» Articles » PMID: 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

Overview
Journal Hippokratia
Specialty General Medicine
Date 2013 Aug 13
PMID 23935270
Citations 2
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

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

Xue C, Zhou C, Dai B, Yu S, Xu C, Mao Z Oncotarget. 2015; 6(40):42515-29.

PMID: 26636542 PMC: 4767449. DOI: 10.18632/oncotarget.6452.


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

Woon C, Bielinski-Bradbury A, OReilly K, Robinson P BMC Nephrol. 2015; 16:140.

PMID: 26275819 PMC: 4536696. DOI: 10.1186/s12882-015-0114-5.

References
1.
van Dijk M, Peters D, Breuning M, Chang P . The angiotensin-converting enzyme genotype and microalbuminuria in autosomal dominant polycystic kidney disease. J Am Soc Nephrol. 1999; 10(9):1916-20. DOI: 10.1681/ASN.V1091916. View

2.
Bae K, Grantham J . Imaging for the prognosis of autosomal dominant polycystic kidney disease. Nat Rev Nephrol. 2010; 6(2):96-106. DOI: 10.1038/nrneph.2009.214. View

3.
Ecder T, Chapman A, Brosnahan G, Edelstein C, Johnson A, Schrier R . Effect of antihypertensive therapy on renal function and urinary albumin excretion in hypertensive patients with autosomal dominant polycystic kidney disease. Am J Kidney Dis. 2000; 35(3):427-32. DOI: 10.1016/s0272-6386(00)70195-8. View

4.
Seeman T, Dusek J, Vondrichova H, Kyncl M, John U, Misselwitz J . Ambulatory blood pressure correlates with renal volume and number of renal cysts in children with autosomal dominant polycystic kidney disease. Blood Press Monit. 2003; 8(3):107-10. DOI: 10.1097/01.mbp.0000085762.28312.4a. View

5.
KLAHR S, Breyer J, Beck G, Dennis V, HARTMAN J, Roth D . Dietary protein restriction, blood pressure control, and the progression of polycystic kidney disease. Modification of Diet in Renal Disease Study Group. J Am Soc Nephrol. 1995; 5(12):2037-47. DOI: 10.1681/ASN.V5122037. View