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Oestrogen and calcium homeostasis in women with hypoparathyroidism

Oestrogen status can affect the requirement for vitamin D in women with hypoparathyroidism

Janet McIlroy, specialist registrar a, Frances Dryburgh, consultant a, John Hinnie, lecturer b, Rosemary Dargie, clinical assistant b, Alaa Al-Rawi, senior house officer b.

a Department of Clinical Biochemistry, Macewen Building, Glasgow Royal Infirmary, Glasgow. G4 0SF, b University Department of Medicine, Glasgow Royal Infirmary

Correspondence to: J McIlroy JMcIlroy@gri-biochem.org.uk

 

Permanent hypoparathyroidism occurs in 0.2%-0.3% of patients who undergo thyroid surgery1; it arises less frequently as an inherited or as an autoimmune disease. The condition is treated with vitamin D analogue drugs, doses of which have to be titrated against the serum calcium concentration while avoiding hypercalciuria. The vitamin D requirements in women with hypoparathyroidism can change if their oestrogen status alters. An awareness of this can avoid hypercalcaemia.

 

Case reports

Case 1

A 54 year old woman had undergone thyroidectomy for Graves' disease 34 years previously and had been treated with vitamin D since that time. She had remained euthyroid, and her serum calcium concentration had been satisfactory and stable for several years on 1- hydroxycholecalciferol treatment (1 µg/day). The patient's parathyroid hormone concentration was below the level of detection, although her calcitonin concentration was measurable (32 ng/l, reference range <45 ng/l). Two months after stopping hormone replacement therapy she developed symptoms of hypercalcaemiaanorexia, nausea, abdominal pain, constipation, and weight loss of 9 kg. Hypercalcaemia was confirmed biochemically; her calcium concentration, adjusted for albumin, was 3.5 mmol/l. Her dose of 1- hydroxycholecalciferol, calcium intake, and compliance with treatment were unchanged. She had been on hormone replacement therapy for 8 yearsa cyclical regimen had been prescribed initially, and thereafter a continuous combined preparation. After 1- hydroxycholecalciferol was stopped, her calcium concentration returned to normal. Her serum calcium concentration subsequently remained within the reference range on a reduced dose of 1- hydroxycholecalciferol (0.25 µg/day).

Case 2

A 52 year old woman with idiopathic hypoparathyroidism had been treated for 30 years with vitamin D analogues. For many years she had been taking 1- hydroxycholecalciferol (3 µg/day). At annual review she was hypercalcaemic (calcium concentration adjusted for albumin, 3.1 mmol/l) and had anorexia, nausea, and weight loss of 12 kg. Before this her serum calcium concentration had consistently been within the reference range. There had been no change in her calcium intake or in compliance with treatment. Her calcium concentration returned to normal values after the dosage of 1- hydroxycholecalciferol was reduced to 1 µg on alternate days. Further inquiry showed that her last menstrual period had been 3 months before the discovery of hypercalcaemia, and her postmenopausal status was confirmed by the finding of raised gonadotrophin concentrations (follicle stimulating hormone 93 U/l, luteinising hormone 109 U/l).

Case 3

A 51 year old woman had been treated with vitamin D analogues and thyroxine supplements for 13 years since developing persistent hypoparathyroidism and hypothyroidism after subtotal thyroidectomy for Graves' disease. Her serum calcium concentrations had been within the reference range until October 1988, when she presented with a 6 month history of weight loss of 9 kg, nausea, vomiting, thirst, and intermittent confusion. She was also menopausal. There had been no change in her dose of 1- hydroxycholecalciferol (2 µg/day), calcium intake, or compliance with treatment. Hypercalcaemia was confirmed (the calcium concentration, adjusted for albumin, was 3.25 mmol/l). Her calcium concentration returned to normal and her symptoms resolved after intravenous rehydration treatment and an interval without vitamin D therapy. Treatment with 1- hydroxycholecalciferol was reintroduced at a reduced daily dose of 0.25 µg, and the patient's calcium concentrations remained within the reference range thereafter.

 

Comment

These three cases show that a change in oestrogen status can alter sensitivity to a potent vitamin D analogue in women who do not have the ability to produce parathyroid hormone. In a similar case, reported in 1979, a patient became hypercalcaemic after stopping the oral contraceptive pill. 2 3 Reintroduction of oestrogen was associated with a fall in her serum calcium concentration. The anti-oestrogenic activity of danazolprescribed for endometriosis in a patient with idiopathic hypoparathyroidism who was being treated with 1- hydroxycholecalciferolresulted in hypercalcaemia and a reduced maintenance requirement for 1- hydroxycholecalciferol.4 Hypercalcaemia can also occur immediately after delivery in women with hypoparathyroidism treated with vitamin D supplements. 5 6 All these observations support a crucial role for oestrogen in calcium regulation in these women.

