<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang J</submitter><funding>Guangdong Basic and Applied Basic Science Foundation</funding><funding>National Natural Science Foundation of China</funding><funding>Swedish Research Council supported by grants from the Swedish Research Council</funding><funding>European Union's Horizon Europe Research and Innovation Programme</funding><funding>National Key Research and Development Program of China</funding><funding>Shenzhen Bay Laboratory</funding><funding>Chongqing Science and Technology Bureau and the Health Commission</funding><funding>Swedish State Support for Clinical Research</funding><pagination>e70038</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11953589</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(3)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>This study was undertaken to evaluate the diagnostic performance of a novel plasma phosphorylated tau (p-tau) 217/amyloid beta (Aβ) 42 ratio test for Alzheimer's disease (AD).&lt;h4>Methods&lt;/h4>The diagnostic performance of the Lumipulse G plasma p-tau217/Aβ42 ratio was evaluated using Aβ and tau positron emission tomography (PET) as reference standards in a clinic cohort (n = 391) and a community cohort (n = 121).&lt;h4>Results&lt;/h4>Plasma p-tau217/Aβ42 exhibited high performance for abnormal statuses of Aβ PET (area under the curve [AUC]: 0.963 to 0.966) and tau PET (AUC: 0.947 to 0.974), which were clinically equivalent to those of cerebrospinal fluid (CSF) p-tau181/Aβ42 and Aβ42/Aβ40 and higher than those of blood p-tau217, Aβ42/Aβ40, p-tau181, and p-tau181/Aβ42 in both c</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>Diagnostic accuracy of plasma p-tau217/Aβ42 for Alzheimer's disease in clinical and community cohorts.</pubmed_title><pmcid>PMC11953589</pmcid><funding_grant_id>2022-01018</funding_grant_id><funding_grant_id>ALFGBG-71320</funding_grant_id><funding_grant_id>81930028</funding_grant_id><funding_grant_id>S241101004-1</funding_grant_id><funding_grant_id>2023YFC3605400</funding_grant_id><funding_grant_id>2019-02397</funding_grant_id><funding_grant_id>82171197</funding_grant_id><funding_grant_id>2023-00356</funding_grant_id><funding_grant_id>2023B1515020113</funding_grant_id><funding_grant_id>82422027</funding_grant_id><funding_grant_id>101053962</funding_grant_id><funding_grant_id>2024GGXM003</funding_grant_id><funding_grant_id>S241101004‐1</funding_grant_id><funding_grant_id>92249305</funding_grant_id><pubmed_authors>Bourgeat P</pubmed_authors><pubmed_authors>Lai YJ</pubmed_authors><pubmed_authors>Guo T</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Zetterberg H</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Dore V</pubmed_authors><pubmed_authors>Sun P</pubmed_authors><pubmed_authors>Translational Biomarker Research of AgIng and Neurodegeneration (TBRAIN)</pubmed_authors><pubmed_authors>Bu XL</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Liu YH</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors><pubmed_authors>Fripp J</pubmed_authors><pubmed_authors>Xiao ZS</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Masters CL</pubmed_authors><pubmed_authors>Wang YJ</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Wang QH</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Yu JT</pubmed_authors><pubmed_authors>Cai Y</pubmed_authors><pubmed_authors>Lan G</pubmed_authors><pubmed_authors>Zeng F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diagnostic accuracy of plasma p-tau217/Aβ42 for Alzheimer's disease in clinical and community cohorts.</name><description>&lt;h4>Introduction&lt;/h4>This study was undertaken to evaluate the diagnostic performance of a novel plasma phosphorylated tau (p-tau) 217/amyloid beta (Aβ) 42 ratio test for Alzheimer's disease (AD).&lt;h4>Methods&lt;/h4>The diagnostic performance of the Lumipulse G plasma p-tau217/Aβ42 ratio was evaluated using Aβ and tau positron emission tomography (PET) as reference standards in a clinic cohort (n = 391) and a community cohort (n = 121).&lt;h4>Results&lt;/h4>Plasma p-tau217/Aβ42 exhibited high performance for abnormal statuses of Aβ PET (area under the curve [AUC]: 0.963 to 0.966) and tau PET (AUC: 0.947 to 0.974), which were clinically equivalent to those of cerebrospinal fluid (CSF) p-tau181/Aβ42 and Aβ42/Aβ40 and higher than those of blood p-tau217, Aβ42/Aβ40, p-tau181, and p-tau181/Aβ42 in both c</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-07-11T03:04:11.38Z</modification><creation>2025-07-11T03:04:11.38Z</creation></dates><accession>S-EPMC11953589</accession><cross_references><pubmed>40156286</pubmed><doi>10.1002/alz.70038</doi></cross_references></HashMap>