Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/118838
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Effect of central sympathoinhibition with moxonidine on sympathetic nervous activity in polycystic ovary syndrome-a randomized controlled trial
Author: Shorakae, S.
Lambert, E.
Jona, E.
Sari, C.
De Courten, B.
Dixon, J.
Lambert, G.
Teede, H.
Citation: Frontiers in Physiology, 2018; 9(OCT):1486-1-1486-10
Publisher: Frontiers
Issue Date: 2018
ISSN: 1664-042X
1664-042X
Statement of
Responsibility: 
Soulmaz Shorakae, Elisabeth A. Lambert, Eveline Jona, Carolina Ika Sari, Barbora de Courten, John B. Dixon, Gavin W. Lambert and Helena J. Teede
Abstract: Sympathetic nervous system (SNS) activity is increased in polycystic ovary syndrome (PCOS). Moxonidine is a centrally acting sympatholytic drug with known beneficial effects on hypertension, insulin sensitivity, dyslipidemia and inflammation. In this double-blind placebo controlled randomized clinical trial we examined the effect of moxonidine on modulating sympathetic activity and downstream metabolic abnormalities in 48 pre-menopausal women with PCOS (Rotterdam diagnostic criteria), recruited from the community (January 2013-August 2015). Participants received moxonidine (0.2 mg daily initially, up titrated to 0.4 mg daily in 2 weeks) (n = 23) or placebo (n = 25) for 12 weeks. Multiunit muscle sympathetic activity (by microneurography) and plasma noradrenaline levels were measured (primary outcomes). Fasting lipids, insulin resistance, serum androgens, and inflammatory markers were measured as secondary outcomes. Forty three women completed the trial (19 moxonidine, 24 placebo). Mean change in burst frequency (-3 ± 7 vs. -3 ± 8 per minute) and burst incidence (-3 ± 10 vs. -4 ± 12 per 100 heartbeat) did not differ significantly between moxonidine and placebo groups. Women on moxonidine had a significant reduction in hs-CRP compared to placebo group (-0.92 ± 2.3 vs. -0.04 ± 1.5) which did not persist post Bonferroni correction. There was a significant association between markers of insulin resistance at baseline and reduction in sympathetic activity with moxonidine. Moxonidine was not effective in modulating sympathetic activity in PCOS. Anti-inflammatory effects of moxonidine and a relationship between insulin resistance and sympathetic response to moxonidine are suggested which need to be further explored. Clinical Trial Registration Number: (NCT01504321).
Keywords: insulin resistance; moxonidine; polycystic ovary syndrome; randomized controlled trial; sympathetic nervous system
Rights: © 2018 Shorakae, Lambert, Jona, Ika Sari, de Courten, Dixon, Lambert and Teede. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
RMID: 0030113620
DOI: 10.3389/fphys.2018.01486
Grant ID: http://purl.org/au-research/grants/nhmrc/1022793
Appears in Collections:Medicine publications

Files in This Item:
File Description SizeFormat 
hdl_118838.pdfPublished version631.61 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.