“…A number of studies have shown that normal aging is associated with mild brain atrophy on structural magnetic resonance (MR) imaging (Jack et al, 1998a(Jack et al, , 1999Jernigan et al, 2001;Pfefferbaum et al, 1994), decreased hemodynamic response on functional MR imaging (D'Esposito et al, 1999), reduced synaptic density (Masliah et al, 1993), increased white matter abnormalities (Guttman et al, 1998;Jernigan et al, 2001;Salat et al, 1999), and a subclinical accumulation of neuritic plaques and neurofibrillary tangles in medial temporal lobe brain regions (Green et al, 2000;Hulette et al, 1998). These brain changes are accompanied by age-related declines in information processing speed, executive functions, and efficiency of learning and recall (Corey-Bloom et al, 1996;Desgranges et al, 1998;Grady et al, 1995;Gunning-Dixon & Raz, 2000;Hulette et al, 1998;Mittenberg et al, 1989;Schacter et al, 1996;Ylikoski et al, 1993). The structural and functional decline that occurs in the Very-Old has led some investigators to suggest that less AD pathology may be needed to produce pathologic cognitive decline in the Very-Old compared to the Young-Old (see .…”