Functional activities of mutant calcium-sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia.

Abstract

OBJECTIVE:

Autosomal dominant hypocalcemia (ADH) is a congenital isolated hypoparathyroidism caused by activating mutations in the calcium-sensing receptor (CASR) gene. The clinical features of ADH are heterogeneous; some patients are asymptomatic, and others show severe hypocalcemia with Bartter's syndrome. We therefore recruited 12 patients with ADH to clarify the determinants of their clinical presentation.

DESIGN AND METHODS:

We studied two sporadic and 10 familial cases of ADH. Serum concentrations of calcium, intact PTH, and magnesium (Mg(2+)) were measured in each patient. Fractional excretion of Mg (FE(Mg)) was calculated in spot urine samples. A nuclear factor of activated T cells luciferase assay was used to analyze the responsiveness of each mutant CaSR to extracellular Ca(2+).

RESULTS:

Genomic analysis revealed five known activating mutations and a novel mutation, E481K, in the CASR. Patients with the A843E, C131W, or F788C mutation showed hypomagnesemia with elevated FE(Mg). Intact PTH in these patients was consistently near the detection limit. In contrast, patients with the P221L, K47N, or E481K mutation exhibited normal Mg(2+) levels. In these patients, intact PTH increased in response to low calcium, and their maximum intact PTH exceeded the lower limit of the reference range. Functional analysis showed an association between the disease severity and the in vitro activity of the mutant CaSR.

CONCLUSIONS:

The functional activity of mutant CaSR determines the serum Mg(2+) level, renal Mg(2+) handling, and intact PTH in patients with ADH. The presence of hypomagnesemia with elevated FE(Mg) may indicate the diagnosis of ADH among patients with PTH-deficient hypoparathyroidism.

• Authors: Yuka Kinoshita, Michiko Hori, Manabu Taguchi, Sumiyo Watanabe, Seiji Fukumoto
• Journal: The Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 99 Issue 2 Pg. E363-8 (Feb 2014) ISSN: 1945-7197 [Electronic] United States
• PMID: 24297799 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Parathyroid Hormone
• Receptors, Calcium-Sensing
• Magnesium
• Calcium

Topics

• Adult
• Calcium (blood)
• Child
• Female
• Humans
• Hypercalciuria (diagnosis, genetics, metabolism)
• Hypocalcemia (diagnosis, genetics, metabolism)
• Hypoparathyroidism (congenital, diagnosis, genetics, metabolism)
• Magnesium (blood)
• Male
• Middle Aged
• Mutation
• Parathyroid Hormone (blood)
• Phenotype
• Receptors, Calcium-Sensing (genetics, metabolism)