Association of premorbid intellectual function with cerebral metabolism in Alzheimer's disease: implications for the cognitive reserve hypothesis.

OBJECTIVE Clinical heterogeneity in Alzheimer's disease has been widely observed. One factor that may influence the expression of dementia in Alzheimer's disease is premorbid intellectual ability. It has been hypothesized that premorbid ability, as measured by educational experience, reflects a cognitive reserve that can affect the clinical expression of Alzheimer's disease. The authors investigated the relation between estimates of premorbid intellectual function and cerebral glucose metabolism in patients with Alzheimer's disease to test the effect of differing levels of premorbid ability on neurophysiological dysfunction. METHOD In a resting state with eyes closed and ears occluded, 46 patients with Alzheimer's disease were evaluated with positron emission tomography and [18F]-2-fluoro-2-deoxy-D-glucose to determine cerebral metabolism. Premorbid intellectual ability was assessed by a demographics-based IQ estimate and performance on a measure of word-reading ability. RESULTS After the authors controlled for demographic characteristics and dementia severity, both estimates of premorbid intellectual ability were inversely correlated with cerebral metabolism in the prefrontal, pre-motor, and left superior parietal association regions. In addition, the performance-based estimate (i.e., reading ability) was inversely correlated with metabolism in the anterior cingulate, paracentral, right orbitofrontal, and left thalamic regions, after demographic and clinical variables were controlled for. CONCLUSIONS The results suggest that higher levels of premorbid ability are associated with greater pathophysiological effects of Alzheimer's disease among patients of similar dementia severity levels. These findings provide support for a cognitive reserve that can alter the clinical expression of dementia and influence the neurophysiological heterogeneity observed in Alzheimer's disease.

[1]  J C Mazziotta,et al.  Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer disease. , 1995, JAMA.

[2]  J. Haxby,et al.  Relations between Neuropsychological and Cerebral Metabolic Asymmetries in Early Alzheimer's Disease , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[3]  A. C. Eycleshymer,et al.  A cross-section anatomy , 1970 .

[4]  P. McKenna,et al.  The use of current reading ability in the assessment of dementia. , 1975, The British journal of social and clinical psychology.

[5]  Leslie G. Ungerleider Two cortical visual systems , 1982 .

[6]  E. J. Green,et al.  chapter 8 – Experience and the Changing Brain1 , 1981 .

[7]  R. Katzman.,et al.  Education and the prevalence of dementia and Alzheimer's disease , 1993, Neurology.

[8]  C. White,et al.  The role of cortical connectivity in Alzheimer's disease pathogenesis: A review and model system , 1993, Neurobiology of Aging.

[9]  J. Haxby,et al.  Activation of cerebral blood flow during a visuoperceptual task in patients with Alzheimer-type dementia , 1993, Neurobiology of Aging.

[10]  J V Haxby,et al.  Visuospatial attention in dementia of the Alzheimer type. , 1992, Brain : a journal of neurology.

[11]  K. Holmen,et al.  Prevalence of Alzheimer's disease and other dementias in an elderly urban population , 1991, Neurology.

[12]  G. V. Van Hoesen,et al.  The topographical and neuroanatomical distribution of neurofibrillary tangles and neuritic plaques in the cerebral cortex of patients with Alzheimer's disease. , 1991, Cerebral cortex.

[13]  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.

[14]  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.

[15]  Cheryl L. Grady,et al.  Dissociation of object and spatial visual processing pathways in , 1993 .

[16]  Z. Khachaturian Diagnosis of Alzheimer's disease. , 1985, Archives of neurology.

[17]  M. Mesulam A cortical network for directed attention and unilateral neglect , 1981, Annals of neurology.

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

[19]  B. Milner,et al.  Interhemispheric differences in the localization of psychological processes in man. , 1971, British medical bulletin.

[20]  R. Reitan Validity of the Trail Making Test as an Indicator of Organic Brain Damage , 1958 .

[21]  R A Brooks,et al.  Alternative formula for glucose utilization using labeled deoxyglucose. , 1982, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[22]  M. Reivich,et al.  THE [14C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1 , 1977, Journal of neurochemistry.

[23]  Bruce G. Link,et al.  Relationship between lifetime occupation and parietal flow , 1995, Neurology.

[24]  G. Alexander,et al.  Inverse relationship between education and parietotemporal perfusion deficit in Alzheimer's disease , 1992, Annals of neurology.

[25]  N L Foster,et al.  Towards a behavioral typology of Alzheimer's patients. , 1986, Journal of clinical and experimental neuropsychology.

[26]  M. Posner,et al.  The attention system of the human brain. , 1990, Annual review of neuroscience.

[27]  R. S. Wilson,et al.  An index of premorbid intelligence. , 1978, Journal of consulting and clinical psychology.

[28]  Herman Buschke,et al.  Selective reminding for analysis of memory and learning , 1973 .

[29]  J V Haxby,et al.  Subgroups in dementia of the Alzheimer type identified using positron emission tomography. , 1990, The Journal of neuropsychiatry and clinical neurosciences.

[30]  D. Salmon,et al.  The prevalence of dementia and Alzheimer's disease in Shanghai, China: Impact of age, gender, and education , 1990, Annals of neurology.

[31]  M. Hamilton,et al.  Development of a rating scale for primary depressive illness. , 1967, The British journal of social and clinical psychology.

[32]  R. Mayeux,et al.  Influence of education and occupation on the incidence of Alzheimer's disease. , 1994, JAMA.

[33]  C. Grady,et al.  Heterogeneous anterior‐posterior metabolic patterns in dementia of the Alzheimer type , 1988, Neurology.

[34]  R. S. J. Frackowiak,et al.  REGIONAL CEREBRAL OXYGEN SUPPLY AND UTILIZATION IN DEMENTIAA CLINICAL AND PHYSIOLOGICAL STUDY WITH OXYGEN-15 AND POSITRON TOMOGRAPHY A CLINICAL AND PHYSIOLOGICAL STUDY WITH OXYGEN - 15 AND POSITRON TOMOHRAPHY , 1981 .

[35]  G. Alexander,et al.  Application of the scaled subprofile model to functional imaging in neuropsychiatric disorders: A principal component approach to modeling brain function in disease , 1994 .

[36]  P. Goldman-Rakic Topography of cognition: parallel distributed networks in primate association cortex. , 1988, Annual review of neuroscience.

[37]  D. Wechsler A Standardized Memory Scale for Clinical Use , 1945 .

[38]  L. R. Hill,et al.  Longitudinal examination of American National Adult Reading Test (AMNART) performance in dementia of the Alzheimer type (DAT): validation and correction based on degree of cognitive decline. , 1996, Journal of clinical and experimental neuropsychology.

[39]  Leslie G. Ungerleider,et al.  Dissociation of object and spatial visual processing pathways in human extrastriate cortex. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[40]  J Marshall,et al.  Cerebral blood flow in dementia. , 1975, Archives of neurology.

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