4.6 Article

Association of NEF2L2 Rs35652124 Polymorphism with Nrf2 Induction and Genotoxic Stress Biomarkers in Autism

Journal

GENES
Volume 14, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/genes14030718

Keywords

Nrf2; autism; ASD; polymorphism; SNP; dimethyl fumarate; antioxidant; oxidative stress; H2AX; rs35652124

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This study investigated the relationship between the functional polymorphism of the Nrf2 gene and genotoxic stress responses in ASD children, as well as the effect of a NRF2 inductor. The results showed that adaptive responses to genotoxic stress were positively correlated with NRF2 content in ASD children, particularly in the T+ genotype. ASD children with the NRF2 rs35652124 CC genotype exhibited higher levels of genotoxic stress and NRF2 induction, lower plasma 8-oxo-dG concentration, and higher cfDNA/plasma nuclease activity ratio. These findings suggest that the NEF2L2 rs35652124 polymorphism may impact adaptive responses and potentially be linked to ASD severity.
Increased oxidative/genotoxic stress is known to impact the pathophysiology of ASD (autism spectrum disorder). Clinical studies, however, reported limited, heterogeneous but promising responses to treatment with antioxidant remedies. We determined whether the functional polymorphism of the Nrf2 gene, master regulator of anti-oxidant adaptive reactions to genotoxic stress, links to the genotoxic stress responses and to an in vitro effect of a NRF2 inductor in ASD children. Oxidative stress biomarkers, adaptive responses to genotoxic/oxidative stress, levels of master antioxidant regulator Nrf2 and its active form pNrf2 before and after inducing by dimethyl fumarate (DMF), and promotor rs35652124 polymorphism of NFE2L2 gene encoding Nrf2 were studied in children with ASD (n = 179). Controls included healthy adults (n = 101). Adaptive responses to genotoxicity as indicated by H2AX and cytoprotection by NRF2 contents positively correlated in ASD children with a Spearman coefficient of R = 0.479 in T+, but not CC genotypes. ASD children with NRF2 rs35652124 CC genotype demonstrated significantly higher H2AX content (0.652 vs. 0.499 in T+) and pNrf2 induction by DMF, lowered 8-oxo-dG concentration in plasma and higher cfDNA/plasma nuclease activity ratio. Our pilot findings suggest that in ASD children the NEF2L2 rs35652124 polymorphism impacts adaptive responses that may potentially link to ASD severity. Our data warrant further studies to reveal the potential for NEF2L2 genotype-specific and age-dependent repurposing of DMF and/or other NRF2-inducing drugs.

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