A randomized, controlled trial of oral intestinal sorbent AST-120 on renal function deterioration in patients with advanced renal dysfunction

  • Cha, Ran-hui ; 
  • Kang, Shin Wook; 
  • Park, Cheol Whee; 
  • Cha, Dae Ryong; 
  • Na, Ki Young; 
  • 외 7명
Citations

WEB OF SCIENCE

86
Citations

SCOPUS

89

초록

Background and objectives The notion that oral intestinal sorbent AST-120 slows renal disease progression has not been evaluated thoroughly. In this study, we investigated the long-term effect of AST-120 on renal disease progression (doubling of serum creatinine, eGFR decrease >50%, or initiation of RRT) in patients with advanced CKD. Design, setting, participants, & measurements We prospectively recruited 579 patients (CKD stage 3 or 4) from 11 medical centers in Korea from March 4, 2009 to August 31, 2010 and randomized them into an AST-120 arm and a control arm. Patients in the AST-120 arm were given 6 g AST-120 in three divided doses per day, and those in the control arm received only standard conventional treatment (open-label design) for 36 months or until the occurrence of primary outcomes. Results Levels of serum and urine indoxyl sulfate and β2-microglobulin decreased throughout the study period in both treatment arms; however, there was not a significant difference in change in uremic toxins in the AST-120 and control arms. The two arms were not different in the occurrence of composite primary outcomes (100 events in 272 individuals in the AST-120 arm and 100 events in 266 individuals in the control arm; hazard ratio, 1.12; 95% confidence interval, 0.85 to 1.48; log-rank P=0.45). The decline in eGFR and change in proteinuria were similar in the two treatment arms over time (Prandomization–time =0.64 and Prandomization–time =0.16, respectively). There was no difference in mortality (nine deaths in the AST-120 arm and 11 deaths in the control arm; log-rank P=0.73) or unplanned hospitalizations (102 in the AST-120 arm and 109 in the control arm; log-rank P=0.76) in the two treatment arms. There was no significant difference of the health–related quality of life score between the two arms. Conclusions Long-term use of AST-120 added to standard treatment did not change renal disease progression, proteinuria, mortality, and health–related quality of life in patients with advanced renal dysfunction. © 2016 by the American Society of Nephrology.

키워드

ast 120; beta 2 microglobulin; calcium channel blocking agent; hemoglobin; indican; sorbent; uremic toxin; ast 120; carbon; oxide; adult; Article; autoinflammatory disease; brain infarction; constipation; controlled study; diabetic nephropathy; diastolic blood pressure; disease course; drug safety; drug withdrawal; estimated glomerular filtration rate; hazard ratio; heart arrhythmia; heart failure; human; inflammatory bowel disease; kidney disease; kidney function; kidney polycystic disease; kidney transplantation; life expectancy; liver cirrhosis; loss of appetite; major clinical study; middle aged; mortality; nausea; obstructive uropathy; proteinuria; quality of life; randomized controlled trial; renin angiotensin aldosterone system; sample size; serum; transient ischemic attack; vomiting; chronic kidney failure; clinical trial; drug effects; female; kidney; male; multicenter study; oral drug administration; pathophysiology; prospective study; Administration, Oral; Carbon; Disease Progression; Female; Humans; Kidney; Kidney Failure, Chronic; Male; Middle Aged; Oxides; Prospective Studies
제목
A randomized, controlled trial of oral intestinal sorbent AST-120 on renal function deterioration in patients with advanced renal dysfunction
저자
Cha, Ran-hui ; Kang, Shin Wook; Park, Cheol Whee; Cha, Dae Ryong; Na, Ki Young; Kim, Sung Gyun; Yoon, Sun Ae; Han, Sang Youb; Chang, Jae Hyun; Park, Sue K; Lim, Chun Soo; Kim, Yon Su
DOI
10.2215/CJN.12011214
발행일
2016-04
유형
Article
저널명
Clinical Journal of the American Society of Nephrology
권
11
호
4
페이지
559 ~ 567