| Literature DB >> 26444757 |
Jonathan Spiegel1,2, Elizabeth Pirraglia1, Ricardo S Osorio1, Lidia Glodzik1, Yi Li1, Wai Tsui1, Leslie A Saint Louis3, Catherine Randall1, Tracy Butler1, Jinfeng Xu1, Raymond P Zinkowski4, Henrik Zetterberg5, Juan Fortea6, Silvia Fossati1,7, Thomas Wisniewski7, Peter Davies8, Kaj Blennow5, Mony J de Leon1,9.
Abstract
Cerebrospinal fluid (CSF) measures of phosphorylated-tau (P-tau) 231 and P-tau181 are two biomarkers for the identification of tau pathology as related to Alzheimer's disease (AD). While both are pathologically validated, their relative diagnostic performances are not well known. This cross-sectional diagnostic study of 87 normal (NL) subjects and 28 AD subjects compared CSF P-tau231 with CSF P-tau181. Logistic regression modeling demonstrated that the P-tau231 was superior to the P-tau181 in the diagnostic classifications. At a fixed 85% sensitivity cutoff, the ROC analysis shows that P-tau231 has greater overall specificity than P-tau181. While both P-tau analytes demonstrated equivalent negative predictive accuracies, P-tau231 yielded significantly fewer false positives. Moreover, P-tau231, but not P-tau181, demonstrated sensitivity to the E4 genotype. A postmortem validation with 9 AD subjects confirmed the superiority of the CSF P-tau231 specificity. This study suggests that P-tau231 has the potential to improve the CSF tau biomarker diagnosis of AD.Entities:
Keywords: Alzheimer’s disease; P-tau181; P-tau231; biomarkers; hyperphosphorylated tau
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Year: 2016 PMID: 26444757 PMCID: PMC4694576 DOI: 10.3233/JAD-150167
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472