Evidence map›Paper›PMID 38863576›Full record

ArticleBrain communications2024

The PREVENT dementia programme: baseline demographic, lifestyle, imaging and cognitive data from a midlife cohort study investigating risk factors for dementia.

Craig W Ritchie, Katie Bridgeman, Sarah Gregory, John T O'Brien, Samuel O Danso, Maria-Eleni Dounavi, Isabelle Carriere, David Driscoll, Robert Hillary, Ivan Koychev and 13 more

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  7. Hypothalamic volume, sleep, and APOE genotype in cognitively healthy adults.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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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

23 authors.

Craig W RitchieEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.ORCID https://orcid.org/0000-0002-6202-6906
Katie BridgemanEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.ORCID https://orcid.org/0000-0002-4168-1493
Sarah GregoryEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.ORCID https://orcid.org/0000-0001-9864-8240
John T O'BrienDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 2QQ, UK.ORCID https://orcid.org/0000-0002-0837-5080
Samuel O DansoEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Maria-Eleni DounaviDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 2QQ, UK.ORCID https://orcid.org/0000-0001-8287-346X
Isabelle CarriereINM, Université de Montpellier, INSERM, Montpellier, 34091, France.
David DriscollPREVENT Participants Panel Member, London, UK.
Robert HillaryEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.ORCID https://orcid.org/0000-0002-2595-552X
Ivan KoychevDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.ORCID https://orcid.org/0000-0001-6813-8493
Brian LawlorGlobal Brain Health Institute, Trinity College Dublin, Dublin 2, Ireland.
Lorina NaciGlobal Brain Health Institute, Trinity College Dublin, Dublin 2, Ireland.
Li SuDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 2QQ, UK.
Audrey LowDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 2QQ, UK.ORCID https://orcid.org/0000-0002-2520-454X
Elijah MakDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 2QQ, UK.ORCID https://orcid.org/0000-0002-6437-8024
Paresh MalhotraImperial College London, UK Dementia Research Institute Care Research and Technology Centre, London, W12 0BZ, UK.ORCID https://orcid.org/0000-0002-1897-0780
Jean MansonEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Riccardo MarioniCentre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Lee MurphyEdinburgh Clinical Research Facility, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Georgios NtailianisEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.
William StewartDepartment of Neuropathology, Queen Elizabeth University Hospital, Glasgow, G51 4TF, UK.ORCID https://orcid.org/0000-0003-2199-2582
Graciela Muniz-TerreraEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Karen RitchieEdinburgh Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH4 2XU, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PREVENT is a multi-centre prospective cohort study in the UK and Ireland that aims to examine midlife risk factors for dementia and identify and describe the earliest indices of disease development. The PREVENT dementia programme is one of the original epidemiological initiatives targeting midlife as a critical window for intervention in neurodegenerative conditions. This paper provides an overview of the study protocol and presents the first summary results from the initial baseline data to describe the cohort. Participants in the PREVENT cohort provide demographic data, biological samples (blood, saliva, urine and optional cerebrospinal fluid), lifestyle and psychological questionnaires, undergo a comprehensive cognitive test battery and are imaged using multi-modal 3-T MRI scanning, with both structural and functional sequences. The PREVENT cohort governance structure is described, which includes a steering committee, a scientific advisory board and core patient and public involvement groups. A number of sub-studies that supplement the main PREVENT cohort are also described. The PREVENT cohort baseline data include 700 participants recruited between 2014 and 2020 across five sites in the UK and Ireland (Cambridge, Dublin, Edinburgh, London and Oxford). At baseline, participants had a mean age of 51.2 years (range 40-59, SD ± 5.47), with the majority female (

Indexed as

Alzheimer’s diseasebrain healthobservational cohortpreclinical dementiarisk factors

Identifiers

PMID38863576
PMCPMC11166176

What OpenQuestion holds

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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.