Chromosome X aneuploidy in Brazilian schizophrenic patients

In Vivo. 2010 May-Jun;24(3):281-6.

Abstract

The identification of cytogenetic abnormalities in schizophrenic patients may provide clues to the genes involved in this disease. For this reason, a chromosomal analysis of samples from 62 schizophrenics and 70 controls was performed with trypsin-Giemsa banding and fluorescence in situ hybridization of the X chromosome. A clonal pericentric inversion on chromosome 9 was detected in one male patient, and we also discovered mosaicism associated with X chromosome aneuploidy in female patients, primarily detected in schizophrenic and normal female controls over 40 years old. When compared with age-matched female controls, the frequency of X chromosome loss was not significantly different between schizophrenics and controls, except for the 40- to 49-year-old age group. Our findings suggest that the X chromosome loss seen in schizophrenic patients is inherent to the normal cellular aging process. However, our data also suggest that X chromosome gain may be correlated with schizophrenia in this Brazilian population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aging / genetics
  • Aneuploidy
  • Brazil
  • Chromosome Aberrations*
  • Chromosomes, Human, X / genetics*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Lymphocytes / physiology
  • Male
  • Middle Aged
  • Mosaicism
  • Schizophrenia / genetics*