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Phosphorylated Tau Levels in Donated Blood

Detection of Elevated Plasma pTau217 in Donated Human Blood Samples: Implications for Blood Transfusion Safety

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07157839
Acronym
pTIDB
Enrollment
250
Registered
2025-09-05
Start date
2025-08-28
Completion date
2026-11-01
Last updated
2026-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer&Amp;#39;s Disease

Keywords

Phosphorylated Tau, donated blood, Alzheimer's disease

Brief summary

Alzheimer's disease (AD) is characterized by the accumulation of tau pathology, and blood-based biomarkers such as phosphorylated tau-217 (pTau217) have been identified as sensitive and specific predictors of AD risk. Recent studies suggest that individuals with elevated pTau217 levels may be at increased risk for developing AD and cognitive dysfunction. This observational study will examine donated human plasma samples to determine whether some units of donated blood contain abnormally elevated pTau217 concentrations. The overarching goal is to evaluate whether transfusion of blood with higher pTau217 may pose risks to recipients and whether such units should be avoided in clinical use.

Detailed description

Study Type: Observational (Laboratory-based biomarker study; no human intervention) Study Design: * Model: Cross-sectional * Time Perspective: Prospective * Sample Source: Donated human blood plasma samples obtained through a blood bank * Enrollment: \ 250 plasma samples; \ 20 plasma samples of AD patients and \ 20 plasma samples of normal control participants, where are purchased from BioIVT (Westbury, NY, USA). Official Title: Observational Measurement of pTau217 in Donated Human Plasma Samples Primary Objective: To determine the prevalence of elevated plasma pTau217 levels in donated blood. Secondary Objectives: 1. To compare pTau217 concentrations with total Tau to assess biomarker distribution in donated blood. 2. To generate preliminary data on whether pTau217 screening could be relevant to transfusion safety guidelines. Primary Outcome Measure: * Proportion of blood samples with plasma pTau217 levels exceeding the threshold established in published Alzheimer's disease biomarker studies (measured by nanoneedle biosensor or equivalent immunoassay). * We will also establish the cut off values of pTau217 of plasma based on the data from 20 AD patients and 30 normal control participants. * Time Frame: At single sample collection Secondary Outcome Measures: * Ratio of pTau217 to total Tau across plasma samples * Distribution of pTau217 levels in the donor population Biospecimen Retention: Samples will be analyzed for biomarker levels; aliquots may be stored for future biomarker validation studies. Eligibility Criteria: * Inclusion: De-identified human plasma samples from standard blood bank donations * Exclusion: Samples failing quality control or insufficient volume Study Population: Approximately 250 de-identified donated plasma samples obtained from healthy adult blood donors. Estimated Enrollment: 250 samples

Interventions

None listed

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* The plasma sample from donators.

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Tau and pTau6 months.Concentration of Tau and pTau217 in plasma.
Concentration of pTau217 and Tau6 months.We will use nanoneedle technology to measure the concentration of Tau and pTau217 in collected plasma samples from blood donators.

Countries

United States

Contacts

CONTACTZhongcong Xie, M.D., Ph.D.
Zhongcong.Xie@uth.tmc.edu17135006207
PRINCIPAL_INVESTIGATORZhongcong Xie, M.D., Ph.D.

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026