Jul 2026· Health & Medical Sciences· Vol 3, pp. 31-46· 0 citations· 23 references
TL;DR
It is shown that plasma p-tau217 serves as a highly accurate biomarker for identifying the biological pathology of Alzheimer's disease, specifically regarding amyloid and tau status, when p-tau217 is paired with Aβ42 or the Aβ42/40 ratio.
Abstract
This systematic review sought to assess the function of the blood biomarker phosphorylated tau 217 (p-tau217) in the early identification of Alzheimer's disease. A systematic review was carried out adhering to the PRISMA 2020 protocols. Literature searches were executed in PubMed, ScienceDirect, and Scopus to locate original studies published between 2023 and 2026. Eligible studies assessed blood p-tau217 in individuals with mild cognitive impairment, suspected Alzheimer's disease, Alzheimer's disease, or at-risk populations and reported diagnostic performance or correlations with established Alzheimer's biomarkers. Study quality was evaluated utilizing QUADAS-2 for diagnostic accuracy studies and the Study Quality Assessment Tools for observational and longitudinal studies. A total of 328 records were retrieved, of which 18 studies met the inclusion criteria. Research consistently demonstrates that plasma p-tau217 serves as a highly accurate biomarker for identifying the biological pathology of Alzheimer's disease, specifically regarding amyloid and tau status. Numerous studies have reported impressive area under the curve (AUC) scores between 0.92 and 0.97. When p-tau217 is paired with Aβ42 or the Aβ42/40 ratio, its diagnostic precision improves significantly, particularly in patients who are cognitively normal or in the preclinical stages of the disease.
P-tau217 has poorer diagnostic performance in the stages of cognitive unimpaired or less cognitively impaired, especially in the Aβ positivity diagnosis of SCD and CU, which is consistent with the guidelines.
Peng Zhang, De-Long Huang, Xing-Yu Lu et al.· European Archives of Psychia...· 0 citations
Plasma p-tau217 showed high diagnostic performance for identifying amyloid and tau pathology and generally outperformed other phosphorylated tau isoforms, but it should not be interpreted as a stand-alone test.
Oliwia Lenkiewicz, Julia Lenkiewicz, Z. Chmielewska et al.· International Journal of Inn...· 0 citations
Overall, current evidence on p-tau217 is derived mainly from selected populations and may not fully reflect real-world clinical diversity, so future studies should prioritize more representative cohorts and standardized reporting of key variables will be essential to strengthen its adoption in clinical practice.
M. T. Blasi, Simona Buscarnera, M. Salzillo et al.· Ageing Research Reviews· 0 citations
Increased serum p-tau217 and decreased ApoE levels were significantly associated with greater AD severity, suggesting that both biomarkers may serve as complementary noninvasive indicators of disease severity in Alzheimer’s disease.
Ahmed Kadom Kalaf, Khawla A. Shemran, Waleed Azeez AlAmeedy· International Journal of Nut...· 0 citations
Plasma biomarkers offer a transformative, non-invasive approach to early AD diagnosis and primary care triage, reducing reliance on CSF and PET scans and overcoming demographic and methodological limitations is essential for their widespread clinical adoption.
Małgorzata Witaszczyk, Alicja Sołtan, Natalia Wiktorzak et al.· International Journal of Inn...· 0 citations
Objective: To analyze the available scientific evidence on neurological biomarkers used for early diagnosis of Alzheimer's disease (AD), evaluating their diagnostic accuracy and predictive capacity for disease progression. Methods: This is an integrative literature review conducted according to the guidelines proposed...
João Pedro Gomes do Nascimento, Maria Luiza de Freitas Serafim, Rhayssa Mylla Barbosa Celestino et al.· Revista de Estudos Interdisc...· 0 citations
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