Your browser doesn't support javascript.
loading
Effects of intensive lifestyle changes on the progression of mild cognitive impairment or early dementia due to Alzheimer's disease: a randomized, controlled clinical trial.
Ornish, Dean; Madison, Catherine; Kivipelto, Miia; Kemp, Colleen; McCulloch, Charles E; Galasko, Douglas; Artz, Jon; Rentz, Dorene; Lin, Jue; Norman, Kim; Ornish, Anne; Tranter, Sarah; DeLamarter, Nancy; Wingers, Noel; Richling, Carra; Kaddurah-Daouk, Rima; Knight, Rob; McDonald, Daniel; Patel, Lucas; Verdin, Eric; E Tanzi, Rudolph; Arnold, Steven E.
Afiliação
  • Ornish D; Preventive Medicine Research Institute, 900 Bridgeway, Sausalito, CA, USA. dean.ornish@pmri.org.
  • Madison C; University of California, San Francisco and University of California, San Diego, USA. dean.ornish@pmri.org.
  • Kivipelto M; Preventive Medicine Research Institute, 900 Bridgeway, Sausalito, CA, USA.
  • Kemp C; Ray Dolby Brain Health Center, California Pacific Medical Center, San Francisco, CA, USA.
  • McCulloch CE; Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Karolinska vägen 37 A, SE-171 64, Solna, Sweden.
  • Galasko D; Theme Inflammation and Aging, Karolinska University Hospital, Karolinska vägen 37 A, SE-171 64, Stockholm, Solna, Sweden.
  • Artz J; The Ageing Epidemiology (AGE) Research Unit, School of Public Health, Imperial College London, St Mary's Hospital, Norfolk Place, London, W2 1PG, United Kingdom.
  • Rentz D; Institute of Public Health and Clinical Nutrition, University of Eastern Finland, Yliopistonranta 8, 70210, Kuopio, Finland.
  • Lin J; Clinical Services, Preventive Medicine Research Institute, Bridgeway, Sausalito, CA, 900, USA.
  • Norman K; Division of Biostatistics, Department of Epidemiology & Biostatistics, UCSF, San Francisco, CA, USA.
  • Ornish A; Neurosciences, University of California, San Diego, CA, USA.
  • Tranter S; Clinical Neurology, School of Medicine, University of Nevada, Reno, USA.
  • DeLamarter N; Renown Health Institute of Neurosciences, Reno, NV, USA.
  • Wingers N; Harvard Medical School, Boston, MA, USA.
  • Richling C; Center for Alzheimer Research and Treatment, Boston, MA, USA.
  • Kaddurah-Daouk R; Mass General Brigham Alzheimer Disease Research Center, Boston, MA, USA.
  • Knight R; Elizabeth Blackburn Lab, UCSF, San Francisco, CA, USA.
  • McDonald D; UCSF, San Francisco, CA, USA.
  • Patel L; Preventive Medicine Research Institute, 900 Bridgeway, Sausalito, CA, USA.
  • Verdin E; Clinical Services, Preventive Medicine Research Institute, Bridgeway, Sausalito, CA, 900, USA.
  • E Tanzi R; Preventive Medicine Research Institute, 900 Bridgeway, Sausalito, CA, USA.
  • Arnold SE; Preventive Medicine Research Institute, 900 Bridgeway, Sausalito, CA, USA.
Alzheimers Res Ther ; 16(1): 122, 2024 06 07.
Article em En | MEDLINE | ID: mdl-38849944
ABSTRACT

BACKGROUND:

Evidence links lifestyle factors with Alzheimer's disease (AD). We report the first randomized, controlled clinical trial to determine if intensive lifestyle changes may beneficially affect the progression of mild cognitive impairment (MCI) or early dementia due to AD.

METHODS:

A 11 multicenter randomized controlled phase 2 trial, ages 45-90 with MCI or early dementia due to AD and a Montreal Cognitive Assessment (MoCA) score of 18 or higher. The primary outcome measures were changes in cognition and function tests Clinical Global Impression of Change (CGIC), Alzheimer's Disease Assessment Scale (ADAS-Cog), Clinical Dementia Rating-Sum of Boxes (CDR-SB), and Clinical Dementia Rating Global (CDR-G) after 20 weeks of an intensive multidomain lifestyle intervention compared to a wait-list usual care control group. ADAS-Cog, CDR-SB, and CDR-Global scales were compared using a Mann-Whitney-Wilcoxon rank-sum test, and CGIC was compared using Fisher's exact test. Secondary outcomes included plasma Aß42/40 ratio, other biomarkers, and correlating lifestyle with the degree of change in these measures.

RESULTS:

Fifty-one AD patients enrolled, mean age 73.5. No significant differences in any measures at baseline. Only two patients withdrew. All patients had plasma Aß42/40 ratios <0.0672 at baseline, strongly supporting AD diagnosis. After 20 weeks, significant between-group differences in the CGIC (p= 0.001), CDR-SB (p= 0.032), and CDR Global (p= 0.037) tests and borderline significance in the ADAS-Cog test (p= 0.053). CGIC, CDR Global, and ADAS-Cog showed improvement in cognition and function and CDR-SB showed significantly less progression, compared to the control group which worsened in all four measures. Aß42/40 ratio increased in the intervention group and decreased in the control group (p = 0.003). There was a significant correlation between lifestyle and both cognitive function and the plasma Aß42/40 ratio. The microbiome improved only in the intervention group (p <0.0001).

CONCLUSIONS:

Comprehensive lifestyle changes may significantly improve cognition and function after 20 weeks in many patients with MCI or early dementia due to AD. TRIAL REGISTRATION Approved by Western Institutional Review Board on 12/31/2017 (#20172897) and by Institutional Review Boards of all sites. This study was registered retrospectively with clinicaltrials.gov on October 8, 2020 (NCT04606420, ID 20172897).
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Doença de Alzheimer / Disfunção Cognitiva / Estilo de Vida Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Doença de Alzheimer / Disfunção Cognitiva / Estilo de Vida Idioma: En Ano de publicação: 2024 Tipo de documento: Article