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Research Article Free access | 10.1172/JCI111016

Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism

M. F. Attie, J. R. Gill Jr., J. L. Stock, A. M. Spiegel, R. W. Downs Jr., M. A. Levine, and S. J. Marx

Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

Digestive and Kidney Diseases, Bethesda, Maryland 20205

Hypertension Endocrine Branch, National Heart Lung and Blood Institute, Bethesda, Maryland 20205

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Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

Digestive and Kidney Diseases, Bethesda, Maryland 20205

Hypertension Endocrine Branch, National Heart Lung and Blood Institute, Bethesda, Maryland 20205

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Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

Digestive and Kidney Diseases, Bethesda, Maryland 20205

Hypertension Endocrine Branch, National Heart Lung and Blood Institute, Bethesda, Maryland 20205

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Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

Digestive and Kidney Diseases, Bethesda, Maryland 20205

Hypertension Endocrine Branch, National Heart Lung and Blood Institute, Bethesda, Maryland 20205

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Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

Digestive and Kidney Diseases, Bethesda, Maryland 20205

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Metabolic Diseases Branch, National Institute of Arthritis, Diabetes, Bethesda, Maryland 20205

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Published August 1, 1983 - More info

Published in Volume 72, Issue 2 on August 1, 1983
J Clin Invest. 1983;72(2):667–676. https://doi.org/10.1172/JCI111016.
© 1983 The American Society for Clinical Investigation
Published August 1, 1983 - Version history
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Abstract

Familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant trait comprising hypercalcemia, hypophosphatemia, parathyroid hyperplasia, and unusually low renal clearance of calcium. We evaluated the role of parathyroid hormone in the relative hypocalciuria of FHH and characterized the renal transport of calcium in this disorder using three previously hypercalcemic FHH patients with surgical hypoparathyroidism and three controls with surgical hypoparathyroidism. Intravenous infusion of calcium chloride in two patients with FHH and in three controls increased serum calcium from a mean basal of 5.0 to a mean peak of 6.8 meq/liter in two FHH patients and from 4.2 to 5.7 in three control subjects. Urinary calcium in a third FHH patient was studied without calcium infusion during recovery from hypercalcemia of vitamin D intoxication. At all serum concentrations of calcium, calcium clearance was lower in FHH than in controls; at base-line serum calcium, the ratio of calcium clearance to inulin clearance (CCa/CIN) in FHH subjects was 32% of that in controls and decreased to 19% during hypercalcemia. Calcium infusion increased the ratio of sodium clearance to inulin clearance in controls from a base line of 0.020 to 0.053 at peak concentrations of calcium in serum, but did not affect this parameter in FHH (0.017 at base-line serum calcium vs. 0.019 at peak).

When calcium infusion studies were performed (in two patients with FHH and one control) during administration of acetazolamide, a drug whose principal renal action causes inhibition of proximal transport of solute, CCa/CIN in the patients with FHH was 29 and 7% of that of the control at base-line and peak serum calcium, respectively. In contrast, ethacrynic acid, a diuretic that acts in the ascending limb of the loop of Henle, increased CCa/CIN more in the FHH patients than in the control subject; CCa/CIN was 65% at base-line and 47% at peak serum calcium, compared with that of the control subject. The greater calciuric response to ethacrynic acid than to acetazolamide or calcium infusion alone in FHH indicates that a major renal locus of abnormal calcium transport in this disorder may be the ascending limb of the loop of Henle.

Decreased clearance of calcium in patients with FHH and hypoparathyroidism when compared with hypoparathyroid controls indicates that relative hypocalciuria in FHH is not dependent on hyperparathyroidism. Since the parathyroid glands in FHH are not appropriately suppressed by calcium, this implies that FHH represents a disorder of abnormal transport of, and/or response to, extracellular calcium in at least two organs, parathyroid gland and kidney.

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