Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9311
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dc.contributor.authorJerums, Georgeen
dc.contributor.authorAllen, Terri Jen
dc.contributor.authorCampbell, D Jen
dc.contributor.authorCooper, Mark Een
dc.contributor.authorGilbert, Richard Een
dc.contributor.authorHammond, J Jen
dc.contributor.authorRaffaele, Jen
dc.contributor.authorTsalamandris, Conen
dc.date.accessioned2015-05-15T22:21:45Z
dc.date.available2015-05-15T22:21:45Z
dc.date.issued2001-05-01en
dc.identifier.citationAmerican Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation; 37(5): 890-9en
dc.identifier.govdoc11325669en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9311en
dc.description.abstractThe aim of this study is to compare the efficacy of an angiotensin-converting enzyme inhibitor with a dihydropyridine calcium channel blocker in preventing progression to macroalbuminuria and/or a decline in renal function in normotensive patients with type 1 diabetes and microalbuminuria. Forty-two patients were randomized to treatment with either perindopril, slow-release nifedipine, or placebo. In the first 3 months, drug dosage was titrated to achieve a decrease in diastolic blood pressure of at least 5 mm HG: Thirty-three patients had a minimum of 24 months' data, and 25 patients were followed up beyond 36 months (mean, 67 +/- 4 months). Patients were studied every 3 months and at the end of the treatment period; those who remained normotensive discontinued therapy and were followed up for an additional 3 months. Baseline geometric mean albumin excretion rates (AERs) were as follows: perindopril, 66 microg/min; nifedipine, 59 microg/min; and placebo, 66 microg/min. During the first 3 years, 7 of the perindopril-treated but none of the placebo or nifedipine-treated patients reverted to normoalbuminuria (P < 0.01). Median AERs at 3 years of treatment in each group were 23 microg/min for perindopril, 122 microg/min for nifedipine, and 112 microg/min for placebo patients (P < 0.01). In patients with more than 3 years' follow-up, median AERs decreased by 45% in the first year and then stabilized in the perindopril group, but increased by 17.6% in the nifedipine group and 27.6% in the placebo group (P < 0.03) in the first year, then increased progressively. In these same patients, there was a significant decline in glomerular filtration rate in the nifedipine group (-7.8 +/- 1.8 mL/min/1.73 m(2)/y), but not in the other two groups (perindopril, -1.0 +/- 1.2 mL/min/1.73 m(2)/y; placebo, -1.3 +/- 1.1 mL/min/1.73 m(2)/y; P = 0.004). At the end of the study, cessation of treatment for 3 months was associated with a doubling of AERs in the perindopril-treated group, but no change in the other two groups (P < 0.001). In conclusion, long-term perindopril therapy is more effective than nifedipine or placebo in delaying the progression of diabetic nephropathy and reducing AER to the normoalbuminuric range (<20 microg/min) in normotensive patients with type 1 diabetes and microalbuminuria.en
dc.language.isoenen
dc.subject.otherAdolescenten
dc.subject.otherAdulten
dc.subject.otherAgeden
dc.subject.otherAlbuminuria.prevention & controlen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.therapeutic useen
dc.subject.otherAntihypertensive Agents.therapeutic useen
dc.subject.otherBlood Pressure.drug effectsen
dc.subject.otherCalcium Channel Blockers.therapeutic useen
dc.subject.otherDiabetes Mellitus, Type 1.complications.urineen
dc.subject.otherDiabetic Nephropathies.prevention & controlen
dc.subject.otherFemaleen
dc.subject.otherFollow-Up Studiesen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherNifedipine.therapeutic useen
dc.subject.otherPerindopril.therapeutic useen
dc.subject.otherProspective Studiesen
dc.subject.otherStatistics as Topicen
dc.titleLong-term comparison between perindopril and nifedipine in normotensive patients with type 1 diabetes and microalbuminuria.en
dc.typeJournal Articleen
dc.identifier.journaltitleAmerican journal of kidney diseases : the official journal of the National Kidney Foundationen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin & Repatriation Medical Centre, Heidelberg 3084, VIC, Australiaen
dc.description.pages890-9en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/11325669en
dc.type.austinJournal Articleen
local.name.researcherJerums, George
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
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