Measuring liability for schizophrenia using optimized antisaccade stimulus parameters

Psychophysiology. 1999 Jan;36(1):138-41. doi: 10.1017/s0048577299980836.

Abstract

The ability to identify unaffected gene carriers within families may be crucial to the success of schizophrenia genetics studies. Data collected from three family samples (N = 365) demonstrated that poor antisaccade performance is an exceptionally promising indicator of liability for schizophrenia. A particular antisaccade task version provides large separations (5-6 sigma) between proband and normal groups. Poor antisaccade performance alone correctly identified 70% of patients in California, Utah, and Micronesia schizophrenia samples. Twenty-five to 50% of these patients' nonpsychotic first-degree relatives also had poor antisaccade performance, yielding risk ratios around 20:1 for simplex and 50:1 for multiplex schizophrenia families. Poor antisaccade performance is associated with dorsolateral prefrontal cortex pathology, suggesting that dysfunction of this circuitry also may predispose individuals to developing this disease.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aging / physiology
  • Antipsychotic Agents / adverse effects
  • Antipsychotic Agents / therapeutic use
  • Eye Movements / physiology
  • Family
  • Female
  • Humans
  • Male
  • Oculomotor Muscles / physiology
  • Photic Stimulation
  • Reaction Time / physiology
  • Saccades / physiology*
  • Schizophrenia / drug therapy
  • Schizophrenia / genetics*
  • Schizophrenia / physiopathology*
  • Sex Characteristics

Substances

  • Antipsychotic Agents