Evidence map›Paper›PMID 42119945›Full record

ArticleBiological psychiatry. Cognitive neuroscience and neuroimaging2026

Hippocampal Total, Subregion, and Subfield Volume Alterations in Late-Life Depression.

Brianca Renfro, Sarah M Szymkowicz, Ke Xu, Kimberly Albert, LaShonda Price, Hakmook Kang, Damian Elson, John Patrick Begnoche, Brian D Boyd, Helmet T Karim and 4 more

Abstract read
In one paragraph

Article in Biological psychiatry. Cognitive neuroscience and neuroimaging, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Brianca RenfroCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
Sarah M SzymkowiczCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: sarah.szymkowicz@vumc.org.
Ke XuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Kimberly AlbertCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
LaShonda PriceCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
Hakmook KangDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Damian ElsonCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
John Patrick BegnocheCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
Brian D BoydCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee.
Helmet T KarimDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
Bennett A LandmanDepartments of Computer Science, Electrical Engineering, and Biomedical Engineering, Vanderbilt University, Nashville, Tennessee; Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Olusola A AjiloreDepartment of Psychiatry, University of Illinois Chicago, Chicago, Illinois.
Carmen AndreescuDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
Warren D TaylorCenter for Cognitive Medicine, Department of Psychiatry and Behavioral Science, Vanderbilt University Medical Center, Nashville, Tennessee; Geriatric Research, Education, and Clinical Center, Veterans Affairs Tennessee Valley Health System, Nashville, Tennessee.

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Expansion of the Dopaminergic Dysfunction in Late-Life Depression Study (The D3 Study)R01MH123662 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TAYLOR, WARREN D · 2020 to 2024
$7.4M
1/3-Recurrence Markers, Cognitive Burden and Neurobiological Homeostasis in Late-life Depression (Rembrandt)R01MH121620 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TAYLOR, WARREN D · 2020 to 2024
$5.3M
Recurrence markers, cognitive burden and neurobiological homeostasis in latelife depression (REMBRANDT) - SupplementR01MH121619 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ANDREESCU, CARMEN · 2020 to 2024
$5.1M
Neural Connectivity Affecting the Antidepressant Response: Testing a Lesion ModelR01MH102246 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TAYLOR, WARREN D · 2015 to 2019
$3.1M
3/3-Recurrence markers, cognitive burden and neurobiological homeostasis in late-life depressionR01MH121384 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI AJILORE, OLUSOLA A. · 2020 to 2024
$3.0M
Nicotinic Modulation of the Cognitive Control System in Late-Life DepressionR33MH122464 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ANDREWS, PATRICIA SERRANO · 2023 to 2025
$2.8M
Nicotinic Modulation of the Cognitive Control System in Late-Life DepressionR61MH122464 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TAYLOR, WARREN D · 2020 to 2021
$1.9M
Frontal hypo perfusion effects on antidepressant outcomes in geriatric depressionR21MH099218 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TAYLOR, WARREN D · 2013 to 2014
$429k
NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1 TR002243NIMH NIH HHS R01 MH102246NIMH NIH HHS R01 MH121384NIMH NIH HHS R01 MH121619NIMH NIH HHS R01 MH121620NIMH NIH HHS R01 MH123662NIMH NIH HHS R21 MH099218NIMH NIH HHS R33 MH122464NIMH NIH HHS R61 MH122464
6 · The paper itself

Abstract

backgroundDespite consistent support for smaller total hippocampal volumes in late-life depression (LLD), there is less consensus on LLD's relationship with hippocampal subregions and subfields. This is particularly relevant for the interactive effects of aging in the context of depression because individuals with LLD may exhibit accelerated aging processes.

methodsWe examined 260 older adults with depression (current and recently remitted) and 140 older adults without depression who completed 3T magnetic resonance imaging, and extracted hippocampal subregion and subfield volumes. Primary analyses investigated the effects of LLD diagnosis, depression status, and age of onset on hippocampal volumes. Secondary analyses evaluated the interactive effects of age and these diagnostic groupings on hippocampal volumes.

resultsCompared with controls, participants with LLD exhibited smaller total hippocampal volumes, with smaller volumes of the bilateral hippocampal head and the right hemisphere body, tail, CA1, and molecular layer. When comparing participants with current and remitted LLD, individuals with current LLD exhibited smaller right total hippocampus, head, body, and molecular layer volumes than controls. They also exhibited smaller CA1, CA2, and CA4/dentate gyrus volumes compared with both control and remitted LLD groups. No regions differed between the control and remitted LLD groups. We did not observe significant group differences in any volume measure between individuals with LLD with an early- or later-life depression onset. There were no significant age-by-diagnostic-group interactions on hippocampal volumes in any analyses.

conclusionsThis cross-sectional work supports diagnostic, but not accelerated aging, effects of depression on hippocampus volumes. In contrast to recently remitted LLD, individuals with current depression exhibited smaller volumes primarily in the right hippocampus.

Indexed as

AgingDepressionDepressive disorderGeriatricHippocampus

Identifiers

PMID42119945
PMCPMC13614850

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