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

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 ma...

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Published inPsychological medicine Vol. 35; no. 12; pp. 1737 - 1746
Main Authors BARRETT, SUZANNE LUCIA, KELLY, CHRISTOPHER, WATSON, DAVID ROBERT, BELL, ROBERT, KING, DAVID JOHN
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 01.12.2005
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Summary: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.
Bibliography:PMID:16300689
ark:/67375/6GQ-NDHF302B-D
PII:S0033291705005702
istex:D65359147BA041D2B54B37F8896FE42661F9413A
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0033-2917
1469-8978
DOI:10.1017/S0033291705005702