The Venular Side of Cerebral Amyloid Angiopathy: Proof of Concept of a Neglected Issue

Author:

Zedde Marialuisa1ORCID,Grisendi Ilaria1ORCID,Assenza Federica1ORCID,Vandelli Gabriele1ORCID,Napoli Manuela2ORCID,Moratti Claudio2ORCID,Lochner Piergiorgio3ORCID,Seiffge David J.4ORCID,Piazza Fabrizio5ORCID,Valzania Franco1ORCID,Pascarella Rosario2ORCID

Affiliation:

1. Neurology Unit, Stroke Unit, AUSL-IRCCS di Reggio Emilia, Via Amendola 2, 42122 Reggio Emilia, Italy

2. Neuroradiology Unit, AUSL-IRCCS di Reggio Emilia, Via Amendola 2, 42122 Reggio Emilia, Italy

3. Department of Neurology, Saarland University Medical Center, 66421 Homburg, Germany

4. Department of Neurology, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland

5. CAA and AD Translational Research and Biomarkers Laboratory, School of Medicine and Surgery, University of Milano-Bicocca, Via Cadore 48, 20900 Monza, Italy

Abstract

Small vessel diseases (SVD) is an umbrella term including several entities affecting small arteries, arterioles, capillaries, and venules in the brain. One of the most relevant and prevalent SVDs is cerebral amyloid angiopathy (CAA), whose pathological hallmark is the deposition of amyloid fragments in the walls of small cortical and leptomeningeal vessels. CAA frequently coexists with Alzheimer’s Disease (AD), and both are associated with cerebrovascular events, cognitive impairment, and dementia. CAA and AD share pathophysiological, histopathological and neuroimaging issues. The venular involvement in both diseases has been neglected, although both animal models and human histopathological studies found a deposition of amyloid beta in cortical venules. This review aimed to summarize the available information about venular involvement in CAA, starting from the biological level with the putative pathomechanisms of cerebral damage, passing through the definition of the peculiar angioarchitecture of the human cortex with the functional organization and consequences of cortical arteriolar and venular occlusion, and ending to the hypothesized links between cortical venular involvement and the main neuroimaging markers of the disease.

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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