第四章

J. Pijl, F. J. Woude, P. Geelhoed-Duijvestijn, M. Frölich, F. V. D. Meer, H. Lemkes, L. Es
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引用次数: 0

摘要

糖尿病肾病是一种以肾小球基底膜增厚和系膜扩张和增生为组织学特征的进行性肾脏疾病。硫酸肝素蛋白多糖的糖胺聚糖侧链是肾小球基底膜的重要组成部分,在糖尿病肾病中与蛋白尿程度成比例地减少。类乙酰肝素钠是一种磺化糖胺聚糖的混合物,主要由硫酸乙酰肝素组成。本研究在糖尿病合并明显蛋白尿患者中应用了丹那帕钠进行随机安慰剂对照交叉研究。该研究的目的是评估对蛋白尿的影响和安全性/耐受性。9名患者完成了研究,无主要副作用,交叉研究包括两个为期6周的治疗,每天一次皮下注射750单位的抗xa钠或安慰剂。服用类达那钠钠后,发现蛋白尿和蛋白尿均显著下降。服用丹那巴苷钠后,以尿肌酐标准衡量的白蛋白排泄率降低了17%,而安慰剂组则增加了23%(差异的95%可信区间为-75.9 3.9%;P = 0.03)。两组治疗组在8周时尿蛋白排泄经尿肌酐校正后的百分比变化差异显著(P = 0.001)。其他安全性参数,如血液学、止血、生化参数和眼底摄影,在两组中没有任何临床显著差异。只有2例患者在使用那那钠钠时,在注射部位有轻微的皮肤血肿。总之,这种补充是可行的,而且没有副作用。蛋白尿明显减少。必须进行更多的前瞻性剂量发现和长期研究,以确定达那那肽钠是否不仅可以诱导蛋白尿减少,还可以阻止肾脏疾病的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CHAPTER 4
Diabetic nephropathy is a progressive renal disease with thickening of the glomerular basement membrane and mesangial expansion and proliferation as histological hallmarks. The presence of the glycosaminoglycan side chains of heparan sulphate proteoglycan, an important constituent of the glomerular basement membrane, is decreased in diabetic nephropathy proportionally to the degree of proteinuria. Danaparoid sodium is a mixture of sulfated glycosaminoglycans, consisting mainly of heparan sulphate. The study presented here involved performing a randomized placebocontrolled crossover study with danaparoid sodium in diabetic patients with overt proteinuria. The aim of the study was to evaluate the effect on proteinuria and safety/tolerability. Nine patients completed the study, without major side-effects, the crossover study consisted of two 6-wk periods of treatment with 750 anti-Xa units danaparoid sodium subcutaneously once-daily or placebo. Following danaparoid sodium, significant declines of both albuminuria and proteinuria were found. After danaparoid sodium, the albumin excretion ratio standardized for urinary creatinine reduced with 17% in comparison with an increase of 23% after placebo (95% confidence interval of the difference, -75.9 3.9%; P = 0.03). The percentage change of the urinary protein excretion corrected for urinary creatinine differed at 8 wk significantly between both treatment arms ( P = 0.001). Additional parameters for safety as hematological, hemostasis, biochemical parameters, and fundusphotography did not show any clinically significant difference for both groups. Only two patients had minor skin hematomas at the injection site while using danaparoid sodium. In conclusion, the supplementation was found to be feasible and was not associated with side effects. A significant decline of proteinuria was found. More prospective dose-finding and long-term studies must be performed to see whether danaparoid sodium could not only induce a reduction of proteinuria but also halt the progression of renal disease.
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