Evidence map›Paper›PMID 31907067›Full record

ArticleAlzheimer's research & therapy2020

Prescreening for European Prevention of Alzheimer Dementia (EPAD) trial-ready cohort: impact of AD risk factors and recruitment settings.

Lisa Vermunt, Graciela Muniz-Terrera, Lea Ter Meulen, Colin Veal, Kaj Blennow, Archie Campbell, Isabelle Carrié, Julien Delrieu, Karine Fauria, Gema Huesa Rodríguez and 16 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  5. Observational
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  7. Review
  8. Article
  9. Application of the ATN classification scheme in a population without dementia: Findings from the EPAD cohort.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
    Article
  10. Article
  11. Article
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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

26 authors at 10 institutions in 6 countries.

Lisa VermuntDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands. l.vermunt@amsterdamumc.nl.ORCID 0000-0001-7420-6384
Graciela Muniz-TerreraCentre for Dementia Prevention, University of Edinburgh, Edinburgh, Scotland.
Lea Ter MeulenDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
Colin VealDepartment of Genetics, University of Leicester, Leicester, UK.
Kaj BlennowDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Archie CampbellMolecular Medicine Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Isabelle CarriéCentre de Recherche Clinique du Gérontopôle, Toulouse University Hospital, Toulouse, France.
Julien DelrieuGérontopôle de Toulouse, UMR INSERM 1027, Toulouse University Hospital, Toulouse, France.
Karine FauriaBarcelonaBeta Brain Research Center, Fundacio Pasqual Maragall, Barcelona, Spain.
Gema Huesa RodríguezBarcelonaBeta Brain Research Center, Fundacio Pasqual Maragall, Barcelona, Spain.
Silvia IngalaDepartment of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
Natalie JenkinsCentre for Dementia Prevention, University of Edinburgh, Edinburgh, Scotland.
José Luis MolinuevoBarcelonaBeta Brain Research Center, Fundacio Pasqual Maragall, Barcelona, Spain.
Pierre-Jean OussetCentre de Recherche Clinique du Gérontopôle, Toulouse University Hospital, Toulouse, France.
David PorteousMolecular Medicine Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Niels D PrinsDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
Alina SolomonInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
Brian D TomMRC Biostatistics Unit, University of Cambridge, Cambridge, UK.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Marissa ZwanDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
Craig W RitchieCentre for Dementia Prevention, University of Edinburgh, Edinburgh, Scotland.
Philip ScheltensDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
Gerald LuscanGlobal Innovative Pharma Business - Clinical Sciences, Pfizer, Paris, France.
Anthony J BrookesDepartment of Genetics, University of Leicester, Leicester, UK.
Pieter Jelle VisserDepartment of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
IMI-EPAD collaborators
Amsterdam Neuroscience · NLUniversity of Leicester · GBPasqual Maragall Foundation · ESUniversité Fédérale de Toulouse Midi-Pyrénées · FRInserm · FRSahlgrenska University Hospital · SEUniversity of Eastern Finland · FIInstitute of Genetics and Cancer · GBMaastricht University · NLUniversity of Cambridge · GB

Funding

Innovative Medicines Initiative 115736Medical Research Council G0700704Medical Research Council MC_UU_00002/2Medical Research Council MR/K026992/1The Dunhill Medical Trust R380R/1114Wellcome Trust 104036/Z/14/Z
6 · The paper itself

Abstract

backgroundRecruitment is often a bottleneck in secondary prevention trials in Alzheimer disease (AD). Furthermore, screen-failure rates in these trials are typically high due to relatively low prevalence of AD pathology in individuals without dementia, especially among cognitively unimpaired. Prescreening on AD risk factors may facilitate recruitment, but the efficiency will depend on how these factors link to participation rates and AD pathology. We investigated whether common AD-related factors predict trial-ready cohort participation and amyloid status across different prescreen settings.

methodsWe monitored the prescreening in four cohorts linked to the European Prevention of Alzheimer Dementia (EPAD) Registry (n = 16,877; mean ± SD age = 64 ± 8 years). These included a clinical cohort, a research in-person cohort, a research online cohort, and a population-based cohort. Individuals were asked to participate in the EPAD longitudinal cohort study (EPAD-LCS), which serves as a trial-ready cohort for secondary prevention trials. Amyloid positivity was measured in cerebrospinal fluid as part of the EPAD-LCS assessment. We calculated participation rates and numbers needed to prescreen (NNPS) per participant that was amyloid-positive. We tested if age, sex, education level, APOE status, family history for dementia, memory complaints or memory scores, previously collected in these cohorts, could predict participation and amyloid status.

resultsA total of 2595 participants were contacted for participation in the EPAD-LCS. Participation rates varied by setting between 3 and 59%. The NNPS were 6.9 (clinical cohort), 7.5 (research in-person cohort), 8.4 (research online cohort), and 88.5 (population-based cohort). Participation in the EPAD-LCS (n = 413 (16%)) was associated with lower age (odds ratio (OR) age = 0.97 [0.95-0.99]), high education (OR = 1.64 [1.23-2.17]), male sex (OR = 1.56 [1.19-2.04]), and positive family history of dementia (OR = 1.66 [1.19-2.31]). Among participants in the EPAD-LCS, amyloid positivity (33%) was associated with higher age (OR = 1.06 [1.02-1.10]) and APOE ɛ4 allele carriership (OR = 2.99 [1.81-4.94]). These results were similar across prescreen settings.

conclusionsNumbers needed to prescreen varied greatly between settings. Understanding how common AD risk factors link to study participation and amyloid positivity is informative for recruitment strategy of studies on secondary prevention of AD.

Indexed as

Patient SelectionAgedAlzheimer DiseaseAmyloidogenic ProteinsBrainCohort StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedRegistriesRisk FactorsAmyloidogenic ProteinsAmyloidEngagementPrescreeningRecruitmentRegistriesSecondary prevention trialsTrial-ready cohort

Identifiers

PMID31907067
PMCPMC6945608
OpenAlexW3000418979

What OpenQuestion holds

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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.