AI Article Synopsis

  • The study examined smooth pursuit eye movement (SPEM) and antisaccade deficits in schizophrenia patients, their healthy siblings, and healthy controls to explore potential genetic links to schizophrenia.
  • Patients displayed marked deficits, including lower SPEM gain and higher antisaccade error rates compared to controls, while siblings showed intermediate performance, particularly in antisaccade gain.
  • Findings suggest that these subtle eye movement deficits could serve as indicators of genetic risk for schizophrenia, emphasizing the importance of considering family relationships in such analyses.

Article Abstract

Smooth pursuit eye movement (SPEM) and antisaccade deficits have been proposed as endophenotypes in the search for schizophrenia genes. We assessed these measures in 24 schizophrenia patients, 24 of their healthy siblings, and 24 healthy controls closely matched to the siblings. Between-group differences were assessed using a random effects regression model taking into account the relatedness between patients and siblings. Patients showed reduced SPEM gain, increased frequency of saccades during pursuit, increased antisaccade error rate, and reduced antisaccade gain compared to controls. Siblings performed intermediate, i.e. between patients and controls, on most measures, but were particularly characterised by reduced antisaccade gain. SPEM gain at one target velocity was significantly correlated between patients and siblings, highlighting the necessity of taking into account within-family correlations in the statistical analysis of between-group differences. It is concluded that subtle SPEM and antisaccade deficits are observed in clinically unaffected siblings of schizophrenia patients; these deficits may be useful markers of genetic liability to schizophrenia.

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http://dx.doi.org/10.1016/s0022-3956(03)00105-5DOI Listing

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