Cha Ran-Hui, Kang Shin Wook, Park Cheol Whee, Cha Dae Ryong, Na Ki Young, Kim Sung Gyun, Yoon Sun Ae, Kim Sejoong, Han Sang Youb, Park Jung Hwan, Chang Jae Hyun, Lim Chun Soo, Kim Yon Su
Department of Internal Medicine, National Medical Center, Seoul, Korea.
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Kidney Res Clin Pract. 2017 Mar;36(1):68-78. doi: 10.23876/j.krcp.2017.36.1.68. Epub 2017 Mar 31.
We investigated the long-term effect of AST-120, which has been proposed as a therapeutic option against renal disease progression, in patients with advanced chronic kidney disease (CKD).
We performed analysis with a per-protocol group of the K-STAR study (Kremezin study against renal disease progression in Korea) that randomized participants into an AST-120 and a control arm. Patients in the AST-120 arm were given 6 g of AST-120 in three divided doses, and those in both arms received standard conventional treatment.
The two arms did not differ significantly in the occurrence of composite primary outcomes (log-rank = 0.41). For AST-120 patients with higher compliance, there were fewer composite primary outcomes: intermediate tertile hazard ratio (HR) 0.62, 95% confidence interval (CI) 0.38 to 1.01, = 0.05; highest tertile HR 0.436, 95% CI 0.25 to 0.76, = 0.003. The estimated glomerular filtration rate level was more stable in the AST-120 arm, especially in diabetic patients. At one year, the AST-120-induced decrease in the serum indoxyl sulfate concentration inversely correlated with the occurrence of composite primary outcomes: second tertile HR 1.59, 95% CI 0.82 to 3.07, = 0.17; third tertile HR 2.11, 95% CI 1.07 to 4.17, = 0.031. Furthermore, AST-120 showed a protective effect against the major cardiovascular adverse events (HR 0.51, 95% CI 0.26 to 0.99, = 0.046).
Long-term use of AST-120 has potential for renal protection, especially in diabetic patients, as well as cardiovascular benefits. Reduction of the serum indoxyl sulfate level may be used to identify patients who would benefit from AST-120 administration.
我们研究了已被提议作为对抗肾病进展治疗选择的AST-120对晚期慢性肾脏病(CKD)患者的长期影响。
我们对K-STAR研究(韩国针对肾病进展的克雷莫辛研究)的符合方案组进行了分析,该研究将参与者随机分为AST-120组和对照组。AST-120组的患者接受6克AST-120,分三次给药,两组患者均接受标准常规治疗。
两组在复合主要结局的发生率上无显著差异(对数秩检验=0.41)。对于依从性较高的AST-120患者,复合主要结局较少:中间三分位数风险比(HR)为0.62,95%置信区间(CI)为0.38至1.01,P=0.05;最高三分位数HR为0.436,95%CI为0.25至0.76,P=0.003。AST-120组的估计肾小球滤过率水平更稳定,尤其是在糖尿病患者中。在一年时,AST-120引起的血清硫酸吲哚酚浓度降低与复合主要结局的发生呈负相关:第二三分位数HR为1.59,95%CI为0.82至3.07,P=0.17;第三三分位数HR为2.11,95%CI为1.07至4.17,P=0.031。此外,AST-120对主要心血管不良事件具有保护作用(HR为0.51,95%CI为0.26至0.99,P=0.046)。
长期使用AST-120具有肾脏保护潜力,尤其是在糖尿病患者中,同时对心血管有益。血清硫酸吲哚酚水平的降低可用于识别可能从AST-120给药中获益的患者。