Hostname: page-component-5c6d5d7d68-wbk2r Total loading time: 0 Render date: 2024-08-15T06:02:45.706Z Has data issue: false hasContentIssue false

Comparative Neuropsychology of Cortical and Subcortical Dementia

Published online by Cambridge University Press:  18 September 2015

Morris Freedman*
Affiliation:
Department of Medicine (Division of Neurology), University of Toronto, Mount Sinai Hospital, and Baycrest Centre for Geriatric Care
Marlene Oscar-Berman
Affiliation:
Psychology Service, Boston Veterans Administration Medical Centre, and Department of Neurology and Division of Psychiatry, Boston University School of Medicine
*
Mount Sinai Hospital, Suite 433, 600 University Avenue, Toronto, Ontario, Canada M5G 1X5
Rights & Permissions [Opens in a new window]

Abstract:

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The terms “cortical” and “subcortical” dementia are controversial; however, the clinical distinction between them is real. For example, although Alzheimer's and Parkinson's disease (prototypical of cortical and subcortical dementia, respectively) share clinical features, they differ in the presence of aphasia, apraxia, and agnosia in Alzheimer's disease but not in Parkinson's dementia. We review our studies aimed at clarifying the mechanisms underlying the differences between these neurological disorders. Experimental paradigms adopted from animal models were used to study the functional anatomy and neuropsychological characteristics of Alzheimer's and Parkinson's disease. The tasks administered include delayed alternation (DA) and delayed response (DR), which are sensitive to frontal system damage, and tactile discrimination learning (TOL) and reversal (TRL) paradigms sensitive to parietal system damage. Alzheimer's patients were significantly impaired on all tasks whereas Parkinsonians with dementia were impaired only on DR and TRL. Consideration of neuroanatomical and neuropsychological mechanisms involved in DA, DR, TOL, and TRL appears to have sharpened the distinction between Alzheimer's and Parkinson's dementia. Dementia in Alzheimer's disease may involve dorsolateral frontal, orbitofrontal and parietal systems. In contrast, dementia in Parkinson's disease may involve prominent dorsolateral frontal system damage.

Type
Neuropsychological Challenges
Copyright
Copyright © Canadian Neurological Sciences Federation 1986

