Test Code P1NP Intact Procollagen I N-Terminal, Serum
Specimen Required
Patient Preparation: For 12 hours before specimen collection, patient should not take multivitamins or dietary supplements (eg, hair, skin, and nail supplements) containing biotin (vitamin B7).
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL Serum
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
Aiding in monitoring antiresorptive and anabolic therapy in patients with osteoporosis
This test should not be used as a screening test for osteoporosis in the general population.
Method Name
Chemiluminescence
Reporting Name
Intact Procollagen I N-Terminal, SSpecimen Type
SerumSpecimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 14 days |
| Frozen | 90 days | |
| Ambient | 7 days |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | OK |
| Gross icterus | OK |
Clinical Information
Procollagen type I propeptides are derived from collagen type I, the most common collagen in mineralized bone. In bone, collagen is synthesized by osteoblasts in the form of procollagen, a precursor that contains a short signal sequence and terminal extension peptides: amino-terminal propeptide (PINP) and carboxy-terminal propeptide. These propeptide extensions are removed by specific proteinases before the collagen molecules form. Both propeptides circulate in blood, and their concentrations reflect the rate of collagen type I synthesis. Although collagen type I propeptides may also originate from other tissues, including skin, vessels, fibrocartilage, and tendons, most nonskeletal tissues exhibit a slower turnover than bone and contribute very little to the circulating pool of PINP. PINP is considered the most sensitive marker of bone formation and is particularly useful for monitoring bone formation and antiresorptive therapies. Testing is recommended at baseline before osteoporosis therapy begins and again 3 to 6 months later.
Reference Values
Adult male: 26-108 ng/mL
Adult female premenopausal: 22-103 ng/mL
Adult female postmenopausal: 18-119 ng/mL
Reference values have not been established for patients who are younger than 18 years.
Day(s) Performed
Monday through Friday
Report Available
1 to 3 daysSpecimen Retention Time
2 weeksPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
83520
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| P1NP | Intact Procollagen I N-Terminal, S | 77370-5 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| P1NP | Intact Procollagen I N-Terminal, S | 77370-5 |