Elsevier, Neurobiology of Aging, 7(33), p. 1486.e9-1486.e15
DOI: 10.1016/j.neurobiolaging.2011.02.008
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Defining cases and controls on the basis of biomarkers rather than clinical diagnosis may reduce sample sizes required for genetic studies. The aim of this study was to assess whether characterizing case/control status on the basis of cerebrospinal fluid (CSF) profile would increase power to replicate known genetic associations for Alzheimer's disease (AD). Independent of clinical diagnosis, Alzheimer's Disease Neuroimaging Initiative (ADNI) subjects with 2 CSF biomarkers for AD (Abeta1-42 23 pg/mL, "CSF-positive") were compared with those without CSF evidence for AD (Abeta1-42 > 192 pg/mL and 181-phosphorylated tau