» Articles » PMID: 27783888

Association of Cortical Microinfarcts and Cerebral Small Vessel Pathology in the Ageing Brain

Overview
Specialty Neurology
Date 2016 Oct 27
PMID 27783888
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Aims: Cortical microinfarcts (CMI) are frequently observed in the ageing brain independent of cognitive decline, but their aetiology is not fully elucidated. To examine the potential role of different vessel pathologies, including cerebral amyloid angiopathy (CAA), arteriolosclerosis-hyalinosis and thromboembolism in the development of CMI, we examined 80 autopsy cases with more than one CMI on routine neuropathological examination.

Methods: Pial and intracortical vessels around CMI were assessed for their integrity with haematoxylin-eosin staining and antibodies against amyloid-β protein and fibrinogen using a semiquantitative four-level rating scale (absent to severe) in the hippocampus, and the frontal, temporal and occipital cortex. Four histological categories of changes were defined: CAA, vessel pathology other than CAA, thromboembolism and absence of vessel pathology near CMI.

Results: A differential distribution of microvascular pathology was observed depending on brain regions. In the occipital cortex, CAA was commonly associated with CMI. In contrast, in the hippocampus and the frontal cortex, cases without any vascular pathology in pial and intracortical vessels were significantly more frequent.

Conclusions: The aetiology of CMI differs depending on brain location. CAA may play a role principally in the occipital cortex. The large number of intact vessels around the CMI (mainly in the frontal cortex and hippocampus) raises the possibility that pathologies other than structural microangiopathy, including hypoperfusion/arterial hypotension or large vessel atherosclerosis, play a role in the development of microvascular lesions. These results are relevant in the context of aetiopathogenesis of vascular changes associated with conditions like vascular dementia.

Citing Articles

Cortical microinfarcts in adults with Down syndrome assessed with 3T-MRI.

Aranha M, Montal V, van den Brink H, Pegueroles J, Carmona-Iragui M, Videla L Alzheimers Dement. 2024; 20(6):3906-3917.

PMID: 38644660 PMC: 11180852. DOI: 10.1002/alz.13797.


Magnetic resonance imaging and neuropsychological findings for predicting of cognitive deterioration in memory clinic patients.

Matsuda K, Shinohara M, Ii Y, Tabei K, Ueda Y, Nakamura N Front Aging Neurosci. 2023; 15:1155122.

PMID: 37600513 PMC: 10435295. DOI: 10.3389/fnagi.2023.1155122.


Insights into the pathological basis of dementia from population-based neuropathology studies.

Wharton S, Simpson J, Ince P, Richardson C, Merrick R, Matthews F Neuropathol Appl Neurobiol. 2023; 49(4):e12923.

PMID: 37462105 PMC: 10946587. DOI: 10.1111/nan.12923.


Arteriolosclerosis differs from venular collagenosis in relation to cerebrovascular parenchymal damages: an autopsy-based study.

Cao Y, Huang M, Mao C, Wang X, Xu Y, Qian X Stroke Vasc Neurol. 2022; 8(4):267-275.

PMID: 36581493 PMC: 10512076. DOI: 10.1136/svn-2022-001924.


Cerebral microinfarct is emergency consequence of Alzheimer's disease: a new insight into development of neurodegenerative diseases.

Lin X, Fan Y, Zhang F, Lin Y Int J Biol Sci. 2022; 18(4):1569-1579.

PMID: 35280690 PMC: 8898357. DOI: 10.7150/ijbs.55419.