Evidence map›Paper›PMID 40238789›Full record

ArticlePloS one2025

Courses of depressive symptoms and diabetes incidence among middle-aged and older adults: A prospective study.

Rachel J Burns, Katherine Ford, Geneviève C Forget, Kimia Fardfini-Ruginets, Richard Ward

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. 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

5 authors.

Rachel J BurnsDepartment of Psychology, Carleton University, Ottawa, Canada.ORCID 0000-0002-5337-7878
Katherine FordDepartment of Psychology, Carleton University, Ottawa, Canada.
Geneviève C ForgetDepartment of Psychology, Carleton University, Ottawa, Canada.
Kimia Fardfini-RuginetsDepartment of Psychology, Carleton University, Ottawa, Canada.
Richard WardDepartment of Psychology, Carleton University, Ottawa, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated depressive symptoms are a risk factor for diabetes. Although depressive symptoms can remit or emerge over time, little work has considered if courses of depressive symptoms are associated with incident diabetes. The purpose of this study was to explore associations between courses of depressive symptoms and incident diabetes. Data came from the English Longitudinal Study of Ageing (n = 4,978), which is an ongoing, cohort study of adults aged 50 years and older residing in private households in England. Depressive symptoms were measured biennially from 2002 to 2008. Participants were categorized into one of six groups: no depressive symptoms, remitted depressive symptoms, incident depressive symptoms with remission, incident depressive symptoms without remission, chronic depressive symptoms, and variable course. Diabetes status was self-reported biennially from 2010 to 2018. After adjusting for covariates, remitted depressive symptoms (HR = 1.52, 95% CI [1.06, 2.22]) and variable course depressive symptoms (HR = 1.83, 95% CI [1.19, 2.81]) remained associated with incident diabetes. In sensitivity analyses, which lowered the cut-off score for depressive symptoms, variable course depressive symptoms (HR = 1.61, 95% CI [1.11, 2.33]) remained associated with incident diabetes. Specific courses of depressive symptoms, including variable course depressive symptoms, were associated with diabetes incidence. Continuing to examine the link between patterns of depressive symptoms over time and incident diabetes may lead to the development of more targeted interventions.

Indexed as

DepressionDiabetes MellitusAgedEnglandFemaleHumansIncidenceLongitudinal StudiesMaleMiddle AgedProspective StudiesRisk Factors

Identifiers

PMID40238789
PMCPMC12002524

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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.