Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs

Genomics. 2017 Jan;109(1):9-15. doi: 10.1016/j.ygeno.2016.12.001. Epub 2016 Dec 9.

Abstract

Parents of children affected with autism spectrum disorders (ASD) often have mild forms of autistic-like characteristics. Past studies have focused on searching for individual genetic risk loci of ASD. Here we studied the overall properties of the genomes of ASD trios by using previously published genome-wide data for common SNPs. The pairwise genetic distance (PGD) between a spousal pair with ASD-affected children was found smaller than that of a random pair selected among the spouses in the ASD trios, and spousal relatedness correlated with severe forms of ASD. Furthermore, for a set of 970 ASD associated SNPs, cases showed higher homozygous minor allele content than parents. These results indicate new genetic elements in the broad phenotypes of parents with ASD-affected offspring and in ASD pathogenesis.

Keywords: Minor allele content (MAC); Pairwise genetic distance (PGD).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Autistic Disorder / genetics*
  • Female
  • Gene Frequency*
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Only Child
  • Parents
  • Polymorphism, Single Nucleotide*