Title of article :
P300 subcomponent abnormalities in schizophrenia: III. Deficits in unaffected siblings of schizophrenic probands
Author/Authors :
Bruce I. Turetsky، نويسنده , , Tyrone D. Cannon، نويسنده , , Raquel E. Gur، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
11
From page :
380
To page :
390
Abstract :
Background: Reduced P300 amplitude is a robust finding in patients with schizophrenia. In previous investigations, we reported reductions of specific subcomponents of the auditory oddball P300 that were independent of acute symptomatology and persistent over time, consistent with a trait abnormality. To clarify whether these stable deficits represented genetic markers of vulnerability to schizophrenia, event-related brain potentials (ERPs) from patients were compared to those from their own healthy siblings and unrelated control subjects. Methods: Auditory P300 ERPs were acquired from 11 schizophrenic patients, 12 healthy siblings and 23 matched control subjects. Five P300 subcomponents were identified using current source density measures: frontal, bilateral parietal, and bilateral temporal. Results: Consistent with previous reports, patients had reduced parietal and frontal P300 amplitudes. The healthy siblings of the schizophrenic probands had an isolated reduction of the frontal P300. Conclusions: Frontal P300 amplitude is a potential endophenotypic marker of genetic vulnerability to schizophrenia in individuals who otherwise show no evidence of clinical symptomatology. Given the functional interpretation of the frontal P300 as a physiological correlate of cognitive orienting, this supports the hypothesis that impairments of the neural substrate underlying attentional mechanisms are selective indicators of genetic susceptibility to schizophrenia in high-risk individuals.
Keywords :
Endophenotype , genetics , P300 , Siblings , Schizophrenia , Evoked potentials
Journal title :
Biological Psychiatry
Serial Year :
2000
Journal title :
Biological Psychiatry
Record number :
501156
Link To Document :
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