Evidence map›Paper›PMID 26982217›Full record

ArticleJAMA psychiatry2016

Trajectories of Depressive Symptoms in Older Adults and Risk of Dementia.

Allison R Kaup, Amy L Byers, Cherie Falvey, Eleanor M Simonsick, Suzanne Satterfield, Hilsa N Ayonayon, Stephen F Smagula, Susan M Rubin, Kristine Yaffe

2 registry-linked trialsAbstract read
In one paragraph

Article in JAMA psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT03550144 nacompletednot on this map

Effects of Awe on Mental Health and Well-Being

TypeinterventionalSponsorUniversity of California, San FranciscoRan2016 to 2018Enrolled60ConditionsAwe, Compassion, AnxietyArmsAwe Walk, Control Walk
NCT06914284 recruitingnot on this mapstarted 2024, after this paper: background citation

Apathy-related Neurobehavioral Markers of Cognitive Decline in Old-age Bipolar Disorders: Proof-of-concept

TypeobservationalSponsorHospital Center Guillaume RégnierRan2024 to 2029Enrolled30ConditionsApathy, Bipolar DisorderArmsActigraphy and MRI
3 · Its place in the literature

Who cites it

140 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Depressive symptom instability predicts incident mild cognitive impairment and dementia in older adults.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Long-term patterns of depressive symptoms and cognitive aging in middle-aged and older adults.Archives of public health = Archives belges de sante publique · 2026
    Article
  11. Article
  12. Trajectories of late-life depression: insights from molecular imaging.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Remission is insufficient: predictors and mechanistic models of recurrence in late-life depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Allison R KaupResearch Service, San Francisco Veterans Affairs Medical Center, San Francisco, California2Department of Psychiatry, University of California, San Francisco.
Amy L ByersResearch Service, San Francisco Veterans Affairs Medical Center, San Francisco, California2Department of Psychiatry, University of California, San Francisco.
Cherie FalveyDepartment of Psychiatry, University of California, San Francisco.
Eleanor M SimonsickIntramural Research Program, National Institute on Aging, Baltimore, Maryland.
Suzanne SatterfieldDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis.
Hilsa N AyonayonDepartment of Epidemiology and Biostatistics, University of California, San Francisco.
Stephen F SmagulaDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
Susan M RubinDepartment of Epidemiology and Biostatistics, University of California, San Francisco.
Kristine YaffeDepartment of Psychiatry, University of California, San Francisco7Department of Neurology, University of California, San Francisco8Department of Epidemiology and Biostatistics, University of California, San Francisco9San Francisco Veterans Affairs Medical.

Funding

CLINICAL RESEARCH TRAINING IN LATE-LIFE MOOD DISORDERST32MH019986 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOWARD J AIZENSTEIN, Carmen Andreescu · 1997 to 2026
$6.9M
Peripheral Nerve Function Decline in an Aged CohortR01AG028050 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STROTMEYER, ELSA S. · 2007 to 2015
$3.5M
End of Life in the Very OldR01NR012459 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALBERT, STEVEN M, LUNNEY, JUNE R · 2011 to 2015
$2.7M
Predictors & Outcomes of Cognitive Trajectories in the Oldest OldK24AG031155 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YAFFE, KRISTINE · 2007 to 2020
$1.5M
Cognitive Reserve and Training in Older Veterans with Traumatic Brain InjuryIK2RX001629 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI KAUP, ALLISON RENEE · 2015 to 2019
–
NIA NIH HHS K24 AG031155NIA NIH HHS R01 AG028050NIMH NIH HHS T32 MH019986NINR NIH HHS R01 NR012459RRD VA IK2 RX001629
6 · The paper itself

Abstract

importanceDepression has been identified as a risk factor for dementia. However, most studies have measured depressive symptoms at only one time point, and older adults may show different patterns of depressive symptoms over time.

objectiveTo investigate the association between trajectories of depressive symptoms and risk of dementia in older adults. DESIGN, SETTING, AND

participantsThis was a prospective cohort investigation of black and white community-dwelling older adults in the Health, Aging, and Body Composition study. Participants were enrolled between May 1997 and June 1998 and followed up through 2001-2002. The dates of this analysis were September 2014 to December 2015. The setting was community research centers in Memphis, Tennessee, and Pittsburgh, Pennsylvania. Trajectories of depressive symptoms were assessed from baseline to year 5. Symptoms were measured with the Center for Epidemiologic Studies Depression Scale Short Form, and trajectories were calculated using latent class growth curve analysis. MAIN OUTCOMES AND MEASURES: Incident dementia through year 11, determined by dementia medication use, hospital records, or significant cognitive decline (≥1.5 SD race-specific decline on the Modified Mini-Mental State Examination). We examined the association between depressive symptom trajectories and dementia incidence using Cox proportional hazards regression models adjusted for demographics, health factors that differed between groups, and cognition during the depressive symptom assessment period (baseline to year 5).

resultsThe analytic cohort included 2488 black and white older adults with repeated depressive symptom assessments from baseline to year 5 who were free of dementia throughout that period. Their mean (SD) age at baseline was 74.0 (2.8) years, and 53.1% (n = 1322) were female. The following 3 depressive symptom trajectories were identified: consistently minimal symptoms (62.0% [n = 1542] of participants), moderate and increasing symptoms (32.2% [n = 801] of participants), and high and increasing symptoms (5.8% [n = 145] of participants). Compared with the consistently minimal trajectory, having a high and increasing depressive symptom trajectory was associated with significantly increased risk of dementia (fully adjusted hazard ratio, 1.94; 95% CI, 1.30-2.90), while the moderate and increasing trajectory was not associated with risk of dementia after full adjustment. Sensitivity analyses indicated that the high and increasing trajectory was associated with dementia incidence, while depressive symptoms at individual time points were not. CONCLUSIONS AND RELEVANCE: Older adults with a longitudinal pattern of high and increasing depressive symptoms are at high risk for dementia. Individuals' trajectory of depressive symptoms may inform dementia risk more accurately than one-time assessment of depressive symptoms.

Indexed as

AgedAlzheimer DiseaseCohort StudiesDepressive DisorderDisease ProgressionFemaleHumansIncidenceMaleProspective StudiesRisk FactorsSensitivity and SpecificityUnited States

Identifiers

PMID26982217
PMCPMC5082978

What OpenQuestion holds

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Registered trials

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.