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Normal Cerebral Oxygen Consumption Despite Elevated Cerebral Blood Flow in Adolescents With Bipolar Disorder: Putative Neuroimaging Evidence of Anomalous Energy Metabolism

Background: Regional cerebral blood flow (CBF) is reportedly altered in both adolescents and adults with bipolar disorder (BD). Whether these CBF differences are part of an overall imbalance in cerebral energy homeostasis remains unknown. Therefore, we examined global cerebral metabolic rate of oxyg...

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Detalles Bibliográficos
Autores principales: Karthikeyan, Sudhir, Fiksenbaum, Lisa, Grigorian, Anahit, Lu, Hanzhang, MacIntosh, Bradley J., Goldstein, Benjamin I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798187/
https://www.ncbi.nlm.nih.gov/pubmed/31681045
http://dx.doi.org/10.3389/fpsyt.2019.00739
Descripción
Sumario:Background: Regional cerebral blood flow (CBF) is reportedly altered in both adolescents and adults with bipolar disorder (BD). Whether these CBF differences are part of an overall imbalance in cerebral energy homeostasis remains unknown. Therefore, we examined global cerebral metabolic rate of oxygen consumption (CMRO(2)) as a physiological index of brain metabolism in adolescents with and without BD. Methods: One hundred and fifteen adolescents (mean age 17.3 ± 1.4 years), including 58 BD (type I, II, or not otherwise specified [NOS]) and 57 age-matched healthy controls (HCs) participated in this magnetic resonance imaging (MRI) study. Global estimates for venous blood oxygenation (Y(v)) and grey matter CBF were measured using T2-relaxation-under-spin-tagging (TRUST) and arterial spin labeling (ASL) MRI, respectively. CMRO(2) was calculated using the Fick principle of arteriovenous difference to test for a group difference. We also examined CMRO(2) in relation to mood states (i.e. euthymic, depressed, or hypomanic/mixed). Results: Although CBF was significantly higher in BD compared to HCs, there was no group difference in global CMRO(2), nor Y(v). Meanwhile, Y(v) significantly decreased with age, and females tended to have greater CBF and CMRO(2) in comparison to males. Lastly, there was no significant association between CMRO(2) and mood states. Conclusions: Our results indicate a potential mismatch between cerebral blood supply and oxygen metabolism in BD, suggesting inefficiency in energy homeostasis in the brain. Mapping CMRO(2) would provide the spatial resolution to investigate regional alterations in metabolism, particularly in the brain regions where CBF is increased.