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From the Departments of Neurology (Drs. Smith, Schmitt, Blonder, and Avison), Anatomy & Neurobiology (Drs. Smith and Andersen), Statistics (Dr. Kryscio), Biochemistry (Drs. Kindy and Avison), and Behavioral Science (Drs. Schmitt and Blonder); the Magnetic Resonance Imaging and Spectroscopy Center (Drs. Smith, Andersen, and Avison); and the Sanders-Brown Center on Aging (Drs. Smith, Kryscio, Schmitt, Kindy, and Blonder), University of Kentucky College of Medicine, Lexington, KY.
Address correspondence and reprint requests to Dr. Charles D. Smith, MRISC 113, University of Kentucky Medical Center, 800 Rose Street, Lexington, KY 40536; e-mail: csmith{at}mri.uky.edu
OBJECTIVE: To determine whether brain function is altered in cognitively normal individuals at high risk for AD several years before the typical age at onset for this illness.
BACKGROUND: Neuropathologic alterations in AD precede cognitive impairment by several years. It is unknown whether functional alterations in neural circuitry accompany these neuropathologic changes, and if so, whether they may be detectable before onset of symptoms.
METHODS: We used functional MRI to compare cortical activation between two groups of cognitively normal women differing only in their risk for developing AD. Visual naming and letter fluency tasks were used to activate brain areas subserving object and face recognition, previously described sites of hypometabolism and neuropathologic alteration in AD. The risk groups differed in family history of AD and apolipoprotein E allele status, but were matched in age, education, and measures of cognitive performance. Average age of the study participants was 52 years.
RESULTS: The regional patterns of brain activation were similar between groups. However, the high risk group showed areas of significantly reduced activation in the mid- and posterior inferotemporal regions bilaterally during both tasks despite identical naming and letter fluency performance.
CONCLUSIONS: Cognitively normal individuals at high risk for AD demonstrate decreased brain activation in key areas engaged during naming and fluency tasks. Decreased activation in the high risk group may be a consequence of the presence of subclinical neuropathology in the inferotemporal region or in the inputs to that region. If so, these findings provide evidence of a window of opportunity for disease-modifying treatment before the onset of symptomatic AD.
Key words: AD—Functional MRI—Apolipoprotein E.
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