Detection of varicella zoster virus antigen and DNA in two cases of cerebral amyloid angiopathy.

J Neurol Sci

Department of Neurology, University of Colorado School of Medicine, Aurora, CO 80045, United States; Department of Ophthalmology, University of Colorado School of Medicine, Aurora, CO 80045, United States. Electronic address:

Published: March 2021

AI Article Synopsis

  • - The study investigates the relationship between varicella zoster virus (VZV) and cerebral amyloid angiopathy (CAA), both of which affect blood vessels in older adults and can lead to cognitive decline.
  • - Researchers analyzed brain tissue from two deceased subjects with confirmed CAA, using techniques to identify the presence of VZV, amyloid-beta (Aβ), and amylin, finding that VZV was present along with Aβ in the affected arteries.
  • - The findings suggest a potential link between VZV infection and the development of CAA, as VZV was detected in some arteries closely associated with Aβ deposits.

Article Abstract

Objective: Varicella zoster virus (VZV) vasculopathy and cerebral amyloid angiopathy (CAA) have similar clinical presentations: both affect cerebrovasculature in the elderly, produce hemorrhage, and can have a protracted course of cognitive decline and other neurological deficits. The cause of CAA is unknown, but amyloid-beta (Aβ) is found within arterial walls. Recent studies show that VZV induces Aβ and amylin expression and an amyloid-promoting environment. Thus, we determined if VZV was present in CAA-affected arteries.

Methods: Two subjects with pathologically-verified CAA were identified postmortem and frontal lobes analyzed by immunohistochemistry for arteries containing VZV, Aβ, and amylin and H&E for pathological changes. VZV antigen detection was confirmed by PCR for VZV DNA in the same region.

Results: In both CAA cases, sections with cerebral arteries containing VZV antigen with corresponding VZV DNA were identified; VZV antigen co-localized with Aβ in media of arteries with histological changes characteristic of CAA. Amylin was also seen in the intima of a VZV-positive artery in the diabetic subject. Not all Aβ-containing arteries had VZV, but all VZV-positive arteries contained Aβ.

Conclusions: VZV antigen co-localized with Aβ in some affected arteries from two CAA cases, suggesting a possible association between VZV infection and CAA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935758PMC
http://dx.doi.org/10.1016/j.jns.2021.117315DOI Listing

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