dc.contributor.author | Griffin, Tomás P. | |
dc.contributor.author | Islam, Md Nahidul | |
dc.contributor.author | Blake, Liam | |
dc.contributor.author | Bell, Marcia | |
dc.contributor.author | Griffin, Matthew D. | |
dc.contributor.author | O’Shea, Paula M. | |
dc.date.accessioned | 2019-03-13T11:14:45Z | |
dc.date.issued | 2018-12-06 | |
dc.identifier.citation | Griffin, Tomás P., Islam, Md Nahidul, Blake, Liam, Bell, Marcia, Griffin, Matthew D., & O’Shea, Paula M. (2019). Effect of Sodium Glucose Co-Transporter-2 Inhibition on the Aldosterone/Renin Ratio in Type 2 Diabetes Mellitus. Horm Metab Res, 51(02), 91-99. doi: 10.1055/a-0794-7026 | en_IE |
dc.identifier.issn | 1439-4286 | |
dc.identifier.uri | http://hdl.handle.net/10379/15016 | |
dc.description.abstract | The aldosterone to renin ratio (ARR) is recommended for case detection of primary aldosteronism (PA). Several factors including medications can undermine its diagnostic accuracy. The objective was to explore the effect of Sodium Glucose Co-Transporter-2 Inhibition on the ARR in patients with type 2 diabetes mellitus (T2DM) who were prescribed a Sodium Glucose Co-Transporter-2 Inhibitor (SGLT-2i) as part of routine clinical care. The primary outcomes were intra-individual changes in aldosterone, renin and ARR. Participants were recruited at routine diabetes outpatient visits as part of a prospective longitudinal study. Eligible participants were prescribed standard doses of empagliflozin and sampled at baseline (pre-SGLT-2i) and at their next routine outpatient visit (post-SGLT-2i). After a mean of 198 (+/- 87) days on SGLT-2i treatment (n=20), there was a significant reduction in HbA(1c) BMI, eGFR and serum triglycerides and a significant increase in serum creatinine and sodium. Compared with baseline, there was a significant increase in median direct renin concentration (mIU/l) [40.3 (6.2-249.5) vs. 70.2 (7.0, 551.0) (p=0.005)] and no significant change in median plasma aldosterone concentration (pmol/l) [296 (101, 685) vs. 273 (101, 794) (p=0.541)] with a significant reduction in median ARR (pmol/mIU) [6.9 (0.6-70.7) vs. 5.3 (0.2-39.3) (p=0.007)]. The proportion of participants with a screen positive ARR decreased from 20% (pre-SGLT-2i) to 5% (post-SGLT-2i) (p=0.248). Although performed in a relatively small cohort of medically complex patients, the study indicates that SGLT-2i therapy has the potential to cause false-negative screening for PA in the setting of T2DM. Future confirmatory studies should include patients with confirmed PA. | en_IE |
dc.description.sponsorship | TPG is supported by a Hardiman Scholarship from the College of
Medicine, Nursing and Health Science, National University of Ireland, Galway and a bursary from the Royal College of Physicians of
Ireland. The authors are supported by grants from the European
Commission [Horizon 2020 Collaborative Health Project NEPHSTROM (grant number 634086; TPG, NI, MDG) and FP7 Collaborative Health Project VISICORT (grant number 602470; MDG)] and
from Science Foundation Ireland [REMEDI Strategic Research Cluster (grant number 09/SRC-B1794; MDG) and CÚRAM Research Centre (grant number 13/RC/2073; MDG)] and by the European Regional Development Fund. The materials presented, and views expressed here are the responsibility of the author(s) only. The EU
Commission takes no responsibility for any use made of the information set out. | en_IE |
dc.format | application/pdf | en_IE |
dc.language.iso | en | en_IE |
dc.publisher | Thieme Publishing | en_IE |
dc.relation.ispartof | Hormone and Metabolic Research | en |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Ireland | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/ie/ | |
dc.subject | sodium glucose co-transporter-2 | en_IE |
dc.subject | type 2 diabetes mellitus | en_IE |
dc.subject | hyperaldosteronism | en_IE |
dc.subject | aldosterone | en_IE |
dc.subject | renin | en_IE |
dc.subject | COTRANSPORTER 2 INHIBITORS | en_IE |
dc.subject | CARDIOVASCULAR EVENTS | en_IE |
dc.subject | SGLT2 INHIBITORS | en_IE |
dc.subject | RENIN-ACTIVITY | en_IE |
dc.subject | MANAGEMENT | en_IE |
dc.subject | SYSTEM | en_IE |
dc.subject | HYPERTENSION | en_IE |
dc.subject | ACTIVATION | en_IE |
dc.subject | DIAGNOSIS | en_IE |
dc.subject | OBESITY | en_IE |
dc.title | Effect of sodium glucose co-transporter-2 inhibition on the Aldosterone/Renin Ratio in Type 2 Diabetes Mellitus | en_IE |
dc.type | Article | en_IE |
dc.date.updated | 2019-03-13T10:56:05Z | |
dc.identifier.doi | 10.1055/a-0794-7026 | |
dc.local.publishedsource | https://dx.doi.org/10.1055/a-0794-7026 | en_IE |
dc.description.peer-reviewed | peer-reviewed | |
dc.contributor.funder | Hardiman Research Scholarship, College of Medicine, Nursing and Health Science, NUI Galway | en_IE |
dc.contributor.funder | Royal College of Physicians of Ireland | en_IE |
dc.contributor.funder | Horizon 2020 | en_IE |
dc.contributor.funder | Seventh Framework Programme | en_IE |
dc.contributor.funder | Science Foundation Ireland | en_IE |
dc.description.embargo | 2019-12-06 | |
dc.internal.rssid | 15968478 | |
dc.local.contact | Matthew Dallas Griffin, Remedi, Biomedical Sciences Buil, Corrib Village, Dangan, Nui Galway. 5436 Email: matthew.griffin@nuigalway.ie | |
dc.local.copyrightchecked | Yes | |
dc.local.version | ACCEPTED | |
dcterms.project | info:eu-repo/grantAgreement/EC/H2020::RIA/634086/EU/Novel Stromal Cell Therapy for Diabetic Kidney Disease/NEPHSTROM | en_IE |
dcterms.project | info:eu-repo/grantAgreement/EC/FP7::SP1::HEALTH/602470/EU/Adverse Immune Signatures and their Prevention in Corneal Transplantation/VISICORT | en_IE |
dcterms.project | info:eu-repo/grantAgreement/SFI/SFI Strategic Research Cluster/09/SRC/B1794/IE/SRC REMEDI: REMEDI-2: From Research to Human Therapy/ | en_IE |
dcterms.project | info:eu-repo/grantAgreement/SFI/SFI Research Centres/13/RC/2073/IE/C�RAM - Centre for Research in Medical Devices/ | en_IE |
nui.item.downloads | 189 | |