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Plasma tau and <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L concentrations were measured using ultra\u2010sensitive single molecule array technology.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Plasma and <jats:styled-content style=\"fixed-case\">CSF<\/jats:styled-content> tau (<jats:italic>R<\/jats:italic> = 0.59, <jats:italic>P<\/jats:italic> &lt; 0.001) and <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L (<jats:italic>R<\/jats:italic> = 0.69, <jats:italic>P<\/jats:italic> &lt; 0.001) levels correlated significantly (Spearman test). Plasma tau and <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L levels were significantly higher in all disease groups compared to healthy controls (<jats:italic>P<\/jats:italic> &lt; 0.001). Receiver operating characteristic curves were used and area under the curve values for comparisons with controls were 0.82 (<jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>), 0.94 (sporadic <jats:styled-content style=\"fixed-case\">CJD<\/jats:styled-content>), 0.92 (genetic <jats:styled-content style=\"fixed-case\">CJD<\/jats:styled-content>) and 0.83 (other neurological disorders) for plasma tau and 0.99, 0.99, 1.00 and 0.96 for plasma <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L, respectively. Molecular subtyping of sporadic <jats:styled-content style=\"fixed-case\">CJD<\/jats:styled-content> showed a strong effect (linear logistic regression) on plasma tau (<jats:italic>P<\/jats:italic> &lt; 0.001) but not <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L levels (<jats:italic>P<\/jats:italic> = 0.19).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Plasma tau and <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L concentrations are strongly increased in <jats:styled-content style=\"fixed-case\">CJD<\/jats:styled-content> and show similar diagnostic performance to the corresponding <jats:styled-content style=\"fixed-case\">CSF<\/jats:styled-content> measure. Molecular subtypes of sporadic <jats:styled-content style=\"fixed-case\">CJD<\/jats:styled-content> show different levels of plasma tau. Although not disease\u2010specific, these findings support the use of plasma tau and <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010L as tools to identify, or to rule out, neurodegeneration.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ene.13389","type":"journal-article","created":{"date-parts":[[2017,8,17]],"date-time":"2017-08-17T07:43:28Z","timestamp":1502955808000},"page":"1326","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":79,"title":["Plasma and cerebrospinal fluid tau and neurofilament concentrations in rapidly progressive neurological syndromes: a neuropathology\u2010based cohort"],"prefix":"10.1111","volume":"24","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3841-5511","authenticated-orcid":false,"given":"G. 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