Affective episodes in recently diagnosed patients with bipolar disorder associated with altered working memory-related prefrontal cortex activity: A longitudinal fMRI study
Research output: Contribution to journal › Journal article › Research › peer-review
Standard
Affective episodes in recently diagnosed patients with bipolar disorder associated with altered working memory-related prefrontal cortex activity : A longitudinal fMRI study. / Macoveanu, Julian; Kjærstad, Hanne Lie; Vinberg, Maj; Harmer, Catherine; Fisher, Patrick Mac Donald; Knudsen, Gitte Moos; Kessing, Lars Vedel; Miskowiak, Kamilla Woznica.
In: Journal of Affective Disorders, Vol. 295, 2021, p. 647-656.Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Affective episodes in recently diagnosed patients with bipolar disorder associated with altered working memory-related prefrontal cortex activity
T2 - A longitudinal fMRI study
AU - Macoveanu, Julian
AU - Kjærstad, Hanne Lie
AU - Vinberg, Maj
AU - Harmer, Catherine
AU - Fisher, Patrick Mac Donald
AU - Knudsen, Gitte Moos
AU - Kessing, Lars Vedel
AU - Miskowiak, Kamilla Woznica
N1 - Publisher Copyright: © 2021
PY - 2021
Y1 - 2021
N2 - Introduction: Bipolar disorder (BD) is often accompanied by trait-related cognitive impairments, but it is unclear which neurocircuitry abnormalities give rise to these impairments and whether neurocircuitry differences are exacerbated with illness progression. This longitudinal fMRI study of recently diagnosed BD patients investigates whether aberrant working memory (WM) related activity in the cognitive control network is accentuated by new affective episodes. Methods: Forty-seven recently diagnosed BD patients in full or partial remission and 38 healthy controls were assessed with neurocognitive tests and fMRI during the performance of a verbal n-back WM task at baseline and follow-up (15.4 months in average). Results: Patients showed WM-related hypo-activity in dorsal prefrontal cortex (dPFC) and impaired cognitive function within attention and psychomotor speed, WM and executive function, and verbal learning and memory compared to controls at baseline. During the follow-up period, 26 patients experienced at least one affective episode (BD+), while 21 remained in remission (BD-). There was no deterioration in cognitive performance in BD+ compared to BD- patients. Nevertheless, BD+ displayed increased WM-related dPFC activity at follow-up compared with BD- patients. This change in dPFC response was independent of mood symptoms and medication. Limitations: The study did not account for type or frequency of affective episodes. Conclusion: The study identifies cognitive impairment and WM-related hypo-activity in dPFC early during the course of BD. Increased high-load WM related dPFC activity over the follow-up period in BD+ versus BD- patients in the absence of changes in cognitive performance may reflect an episode-related reduction in PFC efficiency.
AB - Introduction: Bipolar disorder (BD) is often accompanied by trait-related cognitive impairments, but it is unclear which neurocircuitry abnormalities give rise to these impairments and whether neurocircuitry differences are exacerbated with illness progression. This longitudinal fMRI study of recently diagnosed BD patients investigates whether aberrant working memory (WM) related activity in the cognitive control network is accentuated by new affective episodes. Methods: Forty-seven recently diagnosed BD patients in full or partial remission and 38 healthy controls were assessed with neurocognitive tests and fMRI during the performance of a verbal n-back WM task at baseline and follow-up (15.4 months in average). Results: Patients showed WM-related hypo-activity in dorsal prefrontal cortex (dPFC) and impaired cognitive function within attention and psychomotor speed, WM and executive function, and verbal learning and memory compared to controls at baseline. During the follow-up period, 26 patients experienced at least one affective episode (BD+), while 21 remained in remission (BD-). There was no deterioration in cognitive performance in BD+ compared to BD- patients. Nevertheless, BD+ displayed increased WM-related dPFC activity at follow-up compared with BD- patients. This change in dPFC response was independent of mood symptoms and medication. Limitations: The study did not account for type or frequency of affective episodes. Conclusion: The study identifies cognitive impairment and WM-related hypo-activity in dPFC early during the course of BD. Increased high-load WM related dPFC activity over the follow-up period in BD+ versus BD- patients in the absence of changes in cognitive performance may reflect an episode-related reduction in PFC efficiency.
KW - Bipolar disorder
KW - Cognitive impairment
KW - fMRI
KW - Prefrontal cortex
KW - Working memory
U2 - 10.1016/j.jad.2021.08.110
DO - 10.1016/j.jad.2021.08.110
M3 - Journal article
C2 - 34509780
AN - SCOPUS:85114685347
VL - 295
SP - 647
EP - 656
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
SN - 0165-0327
ER -
ID: 280127869