Differential engagement of cognitive and affective neural systems in pediatric bipolar disorder and attention deficit hyperactivity disorder

This fMRI study investigates the neural bases of cognitive control of emotion processing in pediatric bipolar disorder (PBD) and attention deficit hyperactivity disorder (ADHD). Seventeen un-medicated PBD patients, 15 un-medicated ADHD patients, and 14 healthy controls (HC) (mean age = 13.78 ± 2.47)...

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Published inJournal of the International Neuropsychological Society Vol. 16; no. 1; pp. 106 - 117
Main Authors PASSAROTTI, ALESSANDRA M., SWEENEY, JOHN A., PAVULURI, MANI N.
Format Journal Article
LanguageEnglish
Published New York, USA Cambridge University Press 01.01.2010
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Summary:This fMRI study investigates the neural bases of cognitive control of emotion processing in pediatric bipolar disorder (PBD) and attention deficit hyperactivity disorder (ADHD). Seventeen un-medicated PBD patients, 15 un-medicated ADHD patients, and 14 healthy controls (HC) (mean age = 13.78 ± 2.47) performed an emotional valence Stroop Task, requiring them to match the color of an emotionally valenced word to the color of either of two adjacent circles. Both patient groups responded significantly slower than HC, but there were no group differences in accuracy. A voxel-wise analysis of variance on brain activation revealed a significant interaction of group by word valence [F(2,41) = 4.44; p = .02]. Similar group differences were found for negative and positive words. For negative versus neutral words, both patient groups exhibited greater activation in dorsolateral prefrontal cortex (DLPFC) and parietal cortex relative to HC. The PBD group exhibited greater activation in ventrolateral prefrontal cortex (VLPFC) and anterior cingulate cortex (ACC) relative to HC. The ADHD group exhibited decreased VLPFC activation relative to HC and the PBD group. During cognitive control of emotion processing, PBD patients deployed the VLPFC to a greater extent than HC. The ADHD patients showed decreased VLPFC engagement relative to both HC and PBD patients. (JINS, 2010, 16, 106–117.)
Bibliography:ark:/67375/6GQ-FGKBQS9V-Z
istex:8778A1B4F7DBBD0662DD0AF6DDD56372AA36339B
Dr. Passarotti has no financial relationships to disclose. Dr. Pavuluri’s work unrelated to this manuscript is supported by NARSAD Independent Investigator Award, NICHD, GlaxoSmithKline-NeuroHealth, Abbott Pharmaceuticals, and Janssen Research Foundation. Dr. Sweeney, also unrelated to this work, has received support from NIH, GlaxoSmithKline, AstraZeneca, Janssen and Eli Lilly.
PII:S1355617709991019
ArticleID:99101
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ISSN:1355-6177
1469-7661
DOI:10.1017/S1355617709991019