Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease

<p>Abstract</p> <p>Background</p> <p>The renin-angiotensin-aldosterone system (RAAS) plays an important role in the progression of chronic kidney disease (CKD). Although dual RAAS inhibition results in worse renal outcomes than monotherapy in high risk type 2 diabetes p...

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Main Authors: Li Szu-yuan, Chen Yung-Tai, Yang Wu-Chang, Tarng Der-Cherng, Lin Chih-Ching, Yang Chih-Yu, Liu Wen-Sheng
Format: Article
Language:English
Published: BMC 2012-08-01
Series:BMC Nephrology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2369/13/89
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author Li Szu-yuan
Chen Yung-Tai
Yang Wu-Chang
Tarng Der-Cherng
Lin Chih-Ching
Yang Chih-Yu
Liu Wen-Sheng
author_facet Li Szu-yuan
Chen Yung-Tai
Yang Wu-Chang
Tarng Der-Cherng
Lin Chih-Ching
Yang Chih-Yu
Liu Wen-Sheng
author_sort Li Szu-yuan
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The renin-angiotensin-aldosterone system (RAAS) plays an important role in the progression of chronic kidney disease (CKD). Although dual RAAS inhibition results in worse renal outcomes than monotherapy in high risk type 2 diabetes patients, the effect of dual RAAS inhibition in patients with non-DM CKD is unclear. The aim of this study was to evaluate the potential renoprotective effect of add-on direct renin inhibitor in non-DM CKD patients.</p> <p>Methods</p> <p>We retrospectively enrolled 189 non-DM CKD patients who had been taking angiotensin II receptor blockers (ARBs) for more than six months. Patients were divided into an add-on aliskiren group and an ARB monotherapy group. The primary outcomes were a decline in glomerular filtration rate (GFR) and a reduction in urinary protein-to-creatinine ratio at six months.</p> <p>Results</p> <p>The baseline characteristics of the two groups were similar. Aliskiren 150 mg daily reduced the urinary protein-to-creatinine ratio by 26% (95% confidence interval, 15 to 37%; p < 0.001). The decline in GFR was smaller in the add-on aliskiren group (−2.1 vs. -4.0 ml/min, p = 0.038). Add-on aliskiren had a neutral effect on serum potassium in the non-DM CKD patients. In subgroup analysis, the proteinuria-reducing effect of aliskiren was more prominent in patients with a GFR less than 60 ml/min, and in patients with a urinary protein-to-creatinine ratio greater than 1.8. The effect of aliskiren in retarding the decline in GFR was more prominent in patients with hypertensive nephropathy than in those with glomerulonephritis.</p> <p>Conclusion</p> <p>Add-on direct renin inhibitor aliskiren (150 mg daily) safely reduced proteinuria and attenuated the decline in GFR in the non-DM CKD patients who were receiving ARBs.</p>
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spelling doaj.art-79679977244b432d83bdb1de9bb63c852022-12-22T02:04:08ZengBMCBMC Nephrology1471-23692012-08-011318910.1186/1471-2369-13-89Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney diseaseLi Szu-yuanChen Yung-TaiYang Wu-ChangTarng Der-CherngLin Chih-ChingYang Chih-YuLiu Wen-Sheng<p>Abstract</p> <p>Background</p> <p>The renin-angiotensin-aldosterone system (RAAS) plays an important role in the progression of chronic kidney disease (CKD). Although dual RAAS inhibition results in worse renal outcomes than monotherapy in high risk type 2 diabetes patients, the effect of dual RAAS inhibition in patients with non-DM CKD is unclear. The aim of this study was to evaluate the potential renoprotective effect of add-on direct renin inhibitor in non-DM CKD patients.</p> <p>Methods</p> <p>We retrospectively enrolled 189 non-DM CKD patients who had been taking angiotensin II receptor blockers (ARBs) for more than six months. Patients were divided into an add-on aliskiren group and an ARB monotherapy group. The primary outcomes were a decline in glomerular filtration rate (GFR) and a reduction in urinary protein-to-creatinine ratio at six months.</p> <p>Results</p> <p>The baseline characteristics of the two groups were similar. Aliskiren 150 mg daily reduced the urinary protein-to-creatinine ratio by 26% (95% confidence interval, 15 to 37%; p < 0.001). The decline in GFR was smaller in the add-on aliskiren group (−2.1 vs. -4.0 ml/min, p = 0.038). Add-on aliskiren had a neutral effect on serum potassium in the non-DM CKD patients. In subgroup analysis, the proteinuria-reducing effect of aliskiren was more prominent in patients with a GFR less than 60 ml/min, and in patients with a urinary protein-to-creatinine ratio greater than 1.8. The effect of aliskiren in retarding the decline in GFR was more prominent in patients with hypertensive nephropathy than in those with glomerulonephritis.</p> <p>Conclusion</p> <p>Add-on direct renin inhibitor aliskiren (150 mg daily) safely reduced proteinuria and attenuated the decline in GFR in the non-DM CKD patients who were receiving ARBs.</p>http://www.biomedcentral.com/1471-2369/13/89AliskirenDirect renin inhibitorProteinuriaCKD
spellingShingle Li Szu-yuan
Chen Yung-Tai
Yang Wu-Chang
Tarng Der-Cherng
Lin Chih-Ching
Yang Chih-Yu
Liu Wen-Sheng
Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
BMC Nephrology
Aliskiren
Direct renin inhibitor
Proteinuria
CKD
title Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
title_full Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
title_fullStr Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
title_full_unstemmed Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
title_short Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease
title_sort effect of add on direct renin inhibitor aliskiren in patients with non diabetes related chronic kidney disease
topic Aliskiren
Direct renin inhibitor
Proteinuria
CKD
url http://www.biomedcentral.com/1471-2369/13/89
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