<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shuping JL</submitter><funding>NIA NIH HHS</funding><pagination>e12372</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9983143</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The positron emission tomography (PET) radiotracer [&lt;sup>18&lt;/sup>F]MK-6240 exhibits high specificity for neurofibrillary tangles (NFTs) of tau protein in Alzheimer's disease (AD), high sensitivity to medial temporal and neocortical NFTs, and low within-brain background. Objectives were to develop and validate a reproducible, clinically relevant visual read method supporting [&lt;sup>18&lt;/sup>F]MK-6240 use to identify and stage AD subjects versus non-AD and controls.&lt;h4>Methods&lt;/h4>Five expert readers used their own methods to assess 30 scans of mixed diagnosis (47% cognitively normal, 23% mild cognitive impairment, 20% AD, 10% traumatic brain injury) and provided input regarding regional and global positivity, features influencing assessment, confidence, practicality, and cl</pubmed_abstract><journal>Alzheimer's &amp; dementia (New York, N. Y.)</journal><pubmed_title>Development, initial validation, and application of a visual read method for [&lt;sup>18&lt;/sup>F]MK-6240 tau PET.</pubmed_title><pmcid>PMC9983143</pmcid><funding_grant_id>RF1 AG058067</funding_grant_id><funding_grant_id>K24 AG045334</funding_grant_id><funding_grant_id>R01 AG050436</funding_grant_id><funding_grant_id>R01 AG052414</funding_grant_id><funding_grant_id>R01 AG038465</funding_grant_id><funding_grant_id>R01 AG055299</funding_grant_id><funding_grant_id>R01 AG050440</funding_grant_id><funding_grant_id>P30 AG062715</funding_grant_id><funding_grant_id>RF1 AG051556</funding_grant_id><funding_grant_id>R01 AG055422</funding_grant_id><funding_grant_id>R01 AG062285</funding_grant_id><funding_grant_id>P01 AG025204</funding_grant_id><funding_grant_id>K23 AG052633</funding_grant_id><funding_grant_id>RF1 AG027161</funding_grant_id><funding_grant_id>R01 AG021155</funding_grant_id><funding_grant_id>R01 AG063888</funding_grant_id><funding_grant_id>R00 AG065506</funding_grant_id><funding_grant_id>R01 AG062167</funding_grant_id><pubmed_authors>Wilde CL</pubmed_authors><pubmed_authors>Klunk WE</pubmed_authors><pubmed_authors>Scott D</pubmed_authors><pubmed_authors>Brickman AM</pubmed_authors><pubmed_authors>Lukic AS</pubmed_authors><pubmed_authors>Ward L</pubmed_authors><pubmed_authors>Mathotaarachchi SS</pubmed_authors><pubmed_authors>Rowe CC</pubmed_authors><pubmed_authors>Devanand DP</pubmed_authors><pubmed_authors>Johnson SC</pubmed_authors><pubmed_authors>Johnson KA</pubmed_authors><pubmed_authors>Boxer AL</pubmed_authors><pubmed_authors>Lao PJ</pubmed_authors><pubmed_authors>Sur C</pubmed_authors><pubmed_authors>Price JC</pubmed_authors><pubmed_authors>Cordes L</pubmed_authors><pubmed_authors>Rosa-Neto P</pubmed_authors><pubmed_authors>Stern Y</pubmed_authors><pubmed_authors>Luchsinger JA</pubmed_authors><pubmed_authors>Andrews RD</pubmed_authors><pubmed_authors>Van Laere K</pubmed_authors><pubmed_authors>Evelhoch JL</pubmed_authors><pubmed_authors>Barakos J</pubmed_authors><pubmed_authors>Kreisl WC</pubmed_authors><pubmed_authors>Purcell DD</pubmed_authors><pubmed_authors>Matthews DC</pubmed_authors><pubmed_authors>Shuping JL</pubmed_authors><pubmed_authors>Adamczuk K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development, initial validation, and application of a visual read method for [&lt;sup>18&lt;/sup>F]MK-6240 tau PET.</name><description>&lt;h4>Background&lt;/h4>The positron emission tomography (PET) radiotracer [&lt;sup>18&lt;/sup>F]MK-6240 exhibits high specificity for neurofibrillary tangles (NFTs) of tau protein in Alzheimer's disease (AD), high sensitivity to medial temporal and neocortical NFTs, and low within-brain background. Objectives were to develop and validate a reproducible, clinically relevant visual read method supporting [&lt;sup>18&lt;/sup>F]MK-6240 use to identify and stage AD subjects versus non-AD and controls.&lt;h4>Methods&lt;/h4>Five expert readers used their own methods to assess 30 scans of mixed diagnosis (47% cognitively normal, 23% mild cognitive impairment, 20% AD, 10% traumatic brain injury) and provided input regarding regional and global positivity, features influencing assessment, confidence, practicality, and cl</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan-Mar</publication><modification>2026-03-17T15:23:46.683Z</modification><creation>2025-08-16T03:06:32.324Z</creation></dates><accession>S-EPMC9983143</accession><cross_references><pubmed>36873926</pubmed><doi>10.1002/trc2.12372</doi></cross_references></HashMap>