Literature DB >> 22854099

Bipolar depressed patients show both failure to activate and failure to de-activate during performance of a working memory task.

Paloma Fernández-Corcuera1, Raymond Salvador, Gemma C Monté, S Salvador Sarró, José M Goikolea, Benedikt Amann, Noemí Moro, Bibiana Sans-Sansa, Jordi Ortiz-Gil, Eduard Vieta, Teresa Maristany, Peter J McKenna, Edith Pomarol-Clotet.   

Abstract

BACKGROUND: Bipolar depression has been found to be associated with changes in prefrontal cortex activity during performance of cognitive tasks. However, the role of task-related de-activations has been little investigated.
METHOD: Forty-one bipolar depressed patients and 41 matched normal controls underwent fMRI scanning while performing baseline, 1-back and 2-back versions of the n-back task. Linear models were used to obtain maps of within-group activations and areas of differential activation between the groups.
RESULTS: The bipolar depressed patients showed reduced activation in the dorsolateral prefrontal cortex (DLPFC) bilaterally and several other regions. After controlling for differences in task performance only differences in the DLPFC and cerebellum remained. Left DLPFC activation was inversely correlated with Hamilton and MADRS scores. The patients showed failure to de-activate in the medial prefrontal cortex, an area corresponding to the anterior medial node of the default mode network. LIMITATIONS: To confirm default mode network dysfunction demonstration of resting-state connectivity abnormalities would also be required. The study was carried out on treated patients, and did not assess for presence of depressive symptoms in the healthy controls.
CONCLUSIONS: Both prefrontal cortical and default mode network dysfunction appear to characterise bipolar depression. The former, but not the latter, is associated with symptom severity.
Copyright © 2012 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 22854099     DOI: 10.1016/j.jad.2012.04.009

Source DB:  PubMed          Journal:  J Affect Disord        ISSN: 0165-0327            Impact factor:   4.839


  27 in total

1.  Neurofunctional Correlates of Response to Quetiapine in Adolescents with Bipolar Depression.

Authors:  Kiki Chang; Melissa DelBello; Amy Garrett; Ryan Kelley; Meghan Howe; Cal Adler; Jeffrey Welge; Stephen M Strakowski; Manpreet Singh
Journal:  J Child Adolesc Psychopharmacol       Date:  2018-05-30       Impact factor: 2.576

2.  Prefrontal hypoactivation during working memory in bipolar II depression.

Authors:  J O Brooks; N Vizueta; C Penfold; J D Townsend; S Y Bookheimer; L L Altshuler
Journal:  Psychol Med       Date:  2015-03-10       Impact factor: 7.723

3.  Investigating brain community structure abnormalities in bipolar disorder using path length associated community estimation.

Authors:  Johnson J Gadelkarim; Olusola Ajilore; Dan Schonfeld; Liang Zhan; Paul M Thompson; Jamie D Feusner; Anand Kumar; Lori L Altshuler; Alex D Leow
Journal:  Hum Brain Mapp       Date:  2013-06-25       Impact factor: 5.038

4.  Multimodal Brain Changes in First-Episode Mania: A Voxel-Based Morphometry, Functional Magnetic Resonance Imaging, and Connectivity Study.

Authors:  José M Goikolea; Danai Dima; Ramón Landín-Romero; Imma Torres; Giuseppe DelVecchio; Marc Valentí; Benedikt L Amann; Caterina Mar Bonnín; Peter J McKenna; Edith Pomarol-Clotet; Sophia Frangou; Eduard Vieta
Journal:  Schizophr Bull       Date:  2019-03-07       Impact factor: 9.306

5.  Exposure to childhood trauma is associated with altered n-back activation and performance in healthy adults: implications for a commonly used working memory task.

Authors:  Noah S Philip; Lawrence H Sweet; Audrey R Tyrka; S Louisa Carpenter; Sarah E Albright; Lawrence H Price; Linda L Carpenter
Journal:  Brain Imaging Behav       Date:  2016-03       Impact factor: 3.978

6.  Increased neural activity during overt and continuous semantic verbal fluency in major depression: mainly a failure to deactivate.

Authors:  Heidelore Backes; Bruno Dietsche; Arne Nagels; Mirjam Stratmann; Carsten Konrad; Tilo Kircher; Axel Krug
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2014-02-21       Impact factor: 5.270

7.  Differentiating unipolar and bipolar depression by alterations in large-scale brain networks.

Authors:  Roberto Goya-Maldonado; Katja Brodmann; Maria Keil; Sarah Trost; Peter Dechent; Oliver Gruber
Journal:  Hum Brain Mapp       Date:  2015-11-27       Impact factor: 5.038

Review 8.  Defining biotypes for depression and anxiety based on large-scale circuit dysfunction: a theoretical review of the evidence and future directions for clinical translation.

Authors:  Leanne M Williams
Journal:  Depress Anxiety       Date:  2016-09-21       Impact factor: 6.505

9.  Impact of BDNF and sex on maintaining intact memory function in early midlife.

Authors:  Kyoko Konishi; Sara Cherkerzian; Sarah Aroner; Emily G Jacobs; Dorene M Rentz; Anne Remington; Harlyn Aizley; Mady Hornig; Anne Klibanski; Jill M Goldstein
Journal:  Neurobiol Aging       Date:  2019-12-24       Impact factor: 4.673

10.  A genome-wide supported psychiatric risk variant in NCAN influences brain function and cognitive performance in healthy subjects.

Authors:  Heidelore Raum; Bruno Dietsche; Arne Nagels; Stephanie H Witt; Marcella Rietschel; Tilo Kircher; Axel Krug
Journal:  Hum Brain Mapp       Date:  2014-09-13       Impact factor: 5.038

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.