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NDT Advance Access originally published online on November 4, 2007
Nephrology Dialysis Transplantation 2008 23(2):573-579; doi:10.1093/ndt/gfm731
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© The Author [2007].
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org



Renal and cardiac effects of antihypertensive treatment with ramipril vs metoprolol in autosomal dominant polycystic kidney disease

Raoul Zeltner, Roudolf Poliak, Birgit Stiasny, Roland E. Schmieder and Bernd D. Schulze

Department of Nephrology and Hypertension, University of Erlangen-Nuernberg, Nuernberg, Germany

Correspondence and offprint requests to: Dr. Raoul Zeltner, Medizinische Klinik 4, Universität Erlangen-Nuernberg, Breslauer Strasse 201, D-90471 Nuernberg, Germany. Tel: +49-911-398-2702; Fax: +49-911-398-3183; E-mail: raoul.zeltner{at}klinikum-nuernberg.de



  Abstract

Background. Hypertension is a common complication in autosomal dominant polycystic kidney disease (ADPKD). This prospective randomized double-blind study was performed to compare the renal and cardiac effects of the ACE inhibitor ramipril and the β-blocker metoprolol as first line therapy in ADPKD patients with hypertension.

Methods. Forty-six hypertensive ADPKD patients were randomized to either ramipril (n = 23) or metoprolol (n = 23). Twenty-four hour (24-h) ambulatory blood pressure (BP), glomerular filtration rate (GFR) as calculated by the Cockcroft and Gault formula, urinary albumin excretion (albumin/creatinine ratio), and left ventricular mass index (LVMI) were established at baseline and at yearly intervals. The total follow-up was 3 years. Baseline characteristics were similar in both groups.

Results. Mean arterial pressure (MAP) decreased significantly in both the ramipril and the metoprolol group (–8 ± 2 and –6 ± 2 mmHg; both P < 0.01). There was a significant decline in renal function during follow-up which was similar in patients treated with ramipril or metoprolol (–2.5 ± 0.7 vs –2.9 ± 0.8 ml/min/year; P = NS). After the 3 years follow-up, no differences in GFR, LVMI and urinary albumin excretion were observed between the ramipril and the metoprolol group (80.7 ± 10.7 vs 78.0 ± 7.6 ml/min, 102.6 ± 6.8 vs 100.3 ± 5.4 g/m2; and 42.6 ± 12.3 vs 70.3 ± 32.5 mg/g, respectively; all P = NS). A post-hoc analysis evaluating the effects of BP control, revealed that LVMI increased in patients with standard BP control while it remained stable in patients with rigorous BP control with a significant difference in LVMI between the groups after 3 years of follow-up (110.5 ± 6.3 vs 90.9 ± 4.7 g/m2; P = 0.017). Also, by the end of the study albuminuria was lower in patients with rigorous vs standard BP control (23.5 ± 6.7 vs 94.8 ± 35.4 mg/g; P = 0.05).

Conclusions. In our study population of hypertensive ADPKD patients, no differences in renal function, urinary albumin excretion and LVMI were detected between those treated with ramipril or metoprolol, respectively, during a 3 years follow-up. Rigorous BP control prevented an increase in LVMI and reduced urinary albumin excretion, suggesting a crucial role of BP control for slowing progression of cardiac and renal organ damage in ADPKD.

Keywords: autosomal dominant polycystic kidney disease; hypertension; left ventricular hypertrophy; progression of renal disease

Received for publication: 22. 8.06
Accepted in revised form: 18. 9.07


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Renal and cardiac effects of antihypertensive treatment with ramipril versus metoprolol in autosomal dominant polycystic kidney disease
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