N-Telopeptide, Urine
N-Telopeptide, Urine, Collagen Crosslinks, Crosslinked N-Telopeptide of Type I Collagen, Urine, NTX Creatinine, NTx-Telopeptide, Urine
Test Codes
EPIC: LAB6115, Beaker: XNTXU, Warde: NTXUR
Department
Send Outs
Instructions
For 24 hours before this test do not take multivitamins or dietary supplements containing biotin (Vitamin B7), which is commonly found in hair, skin, and nail supplements and multivitamins.
Specimen Collection Criteria
Collect (preferred specimen): Second morning void urine.
Physician Office/Draw Specimen Preparation
Maintain specimens frozen (-20°C/-4°F or below) prior to transport.
Preparation for Courier Transport
Transport: 2.0 mL second morning void urine, frozen (-20°C/-4°F or below). (Minimum: 1.0 mL)
Rejection Criteria
Specimens not collected and processed as indicated.
In-Lab Processing
Maintain specimens refrigerated (2-8°C or 36-46°F) prior to transport.
Transport: 2.0 mL second morning void urine, frozen (-20°C/-4°F or below). (Minimum: 1.0 mL)
Storage
Specimen Stability for Testing:
Room Temperature (20-26°C or 68-78.8°F): 72 hours
Refrigerated (2-8°C or 36-46°F): 5 days
Frozen (-20°C/-4°F or below): 30 days
Specimen Storage in Department Prior to Disposal:
Specimen retention time is determined by the policy of the reference laboratory. Contact the Send Outs Laboratory with any questions.
Laboratory
Sent to Warde Medical Lab, Ann Arbor, MI and forwarded to Quest Lab, San Juan Capistrano, CA.
Performed
Monday, Wednesday, Friday.
Results available in 3-6 days.
Reference Range
By report.
Test Methodology
Chemiluminescence
Interpretation
By report.
Clinical Utility
This assay measures cross-linked N-telopeptides of collagen type 1 as an indicator of bone resorption. The Negotiated Rulemaking Committee of HCFA has listed the following indications for collagen cross-link assays (any method):
- Identifying individuals with elevated bone resorption who have osteoporosis in whom response to treatment is being monitored.
- Predicting response (as assessed by bone mass measurements) to Food and Drug Administration (FDA)-approved antiresorptive therapy in postmenopausal women.
- Assessing effectiveness of osteoporosis treatment including FDA-approved antiresorptive therapies in postmenopausal women, individuals with osteoporosis, Paget's disease of bone, and antiestrogen or selective estrogen therapies.
CPT Codes
82523 and 82570.
Contacts
Send Outs Laboratory – RO
248-551-9045
Name: Send Outs Laboratory – RO
Location:
Phone: 248-551-9045
Last Updated
9/16/2024
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