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Saccadic eye movement task identifies cognitive deficits in children with schizophrenia, but not in unaffected child relatives
Author(s) -
Ross Randal G.,
Heinlein Shari,
Zerbe Gary O.,
Radant Allen
Publication year - 2005
Publication title -
journal of child psychology and psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.652
H-Index - 211
eISSN - 1469-7610
pISSN - 0021-9630
DOI - 10.1111/j.1469-7610.2005.01437.x
Subject(s) - endophenotype , psychology , saccadic masking , schizophrenia (object oriented programming) , psychosis , proband , cognition , eye movement , gaze , developmental psychology , audiology , psychiatry , neuroscience , medicine , biochemistry , chemistry , psychoanalysis , mutation , gene
Background: The delayed oculomotor response (DOR) task requires response inhibition followed by movement of gaze towards a known spatial location without a current stimulus. Abnormalities in response inhibition and in the spatial accuracy of the eye movement are found in individuals with schizophrenia and in many of their relatives, supporting the use of these saccadic abnormalities as endophenotypes in genetic studies. It is unknown whether school‐age children, either with psychosis or as relatives of a schizophrenic proband, can be included. Method: One hundred eighty‐seven children, ages 5.8–16.0 years – 45 children with childhood‐onset schizophrenia, 64 children with a first‐degree relative with schizophrenia, and 84 typically developing children – completed DOR tasks with 1 and 3 second delays. Results: Children with childhood‐onset schizophrenia demonstrated impaired response inhibition and impaired spatial accuracy compared to both relatives and typicals; however, relatives and typicals did not differ from each other. Conclusions: Children with childhood‐onset schizophrenia have saccadic abnormalities similar to those found in adults with schizophrenia, supporting the continuity of executive function deficits in childhood‐onset with adolescent and adult‐onset schizophrenia. However, saccadic tasks are not sensitive to genetic risk in non‐psychotic children and 6–15‐year‐old children should not be included in genetic studies utilizing this endophenotype.