4.6 Article

Development of multivariable prediction models for institutionalization and mortality in the full spectrum of Alzheimer's disease

Journal

ALZHEIMERS RESEARCH & THERAPY
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13195-022-01053-0

Keywords

Alzheimer's disease; Mild cognitive impairment; Subjective cognitive decline; Prognosis; Mortality; Institutionalization

Funding

  1. EU Joint Programme-Neurodegenerative Disease Research (JPND) ADDITION project (ZonMW) [733051083]
  2. Life Molecular Imaging GmbH [LSHM18075]
  3. ABOARD from ZonMW [73305095007]
  4. Healthsimilar toHolland, Topsector Life Sciences Health [LSHM20106]

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This study developed prediction models for institutionalization and mortality along the Alzheimer's disease cognitive continuum with good accuracy for SCD/MCI patients and moderate accuracy for patients with AD dementia.
Background Patients and caregivers express a desire for accurate prognostic information about time to institutionalization and mortality. Previous studies predicting institutionalization and mortality focused on the dementia stage. However, Alzheimer's disease (AD) is characterized by a long pre-dementia stage. Therefore, we developed prediction models to predict institutionalization and mortality along the AD continuum of cognitively normal to dementia. Methods This study included SCD/MCI patients (subjective cognitive decline (SCD) or mild cognitive impairment (MCI)) and patients with AD dementia from the Amsterdam Dementia Cohort. We developed internally and externally validated prediction models with biomarkers and without biomarkers, stratified by dementia status. Determinants were selected using backward selection (p<0.10). All models included age and sex. Discriminative performance of the models was assessed with Harrell's C statistics. Results We included n=1418 SCD/MCI patients (n=123 died, n=74 were institutionalized) and n=1179 patients with AD dementia (n=413 died, n=453 were institutionalized). For both SCD/MCI and dementia stages, the models for institutionalization and mortality included after backward selection clinical characteristics, imaging, and cerebrospinal fluid (CSF) biomarkers. In SCD/MCI, the Harrell's C-statistics of the models were 0.81 (model without biomarkers: 0.76) for institutionalization and 0.79 (model without biomarker: 0.76) for mortality. In AD-dementia, the Harrell's C-statistics of the models were 0.68 (model without biomarkers: 0.67) for institutionalization and 0.65 (model without biomarker: 0.65) for mortality. Models based on data from amyloid-positive patients only had similar discrimination. Conclusions We constructed prediction models to predict institutionalization and mortality with good accuracy for SCD/MCI patients and moderate accuracy for patients with AD dementia. The developed prediction models can be used to provide patients and their caregivers with prognostic information on time to institutionalization and mortality along the cognitive continuum of AD.

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