Test Directory
| Test Code | ||||
| AD217 | ||||
| Test Name | ||||
| Quest AD Detect ptau217, Plasma | ||||
| CPT Codes | ||||
| 84393 | ||||
| Expected Turnaround Time | ||||
| 2 - 4 days | ||||
| Clinical Utility | ||||
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Current research indicates that plasma p-tau, including p-tau 217, is concordant with amyloid status defined by either CSF biomarker testing or PET scan analysis, and is able to differentiate between AD and non-AD neurodegenerative diseases and to predict progression to AD. Blood-based biomarkers, such as plasma p-tau, could potentially be used as inclusion criteria or to evaluate target engagement and treatment efficacy, and could further advance the development of disease-modifying treatments in the field of AD and related disorders. This assay is designed specifically for the quantitative measurement of tau phosphorylated at threonine 217 (p-tau 217) in human plasma. |
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| Specimen and Container Info | ||||
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Specimen Type: Plasma Collection Container: Lavender Top (EDTA) Desired Specimen Volume: 0.7 mL |
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| Collection Instructions | ||||
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| Processing and Submission Instructions | ||||
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| Patient Preparation | ||||
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Patients should be cautioned to stop biotin consumption at least 72 hours prior to collection of a sample. |
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| Transport Instructions | ||||
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Transport to the laboratory refrigerated. |
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| Stability Requirements | ||||
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| Methodology | ||||
| Immunoassay | ||||
| Reference Intervals | ||||
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See patient report. |
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| Alternate Names | ||||
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| Reference Lab | ||||
| Quest Diagnostics Nichols Institute | ||||
| Testing Schedule | ||||
| Routine, Monday - Saturday | ||||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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