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Longitudinal associations between exercise and biomarkers in autosomal dominant Alzheimer's disease.
Sewell, Kelsey R; Doecke, James D; Xiong, Chengjie; Benzinger, Tammie; Masters, Colin L; Laske, Christoph; Jucker, Mathias; Lopera, Francisco; Gordon, Brian A; Llibre-Guerra, Jorge; Levin, Johannes; Huey, Edward D; Hassenstab, Jason; Schofield, Peter R; Day, Gregory S; Fox, Nick C; Chhatwal, Jasmeer; Ibanez, Laura; Roh, Jee Hoon; Perrin, Richard; Lee, Jae-Hong; Allegri, Ricardo F; Supnet-Bell, Charlene; Berman, Sarah B; Daniels, Alisha; Noble, James; Martins, Ralph N; Rainey-Smith, Stephanie; Peiffer, Jeremiah; Gardener, Samantha L; Bateman, Randall J; Morris, John C; McDade, Eric; Erickson, Kirk I; Sohrabi, Hamid R; Brown, Belinda M.
Afiliação
  • Sewell KR; Centre for Healthy Ageing, Health Futures Institute, Murdoch University, Murdoch, Western Australia, Australia.
  • Doecke JD; Australian E-Health Research Centre, CSIRO, Herston, Queensland, Australia.
  • Xiong C; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Benzinger T; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Masters CL; The Florey Institute, The University of Melbourne, Parkville, Victoria, Australia.
  • Laske C; German Center for Neurodegenerative Diseases, Tubingen, Germany.
  • Jucker M; Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Lopera F; German Center for Neurodegenerative Diseases, Tubingen, Germany.
  • Gordon BA; Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Llibre-Guerra J; Grupo de Neurociencias de Antioquia, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
  • Levin J; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Huey ED; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Hassenstab J; Department of Neurology, LMU University Hospital, LMU, Munich, Germany.
  • Schofield PR; German Center for Neurodegenerative Diseases, Site Munich, Munich, Germany.
  • Day GS; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Fox NC; Department of Psychiatry and Human Behavior, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
  • Chhatwal J; Department of Psychological & Brain Sciences, Washington University in St. Louis, St. Louis, Missouri, USA.
  • Ibanez L; Department of Neurology, Charles F. and Joanne Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Roh JH; Neuroscience Research Australia, Sydney, New South Wales, Australia.
  • Perrin R; School of Medical Sciences, University of New South Wales, Sydney, New South Wales, Australia.
  • Lee JH; Department of Neurology, Mayo Clinic Florida, Jacksonville, Florida, USA.
  • Allegri RF; Dementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.
  • Supnet-Bell C; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Berman SB; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Daniels A; Department of Neurology, Korea University Anam Hospital, Seoul, South Korea.
  • Noble J; Department of Physiology, Korea University College of Medicine, Seoul, South Korea.
  • Martins RN; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Rainey-Smith S; Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Peiffer J; Cognitive Neurology Service of the FLENI Foundation, Foundation for Childhood Neurological Disorders, Cognitive Neurology, Neuropsychology and Neuropsychiatry Section (CONICET-FLENI), Buenos Aires, Argentina.
  • Gardener SL; Washington University in St. Louis, St. Louis, Missouri, USA.
  • Bateman RJ; Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Morris JC; Department of Neurology, Charles F. and Joanne Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • McDade E; Department of Neurology, Columbia University Irving Medical Center, New York, New York, USA.
  • Erickson KI; Centre for Healthy Ageing, Health Futures Institute, Murdoch University, Murdoch, Western Australia, Australia.
  • Sohrabi HR; Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences, Edith Cowan University, Joondalup, Western Australia, Australia.
  • Brown BM; Alzheimer's Research Australia, Ralph and Patricia Sarich Neuroscience Research Institute, Nedlands, Western Australia, Australia.
Alzheimers Dement ; 2024 Sep 26.
Article em En | MEDLINE | ID: mdl-39324510
ABSTRACT

INTRODUCTION:

We investigated longitudinal associations between self-reported exercise and Alzheimer's disease (AD)-related biomarkers in individuals with autosomal dominant AD (ADAD) mutations.

METHODS:

Participants were 308 ADAD mutation carriers aged 39.7 ± 10.8 years from the Dominantly Inherited Alzheimer's Network. Weekly exercise volume was measured via questionnaire and associations with brain volume (magnetic resonance imaging), cerebrospinal fluid biomarkers, and brain amyloid beta (Aß) measured by positron emission tomography were investigated.

RESULTS:

Greater volume of weekly exercise at baseline was associated with slower accumulation of brain Aß at preclinical disease stages ß = -0.16 [-0.23 to -0.08], and a slower decline in multiple brain regions including hippocampal volume ß = 0.06 [0.03 to 0.08].

DISCUSSION:

Exercise is associated with more favorable profiles of AD-related biomarkers in individuals with ADAD mutations. Exercise may have therapeutic potential for delaying the onset of AD; however, randomized controlled trials are vital to determine a causal relationship before a clinical recommendation of exercise is implemented. HIGHLIGHTS Greater self-reported weekly exercise predicts slower declines in brain volume in autosomal dominant Alzheimer's disease (ADAD). Greater self-reported weekly exercise predicts slower accumulation of brain amyloid beta in ADAD. Associations varied depending on closeness to estimated symptom onset.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article