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.
Effect of eplerenone on markers of bone turnover in patients with primary hyperparathyroidism â The randomized, placebo-controlled EPATH trial
Catena, Cristiana;
2017-01-01
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.File | Dimensione | Formato | |
---|---|---|---|
Bone 2017.pdf
non disponibili
Descrizione: Bone 2017 EPATH
Tipologia:
Versione Editoriale (PDF)
Licenza:
Non pubblico
Dimensione
358.78 kB
Formato
Adobe PDF
|
358.78 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.