Evidence map›Paper›PMID 36445876›Full record

Trial reportPloS one2022

Depressive symptoms exacerbate disability in older adults: A prospective cohort analysis of participants in the MemAID trial.

Stephanie S Buss, Laura Aponte Becerra, Jorge Trevino, Catherine B Fortier, Long H Ngo, Vera Novak

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. [Prevention of depression in old age: individual and societal relevance].Zeitschrift fur Gerontologie und Geriatrie · 2024
    Article
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 2 institutions in 1 country.

Stephanie S BussDepartment of Neurology, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School Boston (HMS), Boston, Massachusetts, United States of America.ORCID 0000-0002-9912-063X
Laura Aponte BecerraDepartment of Neurology, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School Boston (HMS), Boston, Massachusetts, United States of America.ORCID 0000-0003-4106-0483
Jorge TrevinoDepartment of Neurology, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School Boston (HMS), Boston, Massachusetts, United States of America.ORCID 0000-0001-8586-0197
Catherine B FortierTranslational Research Center for TBI and Stress Disorders (TRACTS) and Geriatric Research Educational and Clinical Research Center (GRECC) VA Boston Healthcare System, Boston, Massachusetts, United States of America.
Long H NgoDepartment of Medicine, Beth Israel Deaconess Medical Center and School of Public Health, Harvard Medical School Boston, Boston, Massachusetts, United States of America.
Vera NovakDepartment of Neurology, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School Boston (HMS), Boston, Massachusetts, United States of America.
Beth Israel Deaconess Medical Center · USHarvard University · US

Funding

Memory Advancement by Intranasal Insulin in Type 2 Diabetes (MemAID)R01DK103902 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI NOVAK, VERA · 2015 to 2019
$3.7M
Boston Children's Hospital and Beth Israel Deaconess Medical Center NeuroNEXT Clinical Research SiteU24NS107183 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI DARRAS, BASIL T, FRANK, SAMUEL ARTHUR · 2018 to 2022
$1.8M
Understanding the structural, functional, and prognostic implications of cortical excitability in Alzheimer's diseaseK23AG068364 · NIA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BUSS, STEPHANIE · 2021 to 2025
$921k
EPA EP-C-15-031NIA NIH HHS K23 AG068364NIDDK NIH HHS R01 DK103902NINDS NIH HHS U24 NS107183
6 · The paper itself

Abstract

backgroundMaintaining independence in older age is an important aspect of quality of life. We investigated depressive symptoms as an important modifiable risk factor that may mediate the effects of physical and cognitive decline on disability.

methodsWe prospectively analyzed data from 223 adults (age 50-85; 117 controls and 106 with type-2 diabetes) over 48 weeks who were participating in a clinical trial "Memory Advancement by Intranasal Insulin in Type 2 Diabetes." Data from self-reported disability (World Health Organization Disability Assessment Schedule) and depressive symptoms (Geriatric Depression Scale) were obtained from baseline, week 25, and week 48 visits. Cognition (Mini-mental status examination) and medical comorbidities (Charlson Comorbidity Index) were assessed at baseline. Longitudinal analysis assessed the extent to which change in depressive symptoms predicted worsening disability. Mediation analyses were performed to determine the extent to which depressive symptoms accounted for disability associated with worse cognition, walking speed, and comorbidities.

resultsAt baseline, depressive symptoms, cognition, and walking speed were within normal limits, but participants had a high 10-year risk of cardiovascular mortality. Depressive symptoms were related to disability at baseline (p<0.001), and longitudinally (p<0.001). Cognition, walking speed, and comorbidities were associated with disability at baseline (p-values = 0.027-0.001). Depressive symptoms had a large mediating effect on disability longitudinally: the indirect effect on disability via depression accounts for 51% of the effect of cognition, 34% of the effect of mobility, and 24% of the effect of comorbidities.

conclusionsDepressive symptoms substantially exacerbated the effects of worsening cognition, gait speed, and comorbidities on disability. In our sample, most individuals scored within the "normal" range of the Geriatric Depression Scale, suggesting that even subclinical symptoms can lead to disability. Treating subclinical depression, which may be under-recognized in older adults, should be a public health priority to help preserve independence with aging.

Indexed as

DepressionDiabetes Mellitus, Type 2AgedAged, 80 and overCognitionHumansMiddle AgedProspective StudiesQuality of Life

Identifiers

PMID36445876
PMCPMC9707770
OpenAlexW4310358386

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.