Increasing required neural response to expose abnormal brain function in mild versus moderate or severe Alzheimer's disease: PET study using parametric visual stimulation.

OBJECTIVE The authors examined the interaction of Alzheimer's disease severity and visual stimulus complexity in relation to regional brain function. METHOD Each subject had five positron emission tomography [15]H2O scans while wearing goggles containing a grid of red lights embedded into each lens. Regional cerebral blood flow (CBF) was measured at 0 Hz and while lights were flashed alternately into the two eyes at 1, 4, 7, and 14 Hz. Changes in regional CBF from the 0-Hz baseline were measured at each frequency in 19 healthy subjects (mean age = 65 years, SD = 11), 10 patients with mild Alzheimer's disease (mean age = 69, SD = 5; Mini-Mental State score > or = 20), and 11 patients with moderate to severe Alzheimer's disease (mean age = 73, SD = 12; Mini-Mental State score < or = 19). RESULTS As pattern-flash frequency increased, CBF responses in the comparison group included biphasic rising then falling in the striate cortex, linear increase in visual association areas, linear decrease in many anterior areas, and a peak at 1 Hz in V5/MT. Despite equivalent resting CBF and CBF responses to low frequencies among all groups, the groups with Alzheimer's disease had significantly smaller CBF responses than the comparison group at the frequency producing the largest response in the comparison group in many brain regions. Also, patients with moderate/severe dementia had smaller responses at frequencies producing intermediate responses in comparison subjects. CONCLUSIONS Functional failure was demonstrated in patients with mild dementia when large neural responses were required and in patients with moderate/severe dementia when large and intermediate responses were required.

[1]  W J Schwartz,et al.  Metabolic mapping of functional activity in the hypothalamo-neurohypophysial system of the rat. , 1979, Science.

[2]  R H Huesman,et al.  Regional Cerebral Metabolic Alterations in Dementia of the Alzheimer Type: Positron Emission Tomography with [1818] Fluorodeoxyglucose , 1983, Journal of computer assisted tomography.

[3]  J E Holden,et al.  Cerebral blood flow using PET measurements of fluoromethane kinetics. , 1981, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[4]  W. H. Vance,et al.  Effects of antidromic stimulation of the ventral root on glucose utilization in the ventral horn of the spinal cord in the rat. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[5]  J. Penney,et al.  Dementia of the Alzheimer's Type: Changes in Hippocampal L‐[3H]Glutamate Binding , 1987, Journal of neurochemistry.

[6]  S. DeKosky,et al.  Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity , 1990, Annals of neurology.

[7]  S. DeKosky,et al.  Laminar organization of cholinergic circuits in human frontal cortex in Alzheimer's disease and aging , 1985, Neurology.

[8]  M. Reivich,et al.  Blood flow metabolism couple in brain. , 1974, Research publications - Association for Research in Nervous and Mental Disease.

[9]  C. Grady,et al.  Parametric in vivo brain imaging during activation to examine pathological mechanisms of functional failure in Alzheimer disease. , 1993, The International journal of neuroscience.

[10]  E. Mohr,et al.  Cortical glucose utilization patterns in primary degenerative dementias of the anterior and posterior type. , 1987, Archives of gerontology and geriatrics.

[11]  A. Crane,et al.  Differential effects of electrical stimulation of sciatic nerve on metabolic activity in spinal cord and dorsal root ganglion in the rat. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[12]  R. DeTeresa,et al.  Some morphometric aspects of the brain in senile dementia of the alzheimer type , 1981, Annals of neurology.

[13]  C. Cotman,et al.  Plasticity of hippocampal circuitry in Alzheimer's disease. , 1985, Science.

[14]  J. Maunsell,et al.  Magnocellular and parvocellular contributions to the responses of neurons in macaque striate cortex , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  Karl J. Friston,et al.  Assessing the significance of focal activations using their spatial extent , 1994, Human brain mapping.

[16]  J. Coyle,et al.  Alzheimer's disease and senile dementia: loss of neurons in the basal forebrain. , 1982, Science.

[17]  D. Salmon,et al.  Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment , 1991, Annals of neurology.

[18]  C. Sherrington,et al.  On the Regulation of the Blood‐supply of the Brain , 1890, The Journal of physiology.

