An investigation of mitochondrial haplogroups in autism

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):987-9. doi: 10.1002/ajmg.b.30687.

Abstract

Family and twin studies provide strong evidence of a major genetic influence in autism, but the underlying gene defects have yet to be characterized. The mothers of boys with autism share autistic traits, raising the possibility of a maternally inherited factor. Mitochondrial DNA (mtDNA) is almost exclusively inherited down the maternal line. We therefore explored the possibility that a particular mtDNA lineage contributes to the risk of developing autism. The mtDNA haplogroup was determined in 162 autism probands, and compared to two sets of population controls. Results show no compelling evidence of an association of any mitochondrial haplogroup in autism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autistic Disorder / etiology
  • Autistic Disorder / genetics*
  • Case-Control Studies
  • Child
  • Child of Impaired Parents
  • DNA, Mitochondrial*
  • Female
  • Gene Frequency
  • Haplotypes*
  • Humans
  • Male
  • Mitochondrial Diseases / complications
  • Mitochondrial Diseases / genetics

Substances

  • DNA, Mitochondrial