TY - JOUR
T1 - The relationship between fMRI activation and cerebral atrophy
T2 - Comparison of normal aging and Alzheimer disease
AU - Johnson, Sterling C.
AU - Saykin, Andrew J.
AU - Baxter, Leslie C.
AU - Flashman, Laura A.
AU - Santulli, Robert B.
AU - McAllister, Thomas W.
AU - Mamourian, Alexander C.
N1 - Funding Information:
This work was supported by the Alzheimer’s Association (A.J.S., IIRG-133), the National Institutes of Health (S.C.J., F32NS10563), a National Alliance for Research on Schizophrenia and Affective Disorders Younger Investigator Award (L.A.F.), the National Institute of Disability and Rehabilitation Research (T.W.M., H-133670031), the Ira DeCamp Foundation, and the New Hampshire Hospital. The authors gratefully acknowledge the assistance of Chad H. Moritz, R.T., for data collection and image processing; Nancy C. Andreasen and colleagues for providing the BRAINS software package; Henry J. Riordan, Ph.D., Sally A. Frutiger, Ph.D., Judy O’Jile, Ph.D., and Cynthia Smith, Ph.D., for contributions to task design; James C. Ford, Fillia Makedon, Ph.D., and Charles B. Owen, Ph.D., for multimedia presentation software; and John B. Weaver, Ph.D., for technical assistance with scanner software and coil installation. Dr. Johnson is now at the Barrow Neurological Institute (Phoenix, AZ).
PY - 2000/3
Y1 - 2000/3
N2 - Functional MRI has recently been used to examine activation associated with aging and dementia, yet little is known regarding the effect of cerebral atrophy on fMRI signal. The purpose of this study was to examine the relationship between measures of global and regionally specific atrophy and fMRI activation in normal aging and in Alzheimer disease (AD). Two groups of subjects were studied with echoplanar imaging and quantitative structural volumetry: healthy controls spanning a broad age and atrophy range (n = 16) and patients with mild AD (n = 8). Results from a semantic task previously found to activate left inferior frontal (LIFG) and left superior temporal (LSTG) gyri were analyzed. The correlations between clusters of activation in the LIFG and LSTG and measures of local atrophy in the LIFG and LSTG regions were evaluated. For control subjects, there was no significant correlation between activation and regional or total brain atrophy (for LIFG r = -0.03, NS; for LSTG r - 0.20, NS). In contrast, for AD patients, there was a significant positive correlation between atrophy and activation in LIFG (r = 0.70, P = 0.05) but not LSTG (r = 0.00, NS). These results suggest that activation of language regions and atrophy within those regions may be independent among healthy adults spanning a broad age and atrophy range. However, in AD, a relationship exists in the LIFG that may reflect compensatory recruitment of cortical units or disease-specific changes in the hemodynamic response. (C) 2000 Academic Press.
AB - Functional MRI has recently been used to examine activation associated with aging and dementia, yet little is known regarding the effect of cerebral atrophy on fMRI signal. The purpose of this study was to examine the relationship between measures of global and regionally specific atrophy and fMRI activation in normal aging and in Alzheimer disease (AD). Two groups of subjects were studied with echoplanar imaging and quantitative structural volumetry: healthy controls spanning a broad age and atrophy range (n = 16) and patients with mild AD (n = 8). Results from a semantic task previously found to activate left inferior frontal (LIFG) and left superior temporal (LSTG) gyri were analyzed. The correlations between clusters of activation in the LIFG and LSTG and measures of local atrophy in the LIFG and LSTG regions were evaluated. For control subjects, there was no significant correlation between activation and regional or total brain atrophy (for LIFG r = -0.03, NS; for LSTG r - 0.20, NS). In contrast, for AD patients, there was a significant positive correlation between atrophy and activation in LIFG (r = 0.70, P = 0.05) but not LSTG (r = 0.00, NS). These results suggest that activation of language regions and atrophy within those regions may be independent among healthy adults spanning a broad age and atrophy range. However, in AD, a relationship exists in the LIFG that may reflect compensatory recruitment of cortical units or disease-specific changes in the hemodynamic response. (C) 2000 Academic Press.
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U2 - 10.1006/nimg.1999.0530
DO - 10.1006/nimg.1999.0530
M3 - Article
C2 - 10694460
AN - SCOPUS:0034116224
SN - 1053-8119
VL - 11
SP - 179
EP - 187
JO - NeuroImage
JF - NeuroImage
IS - 3
ER -