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https://ahro.austin.org.au/austinjspui/handle/1/10845
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DC Field | Value | Language |
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dc.contributor.author | Ekinci, Elif I | en |
dc.contributor.author | Thomas, Georgina | en |
dc.contributor.author | Thomas, David | en |
dc.contributor.author | Johnson, Cameron | en |
dc.contributor.author | Macisaac, Richard J | en |
dc.contributor.author | Houlihan, Christine A | en |
dc.contributor.author | Finch, Sue | en |
dc.contributor.author | Panagiotopoulos, Sianna | en |
dc.contributor.author | O'Callaghan, Christopher J | en |
dc.contributor.author | Jerums, George | en |
dc.date.accessioned | 2015-05-16T00:25:24Z | - |
dc.date.available | 2015-05-16T00:25:24Z | - |
dc.date.issued | 2009-06-23 | en |
dc.identifier.citation | Diabetes Care 2009; 32(8): 1398-403 | en |
dc.identifier.govdoc | 19549737 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/10845 | en |
dc.description.abstract | OBJECTIVE 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.iso | en | en |
dc.subject.other | Aged | en |
dc.subject.other | Albuminuria.drug therapy.physiopathology | en |
dc.subject.other | Angiotensin-Converting Enzyme Inhibitors.therapeutic use | en |
dc.subject.other | Antihypertensive Agents.therapeutic use | en |
dc.subject.other | Benzimidazoles.therapeutic use | en |
dc.subject.other | Benzoates.therapeutic use | en |
dc.subject.other | Blood Pressure.drug effects.physiology | en |
dc.subject.other | Cross-Over Studies | en |
dc.subject.other | Diabetes Mellitus, Type 2.complications | en |
dc.subject.other | Dietary Supplements | en |
dc.subject.other | Female | en |
dc.subject.other | Glomerular Filtration Rate.drug effects | en |
dc.subject.other | Humans | en |
dc.subject.other | Hydrochlorothiazide.therapeutic use | en |
dc.subject.other | Hypertension.drug therapy | en |
dc.subject.other | Male | en |
dc.subject.other | Middle Aged | en |
dc.subject.other | Sodium Chloride.administration & dosage.therapeutic use | en |
dc.subject.other | Sodium, Dietary | en |
dc.title | Effects 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.type | Journal Article | en |
dc.identifier.journaltitle | Diabetes Care | en |
dc.identifier.affiliation | Endocrine Centre, Austin Health and University of Melbourne, Heidelberg Repatriation Hospital, Heidelberg West, Victoria, Australia | en |
dc.identifier.doi | 10.2337/dc08-2297 | en |
dc.description.pages | 1398-403 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/19549737 | en |
dc.identifier.orcid | 0000-0002-0845-0001 | - |
dc.type.austin | Journal Article | en |
local.name.researcher | Ekinci, Elif I | |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Endocrinology | - |
crisitem.author.dept | Endocrinology | - |
crisitem.author.dept | Office for Research | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
crisitem.author.dept | Endocrinology | - |
Appears in Collections: | Journal articles |
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