Prepulse inhibition in euthymic bipolar disorder patients in comparison with control subjects

Objective Deficient prepulse inhibition (PPI) of the startle response, indicating sensorimotor gating deficits, has been reported in schizophrenia and other neuropsychiatric disorders. This study aimed to assess sensorimotor gating deficits in patients with euthymic bipolar. Furthermore, we analysed...

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Veröffentlicht in:Acta psychiatrica Scandinavica 2016-10, Vol.134 (4), p.350-359
Hauptverfasser: Sánchez-Morla, E. M., Mateo, J., Aparicio, A., García-Jiménez, M. Á., Jiménez, E., Santos, J. L.
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Sprache:eng
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Zusammenfassung:Objective Deficient prepulse inhibition (PPI) of the startle response, indicating sensorimotor gating deficits, has been reported in schizophrenia and other neuropsychiatric disorders. This study aimed to assess sensorimotor gating deficits in patients with euthymic bipolar. Furthermore, we analysed the relationships between PPI and clinical and cognitive measures. Method Prepulse inhibition was measured in 64 patients with euthymic bipolar and in 64 control subjects matched for age, gender, education level and smoking status. Clinical characteristics and level of functioning were assessed in all participants using Hamilton Depression Rating Scale (HDRS), Young Mania Rating Scale (YMRS) and Functioning Assessment Short Test (FAST). Cognition was evaluated using the Measurement and Treatment Research to Improve Cognition in Schizophrenia Consensus Cognitive Battery (MCCB) and the Stroop test as an additional measure of executive function. Results Compared with controls, patients with bipolar disorder exhibited PPI deficits at 60‐ and 120‐millisecond prepulse–pulse intervals. Among patients with bipolar disorder, PPI was correlated with the social cognition domain of the MCCB. PPI was not significantly correlated with other clinical, functional and neurocognitive variables in either group. Conclusions Our data suggest that PPI deficit is a neurobiological marker in euthymic bipolar disorder, which is associated with social cognition but not with other clinical, functional or cognitive measures.
ISSN:0001-690X
1600-0447
DOI:10.1111/acps.12604