Human homeostatic iron regulator gene polymorphism in autistic population of India; a case-control study
Highlights
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Autism is a complex heterogeneous neurodevelopmental disorder.
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C282Y and H63D SNPs of the HFE gene were screened for the first time in autistic children from India.
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TXRF analysis shows a significantly very low concentration of iron in autistic children compared to the controls.
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C28Y and H63D SNPs were not found to be the risk factors for autism in our study cohort with a negative association.
Abstract
Background
Autism is a heterogeneous neurodevelopmental disorder. Human homeostatic iron regulator (HFE) codes for HFE protein. HFE protein is very essential for inhibitory regulation of the endocytosis of iron.
Objective
Present study aims to screen C282Y and H63D polymorphism of the HFE gene in autistic children.
Method
30 autistic children and 30 healthy age-matched control children were included in the study. TXRF analysis was performed for quantification of Iron in plasma. Genomic DNA was extracted using peripheral blood samples and targeted SNPs were screened using Restriction fragment length polymorphism. Genotype, allelic frequencies and risk ratio were calculated using the statistical method.
Results
TXRF analysis shows a significantly very low concentration of iron in autistic children compared to the control group [1039.6 ± 28 μg/L vs 2372.2 ± 35 μg/L, p-value 0.001]. Genetic Study shows that all the 30 controls and 28 autistic cases showed homozygote C/C allele. Two heterozygote C/Y alleles and no homozygous Y/Y allele were observed for C282Y polymorphism for autistic cases. 29 control and 23 autistic cases showed a homozygote H/H allele. 01 control and 07 autistic cases showed heterozygote H/D allele for H63D polymorphism. C282Y and H63D polymorphisms of HFE gene for heterozygous condition showed non-significant evidence of risk for causing autism OR = 5.35, 95%CI = 0.25–116.3, P-value-0.29 and OR = 8.8, 95%CI = 1.0–76.9, P-value = 0.05 respectively.
Conclusions
Present study found that C282Y and H63D were not found to be the risk factor for autism in the targeted study cohort.