中国糖尿病杂志
中國糖尿病雜誌
중국당뇨병잡지
CHINESE JOURNAL OF DIABETES
2011年
1期
45-48
,共4页
韦玉和%许联红%罗春媛%冯小芬%周斌%戚传平
韋玉和%許聯紅%囉春媛%馮小芬%週斌%慼傳平
위옥화%허련홍%라춘원%풍소분%주빈%척전평
基质细胞衍生因子1%CXCR4%内皮祖细胞%糖尿病,2型%大血管并发症
基質細胞衍生因子1%CXCR4%內皮祖細胞%糖尿病,2型%大血管併髮癥
기질세포연생인자1%CXCR4%내피조세포%당뇨병,2형%대혈관병발증
Stromal cell-derived factor-1%CXCR4% Endothelial progenitor cells% Diabetes mellitus% type 2% Macrovascular complicatins
目的 探讨2型糖尿病(T2DM)患者外周血基质细胞衍生因子1(SDF-1)水平与大血管并发症的关系.方法 测定55例无微血管并发症的T2DM患者和26名健康对照者外周血中SDF-1水平、内皮祖细胞(EPCs)数量、EPCs表面SDF-1的受体CXCR4表达率.糖尿病患者分单纯糖尿病组、大血管病变组.结果 SDF-1水平和EPCs数量对照组、单纯糖尿病组、大血管病变组依次降低(P<0.05或0.01);单纯糖尿病组、对照组、大血管病变组CXCR4表达率依次降低(P<0.05或0.01);SDF-1水平与EPCs数量成正相关(r=0.327,P<0.05),颈动脉内膜中层厚度与SDF-1、EPCs负相关(r=-0.342、-0.298,P<0.05).结论 T2DM患者外周血中SDF-1/CXCR4轴的变化与大血管并发症的发生、发展有关.
目的 探討2型糖尿病(T2DM)患者外週血基質細胞衍生因子1(SDF-1)水平與大血管併髮癥的關繫.方法 測定55例無微血管併髮癥的T2DM患者和26名健康對照者外週血中SDF-1水平、內皮祖細胞(EPCs)數量、EPCs錶麵SDF-1的受體CXCR4錶達率.糖尿病患者分單純糖尿病組、大血管病變組.結果 SDF-1水平和EPCs數量對照組、單純糖尿病組、大血管病變組依次降低(P<0.05或0.01);單純糖尿病組、對照組、大血管病變組CXCR4錶達率依次降低(P<0.05或0.01);SDF-1水平與EPCs數量成正相關(r=0.327,P<0.05),頸動脈內膜中層厚度與SDF-1、EPCs負相關(r=-0.342、-0.298,P<0.05).結論 T2DM患者外週血中SDF-1/CXCR4軸的變化與大血管併髮癥的髮生、髮展有關.
목적 탐토2형당뇨병(T2DM)환자외주혈기질세포연생인자1(SDF-1)수평여대혈관병발증적관계.방법 측정55례무미혈관병발증적T2DM환자화26명건강대조자외주혈중SDF-1수평、내피조세포(EPCs)수량、EPCs표면SDF-1적수체CXCR4표체솔.당뇨병환자분단순당뇨병조、대혈관병변조.결과 SDF-1수평화EPCs수량대조조、단순당뇨병조、대혈관병변조의차강저(P<0.05혹0.01);단순당뇨병조、대조조、대혈관병변조CXCR4표체솔의차강저(P<0.05혹0.01);SDF-1수평여EPCs수량성정상관(r=0.327,P<0.05),경동맥내막중층후도여SDF-1、EPCs부상관(r=-0.342、-0.298,P<0.05).결론 T2DM환자외주혈중SDF-1/CXCR4축적변화여대혈관병발증적발생、발전유관.
Objective To study the association of serum level of stromal cell-derived factor-1(SDF-1) and its receptor CXCR4 of endothelial progenitor cells (EPCs)from peripheral blood with macrovascular complication of type 2 diabetes mellitus(T2DM). Methods The study subjects included simple diabetics (n=25), macrovascular complication group (n)=30) and healthy control (n=26). The level of serum SDF-1, the positive rate of CXCR4 on EPCs and the number of EPCs were determined. Results SDF-1 level and EPCs number were decreased one by one from control group to simple diabetic group and to the macrovascular complications group(P<0.05 or 0.01). CXCR4 expression rate were significantly decreased one by one from the simple diabetic group to the control group and to the macrovascular complications group (P<0.05 or 0.01). SDF-1 level was positively correlated with EPCs number. (r=0.327,P<0.05), carotid intima-media thickness were negatively correlated with SDF-1 and EPCs (r=-0.342,-0.298, P<0.05) in T2DM. Conclusion SDF-1/CXCR4 may be related to macrovascular complications in patients with T2DM.