Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10845
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dc.contributor.authorEkinci, Elif Ien
dc.contributor.authorThomas, Georginaen
dc.contributor.authorThomas, Daviden
dc.contributor.authorJohnson, Cameronen
dc.contributor.authorMacisaac, Richard Jen
dc.contributor.authorHoulihan, Christine Aen
dc.contributor.authorFinch, Sueen
dc.contributor.authorPanagiotopoulos, Siannaen
dc.contributor.authorO'Callaghan, Christopher Jen
dc.contributor.authorJerums, Georgeen
dc.date.accessioned2015-05-16T00:25:24Z-
dc.date.available2015-05-16T00:25:24Z-
dc.date.issued2009-06-23en
dc.identifier.citationDiabetes Care 2009; 32(8): 1398-403en
dc.identifier.govdoc19549737en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10845en
dc.description.abstractOBJECTIVE This prospective randomized double-blind placebo-controlled crossover study examined the effects of sodium chloride (NaCl) supplementation on the antialbuminuric action of telmisartan with or without hydrochlorothiazide (HCT) in hypertensive patients with type 2 diabetes, increased albumin excretion rate (AER), and habitual low dietary salt intake (LDS; <100 mmol sodium/24 h on two of three consecutive occasions) or high dietary salt intake (HDS; >200 mmol sodium/24 h on two of three consecutive occasions). RESEARCH DESIGN AND METHODS Following a washout period, subjects (n = 32) received 40 mg/day telmisartan for 4 weeks followed by 40 mg telmisartan plus 12.5 mg/day HCT for 4 weeks. For the last 2 weeks of each treatment period, patients received either 100 mmol/day NaCl or placebo capsules. After a second washout, the regimen was repeated with supplements in reverse order. AER and ambulatory blood pressure were measured at weeks 0, 4, 8, 14, 18, and 22. RESULTS In LDS, NaCl supplementation reduced the anti-albuminuric effect of telmisartan with or without HCT from 42.3% (placebo) to 9.5% (P = 0.004). By contrast, in HDS, NaCl supplementation did not reduce the AER response to telmisartan with or without HCT (placebo 30.9%, NaCl 28.1%, P = 0.7). Changes in AER were independent of changes in blood pressure. CONCLUSIONS The AER response to telmisartan with or without HCT under habitual low salt intake can be blunted by NaCl supplementation. By contrast, when there is already a suppressed renin angiotensin aldosterone system under habitual high dietary salt intake, the additional NaCl does not alter the AER response.en
dc.language.isoenen
dc.subject.otherAgeden
dc.subject.otherAlbuminuria.drug therapy.physiopathologyen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.therapeutic useen
dc.subject.otherAntihypertensive Agents.therapeutic useen
dc.subject.otherBenzimidazoles.therapeutic useen
dc.subject.otherBenzoates.therapeutic useen
dc.subject.otherBlood Pressure.drug effects.physiologyen
dc.subject.otherCross-Over Studiesen
dc.subject.otherDiabetes Mellitus, Type 2.complicationsen
dc.subject.otherDietary Supplementsen
dc.subject.otherFemaleen
dc.subject.otherGlomerular Filtration Rate.drug effectsen
dc.subject.otherHumansen
dc.subject.otherHydrochlorothiazide.therapeutic useen
dc.subject.otherHypertension.drug therapyen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherSodium Chloride.administration & dosage.therapeutic useen
dc.subject.otherSodium, Dietaryen
dc.titleEffects of salt supplementation on the albuminuric response to telmisartan with or without hydrochlorothiazide therapy in hypertensive patients with type 2 diabetes are modulated by habitual dietary salt intake.en
dc.typeJournal Articleen
dc.identifier.journaltitleDiabetes Careen
dc.identifier.affiliationEndocrine Centre, Austin Health and University of Melbourne, Heidelberg Repatriation Hospital, Heidelberg West, Victoria, Australiaen
dc.identifier.doi10.2337/dc08-2297en
dc.description.pages1398-403en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/19549737en
dc.identifier.orcid0000-0002-0845-0001-
dc.type.austinJournal Articleen
local.name.researcherEkinci, Elif I
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
crisitem.author.deptOffice for Research-
crisitem.author.deptClinical Pharmacology and Therapeutics-
crisitem.author.deptEndocrinology-
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