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  Vascular risk factors, white matter microstructure, and depressive symptoms: A longitudinal analysis in the UK Biobank

Blöchl, M., Schaare, H. L., Kumral, D., Gaebler, M., Nestler, S., & Villringer, A. (2023). Vascular risk factors, white matter microstructure, and depressive symptoms: A longitudinal analysis in the UK Biobank. Psychological Medicine, 54(1), 125-135. doi:10.1017/S0033291723000697.

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 Creators:
Blöchl, Maria1, 2, 3, Author                 
Schaare, Herma Lina4, 5, Author                 
Kumral, Deniz6, 7, Author                 
Gaebler, Michael1, 8, 9, Author                 
Nestler, Steffen3, Author
Villringer, Arno1, 10, 11, Author                 
Affiliations:
1Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              
2International Max Planck Research School on Neuroscience of Communication: Function, Structure, and Plasticity, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_2616696              
3Department of Psychology, Münster University, Germany, ou_persistent22              
4Otto Hahn Group Cognitive Neurogenetics, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_3222264              
5Institute of Neuroscience and Medicine, Research Center Jülich, Germany, ou_persistent22              
6Department of Psychology, Albert Ludwigs University Freiburg, Germany, ou_persistent22              
7Department of Clinical Psychology and Psychotherapy, Albert Ludwigs University Freiburg, Germany, ou_persistent22              
8MindBrainBody Institute, Berlin School of Mind and Brain, Humboldt University Berlin, Germany, ou_persistent22              
9Max Planck Dahlem Campus of Cognition (MPDCC), Berlin, Germany, ou_persistent22              
10Clinic for Cognitive Neurology, University of Leipzig, Germany, ou_persistent22              
11Center for Stroke Research, Charité University Medicine Berlin, Germany, ou_persistent22              

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Free keywords: UK Biobank; Depression; Mediation; Vascular depression; Vascular risk factors; White matter
 Abstract: Background: Cumulative burden from vascular risk factors (VRFs) has been associated with an increased risk of depressive symptoms in mid- and later life. It has been hypothesised that this association arises because VRFs disconnect fronto-subcortical white matter tracts involved in mood regulation, which puts older adults at higher risk of developing depressive symptoms. However, evidence for the hypothesis that disconnection of white matter tracts underlies the association between VRF burden and depressive symptoms from longitudinal studies is scarce.

Methods: This preregistered study analysed longitudinal data from 6,964 middle-aged and older adults from the UK Biobank who participated in consecutive assessments of VRFs, brain imaging, and depressive symptoms. Using mediation modelling, we directly tested to what extend white matter microstructure mediates the longitudinal association between VRF burden and depressive symptoms.

Results: VRF burden showed a small association with depressive symptoms at follow-up. However, there was no evidence that fractional anisotropy (FA) of white matter tracts mediated this association. Additional analyses also yielded no mediating effects using alternative operationalisations of VRF burden, mean diffusivity (MD) of single tracts, or overall average of tract-based white matter microstructure (global FA, global MD, white matter hyperintensity volume).

Conclusions: Our results lend no support to the hypothesis that disconnection of white matter tracts underlies the association between VRF burden and depressive symptoms, while highlighting the relevance of using longitudinal data to directly test pathways linking vascular and mental health.

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Language(s): eng - English
 Dates: 2023-04-052023-04-05
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1017/S0033291723000697
Other: epub 2023
PMID: 37016768
 Degree: -

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Title: Psychological Medicine
Source Genre: Journal
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Publ. Info: Cambridge, England : Cambridge University Press
Pages: - Volume / Issue: 54 (1) Sequence Number: - Start / End Page: 125 - 135 Identifier: ISSN: 0033-2917
CoNE: https://pure.mpg.de/cone/journals/resource/954927634419