The cardiovascular system in familial hypocalciuric hypercalcemia: a cross-sectional study on physiological effects of inactivating variants in the calcium-sensing receptor gene

Author:

Breum Jakobsen Niels Frederik1,Laugesen Esben123,Rolighed Lars4,Nissen Peter H5,Poulsen Per Løgstrup1,Pedersen Erling Bjerregaard36,Mosekilde Leif1,Rejnmark Lars13

Affiliation:

1. 1Department of Endocrinology and Internal MedicineAarhus University Hospital, Aarhus, Denmark

2. 2Danish Diabetes AcademyOdense University Hospital, Odense, Denmark

3. 3Department of Clinical MedicineAarhus University, Aarhus, Denmark

4. 4Departments of Surgery

5. 5Clinical BiochemistryAarhus University Hospital, Aarhus, Denmark

6. 6University Clinic in Nephrology and HypertensionHolstebro Hospital, Hospital Jutland West, Holstebro, Denmark

Abstract

Objective Loss-of-function variants in the gene encoding the calcium-sensing receptor (CASR) result in familial hypocalciuric hypercalcemia (FHH), causing hypercalcemia with high normal or elevated parathyroid hormone levels. The CASR may also influence electrolyte and water homeostasis. It is unknown whether FHH affects cardiovascular health. We, therefore investigated whether FHH is associated with changes in the regulation of the cardiovascular system by measuring 24-h blood pressure (BP), arterial stiffness and vasoactive hormones. Design Cross-sectional study comparing 50 patients with FHH to age- and gender-matched controls. Results Studied subjects (69% women) had a mean age of 56years. A similar number of patients and controls (33%) were on treatment with antihypertensive drugs. Overall, no differences were found between groups in 24-h ambulatory BP or pulse wave velocity. However, compared with controls, diastolic BP during nighttime was lower in FHH females (60±5 vs 66±9mmHg, P<0.01) and higher in FHH males (69±6 vs 64±5mmHg, P=0.02). FHH was associated with a significantly higher plasma osmolality (P<0.01), higher plasma levels of vasopressin (P<0.01) and a higher renal excretion of epithelial sodium channels (ENaCs) (P=0.03), whereas urine aquaporin-2 and plasma sodium, aldosterone and renin did not differ between groups. FHH patients had a lower urinary volume with an increased osmolality if analyses were restricted to those not on treatments with antihypertensive drugs. ConclusionsFHH does not seem to be associated with an increased risk of CVD.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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