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Test Code LAB704 Parathyroid Hormone-Related Peptide, Plasma

Reporting Name

PTH-Related Peptide

Useful For

Aiding in the evaluation of individuals with hypercalcemia of unknown origin

 

Aiding in the evaluation of individuals with suspected humoral hypercalcemia of malignancy

 

The test should not be used to exclude cancer or screen individuals with tumors for humoral hypercalcemia of malignancy.

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Plasma EDTA


Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube: Ice-cooled, lavender top (EDTA)

Submission Container/Tube: Plastic vial

Specimen Volume: 0.7 mL

Collection Instructions:

1. Centrifuge specimen in a refrigerated centrifuge or in chilled centrifuge cups.

2. Aliquot plasma into plastic vial and freeze.


Specimen Minimum Volume

0.25 mL

Specimen Stability Information

Specimen Type Temperature Time
Plasma EDTA Frozen 30 days

Reference Values

≤4.2 pmol/L

 

Reference values have not been established for patients younger than 1 year.

Day(s) Performed

Monday through Thursday

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

82397

LOINC Code Information

Test ID Test Order Name Order LOINC Value
PTHRP PTH-Related Peptide 15087-0

 

Result ID Test Result Name Result LOINC Value
81774 PTH-Related Peptide 15087-0

Cautions

Parathyroid hormone-related peptide (PTHrP) can be elevated in pregnant and lactating women and in newborn infants.

 

Nonmalignant conditions that have been described in association with elevated plasma PTHrP levels include systemic lupus erythematosus, HIV-associated lymphadenopathy, lymphedema of chest or pleural cavities, and with benign tumors of the ovary, kidney, and the neuroendocrine system.

 

Because of the complexity of PTHrP isoforms, the differences between various PTHrP assays and the lack of a common calibration standard, PTHrP measurements performed with different assays cannot be compared easily.

 

The complex isoform mixture of PTHrP can occasionally lead to pronounced nonlinearity on dilution of patient specimens. In these situations an accurate measurement of PTHrP concentrations might be impossible.

 

Like all immunometric assays, PTHrP assays are susceptible to false-low results at extremely high analyte concentrations ("hooking") and to rare false-positive results due to heterophile antibody interference. Therefore, if test results are incongruent with the clinical picture, the laboratory should be contacted.

Report Available

2 to 5 days

Reject Due To

Gross hemolysis Reject
Gross lipemia OK
Gross icterus OK

NY State Approved

Yes

Method Name

Immunochemiluminometric Assay (ICMA)

Forms

If not ordering electronically, complete, print, and send a General Request (T239) with the specimen.

Secondary ID

81774