Evidence map›Paper›PMID 36803400›Full record

ArticleInternational psychogeriatrics2023

Neuroimaging features of depression-frailty phenotype in older adults: a pilot study.

Ethan Shuster, Amy E Miles, Lindsay K Heyland, Navona Calarco, Jerrold Jeyachandra, Salim Mansour, Aristotle N Voineskos, David C Steffens, Yuliya S Nikolova, Breno S Diniz

Open access · diamondAbstract read
In one paragraph

Article in International psychogeriatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Ethan ShusterUConn Center on Aging, University of Connecticut School of Medicine, Farmington, CT, USA.
Amy E MilesCentre for Addiction and Mental Health, Toronto, ON, Canada.
Lindsay K HeylandCentre for Addiction and Mental Health, Toronto, ON, Canada.
Navona CalarcoCentre for Addiction and Mental Health, Toronto, ON, Canada.
Jerrold JeyachandraCentre for Addiction and Mental Health, Toronto, ON, Canada.
Salim MansourCentre for Addiction and Mental Health, Toronto, ON, Canada.
Aristotle N VoineskosCentre for Addiction and Mental Health, Toronto, ON, Canada.
David C SteffensDepartment of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.ORCID 0000-0001-6626-7398
Yuliya S NikolovaCentre for Addiction and Mental Health, Toronto, ON, Canada.
Breno S DinizUConn Center on Aging, University of Connecticut School of Medicine, Farmington, CT, USA.ORCID 0000-0003-0653-1905
Centre for Addiction and Mental Health · CAUniversity of Connecticut · USUConn Health · US

Funding

THE SENDEP STUDY: LINKING MOLECULAR SENESCENCE CHANGES TO DEPRESSION AND COGNITIVE IMPAIRMENT IN LATE LIFER01MH115953 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI DINIZ, BRENO SATLER · 2019 to 2023
$3.0M
NIMH NIH HHS R01 MH115953
6 · The paper itself

Abstract

objectiveFrailty and late-life depression (LLD) often coexist and share several structural brain changes. We aimed to study the joint effect LLD and frailty have on brain structure.

designCross-sectional study.

settingAcademic Health Center.

participantsThirty-one participants (14 LLD+Frail and 17 Never-depressed+Robust). MEASUREMENT: LLD was diagnosed by a geriatric psychiatrist according to the Diagnostic and Statistical Manual of Mental Disorders 5th edition for single episode or recurrent major depressive disorder without psychotic features. Frailty was assessed using the FRAIL scale (0-5), classifying subjects as robust (0), prefrail (1-2), and frail (3-5). Participants underwent T1-weighted magnetic resonance imaging in which covariance analysis of subcortical volumes and vertex-wise analysis of cortical thickness values were performed to access changes in grey matter. Participants also underwent diffusion tensor imaging in which tract-based spatial statistics was used with voxel-wise statistical analysis on fractional anisotropy and mean diffusion values to assess changes in white matter (WM).

resultsWe found a significant difference in mean diffusion values (48,225 voxels; peak voxel: pFWER=0.005, MINI coord. (X,Y,Z) = -26,-11,27) between the LLD-Frail group and comparison group. The corresponding effect size (f=0.808) was large.

conclusionWe showed the LLD+Frailty group is associated with significant microstructural changes within WM tracts compared to Never-depressed+Robust individuals. Our findings indicate the possibility of a heightened neuroinflammatory burden as a potential mechanism underlying the co-occurrence of both conditions and the possibility of a depression-frailty phenotype in older adults.

Indexed as

FrailtyMajor Depressive DisorderAgedCross-Sectional StudiesDepressionDiffusion Tensor ImagingHumansNeuroimagingPilot ProjectsDiffusion Tensor ImagingFrailtyLate-life depression

Identifiers

PMID36803400
PMCPMC10439968
OpenAlexW4321374603

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.