Neuroimaging enrichment strategy for secondary prevention trials in Alzheimer’s disease

Linda K McEvoy, Steven D Edland, Dominic Holland, Donald J Hagler Jr, J Cooper Roddey, Christine Fennema-Notestine, David P Salmon, Alain K Koyama, Paul S Aisen, James B Brewer

Research output: Contribution to journalArticlepeer-review

37 Citations (Scopus)


We examined the improvement in statistical power that could be obtained in therapeutic trials for early (predementia) Alzheimer disease by constraining enrollment to individuals with amnestic mild cognitive impairment (MCI) and an atrophy pattern on a screening magnetic resonance imaging (MRI) scan previously found to be predictive of clinical decline, or to individuals with MCI and the apolipoprotein E [varepsilon]4 genetic risk factor for Alzheimer disease. Treatable effects were defined as absolute change versus change relative to healthy controls (HCs). Data from 168 HC and 299 MCI participants were analyzed to determine sample sizes required to detect 25% slowing in mean rate of decline using global function, cognitive function, and structural measures as outcome variables. Reductions in estimated sample sizes of 10% to 43% were observed using the genetic enrichment strategy; reductions of 43% to 60% were observed with the neuroimaging enrichment strategy. Sample sizes needed to detect slowing in rate of atrophy in MCI relative to HC were dramatically larger than those needed to detect absolute change in atrophy rates. Constraining enrollment to MCI subjects with predictive atrophy on a screening MRI scan could improve the efficiency of clinical trials. Failure to take into account normal age-related changes risks under-powering trials designed to test disease-modifying properties of potential treatments.
Original languageEnglish
Pages (from-to)269-277
Number of pages9
JournalAlzheimer Disease and Associated Disorders
Issue number3
Publication statusPublished - 2010
Externally publishedYes


  • mild cognitive impairment
  • magnetic resonance imaging
  • atrophy
  • clinical trials methodology/ study design
  • apolipoprotein E ε4


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