Melbourne Renal Research Group, 73-75 Pine Street, Reservoir, Melbourne, Victoria 3073, Australia.
J Am Soc Nephrol. 2012 Jan;23(1):123-30. doi: 10.1681/ASN.2011040378. Epub 2011 Oct 27.
Sulodexide, a mixture of naturally occurring glycosaminoglycan polysaccharide components, has been reported to reduce albuminuria in patients with diabetes, but it is unknown whether it is renoprotective. This study reports the results from the randomized, double-blind, placebo-controlled, sulodexide macroalbuminuria (Sun-MACRO) trial, which evaluated the renoprotective effects of sulodexide in patients with type 2 diabetes, renal impairment, and significant proteinuria (>900 mg/d) already receiving maximal therapy with angiotensin II receptor blockers. The primary end point was a composite of a doubling of baseline serum creatinine, development of ESRD, or serum creatinine ≥6.0 mg/dl. We planned to enroll 2240 patients over approximately 24 months but terminated the study after enrolling 1248 patients. After 1029 person-years of follow-up, we did not detect any significant differences between sulodexide and placebo; the primary composite end point occurred in 26 and 30 patients in the sulodexide and placebo groups, respectively. Side effect profiles were similar for both groups. In conclusion, these data do not suggest a renoprotective benefit of sulodexide in patients with type 2 diabetes, renal impairment, and macroalbuminuria.
舒洛地特是一种天然存在的糖胺聚糖多糖成分混合物,据报道可减少糖尿病患者的蛋白尿,但尚不清楚其是否具有肾脏保护作用。本研究报告了一项随机、双盲、安慰剂对照的舒洛地特大量蛋白尿(Sun-MACRO)试验的结果,该试验评估了舒洛地特在 2 型糖尿病、肾功能损害和大量蛋白尿(>900mg/d)患者中的肾脏保护作用,这些患者已经接受了血管紧张素 II 受体阻滞剂的最大治疗。主要终点是基线血清肌酐加倍、终末期肾病发展或血清肌酐≥6.0mg/dl 的复合终点。我们计划在大约 24 个月内招募 2240 名患者,但在招募了 1248 名患者后终止了研究。在 1029 人年的随访后,我们没有发现舒洛地特和安慰剂之间有任何显著差异;主要复合终点分别发生在舒洛地特组和安慰剂组的 26 名和 30 名患者中。两组的副作用谱相似。总之,这些数据表明舒洛地特对 2 型糖尿病、肾功能损害和大量蛋白尿患者没有肾脏保护作用。