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Article type: Short Communication
Authors: Carmona-Iragui, Maríaa; b | Fernández-Arcos, Anaa | Alcolea, Daniela; b | Piazza, Fabrizioc; d | Morenas-Rodriguez, Estrellaa; b | Antón-Aguirre, Sofíaa; b | Sala, Isabela; b | Clarimon, Jordia; b | Dols-Icardo, Oriola; b | Camacho, Vallee | Sampedro, Fredericf | Munuera, Josepg | Nuñez-Marin, Fidelf | Lleó, Albertoa; b | Fortea, Juana; b; * | Gómez-Ansón, Beatrizf; h | Blesa, Rafaela; b
Affiliations: [a] Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain | [b] Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Spain | [c] School of Medicine and Surgery, Milan Center for Neuroscience (NeuroMi), University of Milano-Bicocca, Monza, Italy | [d] The inflammatory Cerebral Amyloid Angiopathy and Alzheimer’s disease βiomarkers International Network (iCAβ), Monza, Italy | [e] Department of Nuclear Medicine, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain | [f] Universitat Autònoma de Barcelona, Facultat de Medicina, Barcelona, Spain | [g] MRI Unit Badalona Institut de Diagnòstic per la Imatge. Hospital Germans Trias i Pujol, Badalona, Spain | [h] Neuroradiology Unit, Department of Radiology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Barcelona, Spain
Correspondence: [*] Correspondence to: Juan Fortea Ormaechea, MD, PhD, Memory Unit, Department of Neurology, Hospital of Sant Pau, Sant Antoni María Claret, 167, 08025, Barcelona, Spain. Tel.: +34 935565986; Fax: +34 935565602; E-mail: jfortea@santpau.cat.
Abstract: We report a biomarker and genetic evaluation of four patients with cerebral amyloid angiopathy-related inflammation (CAA-ri) treated with corticosteroids. Patients presented with focal symptomatology and cognitive impairment. MRI revealed cortical microbleeds and asymmetrical hyperintense white matter lesions (WML). Cerebrospinal fluid (CSF) biomarker analyses showed increased anti-Aβ autoantibodies, t-Tau, and p-Tau and decreased Aβ40 and Aβ42. After treatment, focal symptomatology disappeared, and WML and anti-Aβ autoantibodies decreased. The APOE ɛ4 allele was overrepresented. Florbetapir-PET showed cortical deposition with lower retention in swollen areas. In the case of suspected CAA-ri, both CSF anti-Aβ autoantibodies levels and Florbetapir-PET could provide highly useful data to guide the correct diagnosis.
Keywords: Biomarkers, cerebral amyloid angiopathy, cerebrospinal fluid, Florbetapir-PET, inflammation
DOI: 10.3233/JAD-150614
Journal: Journal of Alzheimer's Disease, vol. 50, no. 1, pp. 1-7, 2016
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