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尿激酶对糖尿病肾脏病患者血纤溶酶原激活物抑制物1的影响

Clinical effect of urokinase on plasminogen activator inhibitor-1 in patients with diabetic kidney disease
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摘要 目的观察尿激酶对糖尿病肾脏病(DKD)患者血纤溶酶原激活物抑制物1(PAI-1)的影响及其临床疗效。方法选择在我院住院的DKD患者88例,其中Ⅲ期43例、Ⅳ期45例。将DKDⅢ、Ⅳ期患者分别分为对照组(DKDⅢ-C组、DKDⅣ—C组)和观察组(DKDⅢ-O组、DKDⅣ—O组)。对照组给予常规降糖、保护肾脏及血管紧张素转化酶抑制剂(ACEI)等药物治疗。观察组在常规治疗的基础上给予尿激酶50000U加入100ml生理盐水中静脉滴注,每天1次,共14d。比较各组24h尿白蛋白量、空腹血糖、血肌酐、D-二聚体和血PAI-1水平。结果DKDⅢ—C组和DKDⅣ—C组治疗前、后24h尿白蛋白量、空腹血糖、血肌酐、D-二聚体和血PAI-1均无统计学差异(P〉0.05)。DKDⅢ-O组和DKDⅣ—O组治疗后24h尿白蛋白量和血PAI-1均降低(P〈0.05),而空腹血糖、血肌酐、D二聚体治疗前、后均无统计学差异(P〉0.05)。治疗后,DKDⅢ-O组血PAI-1及24h尿白蛋白下降程度较DKDⅣ—O组明显(P〈0.01)。结论尿激酶可通过降低血PAI-1水平来减少DKD患者尿白蛋白量,对保护肾功能、延缓DKD进展有积极意义,且小剂量应用未增加出血倾向,对DKD是一种安全有效的治疗方法。 Objective To observe the clinical effect of urokinase on plasminogen activator inhib- itor-1 in patients with diabetic kidney disease (DKD). Methods Eighty-eight DKD inpatients in our hospital were chosen, including 43 cases of DKDⅢ, and 45 cases of DKD IV. The patients with DKDⅢ were divided into control group (DKD Ⅲ-C group) and observation group (DKD Ⅲ-O group), and those with DKD Ⅳ were also divided into control group (DKD Ⅳ-C group) and observation group (DKD Ⅳ-O group). The patients in control groups received routine treatments including blood glu- cose-reducing, kidney protection and angiotensin converting enzyme inhibitors (ACEI), and those in observation groups were given 50 000 U urokinase in 100 ml normal saline, once every day, days in addition to the routine treatments. The amount of 24-h urinary albumin, fasting blood glucose, serum creatinine, D-dimer and blood PAI-1 levels were compared. Results Between DKD Ⅲ-C group and DKD Ⅳ-C group before and after treatments, there was no significant difference in the amount of 24- h urinary albumin, fasting blood glucose, serum creatinine, D dimer and blood PAI-1 levels (P〉0. 05). In DKD Ⅲ-O group and the DKD Ⅳ-O group after treatments, the amount of 24-h urinary al- bumin and blood PAI-1 levels were significantly lower than those before treatments (P〈0. 05), but there was no significant difference in fasting blood glucose, serum creatinine and D-dimer before and after treatments (P〉0. 05). After treatment, blood PAI-1 levels and amount of 24-h urinary albumin were reduced more significantly in DKD Ⅲ-O group than in DKD Ⅳ-O group (P〈0. 01). Conclusions Urokinase can decrease the blood PAI-1 levels, resulting the decrease in 24-h urinary albumin in DKD patients,which can protect renal function, and delay progress of DKD. Low doses of urokinasedo not increase the bleeding tendency in DKD.
出处 《临床肾脏病杂志》 2011年第5期207-209,共3页 Journal Of Clinical Nephrology
关键词 尿纤溶酶原激活物 纤溶酶原激活物抑制物1 糖尿病肾病 Urinary plasminogen activator Plasminogen activator inhibitor 1 Diabetic nephropathies
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参考文献14

