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MAPT STUDY: A MULTIDOMAIN APPROACH FOR PREVENTING ALZHEIMER'S DISEASE: DESIGN AND BASELINE DATA.
Vellas, B; Carrie, I; Gillette-Guyonnet, S; Touchon, J; Dantoine, T; Dartigues, J F; Cuffi, M N; Bordes, S; Gasnier, Y; Robert, P; Bories, L; Rouaud, O; Desclaux, F; Sudres, K; Bonnefoy, M; Pesce, A; Dufouil, C; Lehericy, S; Chupin, M; Mangin, J F; Payoux, P; Adel, D; Legrand, P; Catheline, D; Kanony, C; Zaim, M; Molinier, L; Costa, N; Delrieu, J; Voisin, T; Faisant, C; Lala, F; Nourhashémi, F; Rolland, Y; Van Kan, G Abellan; Dupuy, C; Cantet, C; Cestac, P; Belleville, S; Willis, S; Cesari, M; Weiner, M W; Soto, M E; Ousset, P J; Andrieu, S.
Afiliação
  • Vellas B; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Carrie I; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
  • Gillette-Guyonnet S; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Touchon J; Department of Neurology, Memory Research Resource Center for Alzheimer's Disease, University Hospital of Montpellier, Montpellier, France.
  • Dantoine T; Geriatrics Department, Memory Research Resource Center, University Hospital of Limoges, Limoges, France.
  • Dartigues JF; INSERM U897, Memory Research Resource Center for Alzheimer's Disease, University Hospital of Bordeaux, Bordeaux, France.
  • Cuffi MN; Geriatrics Department, Hospital of Castres, Castres, France.
  • Bordes S; Geriatrics Department, Hospital of Tarbes, Tarbes, France.
  • Gasnier Y; Geriatrics Department, Hospital of Tarbes, Tarbes, France.
  • Robert P; Memory Research Resource Center, University Hospital of Nice, Nice, France.
  • Bories L; Geriatrics Department, Hospital of Foix, Foix, France.
  • Rouaud O; Memory Research Resource Center, Neurology Department, University Hospital of Dijon, Dijon, France.
  • Desclaux F; Geriatrics Department, Hospital of Lavaur, Lavaur, France.
  • Sudres K; Geriatrics Department, Hospital of Montauban, Montauban, France.
  • Bonnefoy M; Geriatrics Department, Centre Hospitalier Lyon-Sud, Lyon, France.
  • Pesce A; Geriatrics Department, Hospital of Princess Grace, Monaco.
  • Dufouil C; INSERM Center U897, CIC-EC7, Bordeaux University, Department of Public Health of CHU Bordeaux, Bordeaux, France.
  • Lehericy S; Neuroradiology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Chupin M; Neuroradiology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Mangin JF; CATI, NeuroSpin, CEA-Saclay Center, Gif-sur-Yvette, France.
  • Payoux P; INSERM UMR 825, Toulouse, France ; Department of Nuclear Medicine, CHU Toulouse, Purpan University Hospital, Toulouse, France.
  • Adel D; INSERM UMR 825, Toulouse, France.
  • Legrand P; Nutrition Department, Agrocampus-INRA, Rennes, France.
  • Catheline D; Nutrition Department, Agrocampus-INRA, Rennes, France.
  • Kanony C; Institut de Recherche Pierre Fabre, Toulouse, France.
  • Zaim M; Institut de Recherche Pierre Fabre, Toulouse, France.
  • Molinier L; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France ; Department of Medical Information, CHU Toulouse, Toulouse, France.
  • Costa N; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France ; Department of Medical Information, CHU Toulouse, Toulouse, France.
  • Delrieu J; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
  • Voisin T; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Faisant C; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
  • Lala F; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
  • Nourhashémi F; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Rolland Y; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Van Kan GA; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Dupuy C; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France.
  • Cantet C; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Cestac P; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Belleville S; Research Center, Institut Universitaire de Gériatrie de Montréal, Montréal, Canada.
  • Willis S; Department of Psychiatry and Behavioral Sciences, University of Washington, Washington, USA.
  • Cesari M; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Weiner MW; University of California, San Francisco, California, United States.
  • Soto ME; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Ousset PJ; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France ; INSERM UMR 1027, Toulouse, France ; University of Toulouse III, Toulouse, France.
  • Andrieu S; Gérontopôle, 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.
J Prev Alzheimers Dis ; 1(1): 13-22, 2014 Jun.
Article em En | MEDLINE | ID: mdl-26594639
ABSTRACT

OBJECTIVE:

The 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).

INTERVENTIONS:

1/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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: J Prev Alzheimers Dis Ano de publicação: 2014 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: J Prev Alzheimers Dis Ano de publicação: 2014 Tipo de documento: Article País de afiliação: França
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