Evidence map›Paper›PMID 40966613›Full record

ArticleAge and ageing2025

The association of retinal vessel calibre, white matter hyperintensities and cognitive decline in community-dwelling older adults.

Catherine Robb, Amy Brodtmann, Robyn L Woods, Ruth E Trevaks, Stephanie A Ward, Meng Law, Suzanne G Orchard, Anne M Murray, Rory Wolfe, Joanne Ryan and 10 more

Abstract read
In one paragraph

Article in Age and ageing, 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

20 authors.

Catherine RobbIndustrial Transformation Training Centre for Optimal Ageing, Monash University, Melbourne, Victoria, Australia.
Amy BrodtmannDepartment of Neuroscience, School of Translational Medicine, Monash, Monash University, Melbourne, Victoria, Australia.
Robyn L WoodsSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0003-1249-6149
Ruth E TrevaksSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Stephanie A WardCentre for Healthy Brain Ageing (CHeBA), School of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia.
Meng LawDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Suzanne G OrchardSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Anne M MurrayGeriatrics Division, Department of Medicine, Hennepin Healthcare, and Berman Center for Outcomes and Clinical Research, Hennepin Healthcare Research Institute, Minneapolis, MN, USA.
Rory WolfeDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0002-2126-1045
Joanne RyanSchool of Public Health & Preventive Medicine, ASPREE, Monash University, Level 5, Alfred Centre 99 Commercial Road Prahran, Melbourne, Victoria 3004, Australia.ORCID 0000-0002-7039-6325
Nigel P StocksAdelaide Medical School, The University of Adelaide Discipline of General Practice, Adelaide, South Australia, Australia.
Noni RupasingheSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Raj C ShahDepartment of Family and Preventive Medicine and the Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, USA.
Christopher M ReidSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Walter P AbhayaratnaSchool of Medicine and Psychology, Australian National University, Canberra, Australian Capital Territory, Australia.
Gary F EganMonash Biomedical Imaging, Monash University, Melbourne, Victoria, Australia.
Mohamed Salah KhlifDepartment of Neuroscience, School of Translational Medicine, Monash, Monash University, Melbourne, Victoria, Australia.
Trevor T J ChongTurner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Victoria, Australia.ORCID 0000-0001-7764-3811
Liubov RobmanSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
John J McNeilDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0002-1049-5129

Funding

ASPirin in Reducing Events in the ElderlyU01AG029824 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI MCNEIL, JOHN JAMES, MURRAY, ANNE M · 2009 to 2018
$64.6M
Main Administrative CoreU19AG062682 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI CHAN, ANDREW T, MCNEIL, JOHN JAMES · 2019 to 2023
$42.9M
NIA NIH HHS U01 AG029824NIA NIH HHS U19 AG062682
6 · The paper itself

Abstract

backgroundRetinal vessel calibres (RVCs) are non-invasive markers of microvascular health and may serve as accessible indicators of cerebral small vessel disease (CSVD) and future cognitive impairment. This study examines whether RVCs are associated with cognitive decline, and how these associations compare with those observed for white matter hyperintensities (WMH), a known marker of CSVD.

methodsData were analysed from community-dwelling participants aged 70+ in the ASPREE trial and sub-studies, free of dementia and cardiovascular disease at baseline. RVCs were measured from fundus photography and WMH volumes from 3 T magnetic resonance imaging. Covariate-adjusted linear mixed-effects models assessed cognitive trajectories relative to baseline RVCs and WMH volumes. Cross-sectional associations between baseline RVCs and WMHs were examined via linear regression.

resultsThis study included 3540 participants with RVC data and 489 with WMH data (median [IQR] age: 73.2 [71.4-76.3] and 72.5 [71.2-75.4] years; female: 52.9% and 47.6%) over a median follow-up of 7.4 [IQR 5.5-8.5] and 3.8 [IQR 2.9-5.3] years, respectively. Baseline RVCs were not significantly associated with cognitive trajectories nor with baseline WMHs. Larger baseline WMH volumes were associated with greater global (Modified Mini-Mental State Examination) decline (mean 0.40 points/year; 95% CI 0.57, 0.22) and declines in delayed memory (HVLT-r) (-0.13 [-0.22, -0.04]), psychomotor function (Symbol Digit Modalities Test) (-0.29 [-0.52, -0.07]) and to a lesser extent, executive function (Controlled Oral Word Association Test) (-0.09 [95% CI -0.22, 0.03]).

conclusionIn contrast to WMH volumes, RVCs were not associated with cognitive decline. Exploring longitudinal changes in a broader range of retinal and brain biomarkers may provide deeper insights into the relationship between ocular and cerebral biomarkers in CSVD and clinical outcomes.

Indexed as

Cerebral Small Vessel DiseasesCognitionCognitive DysfunctionRetinal VesselsWhite MatterAgedCross-Sectional StudiesFemaleHumansIndependent LivingMagnetic Resonance ImagingMaleRisk Factorsageingcognitionmicrovasculatureolder peopleretinal vessel calibrewhite matter hyperintensities

Identifiers

PMID40966613
PMCPMC12423393

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.