Improving Proteinuria, Endothelial Functions and Asymmetric Dimethylarginine Levels in Chronic Kidney Disease: Ramipril versus Valsartan

Background: The aim of this study was to find out whether the beneficial effects of the renin-angiotensin-aldosterone system (RAS) blockage in chronic kidney disease (CKD) has any relation with the alteration of asymmetric dimethylarginine (ADMA) levels. Methods: Sixty-six nondiabetic patients with...

Full description

Saved in:
Bibliographic Details
Published inBlood purification Vol. 25; no. 4; pp. 327 - 335
Main Authors Yilmaz, Mahmut Ilker, Saglam, Mutlu, Sonmez, Alper, Caglar, Kayser, Cakir, Erdinc, Kurt, Yasemin, Eyileten, Tayfun, Tasar, Mustafa, Acikel, Cengizhan, Oguz, Yusuf, Vural, Abdulgaffar, Yenicesu, Mujdat
Format Journal Article
LanguageEnglish
Published Basel, Switzerland Karger 01.01.2007
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background: The aim of this study was to find out whether the beneficial effects of the renin-angiotensin-aldosterone system (RAS) blockage in chronic kidney disease (CKD) has any relation with the alteration of asymmetric dimethylarginine (ADMA) levels. Methods: Sixty-six nondiabetic patients with CKD and proteinuria and 36 healthy subjects were enrolled. Patients were treated with either ramipril 5 mg daily or valsartan 160 mg daily for 3 months. Proteinuria, ADMA, symmetric dimethyl arginine (SDMA), flow-mediated dilatation (FMD) and HOMA index measurements were performed both before and after the treatment. Results: ADMA, SDMA, hsCRP levels, HOMA index and proteinuria of patients were significantly higher (p < 0.001 for all) and FMD, L-arginine and L-arginine/ADMA ratio in CKD were significantly lower than controls. According to the multiple regression analysis, proteinuria levels were independently related to ADMA and SDMA levels. Conclusion: Both drugs were equally effective in reducing elevated ADMA levels and improving endothelial dysfunction in CKD patients.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0253-5068
1421-9735
1421-9735
DOI:10.1159/000107410