Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease
Recent studies have demonstrated the high analytical and diagnostic performance of plasma p-tau217 using well-defined cohorts. We aimed to assess the analytical, diagnostic, and prognostic utility of plasma p-tau217 as a routine biomarker in symptomatic patients attending our memory clinic. We also...
| Authors: | , , , , , , , , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2025 |
| Country: | España |
| Institution: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repository: | Recercat. Dipósit de la Recerca de Catalunya |
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| Online Access: | https://doi.org/10.3390/ijms26146771 https://hdl.handle.net/10459.1/470260 |
| Access Level: | Open access |
| Keyword: | Alzheimer’s disease Lumipulse Biomarker Mild cognitive impairment p-tau181 p-tau217 Plasma Progression |
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Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's DiseaseDakterzada, FaridaLópez Ortega, RicardVilella-Figuerola, AlbaMontero-Castilla, NathaliaRiba-Llena, IolandaRuiz-Julián, MariaArias, AlfonsoSarto, JordiTahan, NuriaPiñol Ripoll, GerardAlzheimer’s diseaseLumipulseBiomarkerMild cognitive impairmentp-tau181p-tau217PlasmaProgressionRecent studies have demonstrated the high analytical and diagnostic performance of plasma p-tau217 using well-defined cohorts. We aimed to assess the analytical, diagnostic, and prognostic utility of plasma p-tau217 as a routine biomarker in symptomatic patients attending our memory clinic. We also sought to identify optimal cutoff points that align with cerebrospinal fluid (CSF) amyloid beta (Aβ) status. A total of 276 cognitively impaired patients were included, with 81 mild cognitive impairment (MCI) patients followed for a mean of 56 (±15.8) months to evaluate progression to Alzheimer's disease (AD). CSF and blood biomarkers of AD were quantified using the Lumipulse G platform. Plasma p-tau217 levels showed strong correlations with CSF Aβ42/Aβ40 ( = -0.707), p-tau181/Aβ42 ( = 0.842), and p-tau181 (r 0.728). Plasma p-tau217 levels were significantly higher in the A + T + group than in A - T +/- ( < 0.001) and outperformed other plasma markers in detecting CSF Aβ pathology (AUC 0.924).Additionally, p-tau217 moderated cognitive changes over time as measured by the Mini-mental state examination (MMSE) (F(2, 70) = 13.995, < 0.001) and outperformed other plasma biomarkers in predicting progression from MCI to AD (AUC 0.876). Using a dual cutoff strategy, 72% of patients were classified with 94.9% concordance with CSF Aβ status. Plasma p-tau217 shows strong potential as a non-invasive, cost-effective diagnostic and prognostic tool in clinical settings.MDPI2025info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://doi.org/10.3390/ijms26146771https://hdl.handle.net/10459.1/470260https://hdl.handle.net/10459.1/470260reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.3390/ijms26146771International Journal of Molecular Sciences, 2025, vol. 26, núm. 14cc-by (c)The Authors, 2025Attribution 4.0 Internationalinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/oai:dnet:recercat____::a36f2359956ad954bd0f0a335139c00d2026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| title |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| spellingShingle |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease Dakterzada, Farida Alzheimer’s disease Lumipulse Biomarker Mild cognitive impairment p-tau181 p-tau217 Plasma Progression |
| title_short |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| title_full |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| title_fullStr |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| title_full_unstemmed |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| title_sort |
Performance of Plasma Phosphorylated tau-217 in Patients on the Continuum of Alzheimer's Disease |
| dc.creator.none.fl_str_mv |
Dakterzada, Farida López Ortega, Ricard Vilella-Figuerola, Alba Montero-Castilla, Nathalia Riba-Llena, Iolanda Ruiz-Julián, Maria Arias, Alfonso Sarto, Jordi Tahan, Nuria Piñol Ripoll, Gerard |
| author |
Dakterzada, Farida |
| author_facet |
Dakterzada, Farida López Ortega, Ricard Vilella-Figuerola, Alba Montero-Castilla, Nathalia Riba-Llena, Iolanda Ruiz-Julián, Maria Arias, Alfonso Sarto, Jordi Tahan, Nuria Piñol Ripoll, Gerard |
| author_role |
author |
| author2 |
López Ortega, Ricard Vilella-Figuerola, Alba Montero-Castilla, Nathalia Riba-Llena, Iolanda Ruiz-Julián, Maria Arias, Alfonso Sarto, Jordi Tahan, Nuria Piñol Ripoll, Gerard |
| author2_role |
author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Alzheimer’s disease Lumipulse Biomarker Mild cognitive impairment p-tau181 p-tau217 Plasma Progression |
| topic |
Alzheimer’s disease Lumipulse Biomarker Mild cognitive impairment p-tau181 p-tau217 Plasma Progression |
| description |
Recent studies have demonstrated the high analytical and diagnostic performance of plasma p-tau217 using well-defined cohorts. We aimed to assess the analytical, diagnostic, and prognostic utility of plasma p-tau217 as a routine biomarker in symptomatic patients attending our memory clinic. We also sought to identify optimal cutoff points that align with cerebrospinal fluid (CSF) amyloid beta (Aβ) status. A total of 276 cognitively impaired patients were included, with 81 mild cognitive impairment (MCI) patients followed for a mean of 56 (±15.8) months to evaluate progression to Alzheimer's disease (AD). CSF and blood biomarkers of AD were quantified using the Lumipulse G platform. Plasma p-tau217 levels showed strong correlations with CSF Aβ42/Aβ40 ( = -0.707), p-tau181/Aβ42 ( = 0.842), and p-tau181 (r 0.728). Plasma p-tau217 levels were significantly higher in the A + T + group than in A - T +/- ( < 0.001) and outperformed other plasma markers in detecting CSF Aβ pathology (AUC 0.924).Additionally, p-tau217 moderated cognitive changes over time as measured by the Mini-mental state examination (MMSE) (F(2, 70) = 13.995, < 0.001) and outperformed other plasma biomarkers in predicting progression from MCI to AD (AUC 0.876). Using a dual cutoff strategy, 72% of patients were classified with 94.9% concordance with CSF Aβ status. Plasma p-tau217 shows strong potential as a non-invasive, cost-effective diagnostic and prognostic tool in clinical settings. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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https://doi.org/10.3390/ijms26146771 https://hdl.handle.net/10459.1/470260 https://hdl.handle.net/10459.1/470260 |
| url |
https://doi.org/10.3390/ijms26146771 https://hdl.handle.net/10459.1/470260 |
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Inglés |
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Inglés |
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Reproducció del document publicat a: https://doi.org/10.3390/ijms26146771 International Journal of Molecular Sciences, 2025, vol. 26, núm. 14 |
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cc-by (c)The Authors, 2025 Attribution 4.0 International info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ |
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cc-by (c)The Authors, 2025 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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MDPI |
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MDPI |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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