Development of a PTHrP chemiluminescent immunoassay to assess humoral hypercalcemia of malignancy

التفاصيل البيبلوغرافية
العنوان: Development of a PTHrP chemiluminescent immunoassay to assess humoral hypercalcemia of malignancy
المؤلفون: Joshua A. Bornhorst, Susan Ashrafzadeh-Kian, Alicia Algeciras-Schimnich
المصدر: Journal of the Endocrine Society
بيانات النشر: Elsevier BV, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Immunoassay, Paraneoplastic Syndromes, business.industry, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Parathyroid Hormone-Related Protein, General Medicine, Malignancy, medicine.disease, Hormone Actions in Tumor Biology: From New Mechanisms to Therapy, Parathyroid Hormone, Chemiluminescent immunoassay, Immunology, Hypercalcemia, medicine, Animals, Tumor Biology, Rabbits, business, AcademicSubjects/MED00250, hormones, hormone substitutes, and hormone antagonists
الوصف: Background: Measurement of parathyroid hormone related peptide (PTHrP) is helpful in the diagnosis and clinical management of patients suspected of humoral hypercalcemia of malignancy (HHM). In these patients uncontrolled release of PTHrP by tumor cells is responsible for the hypercalcemia and PTH concentrations are typically suppressed. Objective: Develop a sensitive and specific assay for quantitation of PTHrP in plasma. Method: Calibrators (PTHrP 1-86) and samples (50uL) were incubated with an anti-PTHrP goat polyclonal acridinium ester labeled antibody. Complexes were transferred and incubated in a microplate coated with an anti-PTHrP polyclonal rabbit antibody. After washing, the acridinium ester generated signal, which is directly proportional to the amount of PTHrP in sample, was quantified. Results: In this assay PTHrp was stable for 24 hours ambient, 3 days refrigerated, 34 days frozen and through 3 freeze/thaws. Intra and inter-assay imprecision in EDTA plasma (~0.16-35.0 pmol/L) ranged from 2.2-8.6% and 5-15%, respectively. The limit of detection was 0.04 pmol/L and the limit of quantitation was 0.16 pmol/L (15% CV). The analytical measuring range was 0.39-50.5 pmol/L (slope of 1.07 and r2 of 0.99). Average spike recovery was 98% (range 85-108%). The assay was not affected by hemoglobin of ≤500 mg/dL, triglycerides of ≤2000 mg/dL, or bilirubin of ≤50mg/dL. No hook effect was noted up to 500 pmol/L. PTH (1-84) did not cross-react in the assay. C-terminal PTHrP(107-139), and N-terminal PTHrP(1-36) had no significant cross-reactivity (≤1.1%). Mid-PTHrP(38-94) had 8.3% cross-reactivity. Comparison with an in-house PTHrP assay (n=267) showed an r2 of 0.96, and slope of 2.25 by Passing-Bablok regression fit. The 97.5% reference interval for PTHrP (n=114) was ≤0.7 pmol/L, however a higher concentration (≤4.2 pmol/L) was identified as a more specific clinical cut-off. A retrospective clinical validation study showed that using ≤4.2 pmol/L resulted in a 91% clinical sensitivity and a 98% clinical specificity. Conclusion: We have developed an analytically and clinically sensitive and specific PTHrP immunoassay. A cutoff of ≤4.2 pmol/L is clinically useful in the evaluation of patients suspected of hypercalcemia of malignancy.
تدمد: 0009-9120
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d8ede8a3685f7f82b0b630a20037c71Test
https://doi.org/10.1016/j.clinbiochem.2022.04.005Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....5d8ede8a3685f7f82b0b630a20037c71
قاعدة البيانات: OpenAIRE