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Effect of eplerenone on markers of bone turnover in patients with primary hyperparathyroidism â The randomized, placebo-controlled EPATH trial

Verheyen, Nicolas
•
Grã1⁄4bler, Martin R.
•
Meinitzer, Andreas
altro
Tomaschitz, Andreas
2017
  • journal article

Periodico
BONE
Abstract
Mineralocorticoid receptor (MR) antagonism may affect bone turnover via direct and indirect pathways involving parathyroid hormone, but randomized controlled trials are lacking. In a pre-specified analysis of the “Eplerenone in primary hyperparathyroidism” placebo-controlled, randomized trial (ISRCTN 33941607), effects of eight weeks MR-blockade with eplerenone on bone turnovermarkers in 97 patients with primary hyperparathyroidism were tested. Mean age was 67.5 ± 9.5 years, and 76 (78.4%) were females. In analysis of covariance with adjustment for baseline values, eplerenone had no significant effect on isoform 5b of the tartrate-resistant acid phosphatase (TRAP), beta-crosslaps, N-terminal propeptide of procollagen type 1 (P1NP), osteocalcin and bone-specific alkaline phosphatase.Therewasnosignificant cross-sectional correlation between plasma aldosterone concentration or the aldosterone-to-renin ratio and markers of bone turnover inmultivariate linear regression models at baseline. These data provide first evidence from a randomized and placebo-controlled trial that short-termMR antagonismmay not affect bone turnover, at least in patientswith primary hyperparathyroidism.
DOI
10.1016/j.bone.2017.08.030
WOS
WOS:000413994500024
Archivio
http://hdl.handle.net/11390/1121163
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85029427107
www.elsevier.com/locate/bone
Diritti
closed access
Soggetti
  • Bone turnover

  • Eplerenone

  • Mineralocorticoid rec...

  • Primary hyperparathyr...

  • Randomized controlled...

  • Endocrinology, Diabet...

  • Physiology

  • Histology

Scopus© citazioni
6
Data di acquisizione
Jun 14, 2022
Vedi dettagli
Web of Science© citazioni
8
Data di acquisizione
Mar 25, 2024
Visualizzazioni
2
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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