Literature DB >> 23935270

A comparison of the effects of losartan and ramipril on blood pressure, renal volume and progression in polycystic kidney disease: A 5-Year follow-up.

S Ulusoy1, G Ozkan, P Kosucu, K Kaynar, I Eyuboglu.   

Abstract

BACKGROUND: The major cause of hereditary renal failure is autosomal dominant polycystic kidney disease (ADPKD). Many factors affect renal progression in these patients. Among these, hypertension and an increase in renal volume are interrelated in terms of their effects on renal progression. We aimed to investigate the effects of losartan and ramipril on renal volume and progression in patients with ADPKD.
MATERIALS AND METHODS: Data from 18 hypertensive patients with ADPKD were evaluated. Eleven of the 18 hypertensive patients were on losartan and 7 on ramipril treatment. Demographic parameters, use of antihypertensives and other medications, the course of blood pressure (BP), biochemical parameters, creatinine clearance (CrCL), findings at computed tomography and renal volume were recorded at baseline and at 1 and 5 years.
RESULTS: Target BP values were maintained over 5 years. The annual decrease in CrCL was 1.33 mL/min in the losartan group compared with 6.59 mL/min in the ramipril group. There was no significant difference between the groups in terms of annual decrease in CrCL. Annual increase in renal volume was 252.04 cm³ in the losartan group and 167.36 cm³ in the ramipril group. There was no significant difference between the groups in terms of the increase in renal volumes at 1 and 5 years.
CONCLUSION: Our study demonstrated that losartan and ramipril provided effective BP control. In addition, the results of our study demonstrated that despite the increase in renal volume, losartan and ramipril may have regressed renal progression via other factors.

Entities:  

Keywords:  autosomal dominant polycystic kidney disease; losartan; ramipril; renal progression; renal volume

Year:  2012        PMID: 23935270      PMCID: PMC3738416     

Source DB:  PubMed          Journal:  Hippokratia        ISSN: 1108-4189            Impact factor:   0.471


  22 in total

1.  Epidemiological study of kidney survival in autosomal dominant polycystic kidney disease.

Authors:  Robert W Schrier; Kimberly K McFann; Ann M Johnson
Journal:  Kidney Int       Date:  2003-02       Impact factor: 10.612

Review 2.  The role of renin-angiotensin-aldosterone system in the progression of chronic kidney disease.

Authors:  Giuseppe Remuzzi; Norberto Perico; Manuel Macia; Piero Ruggenenti
Journal:  Kidney Int Suppl       Date:  2005-12       Impact factor: 10.545

3.  Sirolimus and kidney growth in autosomal dominant polycystic kidney disease.

Authors:  Andreas L Serra; Diane Poster; Andreas D Kistler; Fabienne Krauer; Shagun Raina; James Young; Katharina M Rentsch; Katharina S Spanaus; Oliver Senn; Paulus Kristanto; Hans Scheffel; Dominik Weishaupt; Rudolf P Wüthrich
Journal:  N Engl J Med       Date:  2010-06-26       Impact factor: 91.245

4.  Volumetric determination of progression in autosomal dominant polycystic kidney disease by computed tomography.

Authors:  C Sise; M Kusaka; L H Wetzel; F Winklhofer; B D Cowley; L T Cook; M Gordon; J J Grantham
Journal:  Kidney Int       Date:  2000-12       Impact factor: 10.612

5.  The angiotensin-converting enzyme genotype and microalbuminuria in autosomal dominant polycystic kidney disease.

Authors:  M A van Dijk; D J Peters; M H Breuning; P C Chang
Journal:  J Am Soc Nephrol       Date:  1999-09       Impact factor: 10.121

6.  Effect of antihypertensive therapy on renal function and urinary albumin excretion in hypertensive patients with autosomal dominant polycystic kidney disease.

Authors:  T Ecder; A B Chapman; G M Brosnahan; C L Edelstein; A M Johnson; R W Schrier
Journal:  Am J Kidney Dis       Date:  2000-03       Impact factor: 8.860

7.  Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group.

Authors:  N Hateboer; M A v Dijk; N Bogdanova; E Coto; A K Saggar-Malik; J L San Millan; R Torra; M Breuning; D Ravine
Journal:  Lancet       Date:  1999-01-09       Impact factor: 79.321

8.  Kidney function and volume progression in unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis or hypoplasia: a case series.

Authors:  Diane Poster; Andreas D Kistler; Fabienne Krauer; Jon D Blumenfeld; Hanna Rennert; Dominik Weishaupt; Rudolf P Wüthrich; Andreas L Serra
Journal:  Am J Kidney Dis       Date:  2009-06-10       Impact factor: 8.860

9.  Mammalian target of rapamycin and autosomal dominant polycystic kidney disease.

Authors:  R P Wüthrich; A L Serra
Journal:  Transplant Proc       Date:  2009-07-10       Impact factor: 1.066

10.  Developments in the management of autosomal dominant polycystic kidney disease.

Authors:  Amirali Masoumi; Berenice Reed-Gitomer; Catherine Kelleher; Mir Reza Bekheirnia; Robert W Schrier
Journal:  Ther Clin Risk Manag       Date:  2008-04       Impact factor: 2.423

View more
  2 in total

Review 1.  A systematic review of the predictors of disease progression in patients with autosomal dominant polycystic kidney disease.

Authors:  Claire Woon; Ashleigh Bielinski-Bradbury; Karl O'Reilly; Paul Robinson
Journal:  BMC Nephrol       Date:  2015-08-15       Impact factor: 2.388

2.  Antihypertensive treatments in adult autosomal dominant polycystic kidney disease: network meta-analysis of the randomized controlled trials.

Authors:  Cheng Xue; Chenchen Zhou; Bing Dai; Shengqiang Yu; Chenggang Xu; Zhiguo Mao; Chaoyang Ye; Dongping Chen; Xuezhi Zhao; Jun Wu; Wansheng Chen; Changlin Mei
Journal:  Oncotarget       Date:  2015-12-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.