References

1.Battig, K, Rosvold, HE, Mishkin, M.Comparison of the effects of frontal and caudate lesions on delayed response and alternation in monkeys. J Comp Physiol Psychol 1960; 53: 400404.CrossRefGoogle ScholarPubMed
2.Divac, I, Rosvold, HE, Szwarcbart, MK.Behavioural effects of selective ablation of the caudate nucleus. J Comp Psysiol Psychol 1967; 63: 184190.CrossRefGoogle ScholarPubMed
3.Rosvold, HE.The frontal lobe system: cortical-subcortical interrelationships. Acta Neurobiol Exp 1972; 32: 439460.Google ScholarPubMed
4.Albert, ML, Feldman, RG, Willis, AL.‘The subcortical dementia’ of progressive supranuclear palsy. J Neurol Neurosurg Psychiatry 1974; 37: 121130.CrossRefGoogle ScholarPubMed
5.McHugh, PR, Folstein, MF.Psychiatric syndromes of Huntington’s chorea: A clinical and phenomenologie study. In: Benson, DF, Blumer, D, eds. Psychiatric Aspects of Neurologic Disease. New York: Grune and Stratton 1975: 267286.Google Scholar
6.Olton, DS, et al, eds. Memory Dysfunctions: An Integration of Animal and Human Research from Preclinical and Clinical Perspectives. Annals of the New York Academy of Sciences 1985: vol 44.Google Scholar
7.Benson, DF.The treatable dementias. In: Benson, DF, Blumer, D, eds. Psychiatric Aspects of Neurologic Disease. New York: Grune and Stratton 1975: 123148.Google Scholar
8.Cummings, JL, Benson, DF.Subcortical dementia. Arch Neurol 1984;41: 874889.CrossRefGoogle ScholarPubMed
9.Freedman, M, Albert, ML.Subcortical dementia (Chap 19). In: Frederiks, JAM, ed. Handbook of Clinical Neurology, vol 2(46). Amsterdam: Elsevier Science Publishers 1985: 311316.Google Scholar
10.Whitehouse, PJ, Price, DL, Struble, RG, et al. Alzheimer’s disease and senile dementia: loss of neurons in the basal forebrain. Science 1982; 215: 12371239.CrossRefGoogle ScholarPubMed
11.Divac, I.Magnocellular nuclei of the basal forebrain project to neocortex, brainstem, and olfactory bulb. Review of some functional correlates. Brain Res 1975; 93: 385398.CrossRefGoogle ScholarPubMed
12.Jones, EG, Burton, H, Saper, CB, et al. Midbrain diencephalic and cortical relationships of the basal nucleus of Meynert and associated structures in primates. J Comp Neurol 1976; 167: 385420.CrossRefGoogle ScholarPubMed
13.Kievet, J, Kuypers, HGJM.Basal forebrain and hypothalamic connections to frontal and parietal cortex in the rhesus monkey. Science 1975; 187: 660662.CrossRefGoogle Scholar
14.Shute, CCD, Lewis, PR.The ascending cholinergic reticular system: neocortical, olfactory and subcortical projections. Brain 1967; 90: 497520.CrossRefGoogle ScholarPubMed
15.Arendt, T, Bigl, V, Arendt, A, et al. Loss of neurons in the nucleus basalis of Meynert in Alzheimer’s disease, paralysis agitans and Korsakoff’s Disease. Acta Neuropathol 1983; 61: 101108.CrossRefGoogle ScholarPubMed
16.Davis, KL, Mohs, RC, Tinklenberg, JR, et al. Physostigmine: improvement of long-term memory processes in normal humans. Science 1978; 201: 272274.CrossRefGoogle ScholarPubMed
17.Drachman, DA.Memory and cognitive function in man: does the cholinergic system have a specific role? Neurology 1970; 27: 783790.CrossRefGoogle Scholar
18.Drachman, DA, Leavitt, J.Human memory and the cholinergic system: a relationship to aging? Arch Neurol 1974; 30: 113121.CrossRefGoogle ScholarPubMed
19.Peters, BH, Levin, HS.Memory enhancement after physostigmine treatment in the amnesic syndrome. Arch Neurol 1977; 34:215219.CrossRefGoogle ScholarPubMed
20.Peters, BH, Levin, HS.Effects of physostigmine and lecithen on memory in Alzheimer disease. Ann Neurol 1979; 6: 219221.CrossRefGoogle ScholarPubMed
21.Alvord, EC, Forno, LS, Kusske, JA, et al. The pathology of parkinsonism: a comparison of degenerations in cerebral cortex and brainstem. Adv Neurol 1974; 5: 175193.Google ScholarPubMed
