Multisite immunochemiluminometric assay for simultaneously measuring whole-molecule and amino-terminal fragments of human parathyrin

Clin Chem. 1992 May;38(5):628-35.

Abstract

The immunochemiluminometric assay described uses immobilized anti-human parathyrin (parathyroid hormone, hPTH)(1-44) and anti-hPTH(44-68) antisera and acridinium ester-labeled anti-hPTH(1-34) to simultaneously measure both intact hPTH and its amino-terminal fragments. Results by the assay correlate well with those by a cAMP-based bioassay and the Nichols Allegro immunoradiometric assay. The minimal detection limit is 0.08 pmol/L. The normal range is 1.0-5.0 pmol/L, and values are higher in older women. About 90% of study patients with surgically proven parathyroid adenomas had above-normal preoperative PTH concentrations, whereas patients with hypercalcemia of malignancy had normal or suppressed values. This assay was designed to detect both intact PTH and amino-terminal PTH fragments; however, chromatographic fractionation of pools of primary and secondary hyperparathyroid plasma showed virtually no amino-terminal fragment activity. Nonetheless, the design is important because the absence of carboxyl-terminal binding sites prevents interference by carboxyl-terminal fragments and because bioactive amino-terminal fragments will react in the assay if they are present in the patients' sera or if they are produced by in vitro proteolysis of intact PTH.

Publication types

  • Comparative Study

MeSH terms

  • Chromatography
  • Female
  • Humans
  • Hyperparathyroidism / blood
  • Immunoassay / methods*
  • Immunoassay / statistics & numerical data
  • Kidney Failure, Chronic / blood
  • Luminescent Measurements*
  • Male
  • Parathyroid Hormone / blood*
  • Peptide Fragments / blood*
  • Reference Values

Substances

  • Parathyroid Hormone
  • Peptide Fragments