[19]  Louis Sokoloff,et al.  Circulation and Energy Metabolism of the Brain , 1999 .

[20]  N. Logothetis,et al.  Functions of the colour-opponent and broad-band channels of the visual system , 1990, Nature.

[21]  William H. Merigan,et al.  P and M Pathway Specialization in the Macaque , 1991 .

[22]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.

[23]  B. Reisberg,et al.  Computed Tomography and Positron Emission Transaxial Tomography Evaluations of Normal Aging and Alzheimer's Disease , 1983, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  Luigi Mansi,et al.  Regional cortical dysfunction in Alzheimer's disease as determined by positron emission tomography , 1984, Annals of neurology.

[25]  P. Pietrini,et al.  Frequency Variation of a Pattern-Flash Visual Stimulus during PET Differentially Activates Brain from Striate through Frontal Cortex , 1997, NeuroImage.

[26]  J. Haxby,et al.  Positron emission tomography in Alzheimer's disease , 1986, Neurology.

[27]  J. Simpson,et al.  Catecholamines and cholinergic enzymes in pre-senile and senile Alzheimer-type dementia and down's syndrome , 1983, Brain Research.

[28]  D. V. Essen,et al.  Neural mechanisms of form and motion processing in the primate visual system , 1994, Neuron.

[29]  T. Nealey,et al.  Magnocellular and parvocellular contributions to responses in the middle temporal visual area (MT) of the macaque monkey , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  M. Jüptner,et al.  Review: Does Measurement of Regional Cerebral Blood Flow Reflect Synaptic Activity?—Implications for PET and fMRI , 1995, NeuroImage.

[31]  M J Campbell,et al.  Laminar and regional distributions of neurofibrillary tangles and neuritic plaques in Alzheimer's disease: a quantitative study of visual and auditory cortices , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  M. Torrens Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268 , 1990 .

[33]  C. Cotman,et al.  Axon sprouting in the rodent and Alzheimer's disease brain: a reactivation of developmental mechanisms? , 1990, Progress in brain research.

[34]  R. Nudo,et al.  Stimulation‐induced [14C]2‐deoxyglucose labeling of synaptic activity in the central auditory system , 1986, The Journal of comparative neurology.

[35]  J H Maunsell,et al.  Responses in macaque visual area V4 following inactivation of the parvocellular and magnocellular LGN pathways , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  T Jones,et al.  Regional cerebral oxygen supply and utilization in dementia. A clinical and physiological study with oxygen-15 and positron tomography. , 1981, Brain : a journal of neurology.

[37]  M. Raichle,et al.  Stimulus rate dependence of regional cerebral blood flow in human striate cortex, demonstrated by positron emission tomography. , 1984, Journal of neurophysiology.

[38]  Patrick R. Hof,et al.  Cellular Pathology in Alzheimer’s Disease: Implications for Corticocortical Disconnection and Differential Vulnerability , 1990 .

[39]  M. Folstein,et al.  Clinical diagnosis of Alzheimer's disease , 1984, Neurology.

[40]  S. Rapoport,et al.  Impairment in mitochondrial cytochrome oxidase gene expression in Alzheimer disease. , 1994, Brain research. Molecular brain research.

[41]  P. Whitehouse NEUROTRANSMITTER RECEPTOR ALTERATIONS IN ALZHEIMER DISEASE: A REVIEW , 1987, Alzheimer disease and associated disorders.

[42]  P Pietrini,et al.  Visual cortical dysfunction in Alzheimer's disease evaluated with a temporally graded "stress test" during PET. , 1996, The American journal of psychiatry.

[43]  L. Sokoloff,et al.  Relationships among local functional activity, energy metabolism, and blood flow in the central nervous system. , 1981, Federation proceedings.

[44]  D. Benson,et al.  The fluorodeoxyglucose 18F scan in Alzheimer's disease and multi-infarct dementia. , 1983, Archives of neurology.

[45]  Ingvar Dh,et al.  Symposium summary. Neuronal activity and energy metabolism. , 1981 .

[46]  DH Hubel,et al.  Psychophysical evidence for separate channels for the perception of form, color, movement, and depth , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.