cognitive vulnerability indicators in bipolar disorder and schizophrenia

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BioMed Central Page 1 of 1 (page number not for citation purposes) Annals of General Psychiatry Open Access Poster presentation Cognitive vulnerability indicators in bipolar disorder and schizophrenia Tessa Christodoulou* 1 , Michael Hadjulis 1 , Jigar Jogia 1 , Sam J Gilbert 2 , Sophia Frangou 1 and Paul W Burgess 2 Address: 1 Section of Neurobiology of Psychosis, Department of Psychological Medicine, Institute of Psychiatry King's College London, UK and 2 Institute of Cognitive Neuroscience, University College London, UK * Corresponding author Background The aim of this project was to investigate the cognitive abnormalities in healthy individuals (No Axis I or II dis- orders) at high risk for bipolar disorder (BD) and schizo- phrenia (SZ). Materials and methods Participants were 17 BD and 15 SZ relatives (BD-R and SZ- R) respectively and 23 controls. All participants under- went assessment of Full Scale IQ (Wechsler Adult Intelli- gence Scale Revised, WAIS-R), verbal memory and learning (California Verbal Learning test, CVLT), working memory (N-back), inhibition (Hayling Sentence Comple- tion Task, HSCT), verbal fluency (Controlled Oral Word Association, COWA), working memory and inhibition (alphabet and number words tasks). Lack of lifetime Axis I and II disorders was screened using Structured Clinical Interview for DSM-IV (SCID-I/II) and symptomatology was assessed with the Hamilton Depression Rating Scale (HDRS), Young Mania Rating Scale (YMRS) and Brief Psy- chiatric Rating Scale (BPRS). Results No difference was found in the WAIS-R. Loss of inhibition was found for both relatives' groups compared to controls (HSCT). BD-R and SZ-R underperformed compared to controls in short and long delay recall in the CVLT (CVLT) whereas SZ-R made additionally more intrusions and per- severations. SZ-R and BD-R produced fewer words com- pared to controls whereas the former group also made more errors (COWA). The SZ-R had fewer total correct responses overall and in the 3-back condition. In Alpha- bet and number words tasks the SZ-R failed to inhibit rel- atively fast erroneous responses, leading to an effect on error rates but not in reaction times. Effect of BPRS total score was found only for BD-R across all measures apart from the HSCT. Conclusions Genetic predisposition to SZ may be mediated by deficits in the Ventral Prefrontal Cortex (VPFC), Dorsal Prefrontal Cortex (DPFC) and temporal networks. In BD-R impair- ment was limited in the VPFC whereas the DPFC function was preserved. The two disorders share inhibition deficits associated with the VPFC. Acknowledgements To Professors Sophia Frangou and Paul W Burgess. from International Society on Brain and Behaviour: 3rd International Congress on Brain and Behaviour Thessaloniki, Greece. 28 November – 2 December 2007 Published: 17 April 2008 Annals of General Psychiatry 2008, 7(Suppl 1):S271 doi:10.1186/1744-859X-7-S1-S271 <supplement> <title> <p>International Society on Brain and Behaviour: 3rd International Congress on Brain and Behaviour</p> </title> <note>Meeting abstracts - A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1744-859X-7-S1-full.pdf">here</a>.</note> </supplement> This abstract is available from: http://www.annals-general-psychiatry.com/content/7/S1/S271 © 2008 Christodoulou et al.; licensee BioMed Central Ltd.

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Page 1: Cognitive vulnerability indicators in bipolar disorder and schizophrenia

BioMed Central

Page 1 of 1(page number not for citation purposes)

Annals of General Psychiatry

Open AccessPoster presentationCognitive vulnerability indicators in bipolar disorder and schizophreniaTessa Christodoulou*1, Michael Hadjulis1, Jigar Jogia1, Sam J Gilbert2, Sophia Frangou1 and Paul W Burgess2

Address: 1Section of Neurobiology of Psychosis, Department of Psychological Medicine, Institute of Psychiatry King's College London, UK and 2Institute of Cognitive Neuroscience, University College London, UK

* Corresponding author

BackgroundThe aim of this project was to investigate the cognitiveabnormalities in healthy individuals (No Axis I or II dis-orders) at high risk for bipolar disorder (BD) and schizo-phrenia (SZ).

Materials and methodsParticipants were 17 BD and 15 SZ relatives (BD-R and SZ-R) respectively and 23 controls. All participants under-went assessment of Full Scale IQ (Wechsler Adult Intelli-gence Scale Revised, WAIS-R), verbal memory andlearning (California Verbal Learning test, CVLT), workingmemory (N-back), inhibition (Hayling Sentence Comple-tion Task, HSCT), verbal fluency (Controlled Oral WordAssociation, COWA), working memory and inhibition(alphabet and number words tasks). Lack of lifetime AxisI and II disorders was screened using Structured ClinicalInterview for DSM-IV (SCID-I/II) and symptomatologywas assessed with the Hamilton Depression Rating Scale(HDRS), Young Mania Rating Scale (YMRS) and Brief Psy-chiatric Rating Scale (BPRS).

ResultsNo difference was found in the WAIS-R. Loss of inhibitionwas found for both relatives' groups compared to controls(HSCT). BD-R and SZ-R underperformed compared tocontrols in short and long delay recall in the CVLT (CVLT)whereas SZ-R made additionally more intrusions and per-severations. SZ-R and BD-R produced fewer words com-

pared to controls whereas the former group also mademore errors (COWA). The SZ-R had fewer total correctresponses overall and in the 3-back condition. In Alpha-bet and number words tasks the SZ-R failed to inhibit rel-atively fast erroneous responses, leading to an effect onerror rates but not in reaction times. Effect of BPRS totalscore was found only for BD-R across all measures apartfrom the HSCT.

ConclusionsGenetic predisposition to SZ may be mediated by deficitsin the Ventral Prefrontal Cortex (VPFC), Dorsal PrefrontalCortex (DPFC) and temporal networks. In BD-R impair-ment was limited in the VPFC whereas the DPFC functionwas preserved. The two disorders share inhibition deficitsassociated with the VPFC.

AcknowledgementsTo Professors Sophia Frangou and Paul W Burgess.

from International Society on Brain and Behaviour: 3rd International Congress on Brain and BehaviourThessaloniki, Greece. 28 November – 2 December 2007

Published: 17 April 2008

Annals of General Psychiatry 2008, 7(Suppl 1):S271 doi:10.1186/1744-859X-7-S1-S271

<supplement> <title> <p>International Society on Brain and Behaviour: 3rd International Congress on Brain and Behaviour</p> </title> <note>Meeting abstracts - A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1744-859X-7-S1-full.pdf">here</a>.</note> </supplement>

This abstract is available from: http://www.annals-general-psychiatry.com/content/7/S1/S271

© 2008 Christodoulou et al.; licensee BioMed Central Ltd.