Prevalence of frailty and its association with cognition in preclinical Alzheimer's disease: a cross-sectional analysis of baseline data from the A4 study.

Background The prevalence and role of frailty in preclinical Alzheimer's disease (AD) is unclear. Methods Cross-sectional analyses of pre-randomization data from the Anti-Amyloid Treatment in Asymptomatic AD (A4) study were analysed to derive two models of a frailty index (FI)—full [FI-Full] and cog...

Descripción completa

Detalles Bibliográficos
Publicado en:Age & Ageing Vol. 55; no. 1; pp. 1 - 11
Autores principales: Huynh, Andrew L H, Wang, Shunran, Lee, Kathryn, Amadoru, Sanka, Wrigley, Scott, Zisis, Georgios, Ernstrom, Karin, Raman, Rema, Aisen, Paul, Sperling, Reisa A
Formato: Artículo
Publicado: Oxford University Press / USA Jan2026
Materias:
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ssf&AN=192513119&site=ehost-live
header:
  @attributes:
    shortDbName: ssf
    uiTerm: 192513119
    longDbName: Social Sciences Full Text (H.W. Wilson)
    uiTag: AN
  controlInfo:
    bkinfo:
    jinfo:
      jid:
        00020729
        AGA
      jtl: Age & Ageing
      issn: 00020729
      maglogo: N
    pubinfo:
      dt: Jan2026
      vid: 55
      iid: 1
      pid: 622
      pub: Oxford University Press / USA
    artinfo:
      ui:
        192513119
        10.1093/ageing/afaf378
      ppf: 1
      ppct: 10
      formats:
      tig:
        atl: Prevalence of frailty and its association with cognition in preclinical Alzheimer's disease: a cross-sectional analysis of baseline data from the A4 study.
      aug:
        au:
          Huynh, Andrew L H
          Wang, Shunran
          Lee, Kathryn
          Amadoru, Sanka
          Wrigley, Scott
          Zisis, Georgios
          Ernstrom, Karin
          Raman, Rema
          Aisen, Paul
          Sperling, Reisa A
        affil:
          Department of Geriatric Medicine, Austin Health, Heidelberg, Melbourne, Victoria, AustraliaDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Melbourne, Victoria, AustraliaThe Florey Institute of Neuroscience and Mental Health, Parkville, Melbourne, Victoria, Australia
          Alzheimer's Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA, USA
          Department of Geriatric Medicine, Austin Health, Heidelberg, Melbourne, Victoria, Australia
          Department of Geriatric Medicine, Austin Health, Heidelberg, Melbourne, Victoria, AustraliaDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Melbourne, Victoria, Australia
          The Florey Institute of Neuroscience and Mental Health, Parkville, Melbourne, Victoria, Australia
          Department of Neurology, Massachusetts General Hospital, Boston, MA, USACenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Boston, MA, USAHarvard Medical School, Boston, MA, USA
      su:
        Australia
        Cross-sectional method
        Old age
        Alzheimer's disease diagnosis
        Pearson correlation (Statistics)
        Cognitive testing
        Research funding
        T-test (Statistics)
        Frail elderly
        Brain
        Logistic regression analysis
        Positron emission tomography
        Chi-squared test
        Multivariate analysis
        Descriptive statistics
        Odds ratio
        Amyloid
        Neuropsychological tests
        Cognition disorders
        Early diagnosis
        Data analysis software
        Confidence intervals
        Biomarkers
        Amyloid beta-protein precursor
      sug:
        subj:
          Cross-sectional method
          Old age
          Australia
          Diagnostic Imaging Centers
          Alzheimer's disease diagnosis
          Pearson correlation (Statistics)
          Cognitive testing
          Research funding
          T-test (Statistics)
          Frail elderly
          Brain
          Logistic regression analysis
          Positron emission tomography
          Chi-squared test
          Multivariate analysis
          Descriptive statistics
          Odds ratio
          Amyloid
          Neuropsychological tests
          Cognition disorders
          Early diagnosis
          Data analysis software
          Confidence intervals
          Biomarkers
          Amyloid beta-protein precursor
      keyword:
        alzheimer's disease
        amyloid
        cognition
        cognitive decline
        cognitive impairment
        copyrightHolder:British Geriatrics Society
        copyrightYear:2026
        frailty
        https://dx.doi.org/10.1093/ageing/afaf378
        inLanguage:en
        older adults
        publisher:Oxford University Press
        sameAs:https://pubmed.ncbi.nlm.nih.gov/41569280/
        alzheimer's disease
        amyloid
        cognition
        cognitive decline
        cognitive impairment
        copyrightHolder:British Geriatrics Society
        copyrightYear:2026
        frailty
        https://dx.doi.org/10.1093/ageing/afaf378
        inLanguage:en
        older adults
        publisher:Oxford University Press
        sameAs:https://pubmed.ncbi.nlm.nih.gov/41569280/
      ab: Background The prevalence and role of frailty in preclinical Alzheimer's disease (AD) is unclear. Methods Cross-sectional analyses of pre-randomization data from the Anti-Amyloid Treatment in Asymptomatic AD (A4) study were analysed to derive two models of a frailty index (FI)—full [FI-Full] and cognitive variables removed [FI-CVR]. The prevalence of frailty (FI > 0.25) according to amyloid status (Aβ+/−), and the association of frailty and cognition (determined by the Preclinical Alzheimer Cognitive Composite (PACC) score) and whether frailty moderates the relationship between amyloid status and cognition was assessed, adjusting for age, sex and education. Results Four thousand four hundred eighty-six participants were included (mean age 71.3 ± 4.7 years, 30% participants Aβ+, 59% female). The prevalence of frailty in preclinical AD was 22% (or 44% when cognitive variables were removed from the FI). Using either FI model, in adjusted analyses, Aβ+ participants were more likely to be frail compared to Aβ− [FI-Full—Odds ratio (OR) 1.43 95% confidence interval (CI) 1.20–1.71, P  < .001; FI-CVR—OR 1.21 95% CI 1.05–1.40, P  < .008]. Frail participants had lower PACC scores compared to non-frail participants, on average (FI-Full—PACC score −0.58 95% CI −0.76 to −0.40, P  < .001; FI-CVR—PACC score −0.26 95% CI −0.40 to −0.12, P  < .001). Frailty did not influence the relationship between Aβ status and cognition. Conclusions In a cohort screened for a preclinical AD trial, elevated Aβ levels were associated with frailty and frailty was associated with reduced cognitive performance independent of elevated Aβ levels. These associations, and whether or not frailty is associated with longitudinal cognitive decline independent of Aβ status, warrant further study.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
    refInfo:
    copyright:
      @attributes:
        flag: N
    holdings:
      @attributes:
        islocal: N