Neuroimaging Enrichment Strategy for Secondary Prevention Trials in Alzheimer Disease

Department of Radiology, University of California, San Diego, La Jolla, CA 92093-0841, USA.
Alzheimer disease and associated disorders (Impact Factor: 2.44). 07/2010; 24(3):269-77. DOI: 10.1097/WAD.0b013e3181d1b814
Source: PubMed


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 epsilon 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.

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    • "We hypothesized that a genetic score derived from these top AD risk genes would enrich a hypothetical 2-year clinical trial beyond just selecting ApoE4 carriers. We focused on MCI and healthy controls, similarly to prior enrichment studies (Lorenzi et al., 2010; McEvoy et al., 2010), mainly due to the crucial need for early interventions in AD (Kozauer and Katz, 2013). "
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