Dentate gyrus−cornu ammonis (CA) 4 volume is decreased and associated with depressive episodes and lipid peroxidation in bipolar II disorder: Longitudinal and cross‐sectional analyses. (20th December 2016)

• Record Type: Journal Article
• Authors: Elvsåshagen, Torbjørn; Zuzarte, Pedro; Westlye, Lars T; Bøen, Erlend; Josefsen, Dag; Boye, Birgitte; Hol, Per K; Malt, Ulrik F; Young, L Trevor; Andreazza, Ana C
• Is Part Of: Bipolar disorders. Volume 18:Number 8(2016:Dec.)
• Page Start: 657
• Page End: 668
• Publication Date: 2016-12-20
• Subjects: atrophy -- bipolar disorder -- dentate gyrus -- depression -- depressive episode -- hippocampus -- lipid peroxidation -- oxidative stress; Manic-depressive illness -- Periodicals; Depression, Mental -- Periodicals; 616.895
• DOI: 10.1111/bdi.12457
• Languages: English
• ISSNs: 1398-5647

Abstract

Abstract : Objectives: Reduced dentate gyrus volume and increased oxidative stress have emerged as potential pathophysiological mechanisms in bipolar disorder. However, the relationship between dentate gyrus volume and peripheral oxidative stress markers remains unknown. Here, we examined dentate gyrus–cornu ammonis (CA) 4 volume longitudinally in patients with bipolar II disorder (BD‐II) and healthy controls and investigated whether BD‐II is associated with elevated peripheral levels of oxidative stress. Methods: We acquired high‐resolution structural 3T‐magnetic resonance imaging (MRI) images and quantified hippocampal subfield volumes using an automated segmentation algorithm in individuals with BD‐II (n=29) and controls (n=33). The participants were scanned twice, at study inclusion and on average 2.4 years later. In addition, we measured peripheral levels of two lipid peroxidation markers (4‐hydroxy‐2‐nonenal [4‐HNE] and lipid hydroperoxides [LPH]). Results: First, we demonstrated that the automated hippocampal subfield segmentation technique employed in this work reliably measured dentate gyrus–CA4 volume. Second, we found a decreased left dentate gyrus–CA4 volume in patients and that a larger number of depressive episodes between T1 and T2 predicted greater volume decline. Finally, we showed that 4‐HNE was elevated in BD‐II and that 4‐HNE was negatively associated with left and right dentate gyrus–CA4 volumes in patients. Conclusions: These results are consistent with a role for the dentate gyrus in the pathophysiology of bipolar disorder and suggest that depressive episodes and elevated oxidative stress might contribute to hippocampal volume decreases. In addition, these findings provide further support for the hypothesis that peripheral lipid peroxidation markers may reflect brain alterations in bipolar disorders.