22.Boiler, F, Mizutani, T, Roessmann, U, et al. Parkinson disease, dementia, and Alzheimer disease: clinicopathological correlations. Ann Neurol 1980; 7: 329335.CrossRefGoogle Scholar
23.Hakim, AM, Mathieson, G.Dementia in parkinson disease: a neuro-pathology study. Neurology 1979; 29: 12091214.CrossRefGoogle Scholar
24.Victor, M.Discussion of “subcortical dementia”. In: Katzman, R, Terry, RD, Bick, KL, eds. Alzheimer’s Disease: Senile Dementia and Related Disorders, New York: Raven Press 1978: 194.Google Scholar
25.Oscar-Berman, M.Neuropsychological consequences of long-term chronic alcoholism. American Scientist 1980; 68: 410419.Google ScholarPubMed
26.Oscar-Berman, M, Zola-Morgan, SM.Comparative neuropsychology and Korsakoff’s syndrome. I. Spatial and visual reversal learning. Neuropsychologia 1980; 18: 499512.CrossRefGoogle ScholarPubMed
27.Weiskrantz, LA.A comparison of hippocompal pathology in man and other animals. In: Functions of the Septo-hippocampal System. Ciba Foundation Symposium 58. New York: Elsevier 1978.CrossRefGoogle Scholar
28.Freedman, M, Oscar-Berman, M.Bilateral frontal lobe disease and selective delayed-response deficits in humans. Behav Neuroscience 1986; 100: 337342.CrossRefGoogle ScholarPubMed
29.Oscar-Berman, M, Zola-Morgan, SM.Comparative neuropsychology and Korsakoff s syndrome. II. Two-choice visual discrimination learning. Neuropsychologia 1980; 18: 513526.CrossRefGoogle ScholarPubMed
30.Oscar-Berman, M, Zola-Morgan, SM, ôberg, RGE, et al. Comparative neuropsychology and Korsakoff s syndrome. III. Delayed réponse, delayed alternation and DRL performance. Neuropsychologia 1982; 20: 187202.CrossRefGoogle Scholar
31.Pribram, KH, Ahumada, A, Hartog, J, et al. A progress report on the neurological processes disturbed by frontal lesions in primates. In: Warren, JM, Akert, K, eds. The Frontal Granular Cortex and Behaviour. New York: McGraw-Hill Book Company 1964: 2855.Google Scholar
32.Witt, ED, Goldman-Rakic, PS.Intermittent thiamine deficiency in the rhesus monkey: II. Evidence for memory loss. Ann Neurol 1983; 13: 396401.CrossRefGoogle ScholarPubMed
33.Freedman, M, Oscar-Berman, M.Selective delayed réponse deficits in Parkinson’s and Alzheimer’s disease. Arch Neurol 1986; 43: 886890.CrossRefGoogle Scholar
34.Freedman, M, Oscar-Berman, M.Tactile Discrimination Learning Deficits in Alzheimer’s and Parkinson’s Disease. Submitted for publication.Google Scholar
35.Warren, JM, Akert, K, eds. The Frontal Granular Cortex and Behaviour. New York: McGraw-Hill 1964.Google Scholar
36.Brutkowski, S, Mishkin, M, Rosvold, HE.Positive and inhibitory motor conditioned reflexes in monkeys after ablation of orbital or dorsolateral surfact of the frontal cortex. In: Gutmann, E, Hnik, P, eds. Central and Peripheral Mechanisms of Motor Functions. Prague: Czechoslovak Academy of Sciences 1963.Google Scholar
37.Goldman, PS, Rosvold, HE, Vest, B, et al. Analysis of the delayed-alteration deficit produced by dorsolateral prefrontal lesions in the rhesus monkey. J Comp Physiol Psychol 1971; 77: 212220.CrossRefGoogle Scholar
38.Kling, A, Tucker, TJ.Sparing of function following localized brain lesions in neonatal monkeys. In: Isaacson, RL, ed. The neuropsychology of development. New York: John Wiley & Sons Inc. 1968; 121145.Google Scholar
39.Mishkin, M.Effects of small frontal lesions on delayed alternation in monkeys. J Neurophysiol 1957; 20: 615622.CrossRefGoogle ScholarPubMed
40.Wilson, M.Effects of circumscribed cortical lesions upon somesthetic and visual discrimination in the monkey. J Comp Physiol Psychol 1957; 50: 630635.CrossRefGoogle ScholarPubMed
41.Brun, A, Englund, E.Regional pattern of degeneration in Alzheimer’s disease: Neuronal loss and histopathological grading. Histo-pathology 1981; 5: 549564.Google ScholarPubMed
