Osteoporosis, bone & mineral

Evaluating the clinical and mechanistic effects of eplerenone and amiloride monotherapy, and combination therapy with cinacalcet, in primary hyperparathyroidism: A placebo‐controlled randomized trial

Clin Endocrinol (Oxf)Published Randomised controlled trial

Authors' conclusion

Although maximally tolerated therapy with eplerenone and amiloride induced expected changes in renin, aldosterone and blood pressure, there were no meaningful changes in PTH or serum calcium levels in P-HPT patients. These results suggest that inhibition of aldosterone action does not have a clinically meaningful role in medical therapy for P-HPT.

Study context

Population
Patients with primary hyperparathyroidism (P-HPT); most women (83%) and White (76%)
Comparison
Eplerenone vs amiloride vs placebo for 4 weeks, then each combined with cinacalcet for 2 weeks
Primary endpoint
PTH levels
Follow-up
4 weeks
Methodological detailsdouble-blinded, three parallel-group, placebo-controlled
  • Double-blinded
  • Three parallel-group
  • Placebo-controlled

Primary result

As reported in the abstract

PTH and calcium levels
  • Neither eplerenone nor amiloride induced significant changes in parathyroid hormone (PTH) or calcium levels vs placebo

Further findings

Blood pressure, renin and aldosterone

Eplerenone and amiloride induced significant reductions in blood pressure and increases in renin and aldosterone production

Procollagen type 1 N-terminal propeptide

Both eplerenone and amiloride induced significant reductions in procollagen type 1 N-terminal propeptide vs placebo

PTH and serum calcium with added cinacalcet · additional 2 weeks

PTH and calcium markedly reduced in all groups; no significant difference in PTH or serum calcium reductions between groups

Original publication

Evaluating the clinical and mechanistic effects of eplerenone and amiloride monotherapy, and combination therapy with cinacalcet, in primary hyperparathyroidism: A placebo‐controlled randomized trial. Clin Endocrinol (Oxf). Published 8 November 2022. doi:10.1111/cen.14840

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