4.5 Article

Association of cortical microinfarcts and cerebral small vessel pathology in the ageing brain

期刊

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
卷 43, 期 6, 页码 505-513

出版社

WILEY
DOI: 10.1111/nan.12366

关键词

aetiology; arteriosclerosis; cerebral amyloid angiopathy; cortical microinfarct; hypoperfusion; thromboembolism

资金

  1. Swiss National Foundation [SNF 320030_159990]
  2. NIH [P50 AG005138]
  3. Swiss National Science Foundation (SNF) [320030_159990] Funding Source: Swiss National Science Foundation (SNF)

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AimsCortical 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. MethodsPial and intracortical vessels around CMI were assessed for their integrity with haematoxylin-eosin staining and antibodies against amyloid- 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. ResultsA 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. ConclusionsThe 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.

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