<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chang HI</submitter><funding>National Science and Technology Council</funding><pagination>194</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12366151</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>Early and cost-effective identification of amyloid positivity is crucial for Alzheimer's disease (AD) diagnosis. While amyloid PET is the gold standard, plasma biomarkers such as phosphorylated tau 217 (pTau217) provide a potential alternative. This study evaluates the diagnostic accuracy of a combined-panel approach using machine learning models and evaluated the biomarker significance.&lt;h4>Methods&lt;/h4>We enrolled 371 participants, including AD (n = 143), non-AD (n = 159), and cognitively unimpaired (CU, n = 69) controls. Combined panels of pTau217, pTau181, glial fibrillary acidic protein (GFAP), neurofilament light chain (NFL), Aβ42/40, and total tau were measured prior to the amyloid PET scan. The multiclass logistic (LR) regression, support vector machines, decision trees, and random forests (RF)-were applied to classify amyloid positivity (A+) at all stages or at early clinical stages (1-3). In AD, we tested whether the biomarker may define the clinical stagings.&lt;h4>Results&lt;/h4>When benchmarked against amyloid PET, plasma biomarker-based stratification achieves an optimal balance between diagnostic accuracy and cost-effectiveness. The multi-class LR performed equivalently with RF model in identifying A+. The combined plasma panel reached an > 92% accuracy in identifying A+, with performance increasing to 93.4% at early clinical stages. We ranked the importance of individual biomarkers and pTau217 alone achieved comparable accuracy (> 90%) and was the top-ranked biomarker in the LR or RF model. NFL and GFAP correlated significantly with Mini-Mental State Examination; however, these plasma biomarkers did not enhance clinical staging stratification.&lt;h4>Discussion&lt;/h4>The use of multiclass LR model enhances amyloid classification, particularly at earlier clinical stages. While the combined-panel approach is most accurate, pTau217 alone provides a cost-effective alternative for screening. These findings support the integration of plasma biomarkers and ML into clinical workflows for early detection and patient stratification.</pubmed_abstract><journal>Alzheimer's research &amp; therapy</journal><pubmed_title>Optimizing timing and cost-effective use of plasma biomarkers in Alzheimer's disease.</pubmed_title><pmcid>PMC12366151</pmcid><funding_grant_id>NSTC113-2321-B-182A-005</funding_grant_id><pubmed_authors>Chang CC</pubmed_authors><pubmed_authors>Lin KJ</pubmed_authors><pubmed_authors>Huang KL</pubmed_authors><pubmed_authors>Chang HI</pubmed_authors><pubmed_authors>Huang CG</pubmed_authors><pubmed_authors>Huang CW</pubmed_authors><pubmed_authors>Huang SH</pubmed_authors><pubmed_authors>Ma MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimizing timing and cost-effective use of plasma biomarkers in Alzheimer's disease.</name><description>&lt;h4>Background and objectives&lt;/h4>Early and cost-effective identification of amyloid positivity is crucial for Alzheimer's disease (AD) diagnosis. While amyloid PET is the gold standard, plasma biomarkers such as phosphorylated tau 217 (pTau217) provide a potential alternative. This study evaluates the diagnostic accuracy of a combined-panel approach using machine learning models and evaluated the biomarker significance.&lt;h4>Methods&lt;/h4>We enrolled 371 participants, including AD (n = 143), non-AD (n = 159), and cognitively unimpaired (CU, n = 69) controls. Combined panels of pTau217, pTau181, glial fibrillary acidic protein (GFAP), neurofilament light chain (NFL), Aβ42/40, and total tau were measured prior to the amyloid PET scan. The multiclass logistic (LR) regression, support vector machines, decision trees, and random forests (RF)-were applied to classify amyloid positivity (A+) at all stages or at early clinical stages (1-3). In AD, we tested whether the biomarker may define the clinical stagings.&lt;h4>Results&lt;/h4>When benchmarked against amyloid PET, plasma biomarker-based stratification achieves an optimal balance between diagnostic accuracy and cost-effectiveness. The multi-class LR performed equivalently with RF model in identifying A+. The combined plasma panel reached an > 92% accuracy in identifying A+, with performance increasing to 93.4% at early clinical stages. We ranked the importance of individual biomarkers and pTau217 alone achieved comparable accuracy (> 90%) and was the top-ranked biomarker in the LR or RF model. NFL and GFAP correlated significantly with Mini-Mental State Examination; however, these plasma biomarkers did not enhance clinical staging stratification.&lt;h4>Discussion&lt;/h4>The use of multiclass LR model enhances amyloid classification, particularly at earlier clinical stages. While the combined-panel approach is most accurate, pTau217 alone provides a cost-effective alternative for screening. These findings support the integration of plasma biomarkers and ML into clinical workflows for early detection and patient stratification.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-29T15:04:29.224Z</modification><creation>2026-04-08T05:11:54.687Z</creation></dates><accession>S-EPMC12366151</accession><cross_references><pubmed>40830505</pubmed><doi>10.1186/s13195-025-01851-2</doi></cross_references></HashMap>