Evidence map›Paper›PMID 37872582›Full record

Trial reportAlzheimer's research & therapy2023

Cognitive impact of multidomain intervention and omega 3 according to blood Aβ42/40 ratio: a subgroup analysis from the randomized MAPT trial.

Julien Delrieu, Bruno Vellas, Sophie Guyonnet, Christelle Cantet, Vitaliy Ovod, Yan Li, James Bollinger, Randall Bateman, Sandrine Andrieu, MAPT/DSA group

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Alzheimer's research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01513252 (A 2-years Extension Study of MAPT Trial), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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.

NCT01513252 nacompletednot on this map

A 2-years Extension Study of MAPT Trial : Evaluation of the Long Term Effects of Interventional Strategies to Prevent the Decline in Cognitive Functioning in Frail Older Adults

TypeinterventionalSponsorUniversity Hospital, ToulouseRan2011 to 2020Enrolled1,028ConditionsFrail ElderlyArmsGröber and Buschke test
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
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 9 institutions in 3 countries.

Julien DelrieuMaintain Aging Research team, CERPOP, Université de Toulouse, Inserm, Université Paul Sabatier, Toulouse, France; Gérontopôle, Department of Geriatrics, Toulouse CHU, Toulouse, France. delrieu.j@chu-toulouse.fr.
Bruno VellasMaintain Aging Research team, CERPOP, Université de Toulouse, Inserm, Université Paul Sabatier, Toulouse, France; Gérontopôle, Department of Geriatrics, Toulouse CHU, Toulouse, France.
Sophie GuyonnetMaintain Aging Research team, CERPOP, Université de Toulouse, Inserm, Université Paul Sabatier, Toulouse, France; Gérontopôle, Department of Geriatrics, Toulouse CHU, Toulouse, France.
Christelle CantetMaintain Aging Research team, CERPOP, Université de Toulouse, Inserm, Université Paul Sabatier, Toulouse, France; Gérontopôle, Department of Geriatrics, Toulouse CHU, Toulouse, France.
Vitaliy OvodDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Yan LiDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
James BollingerDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Randall BatemanDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Sandrine AndrieuMaintain Aging Research team, CERPOP, Université de Toulouse, Inserm, Université Paul Sabatier, Toulouse, France; Department of Epidemiology and Public Health, Toulouse CHU, Toulouse, France.
MAPT/DSA group
Université Toulouse III - Paul Sabatier · FRCentre de recherche en Epidémiologie et Santé des Populations · FRWashington University in St. Louis · USCentre Hospitalier Universitaire de Toulouse · FRInstitut Universitaire de Gériatrie de Montréal · CAUniversité de Bordeaux · FRCentre National de la Recherche Scientifique · FRLaboratoire Eau, Environnement et Systèmes Urbains · FRUniversité Paris Cité · FR

Funding

Blood amyloid-beta relationship with amyloid plaques and CSF amyloid-betaRF1AG061900 · NIA · WASHINGTON UNIVERSITY · PI BATEMAN, RANDALL J · 2019 to 2020
$6.9M
Blood amyloid-beta relationship with amyloid plaques and CSF amyloid-betaR56AG061900 · NIA · WASHINGTON UNIVERSITY · PI BATEMAN, RANDALL J · 2018 to 2018
$1.4M
NIA NIH HHS R56 AG061900NIA NIH HHS RF1 AG061900
6 · The paper itself

Abstract

backgroundIn MAPT (Multidomain Alzheimer Preventive Trial), a cognitive effect of multidomain intervention (MI) was showed in non-demented subjects with positive amyloid PET. However, screening eligible patients for multidomain intervention by PET is difficult to generalize in real-world settings.

methodsMAPT study was a 3-year, randomized, placebo-controlled trial followed by a 2-year observational and optional extension. All participants were non-demented and randomly assigned (1:1:1:1) to the MI plus omega 3, MI plus placebo, omega 3 alone, or placebo alone group. The objectives were to assess the cognitive effect of MAPT interventions (omega 3 supplementation, MI, combined intervention) in non-demented subjects according to amyloid blood status at 12, 36, and 60 months. In this subgroup analysis (n = 483), amyloid status was defined by plasma Aβ42/40 ratio (cutoff ≤ 0.0107). The primary outcome measure was the change in cognitive composite score after a 1, 3, and 5-year clinical follow-up.

resultsThe intention-to-treat (ITT) population included 483 subjects (161 positive and 322 negative amyloid participants based on plasma Aβ42/40 ratio). In the positive amyloid ITT population, we showed a positive effect of MI plus omega 3 on the change in composite cognitive score in 12 (raw p = .0350, 0.01917, 95% CI = [0.0136 to 0.3699]) and 36 months (raw p = .0357, 0.2818, 95% CI = [0.0190 to 0.5446]). After correction of multiple comparisons and adjustments, these differences were not significant (adjusted p = .1144 and .0690). In the per-protocol positive amyloid group (n = 154), we observed a significant difference between the combined intervention and placebo groups at 12 (p = .0313, 0.2424, 0.0571 to 0.4276) and 36 months (p = .0195, 0.3747, 0.1055 to 0.6439) persisting after adjustment. In the ITT and per-protocol analyses, no cognitive effect was observed in the positive and negative amyloid group at 60-month visit.

conclusionsThese findings suggest a benefit of MI plus omega 3 in positive blood amyloid subjects. This promising trend needs to be confirmed before using blood biomarkers for screening in preventive trials.

trial registrationClinicalTrials.gov Identifier: NCT01513252 .

Indexed as

Alzheimer DiseaseFatty Acids, Omega-3AmyloidAmyloid beta-PeptidesCognitionHumansPeptide FragmentsResearch DesignAmyloidAmyloid beta-Peptidesamyloid beta-protein (1-42)Fatty Acids, Omega-3Peptide FragmentsAlzheimer’s diseaseAmyloid blood biomarkerClinical trialPrevention

Identifiers

PMID37872582
PMCPMC10594723
OpenAlexW4387874035

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.