Evidence map›Paper›PMID 39107406›Full record

ArticleScientific reports2024

Microstructural brain assessment in late-life depression and apathy using diffusion MRI multi-compartments models and tractometry.

Renaud Hédouin, Jean-Charles Roy, Thomas Desmidt, Gabriel Robert, Julie Coloigner

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Renaud HédouinUniv Rennes, INRIA, CNRS, INSERM, IRISA UMR 6074, Empenn ERL U 1228, 35000, Rennes, France.
Jean-Charles RoyUniv Rennes, INRIA, CNRS, INSERM, IRISA UMR 6074, Empenn ERL U 1228, 35000, Rennes, France.
Thomas DesmidtCHU de Tours, Tours, France.
Gabriel RobertUniv Rennes, INRIA, CNRS, INSERM, IRISA UMR 6074, Empenn ERL U 1228, 35000, Rennes, France.
Julie ColoignerUniv Rennes, INRIA, CNRS, INSERM, IRISA UMR 6074, Empenn ERL U 1228, 35000, Rennes, France. julie.coloigner@irisa.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Late-life depression (LLD) is both common and disabling and doubles the risk of dementia onset. Apathy might constitute an additional risk of cognitive decline but clear understanding of its pathophysiology is lacking. While white matter (WM) alterations have been assessed using diffusion tensor imaging (DTI), this model cannot accurately represent WM microstructure. We hypothesized that a more complex multi-compartment model would provide new biomarkers of LLD and apathy. Fifty-six individuals (LLD n = 35, 26 females, 75.2 ± 6.4 years, apathy evaluation scale scores (41.8 ± 8.7) and Healthy controls, n = 21, 16 females, 74.7 ± 5.2 years) were included. In this article, a tract-based approach was conducted to investigate novel diffusion model biomarkers of LLD and apathy by interpolating microstructural metrics directly along the fiber bundle. We performed multivariate statistical analysis, combined with principal component analysis for dimensional data reduction. We then tested the utility of our framework by demonstrating classically reported from the literature modifications in LDD while reporting new results of biological-basis of apathy in LLD. Finally, we aimed to investigate the relationship between apathy and microstructure in different fiber bundles. Our study suggests that new fiber bundles, such as the striato-premotor tracts, may be involved in LLD and apathy, which bring new light of apathy mechanisms in major depression. We also identified statistical changes in diffusion MRI metrics in 5 different tracts, previously reported in major cognitive disorders dementia, suggesting that these alterations among these tracts are both involved in motivation and cognition and might explain how apathy is a prodromal phase of degenerative disorders.

Indexed as

ApathyBrainDepressionDiffusion Tensor ImagingWhite MatterAgedAged, 80 and overDiffusion Magnetic Resonance ImagingFemaleHumansMaleDiffusion MRILate life depressionMulti-compartment modelsTractometry

Identifiers

PMID39107406
PMCPMC11303796

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.