42.Chase, TN, Foster, NL, Fedio, P, et al. Regional cortical dysfunction in Alzheimer’s disease as determined by positron emission tomography. Ann Neurol 1984; 15 (supplement: S170–74).CrossRefGoogle ScholarPubMed
43.Cutler, NR, Haxby, JV, Duara, R, et al. Brain metabolism as measured with positron emission tomography: serial assessment in a patient with familial Alzheimer’s disease. Neurology 1985; 35: 15561561.CrossRefGoogle Scholar
44.Coblentz, JM, Mattis, S, Zingesser, LH, et al. Presenile dementia: clinical aspects and evaluation of cerebrospinal fluid dynamics. Arch Neurol 1973; 29: 299308.CrossRefGoogle ScholarPubMed
45.Gellermann, LW.Chance order of alternating stimuli in visual discrimination experiments. J Genetic Psychol 1933;42:207208.Google Scholar
46.Oscar-Berman, M.The effects of dorsolateral-frontal and ventrolateral orbitofrontal lesions on spatial discrimination learning and delayed response in two modalities. Neuropsychologia 1975; 13:237246.CrossRefGoogle ScholarPubMed
47.Rosvold, HE, Szwarcbart, MK.Neural structures involved in delayed-response performance. In: Warren, JM, Akert, K, eds. The Frontal Granular Cortex and Behaviour. New York: McGraw-Hill 1964: 115.Google Scholar
48.Isseroff, A, Rosvold, HE, Galkin, TW, et al. Spatial memory impairments following damage to the mediodorsal nucleus of the thalamus in rhesus monkeys. Brain Res 1982; 232: 97113.CrossRefGoogle Scholar
49.Schulman, S.Impaired delayed response from thalamic lesions. Arch Neurol 1964; 11: 477499.CrossRefGoogle ScholarPubMed
50.Johnson, TN, Rosvold, HE, Mishkin, M.Projections of behaviorally defined sectors of the prefrontal cortex to the basal ganglia, septum and diencephalon of the monkey. Exp Neurol 1968; 21: 2034.CrossRefGoogle Scholar
51.Akert, K.Comparative anatomy of frontal cortex and thalamo frontal connections. In: Warren, JM, Akert, K, eds. The Frontal Granular Cortex and Behavior. New York: McGraw-Hill 1964: 372396.Google Scholar
52.Walker, AE.The Primate Thalamus. Chicago: University of Chicago Press 1938.Google Scholar
53.Hornykiewicz, O.Brain dopamine in Parkinson’s disease and other neurological disturbances. In: Horn, AS, Korf, J, Westerink, BHC, eds. The Neurobiology of Dopamine. New York: Academic Press 1979: 633–54.Google Scholar
54.Kish, SJ, Rajput, A, Gilbert, J, et al. Elevated γ-Aminobutyric acid level in striatal but not extrastriatal brain regions in Parkinson’s disease: correlation with striatal dopamine loss. Ann Neurol 1986; 20: 2631.CrossRefGoogle Scholar
55.Mahut, H.Spatial and object reversal learning in monkeys with partial temporal lobe ablations. Neuropsychologia 1971; 9: 409424.CrossRefGoogle ScholarPubMed
56.Mahut, H, Cordeau, JP.Spatial reversal deficit in monkeys with amygdalohippocampal ablations. Exp Neurol 1963; 7: 426434.CrossRefGoogle Scholar
57.Sandson, JS, Albert, ML.Varieties of perseveration. Neuropsychologia 1984; 6: 715732.CrossRefGoogle Scholar
58.Mishkin, M.Perseveration of central sets after frontal lesions in monkeys. In: Warren, JM, Akert, K, eds. The Frontal Granular Cortex and Behavior. New York: McGraw-Hill Book Company 1964: 219241.Google Scholar
59.Tomlinson, PE.The pathology of dementia. In: Wells, CE, ed. Dementia. Philadelphia: FA Davis 1977; 113153.Google ScholarPubMed
60.Albert, ML.Subcortical dementia. In: Katzman, R, Terry, RD, Bick, KL, eds. Alzheimer’s Disease: Senile Dementia and Related Disorders. New York: Raven Press 1978: 173180.Google Scholar
61.Cummings, JL, Benson, DF, eds. Dementia: A Clinical Approach. Boston: Butterworths 1983.Google Scholar
62.Cummings, JL, Benson, DR.Subcortical dementia. Arch Neurol 1984; 41: 874889.CrossRefGoogle ScholarPubMed