Basolateral amygdala volume in affective disorders using 7T MRI in vivo

BackgroundThe basolateral complex of the amygdala is a crucial neurobiological site for Pavlovian conditioning. Investigations into volumetric alterations of the basolateral amygdala in individuals with major depressive disorder (MDD) have yielded conflicting results. These may be reconciled in an i...

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Main Authors: Benedikt Kürzinger, Stephanie Schindler, Martin Meffert, Anja Rosenhahn, Robert Trampel, Robert Turner, Peter Schoenknecht
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Psychiatry
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Online Access:https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1404594/full
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author Benedikt Kürzinger
Stephanie Schindler
Martin Meffert
Anja Rosenhahn
Robert Trampel
Robert Turner
Peter Schoenknecht
Peter Schoenknecht
Peter Schoenknecht
author_facet Benedikt Kürzinger
Stephanie Schindler
Martin Meffert
Anja Rosenhahn
Robert Trampel
Robert Turner
Peter Schoenknecht
Peter Schoenknecht
Peter Schoenknecht
author_sort Benedikt Kürzinger
collection DOAJ
description BackgroundThe basolateral complex of the amygdala is a crucial neurobiological site for Pavlovian conditioning. Investigations into volumetric alterations of the basolateral amygdala in individuals with major depressive disorder (MDD) have yielded conflicting results. These may be reconciled in an inverted U-shape allostatic growth trajectory. This hypothesized trajectory unfolds with an initial phase of volumetric expansion, driven by enhanced dendritic arborization and synaptic plasticity. The increase in volume is followed by a reduction phase, as glucocorticoid exposure cumulatively results in excitotoxic damage, reflecting allostatic load.Methods7T magnetic resonance brain imaging was conducted on a total of 84 participants (mean age 38 ± 12 years), comprising 20 unmedicated and 20 medicated individuals with MDD, 21 individuals suffering from bipolar disorder and 23 healthy controls. We employed FreeSurfer 7.3.2 for automatic high-resolution segmentation of nine amygdala subnuclei. We conducted analyses of covariance, with volumes of the basolateral complex, the lateral nucleus and, exploratively, the whole amygdala, as dependent variables, while controlling for the total intracranial volume and sex. Quadratic regressions were computed within the MDD group and in relevant subgroups to investigate the presence of a U-shaped relationship between the number of preceding major depressive episodes or the duration of the disease since the first episode and the dependent variables.ResultsDiagnostic groups did not exhibit statistically significant differences in the volumes of the basolateral amygdala (left F (3,75) = 0.66, p >.05; right F (3,76) = 1.80, p >.05), the lateral nucleus (left F (3,75) = 1.22, p >.05; right F (3,76) = 2.30, p >.05)), or the whole amygdala (left F (3,75) = 0.48, p >.05; right F (3,76) = 1.58, p >.05). No quadratic associations were observed between surrogate parameters of disease progression and any of the examined amygdala volumes. There were no significant correlations between subregion volumes and clinical characteristics.ConclusionWe found no evidence for the hypothesis of an inverted U-shaped volumetric trajectory of the basolateral amygdala in MDD. Future research with larger sample sizes, including the measurement of genetic and epigenetic markers, will hopefully further elucidate this compelling paradigm.
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spelling doaj-art-791b832bda024ea5a604613cf4a119ed2025-08-20T02:53:51ZengFrontiers Media S.A.Frontiers in Psychiatry1664-06402025-01-011510.3389/fpsyt.2024.14045941404594Basolateral amygdala volume in affective disorders using 7T MRI in vivoBenedikt Kürzinger0Stephanie Schindler1Martin Meffert2Anja Rosenhahn3Robert Trampel4Robert Turner5Peter Schoenknecht6Peter Schoenknecht7Peter Schoenknecht8Department of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, GermanyDepartment of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, GermanyDepartment of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, GermanyDepartment of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, GermanyDepartment of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, GermanyDepartment of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, GermanyDepartment of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, GermanyOut-patient Department for Sexual-therapeutic Prevention and Forensic Psychiatry, University Hospital Leipzig, Leipzig, GermanyDepartment of Psychiatry, Psychotherapy and Psychosomatic, Saxon State Hospital Altscherbitz, Schkeuditz, GermanyBackgroundThe basolateral complex of the amygdala is a crucial neurobiological site for Pavlovian conditioning. Investigations into volumetric alterations of the basolateral amygdala in individuals with major depressive disorder (MDD) have yielded conflicting results. These may be reconciled in an inverted U-shape allostatic growth trajectory. This hypothesized trajectory unfolds with an initial phase of volumetric expansion, driven by enhanced dendritic arborization and synaptic plasticity. The increase in volume is followed by a reduction phase, as glucocorticoid exposure cumulatively results in excitotoxic damage, reflecting allostatic load.Methods7T magnetic resonance brain imaging was conducted on a total of 84 participants (mean age 38 ± 12 years), comprising 20 unmedicated and 20 medicated individuals with MDD, 21 individuals suffering from bipolar disorder and 23 healthy controls. We employed FreeSurfer 7.3.2 for automatic high-resolution segmentation of nine amygdala subnuclei. We conducted analyses of covariance, with volumes of the basolateral complex, the lateral nucleus and, exploratively, the whole amygdala, as dependent variables, while controlling for the total intracranial volume and sex. Quadratic regressions were computed within the MDD group and in relevant subgroups to investigate the presence of a U-shaped relationship between the number of preceding major depressive episodes or the duration of the disease since the first episode and the dependent variables.ResultsDiagnostic groups did not exhibit statistically significant differences in the volumes of the basolateral amygdala (left F (3,75) = 0.66, p >.05; right F (3,76) = 1.80, p >.05), the lateral nucleus (left F (3,75) = 1.22, p >.05; right F (3,76) = 2.30, p >.05)), or the whole amygdala (left F (3,75) = 0.48, p >.05; right F (3,76) = 1.58, p >.05). No quadratic associations were observed between surrogate parameters of disease progression and any of the examined amygdala volumes. There were no significant correlations between subregion volumes and clinical characteristics.ConclusionWe found no evidence for the hypothesis of an inverted U-shaped volumetric trajectory of the basolateral amygdala in MDD. Future research with larger sample sizes, including the measurement of genetic and epigenetic markers, will hopefully further elucidate this compelling paradigm.https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1404594/fullamygdalabasolateral amygdalavolumemajor depressive disorderFreeSurferBLA
spellingShingle Benedikt Kürzinger
Stephanie Schindler
Martin Meffert
Anja Rosenhahn
Robert Trampel
Robert Turner
Peter Schoenknecht
Peter Schoenknecht
Peter Schoenknecht
Basolateral amygdala volume in affective disorders using 7T MRI in vivo
Frontiers in Psychiatry
amygdala
basolateral amygdala
volume
major depressive disorder
FreeSurfer
BLA
title Basolateral amygdala volume in affective disorders using 7T MRI in vivo
title_full Basolateral amygdala volume in affective disorders using 7T MRI in vivo
title_fullStr Basolateral amygdala volume in affective disorders using 7T MRI in vivo
title_full_unstemmed Basolateral amygdala volume in affective disorders using 7T MRI in vivo
title_short Basolateral amygdala volume in affective disorders using 7T MRI in vivo
title_sort basolateral amygdala volume in affective disorders using 7t mri in vivo
topic amygdala
basolateral amygdala
volume
major depressive disorder
FreeSurfer
BLA
url https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1404594/full
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