Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial

<p>Abstract</p> <p>Background</p> <p>Increasing evidence suggests the bidirectional interplay between parathyroid hormone and aldosterone as an important mechanism behind the increased risk of cardiovascular damage and bone disease observed in primary hyperparathyroidis...

Full description

Bibliographic Details
Main Authors: Tomaschitz Andreas, Fahrleitner-Pammer Astrid, Pieske Burkert, Verheyen Nicolas, Amrein Karin, Ritz Eberhard, Kienreich Katharina, Horina Jörg H, Schmidt Albrecht, Kraigher-Krainer Elisabeth, Colantonio Caterina, Meinitzer Andreas, Pilz Stefan
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Endocrine Disorders
Subjects:
Online Access:http://www.biomedcentral.com/1472-6823/12/19
id doaj-3ae69d8ed86c4f61b0896f3a62cf3dee
record_format Article
spelling doaj-3ae69d8ed86c4f61b0896f3a62cf3dee2020-11-25T01:42:42ZengBMCBMC Endocrine Disorders1472-68232012-09-011211910.1186/1472-6823-12-19Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trialTomaschitz AndreasFahrleitner-Pammer AstridPieske BurkertVerheyen NicolasAmrein KarinRitz EberhardKienreich KatharinaHorina Jörg HSchmidt AlbrechtKraigher-Krainer ElisabethColantonio CaterinaMeinitzer AndreasPilz Stefan<p>Abstract</p> <p>Background</p> <p>Increasing evidence suggests the bidirectional interplay between parathyroid hormone and aldosterone as an important mechanism behind the increased risk of cardiovascular damage and bone disease observed in primary hyperparathyroidism. Our primary object is to assess the efficacy of the mineralocorticoid receptor-blocker eplerenone to reduce parathyroid hormone secretion in patients with parathyroid hormone excess.</p> <p>Methods/design</p> <p>Overall, 110 adult male and female patients with primary hyperparathyroidism will be randomly assigned to eplerenone (25 mg once daily for 4 weeks and 4 weeks with 50 mg once daily after dose titration] or placebo, over eight weeks. Each participant will undergo detailed clinical assessment, including anthropometric evaluation, 24-h ambulatory arterial blood pressure monitoring, echocardiography, kidney function and detailed laboratory determination of biomarkers of bone metabolism and cardiovascular disease.</p> <p>The study comprises the following exploratory endpoints: mean change from baseline to week eight in (1) parathyroid hormone(1–84) as the primary endpoint and (2) 24-h systolic and diastolic ambulatory blood pressure levels, NT-pro-BNP, biomarkers of bone metabolism, 24-h urinary protein/albumin excretion and echocardiographic parameters reflecting systolic and diastolic function as well as cardiac dimensions, as secondary endpoints.</p> <p>Discussion</p> <p>In view of the reciprocal interaction between aldosterone and parathyroid hormone and the potentially ensuing target organ damage, the EPATH trial is designed to determine whether eplerenone, compared to placebo, will effectively impact on parathyroid hormone secretion and improve cardiovascular, renal and bone health in patients with primary hyperparathyroidism.</p> <p>Trial registration</p> <p>ISRCTN33941607</p> http://www.biomedcentral.com/1472-6823/12/19AldosteroneMineralocorticoid receptor blockerHyperparathyroidism
collection DOAJ
language English
format Article
sources DOAJ
author Tomaschitz Andreas
Fahrleitner-Pammer Astrid
Pieske Burkert
Verheyen Nicolas
Amrein Karin
Ritz Eberhard
Kienreich Katharina
Horina Jörg H
Schmidt Albrecht
Kraigher-Krainer Elisabeth
Colantonio Caterina
Meinitzer Andreas
Pilz Stefan
spellingShingle Tomaschitz Andreas
Fahrleitner-Pammer Astrid
Pieske Burkert
Verheyen Nicolas
Amrein Karin
Ritz Eberhard
Kienreich Katharina
Horina Jörg H
Schmidt Albrecht
Kraigher-Krainer Elisabeth
Colantonio Caterina
Meinitzer Andreas
Pilz Stefan
Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
BMC Endocrine Disorders
Aldosterone
Mineralocorticoid receptor blocker
Hyperparathyroidism
author_facet Tomaschitz Andreas
Fahrleitner-Pammer Astrid
Pieske Burkert
Verheyen Nicolas
Amrein Karin
Ritz Eberhard
Kienreich Katharina
Horina Jörg H
Schmidt Albrecht
Kraigher-Krainer Elisabeth
Colantonio Caterina
Meinitzer Andreas
Pilz Stefan
author_sort Tomaschitz Andreas
title Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
title_short Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
title_full Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
title_fullStr Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
title_full_unstemmed Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
title_sort effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial
publisher BMC
series BMC Endocrine Disorders
issn 1472-6823
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>Increasing evidence suggests the bidirectional interplay between parathyroid hormone and aldosterone as an important mechanism behind the increased risk of cardiovascular damage and bone disease observed in primary hyperparathyroidism. Our primary object is to assess the efficacy of the mineralocorticoid receptor-blocker eplerenone to reduce parathyroid hormone secretion in patients with parathyroid hormone excess.</p> <p>Methods/design</p> <p>Overall, 110 adult male and female patients with primary hyperparathyroidism will be randomly assigned to eplerenone (25 mg once daily for 4 weeks and 4 weeks with 50 mg once daily after dose titration] or placebo, over eight weeks. Each participant will undergo detailed clinical assessment, including anthropometric evaluation, 24-h ambulatory arterial blood pressure monitoring, echocardiography, kidney function and detailed laboratory determination of biomarkers of bone metabolism and cardiovascular disease.</p> <p>The study comprises the following exploratory endpoints: mean change from baseline to week eight in (1) parathyroid hormone(1–84) as the primary endpoint and (2) 24-h systolic and diastolic ambulatory blood pressure levels, NT-pro-BNP, biomarkers of bone metabolism, 24-h urinary protein/albumin excretion and echocardiographic parameters reflecting systolic and diastolic function as well as cardiac dimensions, as secondary endpoints.</p> <p>Discussion</p> <p>In view of the reciprocal interaction between aldosterone and parathyroid hormone and the potentially ensuing target organ damage, the EPATH trial is designed to determine whether eplerenone, compared to placebo, will effectively impact on parathyroid hormone secretion and improve cardiovascular, renal and bone health in patients with primary hyperparathyroidism.</p> <p>Trial registration</p> <p>ISRCTN33941607</p>
topic Aldosterone
Mineralocorticoid receptor blocker
Hyperparathyroidism
url http://www.biomedcentral.com/1472-6823/12/19
work_keys_str_mv AT tomaschitzandreas effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT fahrleitnerpammerastrid effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT pieskeburkert effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT verheyennicolas effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT amreinkarin effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT ritzeberhard effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT kienreichkatharina effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT horinajorgh effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT schmidtalbrecht effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT kraigherkrainerelisabeth effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT colantoniocaterina effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT meinitzerandreas effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
AT pilzstefan effectofeplerenoneonparathyroidhormonelevelsinpatientswithprimaryhyperparathyroidismarandomizeddoubleblindplacebocontrolledtrial
_version_ 1725034811974746112