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Published on: December 18, 2016
Circle of Willis abnormalities and their clinical importance in ageing brains: A cadaveric anatomical and
P Wijesinghe1, H W M Steinbusch2, S K Shankar3
1Interdisciplinary Center for Innovation in Biotechnology & Neuroscience, Genetic Diagnostic & Research Laboratory and Human Brain Tissue and DNA Repository, Dept. Anatomy, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka; EURON - European Graduate School of Neuroscience, Maastricht, The Netherlands.
Insights
Most elderly brains show circle of Willis abnormalities, like hypoplasia and atherosclerosis. These changes had limited association with neurodegenerative diseases but were linked to microscopic infarcts.
Area of Science:
- Neurology
- Cerebrovascular Research
- Neuroanatomy
Background:
- The circle of Willis (CW) is a critical brain artery network for cerebral blood flow.
- CW morphopathology may correlate with neurodegenerative and cerebrovascular disease severity.
- Understanding CW changes in aging is vital for clinical insights.
Purpose of the Study:
- To investigate circle of Willis abnormalities in aging brains.
- To determine the clinical significance of CW variations in the elderly.
- To explore associations between CW pathology and neurodegenerative conditions.
Main Methods:
- Macroscopic examination of 73 formalin-fixed brains for CW stenosis, atherosclerosis, hypoplasia, variations, and aneurysms.
- Immunohistopathological screening for age-related neurodegenerative and cerebrovascular pathologies.
- Statistical analysis using Fisher's exact test to assess associations.
Main Results:
- 93% of elderly brains had at least one hypoplastic CW component.
- Over 90% exhibited CW atherosclerosis.
- Significant association found between deep white matter microinfarcts and communicating artery hypoplasia (p < 0.05).
- A trend (p=0.05) linked Braak's NFT stages to mild-to-severe CW atherosclerosis.
Conclusions:
- Circle of Willis abnormalities are highly prevalent in aging brains.
- CW pathology shows limited direct association with the severity of neurodegenerative diseases.
- Hypoplasia in communicating arteries may be linked to microscopic white matter infarcts.
Abstract:
The circle of Willis (CW) located at the base of the brain forms an important collateral network to maintain adequate cerebral perfusion, especially in clinical situations requiring compensatory changes in blood flow. Morphopathological changes in the CW may relate to the severity of the symptoms of certain neurodegenerative and cerebrovascular disorders. The purpose of this study was to investigate the CW abnormalities and their clinical importance in ageing brains. The CW was examined macroscopically in 73 formalin-fixed samples to determine the degree of stenosis of each CW component, atherosclerosis of the CW, hypoplasia (threshold diameter < 1 mm), anatomical variations and aneurysms. Age-related neurodegenerative and cerebrovascular pathologies were screened using immunohistopathological techniques on specific neuroanatomical regions based on standard guidelines. The majority of the elderly brains -93 % (68/73) presented at least a single hypoplastic CW component at death. Anatomical variations were mostly identified in communicating arteries, followed by proximal posterior and anterior cerebral arteries. Arterial bifurcations were found to be the predominant sites for cerebral aneurysms. More than 90 % of the elderly brains presented CW atherosclerosis at death. CW abnormalities did not show any strong associations with neurodegenerative pathologies except for an "at risk" significant association observed between Braak's neurofibrillary tangle (NFT) stages 1-VI and CW atherosclerosis grades ≥ mild (p = 0.05). However, a significant association was observed between microscopic infarcts in deep white matter and hypoplasia in communicating arteries with Fisher's exact test (p < 0.05). Overall, CW abnormalities were predominant in the ageing brains, however their relationships to the occurrence and severity of the symptoms of neurodegenerative pathologies were found to be low.
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