DNA fragmentation decreased in schizophrenia but not bipolar disorder

Arch Gen Psychiatry. 2003 Apr;60(4):359-64. doi: 10.1001/archpsyc.60.4.359.

Abstract

Background: Apoptosis is thought to play a role in neuronal pathology in schizophrenia and bipolar disorder.

Methods: To test this hypothesis, the Klenow method for in situ end-labeling of single-stranded DNA breaks was applied to anterior cingulate cortex from 18 healthy controls, 18 schizophrenic subjects, and 10 bipolar subjects.

Results: An unexpected reduction (71%) in Klenow-positive nuclei was found in schizophrenic but not in bipolar cortexes.

Conclusions: To our knowledge to date, this is the first demonstration that there is much less DNA fragmentation in individuals with schizophrenia than in healthy controls and bipolar subjects, which raises a key question as to whether this alteration represents an adaptive or nonadaptive change in the regulation of intracellular signaling and mitochondrial oxidative pathways associated with apoptosis.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Apoptosis / genetics*
  • Bipolar Disorder / genetics*
  • Bipolar Disorder / metabolism
  • Bipolar Disorder / physiopathology
  • Cohort Studies
  • DNA Fragmentation / genetics*
  • Endodeoxyribonucleases / genetics
  • Endodeoxyribonucleases / metabolism
  • Female
  • Gyrus Cinguli / metabolism
  • Gyrus Cinguli / physiopathology
  • Humans
  • In Situ Nick-End Labeling
  • Male
  • Middle Aged
  • Polymorphism, Single-Stranded Conformational
  • Schizophrenia / genetics*
  • Schizophrenia / metabolism
  • Schizophrenia / physiopathology

Substances

  • Endodeoxyribonucleases
  • mitochondrial oxidative damage endonuclease