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Anna Plachti

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YNICL Journal 2022 Journal Article

Associations of depression and regional brain structure across the adult lifespan: Pooled analyses of six population-based and two clinical cohort studies in the European Lifebrain consortium

  • Julia Binnewies
  • Laura Nawijn
  • Andreas M. Brandmaier
  • William F.C. Baaré
  • David Bartrés-Faz
  • Christian A. Drevon
  • Sandra Düzel
  • Anders M. Fjell

OBJECTIVE: Major depressive disorder has been associated with lower prefrontal thickness and hippocampal volume, but it is unknown whether this association also holds for depressive symptoms in the general population. We investigated associations of depressive symptoms and depression status with brain structures across population-based and patient-control cohorts, and explored whether these associations are similar over the lifespan and across sexes. METHODS: We included 3,447 participants aged 18-89 years from six population-based and two clinical patient-control cohorts of the European Lifebrain consortium. Cross-sectional meta-analyses using individual person data were performed for associations of depressive symptoms and depression status with FreeSurfer-derived thickness of bilateral rostral anterior cingulate cortex (rACC) and medial orbitofrontal cortex (mOFC), and hippocampal and total grey matter volume (GMV), separately for population-based and clinical cohorts. RESULTS: = -0.25). Effect sizes were slightly larger for presence of moderate-to-severe depression. Associations were similar across age groups and sex. Across population-based cohorts, no associations between depression and brain structures were observed. CONCLUSIONS: Fitting with previous meta-analyses, depressive symptoms and depression status were associated with lower mOFC, rACC thickness, and hippocampal and total grey matter volume in clinical patient-control cohorts, although effect sizes were small. The absence of consistent associations in population-based cohorts with mostly mild depressive symptoms, suggests that significantly lower thickness and volume of the studied brain structures are only detectable in clinical populations with more severe depressive symptoms.

YNIMG Journal 2020 Journal Article

Characterizing the gradients of structural covariance in the human hippocampus

  • Shahrzad Kharabian Masouleh
  • Anna Plachti
  • Felix Hoffstaedter
  • Simon Eickhoff
  • Sarah Genon

The hippocampus is a plastic brain structure that has been associated with a range of behavioral aspects but also shows vulnerability to the most frequent neurocognitive diseases. Different aspects of its organization have been revealed by studies probing its different neurobiological properties. In particular, histological work has shown a pattern of differentiation along the proximal-distal dimension, while studies examining functional properties and large-scale functional integration have primarily highlighted a pattern of differentiation along the anterior-posterior dimension. To better understand how these organizational dimensions underlie the pattern of structural covariance (SC) in the human hippocampus, we here applied a non-linear decomposition approach, disentangling the major modes of variation, to the pattern of gray matter volume correlation of hippocampus voxels with the rest of the brain in a sample of 377 healthy young adults. We additionally investigated the consistency of the derived gradients in an independent sample of life-span adults and also examined the relationships between these major modes of variations and the patterns derived from microstructure and functional connectivity mapping. Our results showed that similar major modes of SC-variability are identified across the two independent datasets. The major dimension of variation found in SC runs along the hippocampal anterior-posterior axis and followed closely the principal dimension of functional differentiation, suggesting an influence of network level interaction in this major mode of morphological variability. The second main mode of variability in the SC showed a gradient along the dorsal-ventral axis, and was moderately related to variability in hippocampal microstructural properties. Thus our results depicting relatively reliable patterns of SC-variability within the hippocampus show an interplay between the already known organizational principles on the pattern of variability in hippocampus' macrostructural properties. This study hence provides a first insight on the underlying organizational forces generating different co-plastic modes within the human hippocampus that may, in turn, help to better understand different vulnerability patterns of this crucial structure in different neurological and psychiatric diseases.

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