Evidence map›Paper›PMID 37085328›Full record

Trial reportNeurology2023

Association of the Informant-Reported Memory Decline With Cognitive and Brain Deterioration Through the Alzheimer Clinical Continuum.

Elizabeth Kuhn, Audrey Perrotin, Renaud La Joie, Edelweiss Touron, Sophie Dautricourt, Matthieu Vanhoutte, Denis Vivien, Vincent de La Sayette, Gaël Chételat, Alzheimer's Disease Neuroimaging Initiative

Registry-linked trialOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01638949 (Study of the Predictive Markers and the Pathophysiological Mechanisms of Alzheimer's Disease), which is not on this map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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.

NCT01638949 nacompletednot on this map

Study of the Predictive Markers and the Pathophysiological Mechanisms of Alzheimer's Disease: Transverse and Longitudinal Approach in Anatomical and Functional Multimodal Imaging

TypeinterventionalSponsorUniversity Hospital, CaenRan2012 to 2022Enrolled242ConditionsAlzheimer's DiseaseArmsMemory assessment, Circulating biomarkers measure, ApoE4, Brain imaging examination MRI and PET examinations
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Elizabeth KuhnFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0002-3744-1155
Audrey PerrotinFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.
Renaud La JoieFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0003-2581-8100
Edelweiss TouronFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0001-7906-934X
Sophie DautricourtFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0001-8848-8300
Matthieu VanhoutteFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.
Denis VivienFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0002-7636-2185
Vincent de La SayetteFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France.ORCID 0000-0003-0663-092X
Gaël ChételatFrom the Normandie Univ (E.K., A.P., E.T., S.D., M.V., D.V., G.C.), UNICAEN, INSERM, U1237, PhIND "Physiopathology and Imaging of Neurological Disorders," Institut Blood and Brain @ Caen-Normandie, Cyceron, France; Memory and Aging Center (R.L.J.), Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco; Département de Recherche Clinique (D.V.), CHU Caen-Normandie; and Service de Neurologie (V.d.L.S.), CHU de Caen, France. chetelat@cyceron.fr.ORCID 0000-0002-4889-7932
Alzheimer's Disease Neuroimaging Initiative
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesStudies are sparse regarding the association between the informant-reported subjective memory decline (informant report) and Alzheimer disease (AD) biomarkers. This study thus aimed at determining the clinical relevance of the informant report throughout the AD clinical continuum, by assessing its specific relationships with amyloid deposition, cognition, and neurodegeneration.

methodsParticipants from the Imagerie Multimodale de la maladie d'Alzheimer à un stade Précoce (IMAP+) primary cohort and the Alzheimer Disease Neuroimaging Initiative (ADNI) replication cohort were included; all underwent multimodal neuroimaging and neuropsychological assessments. Follow-up data of IMAP+ participants over up to 36 months were also used for longitudinal analyses. The informant report was measured with the Cognitive Difficulties Scale (IMAP+) and Everyday Cognition (ADNI). General linear models were used to assess the cross-sectional associations between the informant report and amyloid-PET, cognitive performances, and neurodegeneration (atrophy and hypometabolism) in Alzheimer signature areas; while longitudinal links were assessed in IMAP+ with linear mixed-effects models.

resultsA total of 110 IMAP+ participants were included, including 32 cognitively unimpaired older individuals (controls, age: 70.91 ± 6.57 years, female: 50%), 25 patients with subjective cognitive decline (SCD, 65.88 ± 6.64, 40%), 35 with mild cognitive impairment (MCI, 72.49 ± 7.5, 34%), and 18 with Alzheimer-type dementia (AD dementia, 68.17 ± 8.59, 28%). Seven hundred thirty-one ADNI participants were included, including 157 controls (74.21 ± 5.95, 55%), 84 with SCD (72.00 ± 5.41, 63%), 369 with MCI (71.84 ± 7.4, 44%), and 121 with AD dementia (74.29 ± 7.75, 40%). In IMAP+, a higher informant report strongly correlated to greater amyloid-PET, specifically in patients with MCI (β = 0.48, DISCUSSION: Altogether, our findings suggest that the informant report is particularly relevant in patients with MCI where it strongly relates to higher amyloid-PET, indicative of impairment due to AD. TRIAL REGISTRATION INFORMATION: ClinicalTrials.gov Identifier: NCT01638949.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAmyloidAmyloid beta-PeptidesBiomarkersBrainCognitionCross-Sectional StudiesFemaleHumansMemory DisordersMiddle AgedPositron-Emission TomographyAmyloidAmyloid beta-PeptidesBiomarkers

Identifiers

PMID37085328
PMCPMC10264050
OpenAlexW4366728513

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.