AST-120 for the management of progression of chronic kidney disease

Gerald Schulman,1 Raymond Vanholder,2 Toshimitsu Niwa31Vanderbilt University School of Medicine, Nashville, TN, USA; 2University Hospital, Ghent, Belgium; 3Nagoya University Graduate School of Medicine, Nagoya, JapanAbstract: Uremic toxins such as indoxyl sulfate contribute to the pathogenesis of c...

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Main Authors: Schulman G, Vanholder R, Niwa T
Format: Article
Language:English
Published: Dove Medical Press 2014-01-01
Series:International Journal of Nephrology and Renovascular Disease
Online Access:http://www.dovepress.com/ast-120-for-the-management-of-progression-of-chronic-kidney-disease-a15666
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spelling doaj-f6145c36557d4089b012a3a5a57adb402020-11-25T02:47:14ZengDove Medical PressInternational Journal of Nephrology and Renovascular Disease1178-70582014-01-012014default495615666AST-120 for the management of progression of chronic kidney diseaseSchulman GVanholder RNiwa T Gerald Schulman,1 Raymond Vanholder,2 Toshimitsu Niwa31Vanderbilt University School of Medicine, Nashville, TN, USA; 2University Hospital, Ghent, Belgium; 3Nagoya University Graduate School of Medicine, Nagoya, JapanAbstract: Uremic toxins such as indoxyl sulfate contribute to the pathogenesis of chronic kidney disease (CKD) by promoting glomerulosclerosis and interstitial fibrosis with loss of nephrons and vascular damage. AST-120, an orally administered intestinal sorbent, adsorbs indole, a precursor of indoxyl sulfate, thereby reducing serum and urinary concentrations of indoxyl sulfate. AST-120 has been available in Japan since 1991, and subsequently Korea (2005), and the Philippines (2010) as an agent to prolong the time to initiation of hemodialysis and for improvement of uremic symptoms in patients with CKD. A Medline search was performed to identify data supporting clinical experience with AST-120 for managing CKD. Prospective open-label and double-blind trials as well as retrospective analyses were included. In prospective trials and retrospective analyses, AST-120 has been shown to prolong the time to initiation of hemodialysis, and slow decline in glomerular filtration rate and the increase serum creatinine. In an initial randomized, double-blind, placebo-controlled trial in the United States, AST-120 was associated with a significant dose-dependent reduction in serum indoxyl sulfate levels and a decrease in uremia-related malaise. The Evaluating Prevention of Progression in CKD (EPPIC) trials, two double-blind, placebo-controlled trials undertaken in North America/Latin America and Europe, are evaluating the efficacy of AST-120 for preventing the progression of CKD. The results of the EPPIC trials will further define the role of AST-120 in this debilitating condition.Keywords: AST-120, chronic kidney disease, hemodialysis, indoxyl sulfate, uremic toxinhttp://www.dovepress.com/ast-120-for-the-management-of-progression-of-chronic-kidney-disease-a15666
collection DOAJ
language English
format Article
sources DOAJ
author Schulman G
Vanholder R
Niwa T
spellingShingle Schulman G
Vanholder R
Niwa T
AST-120 for the management of progression of chronic kidney disease
International Journal of Nephrology and Renovascular Disease
author_facet Schulman G
Vanholder R
Niwa T
author_sort Schulman G
title AST-120 for the management of progression of chronic kidney disease
title_short AST-120 for the management of progression of chronic kidney disease
title_full AST-120 for the management of progression of chronic kidney disease
title_fullStr AST-120 for the management of progression of chronic kidney disease
title_full_unstemmed AST-120 for the management of progression of chronic kidney disease
title_sort ast-120 for the management of progression of chronic kidney disease
publisher Dove Medical Press
series International Journal of Nephrology and Renovascular Disease
issn 1178-7058
publishDate 2014-01-01
description Gerald Schulman,1 Raymond Vanholder,2 Toshimitsu Niwa31Vanderbilt University School of Medicine, Nashville, TN, USA; 2University Hospital, Ghent, Belgium; 3Nagoya University Graduate School of Medicine, Nagoya, JapanAbstract: Uremic toxins such as indoxyl sulfate contribute to the pathogenesis of chronic kidney disease (CKD) by promoting glomerulosclerosis and interstitial fibrosis with loss of nephrons and vascular damage. AST-120, an orally administered intestinal sorbent, adsorbs indole, a precursor of indoxyl sulfate, thereby reducing serum and urinary concentrations of indoxyl sulfate. AST-120 has been available in Japan since 1991, and subsequently Korea (2005), and the Philippines (2010) as an agent to prolong the time to initiation of hemodialysis and for improvement of uremic symptoms in patients with CKD. A Medline search was performed to identify data supporting clinical experience with AST-120 for managing CKD. Prospective open-label and double-blind trials as well as retrospective analyses were included. In prospective trials and retrospective analyses, AST-120 has been shown to prolong the time to initiation of hemodialysis, and slow decline in glomerular filtration rate and the increase serum creatinine. In an initial randomized, double-blind, placebo-controlled trial in the United States, AST-120 was associated with a significant dose-dependent reduction in serum indoxyl sulfate levels and a decrease in uremia-related malaise. The Evaluating Prevention of Progression in CKD (EPPIC) trials, two double-blind, placebo-controlled trials undertaken in North America/Latin America and Europe, are evaluating the efficacy of AST-120 for preventing the progression of CKD. The results of the EPPIC trials will further define the role of AST-120 in this debilitating condition.Keywords: AST-120, chronic kidney disease, hemodialysis, indoxyl sulfate, uremic toxin
url http://www.dovepress.com/ast-120-for-the-management-of-progression-of-chronic-kidney-disease-a15666
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