Caspian Journal of Neurological Sciences (Feb 2017)

MTHFR rs1801133 Gene Polymorphism and Autism Susceptibility

  • Mahsa Delshadpour,
  • Farhad Mashayekhi,
  • Elham Bidabadi,
  • Shirin Shahangian,
  • Zivar Salehi

Journal volume & issue
Vol. 3, no. 8
pp. 39 – 45

Abstract

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Background: It is believed that environmental and genetic factors may be responsible for autism. Methylenetetrahydrofolate reductase (MTHFR) and its gene polymorphisms have been shown to be implicated as risk factors in autism. Objectives: To analyze MTHFR C677T polymorphism (rs1801133) in autistic patients. Materials and Methods: This study was carried out in 2014 and 2015 in northern Iran. One hundred and seventy-one male autistic patients and 198 healthy males were included in this study. Autism was diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV) criteria. Each autism spectrum disorder (ASD) patient was also evaluated by the Childhood Autism Rating Scale (CARS). All participants were tested for C677T polymorphism by using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Statistical analyzes were performed using MedCalc version 12.1 by the χ2 test and logistic regression model. A value of p0.05). The allele frequencies of C and T in children with autism were 73.0% and 27.0%, and in control group were 76.0% and 24.0%, respectively (p>0.05). Conclusion: MTHFR C677T polymorphism is not associated with autism in a population in the north of Iran.

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