Evidence map›Paper›PMID 26594639›Full record

ArticleThe journal of prevention of Alzheimer's disease2014

MAPT STUDY: A MULTIDOMAIN APPROACH FOR PREVENTING ALZHEIMER'S DISEASE: DESIGN AND BASELINE DATA.

B Vellas, I Carrie, S Gillette-Guyonnet, J Touchon, T Dantoine, J F Dartigues, M N Cuffi, S Bordes, Y Gasnier, P Robert and 35 more

3 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 150 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 13 pooled it
15.3field-weighted citation impact, top 1% 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.

NCT03336320 nacompletednot on this mapstarted 2017, after this paper: background citation

Feasibility and Acceptability of a Web-based Multidomain Intervention With Connected Devices Made to Maintain Cognitive Function in Older Adults: a Pilot Randomised Controlled Trial

TypeinterventionalSponsorUniversity Hospital, ToulouseRan2017 to 2019Enrolled120ConditionsAgedArmsICT Multidomain Intervention Training
NCT03978052 nacompletednot on this mapstarted 2019, after this paper: background citation

Prevention of Cognitive Decline in ApoE4 Carriers With Subjective Cognitive Decline After EGCG and a Multimodal Intervention

TypeinterventionalSponsorParc de Salut MarRan2019 to 2023Enrolled129ConditionsAlzheimer Disease, Cognitive DeclineArmsEGCG, Placebo EGCG, Healthy lifestyle recommendations, Multimodal lifestyle intervention
NCT07698431 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Implementation of a Brain Health Service for Personalized Stratification and Prevention of Dementia Risk: The B-HEALTH Project

TypeinterventionalSponsorBarcelonabeta Brain Research Center, Pasqual Maragall FoundationRan2026 to 2028Enrolled120ConditionsSubjective Cognitive Decline (SCD)ArmsMultimodal Lifestyle Intervention, Lifestyle Recommendations and Counseling
3 · Its place in the literature

Who cites it

150 citing papers in PubMed, 13 syntheses or guidelines pooled it, 261 citations in OpenAlex.

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  18. An 18-month multimodal intervention trial for preventing dementia: J-MINT PRIME Tamba.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
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90 more citing papers are in PubMed but not listed here.

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

45 authors at 20 institutions in 4 countries.

B VellasGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
I CarrieGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
S Gillette-GuyonnetGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
J TouchonDepartment of Neurology, Memory Research Resource Center for Alzheimer's Disease, University Hospital of Montpellier, Montpellier, France.
T DantoineGeriatrics Department, Memory Research Resource Center, University Hospital of Limoges, Limoges, France.
J F DartiguesINSERM U897, Memory Research Resource Center for Alzheimer's Disease, University Hospital of Bordeaux, Bordeaux, France.
M N CuffiGeriatrics Department, Hospital of Castres, Castres, France.
S BordesGeriatrics Department, Hospital of Tarbes, Tarbes, France.
Y GasnierGeriatrics Department, Hospital of Tarbes, Tarbes, France.
P RobertMemory Research Resource Center, University Hospital of Nice, Nice, France.
L BoriesGeriatrics Department, Hospital of Foix, Foix, France.
O RouaudMemory Research Resource Center, Neurology Department, University Hospital of Dijon, Dijon, France.
F DesclauxGeriatrics Department, Hospital of Lavaur, Lavaur, France.
K SudresGeriatrics Department, Hospital of Montauban, Montauban, France.
M BonnefoyGeriatrics Department, Centre Hospitalier Lyon-Sud, Lyon, France.
A PesceGeriatrics Department, Hospital of Princess Grace, Monaco.
C DufouilINSERM Center U897, CIC-EC7, Bordeaux University, Department of Public Health of CHU Bordeaux, Bordeaux, France.
S LehericyNeuroradiology Department, Pitié-Salpêtrière Hospital, Paris, France.
M ChupinNeuroradiology Department, Pitié-Salpêtrière Hospital, Paris, France.
J F ManginCATI, NeuroSpin, CEA-Saclay Center, Gif-sur-Yvette, France.
P PayouxINSERM UMR 825, Toulouse, France ; Department of Nuclear Medicine, CHU Toulouse, Purpan University Hospital, Toulouse, France.
D AdelINSERM UMR 825, Toulouse, France.
P LegrandNutrition Department, Agrocampus-INRA, Rennes, France.
D CathelineNutrition Department, Agrocampus-INRA, Rennes, France.
C KanonyInstitut de Recherche Pierre Fabre, Toulouse, France.
M ZaimInstitut de Recherche Pierre Fabre, Toulouse, France.
L MolinierINSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France ; Department of Medical Information, CHU Toulouse, Toulouse, France.
N CostaINSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France ; Department of Medical Information, CHU Toulouse, Toulouse, France.
J DelrieuGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
T VoisinGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
C FaisantGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
F LalaGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
F NourhashémiGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
Y RollandGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
G Abellan Van KanGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
C DupuyGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France.
C CantetGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
P CestacGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
S BellevilleResearch Center, Institut Universitaire de Gériatrie de Montréal, Montréal, Canada.
S WillisDepartment of Psychiatry and Behavioral Sciences, University of Washington, Washington, USA.
M CesariGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
M W WeinerUniversity of California, San Francisco, California, United States.
M E SotoGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
P J OussetGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
S AndrieuGérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France ; Department of Epidemiology and Public Health, CHU Toulouse, Toulouse, France.
Université Toulouse III - Paul Sabatier · FRInserm · FRHôpital Purpan · FRCentre Hospitalier de Bigorre · FRCentre National de la Recherche Scientifique · FRInstitut Agro Rennes-Angers · FRPierre Fabre (France) · FRATECA - Applications Technologie Avancée · FRCentre Hospitalier Intercommunal Castres-Mazamet · FRCentre Hospitalier Universitaire de Montpellier · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRHôpital Lyon Sud · FRInstitut Universitaire de Gériatrie de Montréal · CAMaison des Sciences sociales et des Humanités de Dijon · FRMédipole Garonne · FRPrincess Grace Hospital Centre · MCSorbonne Université · FRUniversité de Limoges · FRUniversity of California, San Francisco · USUniversity of Washington · US

