Disentangling relationships between Alzheimer's disease plasma biomarkers and established biomarkers in patients of tertiary memory clinics

dc.contributor.authorBluma, M
dc.contributor.authorChiotis, K
dc.contributor.authorBucci, M
dc.contributor.authorSavitcheva, I
dc.contributor.authorMatton, A
dc.contributor.authorKivipelto, M
dc.contributor.authorJeromin, A
dc.contributor.authorDe Santis, G
dc.contributor.authorDi Molfetta, G
dc.contributor.authorAshton, NJ
dc.contributor.authorBlennow, K
dc.contributor.authorZetterberg, H
dc.contributor.authorNordberg, A
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.14646305228
dc.converis.publication-id484250817
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/484250817
dc.date.accessioned2025-08-27T21:36:28Z
dc.date.available2025-08-27T21:36:28Z
dc.description.abstract<p><b>Background </b>Several plasma biomarkers for Alzheimer's disease (AD) have demonstrated diagnostic and analytical robustness. Yet, contradictory results have been obtained regarding their association with standard diagnostic markers of AD. This study aims to investigate the specific relationship between the AD biomarkers currently used in clinical practice and the plasma biomarkers.<br></p><p><b>Methods </b>In a memory clinic cohort, we analysed plasma pTau181, pTau217, pTau231, respectively, GFAP, NfL, CSF pTau181, Aβ-PET scans, and MRI/CT visual read of atrophy. We utilized methods based on multiple linear regression to evaluate the specific associations between clinically used and recently developed plasma biomarkers, while also considering demographic variables such as age and sex.<br></p><p><b>Findings </b>Although plasma pTau181, pTau217, pTau231, and GFAP were significantly associated with both Aβ-PET and CSF pTau181, Aβ-PET explained more variance in the levels of these biomarkers. The effect of CSF pTau181 on plasma GFAP and pTau181 was completely attenuated by Aβ-PET, whereas pTau231 and pTau217 were affected by both Aβ-PET and CSF pTau181 levels. Unlike these biomarkers, increased NfL was rather indicative of brain atrophy and older age. Based on the effect sizes, plasma pTau217 emerged as highly effective in distinguishing between A+ and A-, and T+ and T- individuals, with 60% of variance in plasma pTau217 explained by clinical AD biomarkers.<br></p><p><b>Interpretation </b>Amyloid burden primarily drives the changes in plasma pTau181, pTau217, pTau231, and GFAP. In contrast to plasma pTau217, a significant portion of variance in plasma pTau181, pTau231, GFAP, NfL remains unexplained by clinical AD biomarkers.<br></p><p><b>Funding </b>This research is supported by the Swedish Research Council VR: 2017-06086, 2020-4-3018, 2024-2027; Swedish Brain Foundation, Swedish Alzhzeimer Foundation, CIMED Region Stockholm/Karolinska Institutet; the Region Stockholm - Karolinska Institutet regional agreement on medical training and clinical research (ALF), Fondation Recherche sur Alzheimer (France).<br></p>
dc.identifier.eissn2352-3964
dc.identifier.jour-issn2352-3964
dc.identifier.olddbid200727
dc.identifier.oldhandle10024/183754
dc.identifier.urihttps://www.utupub.fi/handle/11111/46755
dc.identifier.urlhttps://doi.org/10.1016/j.ebiom.2024.105504
dc.identifier.urnURN:NBN:fi-fe2025082789213
dc.language.isoen
dc.okm.affiliatedauthorBucci, Marco
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.articlenumber105504
dc.relation.doi10.1016/j.ebiom.2024.105504
dc.relation.ispartofjournalEBioMedicine
dc.relation.volume112
dc.source.identifierhttps://www.utupub.fi/handle/10024/183754
dc.titleDisentangling relationships between Alzheimer's disease plasma biomarkers and established biomarkers in patients of tertiary memory clinics
dc.year.issued2025

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