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There were no differences in A\u03b2040 levels between groups or between subjects with and without CAA.<\/jats:p><\/jats:sec><jats:sec><jats:title>Discussion<\/jats:title><jats:p>CAA is more frequently found in genetically determined AD than in sporadic EOAD. Cerebrospinal fluid A\u03b240 levels are not a useful biomarker for CAA in AD.<\/jats:p><\/jats:sec>","DOI":"10.1016\/j.jalz.2017.03.007","type":"journal-article","created":{"date-parts":[[2017,4,29]],"date-time":"2017-04-29T17:00:12Z","timestamp":1493485212000},"page":"1251-1260","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":89,"title":["Cerebral amyloid angiopathy in Down syndrome and sporadic and autosomal\u2010dominant Alzheimer's disease"],"prefix":"10.1002","volume":"13","author":[{"given":"Mar\u00eda","family":"Carmona\u2010Iragui","sequence":"first","affiliation":[{"name":"Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau Biomedical Research Institute Sant Pau, Universitat Aut\u00f2noma de Barcelona  Barcelona Spain"},{"name":"Barcelona Down Medical Center, Fundaci\u00f3 Catalana de S\u00edndrome de Down  Barcelona Spain"},{"name":"Centro de Investigaci\u00f3n Biom\u00e9dica en Red de 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