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| ID | Type | Description | Link |
|---|---|---|---|
| 5R01AG062509 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Aging (NIA) | NIH |
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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.
Study Type:
Observational (Laboratory-based biomarker study; no human intervention)
Study Design:
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:
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.
Secondary Outcome Measures:
Biospecimen Retention:
Samples will be analyzed for biomarker levels; aliquots may be stored for future biomarker validation studies.
Eligibility Criteria:
Study Population:
Approximately 250 de-identified donated plasma samples obtained from healthy adult blood donors.
Estimated Enrollment: 250 samples
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| Measure | Description | Time Frame |
|---|---|---|
| Tau and pTau | Concentration of Tau and pTau217 in plasma. | 6 months. |
| Concentration of pTau217 and Tau | We will use nanoneedle technology to measure the concentration of Tau and pTau217 in collected plasma samples from blood donators. | 6 months. |
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Inclusion Criteria:
Exclusion Criteria:
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Anybody who can donate blood.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Zhongcong Xie, M.D., Ph.D. | Contact | 17135006207 | Zhongcong.Xie@uth.tmc.edu |
| Name | Affiliation | Role |
|---|---|---|
| Zhongcong Xie, M.D., Ph.D. | The University of Texas Health Science Center, Houston | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Texas Health Science Center at Houston | Recruiting | Houston | Texas | 77030 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Result | 40. Tatebe H, Kasai T, Ohmichi T, et al. Quantification of plasma phosphorylated tau to use as a biomarker for brain Alzheimer pathology: pilot case-control studies including patients with Alzheimer's disease and down syndrome. Mol Neurodegener. Sep 4 2017;12(1):63. doi:10.1186/s13024-017-0206-8 41. Mielke MM, Hagen CE, Xu J, et al. Plasma phospho-tau181 increases with Alzheimer's disease clinical severity and is associated with tau- and amyloid-positron emission tomography. Alzheimers Dement. Aug 2018;14(8):989-997. doi:10.1016/j.jalz.2018.02.013 42. Janelidze S, Mattsson N, Palmqvist S, et al. Plasma P-tau181 in Alzheimer's disease: relationship to other biomarkers, differential diagnosis, neuropathology and longitudinal progression to Alzheimer's dementia. Nat Med. Mar 2020;26(3):379-386. doi:10.1038/s41591-020-0755-1 43. Karikari TK, Pascoal TA, Ashton NJ, et al. Blood phosphorylated tau 181 as a biomarker for Alzheimer's disease: a diagnostic performance and prediction modelling study using data from four prospective cohorts. Lancet Neurol. May 2020;19(5):422-433. doi:10.1016/S1474-4422(20)30071-5 44. Palmqvist S, Insel PS, Stomrud E, et al. Cerebrospinal fluid and plasma biomarker trajectories with increasing amyloid deposition in Alzheimer's disease. EMBO Mol Med. Dec 2019;11(12):e11170. doi:10.15252/emmm.201911170 45. Palmqvist S, Janelidze S, Quiroz YT, et al. Discriminative Accuracy of Plasma Phospho-tau217 for Alzheimer Disease vs Other Neurodegenerative Disorders. JAMA. Aug 25 2020;324(8):772-781. doi:10.1001/jama.2020.12134 46. Janelidze S, Berron D, Smith R, et al. Associations of Plasma Phospho-Tau217 Levels With Tau Positron Emission Tomography in Early Alzheimer Disease. JAMA Neurol. Nov 9 2020;doi:10.1001/jamaneurol.2020.4201 47. Thijssen EH, La Joie R, Strom A, et al. Plasma phosphorylated tau 217 and phosphorylated tau 181 as biomarkers in Alzheimer's disease and frontotemporal lobar degeneration: a retrospective diagnostic performance study. Lan |
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We do not know the names of any blood donators who provide samples of plasma.
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Donated plasma.