A twin and family study of the association between immune system dysfunction and dyslexia using blood serum immunoassay and survey data

Brain Cogn. 1998 Apr;36(3):310-33. doi: 10.1006/brcg.1997.0972.

Abstract

We conducted a study of the association between developmental reading disability (DRD) and immune disorders (ID) using both survey and immunoassay data in two separate samples of families. One sample was made up of twins and their parents and was ascertained through a population-based sampling scheme. The other sample was a set of extended pedigrees selected for apparent autosomal dominant transmission of DRD. We failed to find an association between DRD and ID in either sample, regardless of the method used to assess immune system function. Even though our twin sample provided evidence that both DRD and immune conditions were significantly heritable, there was no evidence for a genetic correlation between ID and DRD nor was there any clear indication that a special subgroup of individuals may be comorbid for these conditions because of genetic reasons. How these negative findings can be reconciled with the developmental hypothesis of Geschwind, Behan, Galaburda, and colleagues, and how they may relate to the gene locus influencing DRD that has been recently located in the HLA region of the short arm of chromosome 6 is discussed.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Twin Study

MeSH terms

  • Adolescent
  • Antibodies, Antinuclear / blood
  • Autoimmune Diseases / complications*
  • Autoimmune Diseases / genetics
  • Child
  • Colorado / epidemiology
  • Diseases in Twins / epidemiology
  • Diseases in Twins / genetics*
  • Dyslexia / epidemiology
  • Dyslexia / genetics
  • Dyslexia / immunology*
  • Female
  • Genetic Linkage*
  • HLA Antigens / genetics
  • Humans
  • Hypersensitivity / complications*
  • Hypersensitivity / epidemiology
  • Hypersensitivity / genetics
  • Male
  • Pedigree
  • Phenotype
  • Rheumatoid Factor / blood

Substances

  • Antibodies, Antinuclear
  • HLA Antigens
  • Rheumatoid Factor