<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Fandos N</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Plasma amyloid β (Aβ) peptides have been previously studied as candidate biomarkers to increase recruitment efficiency in secondary prevention clinical trials for Alzheimer's disease.&lt;h4>Methods&lt;/h4>Free and total Aβ42/40 plasma ratios (FP42/40 and TP42/40, respectively) were determined using ABtest assays in cognitively normal subjects from the Australian Imaging, Biomarker and Lifestyle Flagship Study. This population was followed-up for 72 months and their cortical Aβ burden was assessed with positron emission tomography.&lt;h4>Results&lt;/h4>Cross-sectional and longitudinal analyses showed an inverse association of Aβ42/40 plasma ratios and cortical Aβ burden. Optimized as a screening tool, TP42/40 reached 81% positive predictive value of high cortical Aβ burden, which r</pubmed_abstract><journal>Alzheimer's &amp; dementia (Amsterdam, Netherlands)</journal><pagination>179-187</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5602863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals.</pubmed_title><pmcid>PMC5602863</pmcid><pubmed_authors>AIBL Research Group</pubmed_authors><pubmed_authors>Perez-Grijalba V</pubmed_authors><pubmed_authors>Fowler C</pubmed_authors><pubmed_authors>Fandos N</pubmed_authors><pubmed_authors>Villemagne VL</pubmed_authors><pubmed_authors>Masters CL</pubmed_authors><pubmed_authors>Sarasa M</pubmed_authors><pubmed_authors>Olmos S</pubmed_authors><pubmed_authors>Pesini P</pubmed_authors><pubmed_authors>Bossa M</pubmed_authors><pubmed_authors>Doecke J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals.</name><description>&lt;h4>Introduction&lt;/h4>Plasma amyloid β (Aβ) peptides have been previously studied as candidate biomarkers to increase recruitment efficiency in secondary prevention clinical trials for Alzheimer's disease.&lt;h4>Methods&lt;/h4>Free and total Aβ42/40 plasma ratios (FP42/40 and TP42/40, respectively) were determined using ABtest assays in cognitively normal subjects from the Australian Imaging, Biomarker and Lifestyle Flagship Study. This population was followed-up for 72 months and their cortical Aβ burden was assessed with positron emission tomography.&lt;h4>Results&lt;/h4>Cross-sectional and longitudinal analyses showed an inverse association of Aβ42/40 plasma ratios and cortical Aβ burden. Optimized as a screening tool, TP42/40 reached 81% positive predictive value of high cortical Aβ burden, which r</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-05T14:31:12.649Z</modification><creation>2019-03-27T02:56:39Z</creation></dates><accession>S-EPMC5602863</accession><cross_references><pubmed>28948206</pubmed><doi>10.1016/j.dadm.2017.07.004</doi></cross_references></HashMap>