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
UC Davis Alzheimer's Disease Core CenterP30AG010129 · NIA · UNIVERSITY OF CALIFORNIA DAVIS · PI DECARLI, CHARLES · 1991 to 2020
$28.3M
Prediction of cognitive decline with structural, diffusion, and perfusion MRIR01AG010897 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI WEINER, MICHAEL W · 1992 to 2013
$9.4M
NIA NIH HHS P30 AG010129NIA NIH HHS R01 AG010897NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

objectiveThe Multidomain Alzheimer Preventive Trial (MAPT study) was designed to assess the efficacy of isolated supplementation with omega-3 fatty acid, an isolated multidomain intervention (consisting of nutritional counseling, physical exercise, cognitive stimulation) or a combination of the two interventions on the change of cognitive functions in frail subjects aged 70 years and older for a period of 3 years. Ancillary neuroimaging studies were additionally implemented to evaluate the impact of interventions on cerebral metabolism (FDG PET scans) and atrophy rate (MRIs), as well as brain amyloïd deposit (AV45 PET scans). DESIGN PATIENTS: 1680 subjects (mean age: 75.3 years; female: 64.8 %), enrolled by 13 memory clinics, were randomized into one of the following four groups: omega-3 supplementation alone, multidomain intervention alone, omega-3 plus multidomain intervention, or placebo. Participants underwent cognitive, functional and biological assessments at M6, M12, M24 and M36 visits. The primary endpoint is a change of memory function at 3 years, as assessed by the Free and Cued Selective Reminding test. All participants will be followed for 2 additional years after the 3-years intervention (MAPT PLUS extension study).

interventions1/Omega-3 supplementation: two soft capsules daily as a single dose, containing a total of 400 mg docosahexaenoic acid (DHA), i.e., 800 mg docosahexaenoic acid per day, for 3 years. 2/ Multidomain intervention: collective training sessions conducted in small groups (6-8 participants) in twelve 120-minute sessions over the first 2 months (two sessions a week for the first month, and one session a week the second month) then a 60-minute session per month in the following three areas: nutrition, physical activity, and cognition until the end of the 3 years. In addition to the collective sessions, individualized preventive outpatient visits exploring possible risk factors for cognitive decline are performed at baseline, M12 and M24. BASELINE POPULATION: For cognition, the mean MMSE at baseline was 28.1 (± 1.6). About 58% and 42% of participants had a CDR score equal to 0 and 0.5, respectively. Regarding mobility status, 200 (11.9%) had a 4-m gait speed lower or equal to 0.8 m/s. According to the Fried criteria, 673 (42.1%) participants were considered pre frail, and 51 (3.2%) frail. The red blood cell DHA content was 26.1 ± 8.1 µg/g. Five hundred and three participants underwent baseline MRI. AV45 PET scans were performed in 271 individuals and preliminary results showed that 38.0% had a cortical SUVR > 1.17, which gave an indication of significant brain amyloïd deposit. DISCUSSION: The MAPT trial is presently the first largest and longest multidomain preventive trial relevant to cognitive decline in older adults with subjective memory complaints. The multidomain intervention designed for the MAPT trial is likely to be easily implemented within the general population.

Indexed as

Alzheimer’s diseaseMultidomain interventionOmega-3 fatty acidsPrevention

Identifiers

PMID26594639
PMCPMC4652787
OpenAlexW2183174223

What OpenQuestion holds

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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 OpenQuestion graph.