Parathyroid hormone‐related protein in hypercalcaemia associated with haematological malignancy

F Firkin, JF Seymour, AM Watson… - British Journal of …, 1996 - Wiley Online Library
F Firkin, JF Seymour, AM Watson, V Grill, TJ Martin
British Journal of Haematology, 1996Wiley Online Library
The incidence of hypercalcaemia and its association with humoral mechanisms involving
parathyroid hormone‐related protein (PTHrP), parathyroid hormone (PTH), or 1, 25 (OH) 2
vitamin D were assessed in a prospective study of patients admitted to a clinical
haematology unit. Hypercalcaemia was detected in 18/165 patients, and was due to primary
hyperparathyroidism in 3/17 patients in whom results of humoral mediator assessments
were obtained. In the other patients, hypercalcaemia was associated in nine instances with …
The incidence of hypercalcaemia and its association with humoral mechanisms involving parathyroid hormone‐related protein (PTHrP), parathyroid hormone (PTH), or 1,25(OH)2 vitamin D were assessed in a prospective study of patients admitted to a clinical haematology unit. Hypercalcaemia was detected in 18/165 patients, and was due to primary hyperparathyroidism in 3/17 patients in whom results of humoral mediator assessments were obtained. In the other patients, hypercalcaemia was associated in nine instances with myeloma, in five with B‐cell non‐Hodgkin's lymphoma (NHL), and in one with myeloid neoplasia. No evidence was obtained of a humoral mechanism involving 1,25(OH)2 vitamin D, but elevated circulating levels of PTHrP, comparable with those in humoral hypercalcaemia of malignancy, were present in 2/4 patients with NHL, and in 3/9 with myeloma. The relationship between presence or absence of elevated circulating PTHrP, and presence or absence of hypercalcaemia during the course of treatment, indicated PTHrP was involved in the production of hypercalcaemia. Such an association raises the possibility that PTHrP released by neoplastic cells in these disorders acts in a paracrine manner to produce local bone resorption, and when produced in greater amounts causes elevated circulating levels which make an additional humorally‐mediated contribution to the development of hypercalcaemia.
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