Fetal and Pediatric Pathology | 2019

Association of MTHFR 677C\u2009>\u2009T and 1298A\u2009>\u2009C polymorphisms with susceptibility to attention deficit and hyperactivity disorder

 
 
 
 
 
 
 
 

Abstract


Abstract Background: The associations of MTHFR polymorphisms with risk of attention deficit and hyperactivity disorder (ADHD) are poorly elucidated. This study was performed to evaluate the association of MTHFR polymorphisms with ADHD risk in Iranian children. Methods: This case–control study included 214 children with ADHD and 220 healthy subjects. The MTHFR 677C\u2009>\u2009T and 1298A\u2009>\u2009C polymorphisms were genotyped by an ABI PRISMs 7500 real-time PCR System. The odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association. Results: The MTHFR 1298A\u2009>\u2009C polymorphism CC genotype (OR= 1.526, 95% CI 1.004–2.320, p\u2009=\u20090.048) and C allele (OR= 1.336, 95% CI 0.1023–1.745, p\u2009=\u20090.034) were associated with an increased risk of ADHD. There was no significant association between MTHFR 677C\u2009>\u2009T polymorphism and increased risk of ADHD. Conclusions: Our results revealed that the MTHFR 1298A\u2009>\u2009C polymorphism but not the MTHFR 677\u2009C\u2009>\u2009T is associated with increased risk of ADHD in Iranian children.

Volume 39
Pages 422 - 429
DOI 10.1080/15513815.2019.1666330
Language English
Journal Fetal and Pediatric Pathology

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