VIII Conferencia Bienal
Barcelona/Pittsburgh
La demencia hoy23-25 Mayo 2012
VIII Barcelona/Pittsburgh
Biennial Conference
Dementia today23TH-25TH May 2012
Próxima edición de la Conferencia Barcelona-Pittsburgh: 23-25 Mayo 2012 - Next edition of the Barcelona/Pittsburgh Conference 23th-25th May 2012.

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Agenda

Charla "La memoria y la atención. Cambios en la edad adulta" - Jornadas de Puertas Abiertas - Fundació ACE. Institut Català de Neurociències Aplicades

Fecha
22-09-2011 al 22-09-2011

Lugar
Centro Cívico Cotxeres de Sants - Barcelona - España

Organizado por
Fundació ACE. Institut Català de Neurociències Aplicades

Más información

Charla "Tipos de memoria y por qué se afectan"- "La respuesta social ante la demencia" - Jornadas de Puertas Abiertas - Fundació ACE. Institut Català de Neurociències Aplicades

Fecha
13-09-2011 al 13-09-2011

Lugar
Centro Cívico Can Deu - Barcelona - España

Organizado por
Fundació ACE. Institut Català de Neurociències Aplicades

Más información

"Ageing and Neurodegeneration"

Fecha
01-09-2011 al 04-09-2011

Lugar
Bergisch Gladbach - Alemania

Organizado por
DZNE, the German Center for Neurodegenerative Diseases and the Max Planck Institute for Biology of Ageing

Más información



Haga clic aquí­ para iniciar La Cochrane Library Plus en Español - la información más fiable y completa sobre los efectos de la atención sanitaria

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Vitamin E and Donepezil for the Treatment of Mild Cognitive Impairment

Ronald C. Petersen, Ph.D., M.D., Ronald G. Thomas, Ph.D., Michael Grundman, M.D., M.P.H., David Bennett, M.D., Rachelle Doody, M.D., Ph.D., Steven Ferris, Ph.D., Douglas Galasko, M.D., Shelia Jin, M.D., M.P.H., Jeffrey Kaye, M.D., Allan Levey, M.D.,

The New England Journal of Medicine, Volume 352, 2379-2388

Año: 2005

Background Mild cognitive impairment is a transitional state between the cognitive changes of normal aging and early Alzheimer's disease.

Methods In a double-blind study, we evaluated subjects with the amnestic subtype of mild cognitive impairment. Subjects were randomly assigned to receive 2000 IU of vitamin E daily, 10 mg of donepezil daily, or placebo for three years. The primary outcome was clinically possible or probable Alzheimer's disease; secondary outcomes were cognition and function.

Results A total of 769 subjects were enrolled, and possible or probable Alzheimer's disease developed in 212. The overall rate of progression from mild cognitive impairment to Alzheimer's disease was 16 percent per year. As compared with the placebo group, there were no significant differences in the probability of progression to Alzheimer's disease in the vitamin E group (hazard ratio, 1.02; 95 percent confidence interval, 0.74 to 1.41; P=0.91) or the donepezil group (hazard ratio, 0.80; 95 percent confidence interval, 0.57 to 1.13; P=0.42) during the three years of treatment. Prespecified analyses of the treatment effects at 6-month intervals showed that as compared with the placebo group, the donepezil group had a reduced likelihood of progression to Alzheimer's disease during the first 12 months of the study (P=0.04), a finding supported by the secondary outcome measures. Among carriers of one or more apolipoprotein E 4 alleles, the benefit of donepezil was evident throughout the three-year follow-up. There were no significant differences in the rate of progression to Alzheimer's disease between the vitamin E and placebo groups at any point, either among all patients or among apolipoprotein E 4 carriers.

Conclusions Vitamin E had no benefit in patients with mild cognitive impairment. Although donepezil therapy was associated with a lower rate of progression to Alzheimer's disease during the first 12 months of treatment, the rate of progression to Alzheimer's disease after three years was not lower among patients treated with donepezil than among those given placebo.

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