Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/123704
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dc.contributor.authorChen, A.X.-
dc.contributor.authorMoran, J.L.-
dc.contributor.authorLibianto, R.-
dc.contributor.authorBaqar, S.-
dc.contributor.authorO Callaghan, C.-
dc.contributor.authorMacIsaac, R.J.-
dc.contributor.authorJerums, G.-
dc.contributor.authorEkinci, E.I.-
dc.date.issued2019-
dc.identifier.citationJournal of Human Hypertension, 2019; 34(2):143-150-
dc.identifier.issn0950-9240-
dc.identifier.issn1476-5527-
dc.identifier.urihttp://hdl.handle.net/2440/123704-
dc.description.abstractHigh blood pressure variability (BPV) has been associated with increased cardiovascular (CV) risk. The effect of dietary salt and renin-angiotensin-aldosterone system (RAAS) activity on short-term BPV in type 2 diabetes mellitus (T2DM) is not well characterised. We aimed to determine the effect of dietary salt (sodium chloride, NaCl) supplementation on 24-h mean arterial BPV (24hBPV) during angiotensin II receptor blocker (telmisartan) use and to evaluate the effects of age, sex, plasma renin activity (PRA) and serum aldosterone on 24hBPV. In a randomised, double-blind, crossover study, patients with T2DM (n = 28), treated with telmisartan received NaCl (100 mmol/24 h) or placebo capsules during 2 weeks of telmisartan. Following a 6-week washout, the protocol was repeated in reverse. 24hBPV was evaluated as a co-efficient of variation [CV (%) = mean/standard deviation] × 100). Twenty-four hour urinary sodium excretion, ambulatory BP and biochemical tests were performed at each phase. Results were analysed using a linear mixed model to generate predicted values for 24hBPV. Predicted 24hBPV was higher with telmisartan vs baseline (p = 0.01), with a trend towards reduced 24hBPV with salt (p = 0.052). Predicted 24hBPV was lower in females (p = 0.017), increasing age (p = 0.001) and increasing PRA (p = 0.011). In patients with T2DM, predicted 24hBPV increased from baseline with telmisartan, but there was no additional increase in predicted 24hBPV with salt supplementation. This suggests that in the short-term, salt supplementation has no apparent deleterious effects on 24hBPV. Long-term studies are required to evaluate the effect of 24hBPV on CV outcomes in patients with T2DM.-
dc.description.statementofresponsibilityAngela X. Chen, John L. Moran, Renata Libianto, Sara Baqar, Christopher O'Callaghan, Richard J. MacIsaac, George Jerums, Elif I. Ekinci-
dc.language.isoen-
dc.publisherSpringer Nature-
dc.rights© The Author(s), under exclusive licence to Springer Nature Limited 2019.-
dc.source.urihttp://dx.doi.org/10.1038/s41371-019-0238-3-
dc.subjectHumans-
dc.subjectHypertension-
dc.subjectDiabetes Mellitus, Type 2-
dc.subjectSodium Chloride-
dc.subjectSodium Chloride, Dietary-
dc.subjectAldosterone-
dc.subjectRenin-
dc.subjectAngiotensin II-
dc.subjectCross-Over Studies-
dc.subjectRenin-Angiotensin System-
dc.subjectBlood Pressure-
dc.subjectDietary Supplements-
dc.subjectFemale-
dc.subjectAngiotensin Receptor Antagonists-
dc.titleEffect of angiotensin II receptor blocker and salt supplementation on short-term blood pressure variability in type 2 diabetes-
dc.typeJournal article-
dc.identifier.doi10.1038/s41371-019-0238-3-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/466611-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1054312-
pubs.publication-statusPublished-
dc.identifier.orcidMoran, J.L. [0000-0003-2311-0440]-
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