  • 1McCrary EB. The road to renal failures An overview of diabetic nephropathy. Adv Nurse Pract, 2008,16: 61-63.
  • 2Najafian B, Mauer M. Progression of diabetic nephropathy in type 1 diabetic patients. Diabetes Res Clin Pract, 2009,83 : 1-8.
  • 3孙艺.糖尿病肾病发病机理与临床的新认识[J].沈阳医学院学报,2006,8(2):81-82. 被引量:6
  • 4Soldatos G, Cooper ME. Diabetic nephropathy.. Important pathophysiologic mechanisms. Diabetes Res Clin Pract, 2008,82 (suppl 1 ) :S75-S79.
  • 5王蜀鄂,李竞.生长因子与糖尿病肾病[J].武汉大学学报(医学版),2006,27(1):130-134. 被引量:5
  • 6Chen S,Ziyadeb FN. Vascular endothelial growth factor and diabetic nephropathy. Curr Diab Rep, 2008,8 : 470-476.
  • 7Lee HB, Ha H, Kim SI, et al. Diabetic kidney disease research: Where do we stand at the turn of the century? Kidney Int,2000, 58(suppl 77) : 1-2.
  • 8Dalla Vestra M,Simioni N,Masiero A. Renal effects of dual rennin-angiotensin-aldosterone system blockade in patients with diabetic nephropathy. Int Urol Nephrol, 2009,41 : 119-126.
  • 9Eddy AA. Plasminogen activator inhibitor-1 and he kidney. Am J Physiol Renal Physiol, 2002,283:209-220.
  • 10Kamgar M, Nobakhthaghighi N, Shamshirsaz AA, et al. Impaired fibrinolytic activity in type II diabetes: Correlation with urinary albumin excretion and progression of renal disease. Kidney Int, 2006,69:1899-1903.

二级参考文献36

  • 1Flyvbjerg A. Putative pathophysiological role of growth factor and cytokines in experimental diabetic kidney diseases[J]. Diabetologia, 2000,43(10) : 1 205.
  • 2Cooper ME, Vranes D,Youssef S, et al. Increased renal expression of vascular endothelial growth factor(VEGF) and its receptor VEGFR-2 in experimental diahetes[J]. Diabetes, 1999,48 : 2 229.
  • 3Senthil D,Choudhury GG,Mclaurin C, et al. Vascular endothelial growth factor induces protein synthesis in renal epithelial cells: A potential role in diabetic nephropathy[J]. Kidney International, 2003, 64 (2)468.
  • 4Chen S, Kasama Y, Lee JS, et al. Podocyte-derived vascular endothelial growth factor mediates the stimulation of alpha 3(IV) collagen production by transforming growth factor-beta 1 in mouse podocytes[J]. Diabetes,2004,53 (11): 2 939.
  • 5Vriese AS, Tilton RG, Elger M, et al. Antibodies against vascular endothelial growth factor improve early renal dysfunction in experimental diabetes[J]. J Am Soc Nephrol, 2001,12 : 993.
  • 6Vavrinec J. Increased level of TGF heta 1 in recently diagnosed diabetes mellitus in adults and in patients with diabetic complications [J]. Diabetes, 2005, 54(Suppl 1): A614.
  • 7Wolf G,schanze A,Stahl R, et al. p27(Kipl) knockout mice are protected from diabetic nephropathy: Evidence for p27 (Kip1) haplotype insufficiency[J]. Kidney International, 2005,68 (4):1 583.
  • 8Akahori H, Ota T, Torita M,et al. Tranilast prevents the progression of experimental diabetic nephropathy through suppression of enhanced extracellular matrixgene expression[J]. Journal of Pharmacology and Experimental Theraperimental Therapeutics, 2005, 314(2) : 514.
  • 9McLennan SV, Death AK, Fisher EJ, et al. The role of the mesangial cell and its matrix in the pathogenesis of diabetic nephropathy[J]. Cellular and Molecular Biology, 2001, 45 (1): 123.
  • 10Cingel-Ristic V, Flyvbjerg A, Drop SLS. The physiological and pathophysiological roles of the GH/IGF-axis in the kidney: Lessons from experimental rodent models[J]. Growth Hormone & IGF Research, 2004,14(6) : 418.

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