Hostname: page-component-848d4c4894-4rdrl Total loading time: 0 Render date: 2024-06-26T06:33:56.584Z Has data issue: false hasContentIssue false

Normal levels of prepulse inhibition in the euthymic phase of bipolar disorder

Published online by Cambridge University Press:  28 July 2005

SUZANNE LUCIA BARRETT
Affiliation:
Department of Psychology, University of Ulster, Jordanstown Campus, Co. Antrim, UK
CHRISTOPHER KELLY
Affiliation:
Division of Psychiatry & Neuroscience, Queen's University Belfast, UK
DAVID ROBERT WATSON
Affiliation:
Division of Psychiatry & Neuroscience, Queen's University Belfast, UK
ROBERT BELL
Affiliation:
School of Psychology, Queen's University Belfast, UK
DAVID JOHN KING
Affiliation:
Department of Therapeutics and Pharmacology, Queen's University Belfast, UK

Abstract

Background. Deficits in prepulse inhibition (PPI) of the acoustic startle response have been suggested as a potentially useful endophenotype for schizophrenia spectrum disorders and may explain certain symptoms and cognitive deficits observed in the psychoses. PPI deficits have also been found in mania, but it remains to be confirmed whether this dysfunction is present in the euthymic phase of bipolar disorder.

Method. Twenty-three adult patients with DSM-IV bipolar disorder were compared to 20 controls on tests of acoustic startle reactivity and PPI of the startle response. Sociodemographic and treatment variables were recorded and symptom scores assessed using the Hamilton Depression Inventory and the Young Mania Rating Scale.

Results. Overall, the patient and control groups demonstrated similar levels of startle reactivity and PPI, although there was a trend for the inter-stimulus interval to differentially affect levels of PPI in the two groups.

Conclusions. In contrast to bipolar patients experiencing a manic episode, general levels of PPI were normal in this euthymic sample. Further studies are required to confirm this finding and to determine the mechanisms by which this potential disruption/normalization occurs. It is suggested that an examination of PPI in a high-risk group is required to fully discount dysfunctional PPI as a potentially useful endophenotype for bipolar disorder.

Type
Original Article
Copyright
2005 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)