Evidence map›Paper›PMID 24378256›Full record

ArticleThe American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry2014

Hippocampus atrophy and the longitudinal course of late-life depression.

Warren D Taylor, Douglas R McQuoid, Martha E Payne, Anthony S Zannas, James R MacFall, David C Steffens

Open access · greenAbstract read
In one paragraph

Article in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 4 pooled it
2.1field-weighted citation impact, top 15% 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

72 citing papers in PubMed, 4 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Structural MRI-Based Measures of Accelerated Brain Aging do not Moderate the Acute Antidepressant Response in Late-Life Depression.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2022
    Trial
  7. Article
  8. Article
  9. Hippocampal Total, Subregion, and Subfield Volume Alterations in Late-Life Depression.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
    Article
  10. Synaptic density in the hippocampus of depressed patients: A quantitative electron microscopic study.Progress in neuro-psychopharmacology & biological psychiatry · 2026
    Article
  11. Moderators of treatment response in late-life depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  12. Remission is insufficient: predictors and mechanistic models of recurrence in late-life depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Review
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  18. Article
  19. Article
  20. Effects of Persistent Depression on Recall Memory are Moderated by Subjective Age Levels: Evidence From Community-Dwelling Older Adults.Stress and health : journal of the International Society for the Investigation of Stress · 2025
    Article

12 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 1 country.

Warren D TaylorDepartment of Psychiatry, Vanderbilt University Medical Center, Nashville, TN. Electronic address: warren.d.taylor@vanderbilt.edu.
Douglas R McQuoidDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC.
Martha E PayneDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC.
Anthony S ZannasDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC.
James R MacFallDepartment of Radiology, Duke University Medical Center, Durham, NC.
David C SteffensDepartment of Psychiatry, University of Connecticut Health Center, Farmington, CT.
Duke Medical Center · USDuke University Hospital · USUConn Health · USVanderbilt University Medical Center · US

Funding

Recruitment and Assessment Core Patient RecruitmentP50MH060451 · NIMH · DUKE UNIVERSITY · PI MCCARTHY, GREGORY E · 2001 to 2010
$22.3M
Geriatric Depression: Risk Factors for Adverse OutcomesR01MH054846 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI STEFFENS, DAVID C. · 1995 to 2016
$10.1M
Genes and Alterations in Brain Structure and Function in DepressionR01MH077745 · NIMH · VANDERBILT UNIVERSITY · PI TAYLOR, WARREN D · 2008 to 2012
$2.6M
Midcareer Investigator Award in Geriatric DepressionK24MH070027 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI STEFFENS, DAVID C. · 2004 to 2013
$1.6M
NIMH NIH HHS K24 MH070027NIMH NIH HHS P50 MH060451NIMH NIH HHS P50 MH60451NIMH NIH HHS R01 MH054846NIMH NIH HHS R01 MH077745
6 · The paper itself

Abstract

objectivesSmaller hippocampal volumes are observed in depression but it remains unclear how antidepressant response and persistent depression relate to changes in hippocampal volume. We examined the longitudinal relationship between hippocampal atrophy and course of late-life depression.

settingAcademic medical center.

participantsDepressed and never-depressed cognitively intact subjects age 60 years or older. MEASUREMENTS: Depression severity was measured every three months with the Montgomery-Asberg Depression Rating Scale (MADRS). Participants also completed cranial 1.5-T magnetic resonance imaging every 2 years. We compared 2-year change in hippocampal volume based on remission status, then in expanded analyses examined how hippocampal volumes predicted MADRS score.

resultsIn analyses of 92 depressed and 70 never-depressed subjects, over 2 years the cohort whose depression never remitted exhibited greater hippocampal atrophy than the never-depressed cohort. In expanded analyses of a broader sample of 152 depressed elders, depression severity was significantly predicted by a hippocampus × time interaction where smaller hippocampus volumes over time were associated with greater depression severity.

conclusionsHippocampal atrophy is associated with greater and persistent depression severity. Neuropathological studies are needed to determine if this atrophy is related to the toxic effects of persistent depression or related to underlying Alzheimer disease.

Indexed as

Disease ProgressionAgedAged, 80 and overAntidepressive AgentsAtrophyFemaleHippocampusHumansLongitudinal StudiesMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedRecurrenceRemission InductionSeverity of Illness IndexAntidepressive AgentsdepressionGeriatricshippocampuslongitudinalMRIneuroimaging

Identifiers

PMID24378256
PMCPMC4031313
OpenAlexW2013004783

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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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.