[article]
Titre : |
Synergic effect of GSTP1 and blood manganese concentrations in Autism Spectrum Disorder |
Type de document : |
Texte imprimé et/ou numérique |
Auteurs : |
Mohammad H. RAHBAR, Auteur ; Maureen SAMMS-VAUGHAN, Auteur ; Jianzhong MA, Auteur ; Jan BRESSLER, Auteur ; Aisha S. DICKERSON, Auteur ; Manouchehr HESSABI, Auteur ; Katherine A. LOVELAND, Auteur ; Megan L. GROVE, Auteur ; Sydonnie SHAKESPEARE-PELLINGTON, Auteur ; Compton BEECHER, Auteur ; Wayne MCLAUGHLIN, Auteur ; Eric BOERWINKLE, Auteur |
Article en page(s) : |
p.73-82 |
Langues : |
Anglais (eng) |
Mots-clés : |
Manganese Autism Spectrum Disorder (ASD) Glutathione-S-transferase (GST) genes Oxidative stress Interactions Jamaica |
Index. décimale : |
PER Périodiques |
Résumé : |
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 ? 12 ?g/L had about 4 times higher odds of ASD than those with BMC < 12 ?g/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 ? 12 ?g/L had about six times higher odds of ASD than those with BMC < 12 ?g/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. |
En ligne : |
http://dx.doi.org/10.1016/j.rasd.2015.08.001 |
Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=268 |
in Research in Autism Spectrum Disorders > 18 (October 2015) . - p.73-82
[article] Synergic effect of GSTP1 and blood manganese concentrations in Autism Spectrum Disorder [Texte imprimé et/ou numérique] / Mohammad H. RAHBAR, Auteur ; Maureen SAMMS-VAUGHAN, Auteur ; Jianzhong MA, Auteur ; Jan BRESSLER, Auteur ; Aisha S. DICKERSON, Auteur ; Manouchehr HESSABI, Auteur ; Katherine A. LOVELAND, Auteur ; Megan L. GROVE, Auteur ; Sydonnie SHAKESPEARE-PELLINGTON, Auteur ; Compton BEECHER, Auteur ; Wayne MCLAUGHLIN, Auteur ; Eric BOERWINKLE, Auteur . - p.73-82. Langues : Anglais ( eng) in Research in Autism Spectrum Disorders > 18 (October 2015) . - p.73-82
Mots-clés : |
Manganese Autism Spectrum Disorder (ASD) Glutathione-S-transferase (GST) genes Oxidative stress Interactions Jamaica |
Index. décimale : |
PER Périodiques |
Résumé : |
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 ? 12 ?g/L had about 4 times higher odds of ASD than those with BMC < 12 ?g/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 ? 12 ?g/L had about six times higher odds of ASD than those with BMC < 12 ?g/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. |
En ligne : |
http://dx.doi.org/10.1016/j.rasd.2015.08.001 |
Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=268 |
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