Laboratory Services

Parathyroid Hormone-Related Peptide (PTHrP), Plasma

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Updated Test Information:

Test Description
Parathyroid Hormone-Related Peptide (PTHrP), Plasma
Synonym(s)

Humoral Hypercalcemia of Malignancy Factor; Parathyroid Related Polypeptide; Parathyroid Related Protein; PRP; PTH Related Peptide; PTHRP, Plasma; PTH Related Protein; Parathyroid Hormone Related Peptide

Test ID
PTHRP
General Information

Useful for:



  • As an aid in the evaluation of patients with hypercalcemia of unknown origin

  • As an aid in the evaluation of patients with suspected humoral hypercalcemia of malignancy

  • The test should not be used to exclude cancer or screen tumor patients for humoral hypercalcemia of malignancy.

Specimen Type

EDTA Plasma

Specimen Requirements

Ice-cooled, lavender top (EDTA)

Specimen Collection / Processing Instructions

  • Centrifuge specimen in a refrigerated centrifuge or in chilled centrifuge cups

  • Aliquot plasma into plastic vial and freeze

Minimum Sample Volume

0.25 mL

Stability

Frozen: 30 days

Unacceptable Specimen Conditions

Gross hemolysis

Limitations

  • 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

Methodology

Immunochemiluminometric Assay (ICMA)

Estimated TAT

2-5 days

Testing Schedule

Monday-Thursday

Retention

3 months

CPT Code(s)

82397

Reference Range

≤ 4.2 pmol/L

Performing Lab

Mayo

LOINC Code(s)

15087-0

Additional Information