中国药物评价
中國藥物評價
중국약물평개
Chinese Journal of Drug Evaluation
2015年
5期
280-283
,共4页
冯然%李莉%王宁%田静%孙娜%刘涛%刘静芹
馮然%李莉%王寧%田靜%孫娜%劉濤%劉靜芹
풍연%리리%왕저%전정%손나%류도%류정근
糖尿病肾病%转化生长因子-β1%D-二聚体%胱抑素C%缬沙坦
糖尿病腎病%轉化生長因子-β1%D-二聚體%胱抑素C%纈沙坦
당뇨병신병%전화생장인자-β1%D-이취체%광억소C%힐사탄
Diabetic nephropathies%Transforming growth factor betal%D-Dimer%CystatinC%Valsartan
目的:探讨缬沙坦对早期糖尿病肾病患者血清转化生长因子-β1( TGF-β1)、D-二聚体( D-D)及胱抑素C( CysC)水平的影响。方法:30例体检健康者作为对照组( NC组),90例合并糖尿病肾病的2型糖尿病患者分为正常白蛋白尿1组( NA1组, UMA/Cr<10μg/mg)22例,正常白蛋白尿2组(NA2组,UMA/Cr 10~30μg/mg)29例,微量白蛋白尿组(MA组,UMA/Cr 31~300μg/mg)39例,均合并DR、高血压,应用缬沙坦80mg/d共4周。分别采血测定用药前后血清TGF-β1、D-D及CysC水平。结果:NA1组、NA2组、MA组血清TGF-β1、D-D、CysC水平明显升高(P<0.05),且3组间比较差异也均有统计学意义(P<0.05)。DN各组中应用缬沙坦后血清TGF-β1、D-D及CysC水平明显下降( P<0.05)。结论:血清TGF-β1、D-D及CysC有可能作为早期糖尿病肾病的特异性指标。早期应用缬沙坦可能通过降低DN患者血清TGF-β1、D-D及CysC的水平延缓DN的发生、发展。
目的:探討纈沙坦對早期糖尿病腎病患者血清轉化生長因子-β1( TGF-β1)、D-二聚體( D-D)及胱抑素C( CysC)水平的影響。方法:30例體檢健康者作為對照組( NC組),90例閤併糖尿病腎病的2型糖尿病患者分為正常白蛋白尿1組( NA1組, UMA/Cr<10μg/mg)22例,正常白蛋白尿2組(NA2組,UMA/Cr 10~30μg/mg)29例,微量白蛋白尿組(MA組,UMA/Cr 31~300μg/mg)39例,均閤併DR、高血壓,應用纈沙坦80mg/d共4週。分彆採血測定用藥前後血清TGF-β1、D-D及CysC水平。結果:NA1組、NA2組、MA組血清TGF-β1、D-D、CysC水平明顯升高(P<0.05),且3組間比較差異也均有統計學意義(P<0.05)。DN各組中應用纈沙坦後血清TGF-β1、D-D及CysC水平明顯下降( P<0.05)。結論:血清TGF-β1、D-D及CysC有可能作為早期糖尿病腎病的特異性指標。早期應用纈沙坦可能通過降低DN患者血清TGF-β1、D-D及CysC的水平延緩DN的髮生、髮展。
목적:탐토힐사탄대조기당뇨병신병환자혈청전화생장인자-β1( TGF-β1)、D-이취체( D-D)급광억소C( CysC)수평적영향。방법:30례체검건강자작위대조조( NC조),90례합병당뇨병신병적2형당뇨병환자분위정상백단백뇨1조( NA1조, UMA/Cr<10μg/mg)22례,정상백단백뇨2조(NA2조,UMA/Cr 10~30μg/mg)29례,미량백단백뇨조(MA조,UMA/Cr 31~300μg/mg)39례,균합병DR、고혈압,응용힐사탄80mg/d공4주。분별채혈측정용약전후혈청TGF-β1、D-D급CysC수평。결과:NA1조、NA2조、MA조혈청TGF-β1、D-D、CysC수평명현승고(P<0.05),차3조간비교차이야균유통계학의의(P<0.05)。DN각조중응용힐사탄후혈청TGF-β1、D-D급CysC수평명현하강( P<0.05)。결론:혈청TGF-β1、D-D급CysC유가능작위조기당뇨병신병적특이성지표。조기응용힐사탄가능통과강저DN환자혈청TGF-β1、D-D급CysC적수평연완DN적발생、발전。
Objective:To investigate the relationship between serum transforming growth factor-β1(TGF-β1), D-Dimer(D-D), cys-tatinC(CysC) levels and early and early diabetic nephropathy and clarify whether valsartan plays a role in renal protection by reducing the level of serum TGF-β1, D-D, CysC.Methods:The study subjects were divided into 4 groups:control group (30 cases);normal albumi-nuria group 1( NA1 group with 22 cases, UMA /Cr <10 μg/mg combined with type 2 diabetes) ;normal alb-uminuria grop 2 ( NA2 group with 29 cases, UMA/Cr10~30μg/mg combined with type 2 diabetes);mieroalbuminuria group ( MA group with 39 cases, UMA/Cr31~300 μg/mg combined with type 2 diabetes).All these type 2 diabetic patients were suffering from diabetic refinopathy and hyper-tension.Valsartan (80 mg/d) were medicated for patients.The serum TGF-β1, D-D, CysC levels were measured in all subjects before and after treatment.Results:Serum TGF-β1, D-D, CysC levels in 3 diabetes groups were higher than those in control group(P<0.05). There were significant differences in serum TGF-β1, D-D, CysC levels among MA group, NA 2 group and NA1 group (P<0.05). Serum TGF-β1, D-D, CysC levels in NA1 group with valsartan treatment significantly decreased compared with those before treatment ( P<0.05).Conlusion:High serum TGF-β1, D-D, CysC level may be associated with type 2 diabetes and early diabetic nephropathy. Valsartan may be delay the onset and development of early diabetic nephropathy by decreasing the serum TGF-β1, D-D, CysC level.