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Neuropsychological testing of cognitive impairment in euthymic bipolar disorder: an individual patient data meta-analysis

Bourne, C., Aydemir, Ö., Balanzá-Martínez, V., Bora, E., Brissos, S., Cavanagh, J., Clark, L., Cubukcuoglu, Z., Dias, V., Dittmann, S., Ferrier, I., Fleck, D., Frangou, S., Gallagher, P., Jones, L., Kieseppä, T., Martínez-Aran, A., Melle, I., Moore, P., Mur, M., Pfennig, A., Raust, A., Senturk, V., Simonsen, C., Smith, D., Bio, D., Soeiro-de-Souza, M., Stoddart, S., Sundet, K., Szöke, A., Thompson, J., Torrent, C., Zalla, T., Craddock, Nicholas John, Andreassen, O., Leboyer, M., Vieta, E., Bauer, M., Worhunsky, P., Tzagarakis, C., Rogers, R., Geddes, J. and Goodwin, G. 2013. Neuropsychological testing of cognitive impairment in euthymic bipolar disorder: an individual patient data meta-analysis. Acta Psychiatrica Scandinavica 128 (3) , pp. 149-162. 10.1111/acps.12133

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Objective: An association between bipolar disorder and cognitive impairment has repeatedly been described, even for euthymic patients. Findings are inconsistent both across primary studies and previous meta-analyses. This study reanalysed 31 primary data sets as a single large sample (N = 2876) to provide a more definitive view. Method: Individual patient and control data were obtained from original authors for 11 measures from four common neuropsychological tests: California or Rey Verbal Learning Task (VLT), Trail Making Test (TMT), Digit Span and/or Wisconsin Card Sorting Task. Results: Impairments were found for all 11 test-measures in the bipolar group after controlling for age, IQ and gender (Ps ≤ 0.001, E.S. = 0.26-0.63). Residual mood symptoms confound this result but cannot account for the effect sizes found. Impairments also seem unrelated to drug treatment. Some test-measures were weakly correlated with illness severity measures suggesting that some impairments may track illness progression. Conclusion: This reanalysis supports VLT, Digit Span and TMT as robust measures of cognitive impairments in bipolar disorder patients. The heterogeneity of some test results explains previous differences in meta-analyses. Better controlling for confounds suggests deficits may be smaller than previously reported but should be tracked longitudinally across illness progression and treatment.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Subjects: R Medicine > R Medicine (General)
R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
R Medicine > RZ Other systems of medicine
Uncontrolled Keywords: Adult; Affect; Affective Symptoms; Age of Onset; Bipolar Disorder; Cognition Disorders; Confounding Factors (Epidemiology); Female; Humans; Male; Mental Competency; Mental Processes; Middle Aged; Neuropsychological Tests; Psychiatric Status Rating Scales; Psychotropic Drugs; Risk Factors
Publisher: Wiley-Blackwell
ISSN: 0001-690X
Last Modified: 04 Jun 2017 08:22

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