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dc.contributor.authorGriffin, Tomás P.
dc.contributor.authorIslam, Md Nahidul
dc.contributor.authorBlake, Liam
dc.contributor.authorBell, Marcia
dc.contributor.authorGriffin, Matthew D.
dc.contributor.authorO’Shea, Paula M.
dc.date.accessioned2019-03-13T11:14:45Z
dc.date.issued2018-12-06
dc.identifier.citationGriffin, 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-0794-7026en_IE
dc.identifier.issn1439-4286
dc.identifier.urihttp://hdl.handle.net/10379/15016
dc.description.abstractThe 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.sponsorshipTPG 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.formatapplication/pdfen_IE
dc.language.isoenen_IE
dc.publisherThieme Publishingen_IE
dc.relation.ispartofHormone and Metabolic Researchen
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectsodium glucose co-transporter-2en_IE
dc.subjecttype 2 diabetes mellitusen_IE
dc.subjecthyperaldosteronismen_IE
dc.subjectaldosteroneen_IE
dc.subjectreninen_IE
dc.subjectCOTRANSPORTER 2 INHIBITORSen_IE
dc.subjectCARDIOVASCULAR EVENTSen_IE
dc.subjectSGLT2 INHIBITORSen_IE
dc.subjectRENIN-ACTIVITYen_IE
dc.subjectMANAGEMENTen_IE
dc.subjectSYSTEMen_IE
dc.subjectHYPERTENSIONen_IE
dc.subjectACTIVATIONen_IE
dc.subjectDIAGNOSISen_IE
dc.subjectOBESITYen_IE
dc.titleEffect of sodium glucose co-transporter-2 inhibition on the Aldosterone/Renin Ratio in Type 2 Diabetes Mellitusen_IE
dc.typeArticleen_IE
dc.date.updated2019-03-13T10:56:05Z
dc.identifier.doi10.1055/a-0794-7026
dc.local.publishedsourcehttps://dx.doi.org/10.1055/a-0794-7026en_IE
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funderHardiman Research Scholarship, College of Medicine, Nursing and Health Science, NUI Galwayen_IE
dc.contributor.funderRoyal College of Physicians of Irelanden_IE
dc.contributor.funderHorizon 2020en_IE
dc.contributor.funderSeventh Framework Programmeen_IE
dc.contributor.funderScience Foundation Irelanden_IE
dc.description.embargo2019-12-06
dc.internal.rssid15968478
dc.local.contactMatthew Dallas Griffin, Remedi, Biomedical Sciences Buil, Corrib Village, Dangan, Nui Galway. 5436 Email: matthew.griffin@nuigalway.ie
dc.local.copyrightcheckedYes
dc.local.versionACCEPTED
dcterms.projectinfo:eu-repo/grantAgreement/EC/H2020::RIA/634086/EU/Novel Stromal Cell Therapy for Diabetic Kidney Disease/NEPHSTROMen_IE
dcterms.projectinfo:eu-repo/grantAgreement/EC/FP7::SP1::HEALTH/602470/EU/Adverse Immune Signatures and their Prevention in Corneal Transplantation/VISICORTen_IE
dcterms.projectinfo:eu-repo/grantAgreement/SFI/SFI Strategic Research Cluster/09/SRC/B1794/IE/SRC REMEDI: REMEDI-2: From Research to Human Therapy/en_IE
dcterms.projectinfo:eu-repo/grantAgreement/SFI/SFI Research Centres/13/RC/2073/IE/C�RAM - Centre for Research in Medical Devices/en_IE
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