Evidence map›Paper›PMID 32527600›Full record

ArticleThe American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry2020

Aging and Positive Mood: Longitudinal Neurobiological and Cognitive Correlates.

Devyn L Cotter, Samantha M Walters, Corrina Fonseca, Amy Wolf, Yann Cobigo, Emily C Fox, Michelle Y You, Marie Altendahl, Nina Djukic, Adam M Staffaroni and 4 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Tracking the Continuous Time Dynamics of Tau and Depressive Symptoms across the Alzheimer's Disease Continuum.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
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  3. Defining the contributions of tau pathology in the amygdala to increasing depressive symptoms in aging.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Devyn L CotterMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Samantha M WaltersMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Corrina FonsecaMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Amy WolfMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Yann CobigoMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Emily C FoxMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Michelle Y YouMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Marie AltendahlMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Nina DjukicMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Adam M StaffaroniMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Fanny M ElahiMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Joel H KramerMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Kaitlin B CasalettoMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA. Electronic address: Kaitlin.casaletto@ucsf.edu.
Hillblom Aging NetworkMemory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
University of California, San Francisco · USUniversity Memory and Aging Center · US

Funding

Research Education ComponentP30AG062422 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HOWARD J ROSEN · 2019 to 2026
$36.9M
Mechanisms of Executive Decline in Normal AgingR01AG032289 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Kaitlin B Casaletto, JOEL H KRAMER · 2009 to 2026
$8.3M
Biological Predictors Of Brain Aging Trajectories Diversity Supplement: African American Outreach And The Intersection Between Social Determinants Of Health And Biomarkers Of Degenerative DiseaseRF1AG032289 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRAMER, JOEL H · 2020 to 2021
$5.3M
Effects of chronic inflammation on brain structure and functionR01AG048234 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRAMER, JOEL H · 2015 to 2019
$3.2M
Can Behavior Shape Neural Health? Identifying Modifiable Factors to Prevent Cognitive Decline in AgeK23AG058752 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CASALETTO, KAITLIN B · 2018 to 2022
$994k
NIA NIH HHS K23 AG058752NIA NIH HHS P30 AG062422NIA NIH HHS R01 AG032289NIA NIH HHS R01 AG048234NIA NIH HHS RF1 AG032289
6 · The paper itself

Abstract

objectiveDespite the losses commonly associated with aging, older adults seem to possess particularly preserved emotional regulation. To further understand this phenomenon, the authors examined longitudinal trajectories between age, depressive symptoms, brain structure, and cognition.

methodsSeven hundred and sixteen functionally intact older adults (age M = 67.9, 56.8% female), followed longitudinally (visit range: 1-13, M = 2.5), completed cognitive testing and the Geriatric Depression Scale (GDS). A subset (N = 327) underwent 3T brain MRI. Mixed-effects linear regression models were conducted controlling for sex, education, and total intracranial volume.

resultsThere was a significant interaction between age and time on GDS, such that GDS improved with increasing age over time, but attenuated around age 71 (age*time b = 0.10, p <0.001). Fractional anisotropy (FA) and mean diffusivity interacted with age to predict longitudinal changes in GDS (FA: b = -0.02, p = 0.01; MD: b = 0.03, p = 0.007), such that age-related benefits on GDS were attenuated in those with declining FA. Executive function (EF) and processing speed also interacted with age to predict longitudinal changes in GDS (EF: b = -0.04, p = 0.03; speed: b = 0.04, p = 0.04). Again, the positive effect of age on GDS attenuated in those with worsening EF and speed. There were no associations with memory, semantic fluency, or gray matter (p values >0.05).

conclusionEF, processing speed, and white matter integrity moderated the longitudinal relationship between age and mood. Previous studies demonstrate the link between positivity and better cognitive control, leading to improved mood in older adults. Our results are not only consistent, but establish a potential neurobiological correlate. Future research further exploring biological mechanisms driving psychological processes may have important therapeutic implications.

Indexed as

BrainDepressionEmotional RegulationAffectAgedAgingCognitionCorrelation of DataExecutive FunctionFemaleFunctional NeuroimagingHumansLongitudinal StudiesMaleNeuropsychological TestsOptimismexecutive functionmoodprocessing speedwhite matter microstructural integrity

Identifiers

PMID32527600
PMCPMC7484115
OpenAlexW3024945859

What OpenQuestion holds

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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.