Clinical Characteristics, Neuroimaging Markers, and Outcomes in Patients with Cerebral Amyloid Angiopathy: A Prospective Cohort Study

Author:

Theodorou Aikaterini1ORCID,Palaiodimou Lina1ORCID,Papagiannopoulou Georgia1,Kargiotis Odysseas2ORCID,Psychogios Klearchos2ORCID,Safouris Apostolos2ORCID,Bakola Eleni1ORCID,Chondrogianni Maria1,Kotsali-Peteinelli Vasiliki1,Melanis Konstantinos1ORCID,Tsibonakis Athanasios1,Andreadou Elissavet3,Vasilopoulou Sofia3,Lachanis Stefanos4,Velonakis Georgios5ORCID,Tzavellas Elias6,Tzartos John S.1,Voumvourakis Konstantinos1,Paraskevas Georgios P.1ORCID,Tsivgoulis Georgios17ORCID

Affiliation:

1. Second Department of Neurology, “Attikon” University Hospital, School of Medicine, National and Kapodistrian University of Athens, 12462 Athens, Greece

2. Stroke Unit, Metropolitan Hospital, 18547 Piraeus, Greece

3. First Department of Neurology, “Eginition” Hospital, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece

4. Iatropolis Magnetic Resonance Diagnostic Centre, 15231 Athens, Greece

5. Second Department of Radiology, “Attikon” University Hospital, School of Medicine, National and Kapodistrian University of Athens, 12462 Athens, Greece

6. First Department of Psychiatry, “Aiginition” Hospital, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece

7. Department of Neurology, University of Tennessee Health Science Center, Memphis, TN 38163, USA

Abstract

Background and purpose: Sporadic cerebral amyloid angiopathy (CAA) is a small vessel disease, resulting from progressive amyloid-β deposition in the media/adventitia of cortical and leptomeningeal arterioles. We sought to assess the prevalence of baseline characteristics, clinical and radiological findings, as well as outcomes among patients with CAA, in the largest study to date conducted in Greece. Methods: Sixty-eight patients fulfilling the Boston Criteria v1.5 for probable/possible CAA were enrolled and followed for at least twelve months. Magnetic Resonance Imaging was used to assess specific neuroimaging markers. Data regarding cerebrospinal fluid biomarker profile and Apolipoprotein-E genotype were collected. Multiple logistic regression analyses were performed to identify predictors of clinical phenotypes. Cox-proportional hazard regression models were used to calculate associations with the risk of recurrent intracerebral hemorrhage (ICH). Results: Focal neurological deficits (75%), cognitive decline (57%), and transient focal neurological episodes (TFNEs; 21%) were the most common clinical manifestations. Hemorrhagic lesions, including lobar cerebral microbleeds (CMBs; 93%), cortical superficial siderosis (cSS; 48%), and lobar ICH (43%) were the most prevalent neuroimaging findings. cSS was independently associated with the likelihood of TFNEs at presentation (OR: 4.504, 95%CI:1.258–19.088), while multiple (>10) lobar CMBs were independently associated with cognitive decline at presentation (OR:5.418, 95%CI:1.316–28.497). cSS emerged as the only risk factor of recurrent ICH (HR:4.238, 95%CI:1.509–11.900) during a median follow-up of 20 months. Conclusions: cSS was independently associated with TFNEs at presentation and ICH recurrence at follow-up, while a higher burden of lobar CMBs with cognitive decline at baseline. These findings highlight the prognostic value of neuroimaging markers, which may influence clinical decision-making.

Publisher

MDPI AG

Subject

General Medicine

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