Cerebral amyloid angiopathy (CAA) is a small vessel disease characterized by the deposition
of amyloid-beta in small cerebral vessels, which can lead to intracerebral hemorrhages
and cognitive impairment. Rare variants, such as cerebral amyloid angiopathy-related
inflammation (CAA-ri) and iatrogenic CAA (ICAA), may mimic other neurological conditions
and challenge diagnosis in clinical practice. We present three cases that illustrate
distinct CAA syndromes, along with CSF biomarker analysis. One patient experienced
recurrent hemorrhagic strokes with a history of dural graft, raising concerns about
amyloid transmission. Two patients presented with rapidly progressive dementia that
fulfilled CAA-ri criteria. All cases exhibited decreased levels of CSF Aβ40 and Aβ42,
with one showing elevated p-tau, suggesting comorbid Alzheimer's pathology. Cerebrospinal
fluid biomarkers complement neuroimaging in the diagnosis of CAA, aiding in differentiation
from other dementias. Early recognition and diagnosis of CAA-ri variants is crucial,
because immunotherapy may improve outcomes. Further research is necessary to establish
biomarker thresholds and their clinical applicability.
Keywords
Cerebral Amyloid Angiopathy - Biomarkers - Amyloid Beta-Peptides - Cerebrospinal Fluid
Bibliographical Record
Ana Silvia Sobreira Lima Verde, Alessandra Braga Cruz Guedes de Morais, Amanda Vale
Catunda, João Igor Dantas Landim, Ian Silva Ribeiro, Bruno Diógenes Iepsen, Norberto
Anízio Ferreira Frota. Cerebrospinal fluid biomarkers in cerebral amyloid angiopathy:
insights from a clinical case series. Arq Neuropsiquiatr 2025; 83: s00451812887.
DOI: 10.1055/s-0045-1812887