APP-Aβ Metabolism in Rare Cerebral Small Vessel Vasculitides

A special issue of Metabolites (ISSN 2218-1989).

Deadline for manuscript submissions: closed (15 November 2022) | Viewed by 1069

Special Issue Editor


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Guest Editor
Department of Experimental Neurology, Charité – Universität smedizin Berlin, 1, 10117 Berlin, Germany
Interests: genetics; Alzheimer’s disease; neurodegenerative diseases; dementia; vascular
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Special Issue Information

Dear Colleagues,

An imbalance between amyloid precursor protein (APP) production and degradation is the leading cause of familial and sporadic Alzheimer’s disease (AD), respectively. Importantly, cerebral small-vessel disease (cSVD) represents a critical factor that significantly influences AD onset and progression, and frequently co-exists with AD. A growing body of literature has described APP-Aβ metabolism in the classical sporadic and monogenic forms of cSVD. However, the association of APP-Aβ catabolism with rare inflammatory and immunologically mediated cSVD has not been deeply investigated. Therefore, the aim of this Special Issue is to describe clinical-pathological and laboratory features associated with APP-Aβ dysmetabolism in rare cerebral small-vessel Vasculitides, with a particular focus on cerebral amyloid angiopathy (CAA)-related inflammation (CAA-RI), amyloid-β-related angiitis (ABRA), eosinophilic granulomatosis with polyangiitis (EGPA), and rheumatoid vasculitis.

Dr. Celeste Sassi
Guest Editor

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Keywords

  • APP-Aβ metabolism
  • Alzheimer’s disease (AD)
  • cerebral small-vessel disease (cSVD)
  • amyloid angiopathy (CAA)-related inflammation (CAA-RI)
  • amyloid-β-related angiitis (ABRA)
  • eosinophilic granulomatosis with polyangiitis (EGPA)
  • rheumatoid vasculitis

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