Increased Timing Variability in Schizophrenia and Bipolar Disorder

dc.contributor.authorBolbecker, Amanda R.
dc.contributor.authorWestfall, Daniel R.
dc.contributor.authorHowell, Josselyn M.
dc.contributor.authorLackner, Ryan J.
dc.contributor.authorCarroll, Christine A.
dc.contributor.authorO’Donnell, Brian F.
dc.contributor.authorHetrick, William P.
dc.contributor.departmentPsychiatry, School of Medicine
dc.date.accessioned2025-04-03T14:40:05Z
dc.date.available2025-04-03T14:40:05Z
dc.date.issued2014-05-21
dc.description.abstractTheoretical and empirical evidence suggests that impaired time perception and the neural circuitry underlying internal timing mechanisms may contribute to severe psychiatric disorders, including psychotic and mood disorders. The degree to which alterations in temporal perceptions reflect deficits that exist across psychosis-related phenotypes and the extent to which mood symptoms contribute to these deficits is currently unknown. In addition, compared to schizophrenia, where timing deficits have been more extensively investigated, sub-second timing has been studied relatively infrequently in bipolar disorder. The present study compared sub-second duration estimates of schizophrenia (SZ), schizoaffective disorder (SA), non-psychotic bipolar disorder (BDNP), bipolar disorder with psychotic features (BDP), and healthy non-psychiatric controls (HC) on a well-established time perception task using sub-second durations. Participants included 66 SZ, 37 BDNP, 34 BDP, 31 SA, and 73 HC who participated in a temporal bisection task that required temporal judgements about auditory durations ranging from 300 to 600 milliseconds. Timing variability was significantly higher in SZ, BDP, and BDNP groups compared to healthy controls. The bisection point did not differ across groups. These findings suggest that both psychotic and mood symptoms may be associated with disruptions in internal timing mechanisms. Yet unexpected findings emerged. Specifically, the BDNP group had significantly increased variability compared to controls, but the SA group did not. In addition, these deficits appeared to exist independent of current symptom status. The absence of between group differences in bisection point suggests that increased variability in the SZ and bipolar disorder groups are due to alterations in perceptual timing in the sub-second range, possibly mediated by the cerebellum, rather than cognitive deficits.
dc.eprint.versionFinal published version
dc.identifier.citationBolbecker AR, Westfall DR, Howell JM, et al. Increased timing variability in schizophrenia and bipolar disorder. PLoS One. 2014;9(5):e97964. Published 2014 May 21. doi:10.1371/journal.pone.0097964
dc.identifier.urihttps://hdl.handle.net/1805/46807
dc.language.isoen_US
dc.publisherPublic Library of Science
dc.relation.isversionof10.1371/journal.pone.0097964
dc.relation.journalPLoS One
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectBipolar disorder
dc.subjectPsychotic disorders
dc.subjectSchizophrenia
dc.subjectPsychotropic drugs
dc.titleIncreased Timing Variability in Schizophrenia and Bipolar Disorder
dc.typeArticle
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