectr Disord