Oestrogen, 1,25-dihydroxyvitamin D, and parathyroid hormone influence bone metabolism. Cytokines are now recognised as pivotal mediators of oestrogen, which acts on oestrogen receptors on osteoblasts7 and osteoclasts8 to inhibit bone resorption.9 In normal women, oestrogen withdrawal increases bone resorption and causes a rise in serum calcium. 1,25-dihydroxyvitamin D is now known to be the major direct regulator of active transcellular calcium absorption via vitamin D receptors in intestinal mucosal cells.10 Oestrogen can increase calcium absorption directly and indirectly by stimulating 1- hydroxylase activity in the kidney.11 Withdrawal of oestrogens would theoretically reduce calcium absorption, and hypercalcaemia in these cases cannot be explained by this mechanism. Ultimately, the effects of oestrogen on bone and calcium metabolism are monitored by the calcium sensing receptor on parathyroid cells,12 which respond by altering parathyroid hormone secretion. Parathyroid hormone is a major modulator of osteoclast activity. In the absence of parathyroid hormone, the positive effect on osteoclast activity and bone resorption of withdrawal of oestrogen becomes much more important for calcium regulation. In the absence of parathyroid hormone, the balance between the action of 1,25-dihydroxyvitamin D, which is a potent inducer of bone resorption,13 and of oestrogen, which inhibits bone resorption, may become more crucial. A clinical awareness of this phenomenon allows appropriate monitoring of patients and adjustment of their dose of vitamin D at the menopause or while starting or stopping hormone replacement therapy.

 

Acknowledgments

Contributors: JM, RD and AA collected cases. JM, FD and JH wrote the manuscript and are guarantors for the paper.

 

References

  1. Gann DS, Paone JF. Delayed hypocalcemia after thyroidectomy for Graves' disease is prevented by parathyroid autotransplanation. Ann Surg 1979; 190: 508-513[Medline].
  2. Verbeelen D, Fuss M. Hypercalcaemia induced by oestrogen withdrawal in vitamin D-treated hypoparathyroidism. BMJ 1979; i: 522-523.
  3. Nagant de Deuxchaisnes C. Oestrogen-induced hypocalcaemia in hypoparathyroidism. BMJ 1979; i: 1563.
  4. Hepburn NC, Abdul-Aziz LAS, Whiteoak R. Danazol-induced hypercalcaemia in alphacalcidol-treated hypoparathyoidism. Postgrad Med J 1989; 65: 849-850[Abstract].
  5. Cundy T, Haining SA, Guilland-Cumming DF, Butler J, Kanis JA. Remission of hypoparathyroidism during lactation: evidence for a physiological role for prolactin in the regulation of vitamin D metabolism. Clin Endocrinol 1987; 26: 667-674[Medline].
  6. Wright AD, Joplin GF, Dixon HG. Postpartum hypercalcaemia in treated hypoparathyroidism. BMJ 1969; i: 23-25.
  7. Eriksen EF, Colvard DS, Berg NJ, Graham ML, Mann KG, Spelsberg TC, et al. Evidence of oestrogen receptors on normal human osteoblast-like cells. Science 1988; 241: 84-86[Abstract/Free Full Text].
  8. Oursler MJ, Pederson L, Pyfferoen J, Osdoby P, Fitzpatrick L, Spelsberg TC. Oestrogen modulation of avian osteoclast lysosomal gene expression. Endocrinology 1993; 132: 1373-1380[Abstract].
  9. Manolagas SC, Jilka RL. Bone marrow cytokines and bone remodelling. Emerging insights into the pathophysiology of osteoporosis. N Engl J Med 1995; 332: 305-311[Free Full Text].
  10. Reichel H, Koeffler HP, Norman AW. Role of vitamin D endocrine system in health and disease. N Engl J Med 1989; 320: 980[Medline].
  11. Gennari C, Agnusdei D, Nardi P, Givirelli R. Estrogen preserves a normal intestinal responsiveness to 1,25-dihydroxyvitamin D3 in oophorectomized women J Clin Endocrinol Metab 1990; 71: 1288-1293[Abstract].
  12. Brown EM, Gamba G, Riccardi D, Lambardi M, Butters R, Kifor O, et al. Cloning and characterisation of an extracellular calcium sensing receptor from bovine parathyroid. Nature 1993; 366: 575-580[Medline].
  13. Reynolds JJ, Pavlovitch H, Balsan S. 1,25-dihydroxycholecalciferol increases bone resorption on thyroparathyroidectomised mice. Calcified Tiss Res 1976; 21: 207-212.

(Accepted 12 May 1999)

 Published here with permission from BMJ Publishing Group Ltd

License number 1656141335898

© BMJ 1999


   
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