Cited by 397Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration Mechanisms

Distribution of cerebral degeneration in Alzheimer's disease: A clinico-pathological study

Brun, A., Gustafson, L.·1976·Archiv f�r Psychiatrie und Nervenkrankheiten

Abstract

Seven cases of Alzheimer's disease were studied in detail from a clinical and neuropathological point of view. The degenerative process was mapped with regard to regional variations in the intensity, extent and consistency of focal accentuations. The degeneration was regularly found to be most pronounced in certain areas: maximal cortical degeneration occurred in the medial temporal (limbic) area and, in the lateral hemisphere, consistently within a field expanding from the posterior inferior temporal areas to the adjoining portions of the parieto occipital lobes. In addition, the posterior cingulate gyrus was severely involved. On the other hand certain areas were notably and consistently spared or less involved, mainly the anterior cingulate gyrus and the calcarine and central sensory motor areas (primary projection areas). The frontal lobes occupied an intermediate position, being less severely involved than is usually reported. The clinical symptoms correlated well with this pattern of degeneration. Thus groups of symptoms such as memory dysfunction, emotional and personality alterations, and some symptoms of the Klüver-Bucy syndrome, were referable to the limbic lesions. The cortical lesions of the temporo-parieto-occipital association cortex correlated with the symptoms of agnosia, aphasia and apraxia, which were recorded in all cases. The relative sparing of the primary projection areas correspond well to findings of retained motility and perception even in later stages of the disease. The relative sparing of the frontal lobes and the anterior cingulate gyrus was related to the preservation of habitual personality traits. The pattern described may be related to ontogenetic features, and the tendency to focalization to the age of disease onset. The role of genetic factors and of other diseases is discussed.

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Crossref · 10.1007/bf00367450

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References 75 · Cited by 397

Authors
Brun, A., & Gustafson, L.
Affiliations
Skåne University Hospital (SE)
Venue
Archiv f�r Psychiatrie und Nervenkrankheiten
Published
1976
Volume
223
Issue
1
Pages
15-33
ISSN
  • 0003-9373 (ISSN-L)
  • 1433-8491
OpenAlex
W2315630201
Cited by
397
References
75
Citations by year
2026: 1 · 2025: 6 · 2024: 2 · 2023: 6 · 2022: 2 · 2021: 12 · 2020: 6 · 2019: 6 · 2018: 2 · 2017: 2 · 2016: 5 · 2015: 5 · 2014: 5 · 2013: 2 · 2012: 4
FWCI
2.99
Type
journal article
Language
en
Open access
closed
Locations
  • European Archives of Psychiatry and Clinical Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
Alzheimer's disease, cerebral degeneration, medial temporal lobe, limbic system, posterior cingulate cortex, Klüver-Bucy syndrome, memory impairment, agnosia, aphasia, apraxia, age of disease onset, genetic factors
MeSH terms
Aged, Alzheimer Disease, Autopsy, Basal Ganglia, Brain Stem, Cerebellar Cortex, Cerebral Cortex, Dementia, Female, Humans, Limbic System, Male, Mammillary Bodies, Middle Aged, Nerve Degeneration

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