TY - JOUR
T1 - Pursuit eye movements as an intermediate phenotype across psychotic disorders
T2 - Evidence from the B-SNIP study
AU - Lencer, Rebekka
AU - Sprenger, Andreas
AU - Reilly, James L.
AU - McDowell, Jennifer E.
AU - Rubin, Leah H.
AU - Badner, Judith A.
AU - Keshavan, Matcheri S.
AU - Pearlson, Godfrey D.
AU - Tamminga, Carol A.
AU - Gershon, Elliot S.
AU - Clementz, Brett A.
AU - Sweeney, John A.
N1 - Funding Information:
American Psychiatric Association — Deputy Editor; Astellas — Ad Hoc Consultant; Autifony — Ad Hoc Consultant; The Brain and Behavior Foundation — Council Member; Eli Lilly Pharmaceuticals — Ad Hoc Consultant; Intra-cellular Therapies (ITI, Inc.) — Advisory Board, drug development; Institute of Medicine — Council Member; National Academy of Medicine — Council Member; Pfizer — Ad Hoc Consultant; Sunovion — Investigator Initiated grant funding.
Funding Information:
This work was supported by the National Institute of Mental Health [grant numbers: MH077851 (CAT), MH078113 (MSK), MH077945 (GDP), MH077852 (GKT) and MH077862 (JAS)]. The NIMH has no role in study design; in the collection, analysis and interpretation of data; in the writing of the report; or the decision to submit the manuscript for publication. Research reported in this publication was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award Number TL1TR001104 . The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Smooth pursuit eye tracking deficits are a promising intermediate phenotype for schizophrenia and possibly for psychotic disorders more broadly. The Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) consortium investigated the severity and familiality of different pursuit parameters across psychotic disorders. Probands with schizophrenia (N=265), schizoaffective disorder (N=178), psychotic bipolar disorder (N=231), their first-degree relatives (N=306, N=217, N=273, respectively) and healthy controls (N=305) performed pursuit tracking tasks designed to evaluate sensorimotor and cognitive/predictive aspects of pursuit. Probands from all diagnostic groups were impaired on all pursuit measures of interest compared to controls (p<0.001). Schizophrenia probands were more impaired than other proband groups on both early pursuit gain and predictive gain. Relatives with and without enhanced psychosis spectrum personality traits were impaired on initial eye acceleration, the most direct sensorimotor pursuit measure, but not on pursuit gain measures. This suggests that alterations in early sensorimotor function may track susceptibility to psychosis even in the absence of psychosis related personality traits. There were no differences in pursuit measures between relatives of the three proband groups. Familiality estimates of pursuit deficits indicate that early pursuit gain was more familial than predictive gain, which has been the most widely used measure in previous family studies of psychotic disorders. Thus, while disease-related factors may induce significant impairments of pursuit gain, especially in schizophrenia, the pattern of deficits in relatives and their familiality estimates suggest that alterations in sensorimotor function at pursuit onset may indicate increased susceptibility across psychotic disorders.
AB - Smooth pursuit eye tracking deficits are a promising intermediate phenotype for schizophrenia and possibly for psychotic disorders more broadly. The Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) consortium investigated the severity and familiality of different pursuit parameters across psychotic disorders. Probands with schizophrenia (N=265), schizoaffective disorder (N=178), psychotic bipolar disorder (N=231), their first-degree relatives (N=306, N=217, N=273, respectively) and healthy controls (N=305) performed pursuit tracking tasks designed to evaluate sensorimotor and cognitive/predictive aspects of pursuit. Probands from all diagnostic groups were impaired on all pursuit measures of interest compared to controls (p<0.001). Schizophrenia probands were more impaired than other proband groups on both early pursuit gain and predictive gain. Relatives with and without enhanced psychosis spectrum personality traits were impaired on initial eye acceleration, the most direct sensorimotor pursuit measure, but not on pursuit gain measures. This suggests that alterations in early sensorimotor function may track susceptibility to psychosis even in the absence of psychosis related personality traits. There were no differences in pursuit measures between relatives of the three proband groups. Familiality estimates of pursuit deficits indicate that early pursuit gain was more familial than predictive gain, which has been the most widely used measure in previous family studies of psychotic disorders. Thus, while disease-related factors may induce significant impairments of pursuit gain, especially in schizophrenia, the pattern of deficits in relatives and their familiality estimates suggest that alterations in sensorimotor function at pursuit onset may indicate increased susceptibility across psychotic disorders.
KW - Bipolar disorder
KW - Familiality
KW - Predictive pursuit eye movements
KW - Schizoaffective disorder
KW - Schizophrenia
KW - Sensorimotor processing
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U2 - 10.1016/j.schres.2015.09.032
DO - 10.1016/j.schres.2015.09.032
M3 - Article
C2 - 26481615
AN - SCOPUS:84953839220
SN - 0920-9964
VL - 169
SP - 326
EP - 333
JO - Schizophrenia Research
JF - Schizophrenia Research
IS - 1-3
ER -