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Saccadic distractibility is elevated in schizophrenia patients, but not in their unaffected relatives

Published online by Cambridge University Press:  28 July 2005

JAMES H. MacCABE
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UK
HELEN SIMON
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UK
JOLANTA W. ZANELLI
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UK
REBECCA WALWYN
Affiliation:
Department of Biostatistics and Computing, Institute of Psychiatry, London, UK
COLM D. McDONALD
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UK
ROBIN M. MURRAY
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UK

Abstract

Background. Saccadic distractibility, as measured by the antisaccade task, has attracted attention as a putative endophenotypic marker for schizophrenia. Some studies have suggested that this measure is elevated in the unaffected relatives of schizophrenia patients. However, recent studies have called this into question and the topic remains controversial.

Method. Saccadic distractibility was measured in 53 patients with DSM-IV schizophrenia, 80 unaffected first-degree relatives and 41 unaffected controls.

Results. Schizophrenia patients performed worse than relatives and controls combined (p<0·00001), but relatives did not differ significantly from controls. Performance in multiply affected families was no worse than that in singly affected families. Relatives with a high presumed genetic risk for schizophrenia performed no worse than other relatives. The performance of the patients did not predict that of their relatives.

Conclusions. These results demonstrate that saccadic distractibility is strongly associated with disease status but not with genetic loading for schizophrenia. We conclude that saccadic distractibility is unlikely to be useful as an endophenotypic marker in schizophrenia.

Type
Original Article
Copyright
2005 Cambridge University Press

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