2型糖尿病下肢血管病变与kruppel样因子4%2c可溶性p选择素%2c超敏C反应蛋白关系的的研究.doc

2型糖尿病下肢血管病变与kruppel样因子4%2c可溶性p选择素%2c超敏C反应蛋白关系的的研究.doc

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组 117.87±14.27 vs 90.91±8.09, P=0.001);而血清 KLF4 则明显降低, 差异具有统计学意义(N-PVD vs 对照组 44.88±7.05 vs 53.74±7.38, P=0.04)。结论:hsCRP、Ps 及 KLF4 在 2 型糖尿病下肢血管病变的 发生发展中具有临床价值。血清高 Ps 及 hsCRP 水平可能是 2 型糖 尿病 PAD 发病的重要危险因素,与 PAD 严重程度密切相关;而 KLF4 则可能具有延缓糖尿病下肢血管病变发生发展的作用。Ps、CRP 及 KLF4 能否作为早期糖尿病下肢血管病变发生的预测指标,KLF4 是否可作为新的防治糖尿病合并下肢血管病变的干预指标还有待进 一步的研究。 关键词:2 型糖尿病;下肢血管病变;超敏 C 反应蛋白;可溶性 P 选择素;kruppel 样因子 4 Relationship Among High-sensitivity C-reactive Protein, soluble P-selection, Kruppel-like factor 4 and peripheral vascular disease in Type 2 diabetes patients Abstract Objective:Toinvestigate the relationship Among high-sensitivity C-reactive Protein, soluble P-selection, Kruppel-like factor 4 and peripheral vascular  disease in Type 2 diabetes patients. Method:The level of inflammation hctors including hsCRP,Ps,KLF4 were compared among PVD patients(ABI0.9) , N-PVD patients(ABI≥0.9) as well as the control group,and the differences in body mass index(BMI),blood pressure(BP),serum glucofe,HbA lc, and Bloodlipid were also observed. Result: Compared with the N-PVD group and the control group, the level of hsCRP and Ps were both significantly incressed(the hsCRP level: PAD vs N-PVD 77.44±8.59 vs 61.16±9.41 , P=0.003;  PAD vs control 77.44±8.59 vs 44.48±6.15,P<0.001. the Ps level:PAD vs N-PVD 142.42±13.46 vs 117.87±14.27,P=0.002; PAD vs control 142.42±13.46 vs 90.91±8.09,P<0.001); however, the KLF4 level in PVD group was significantly lower than that of N-PVD group and control group( PAD vs N-PVD 34.72±5.41vs 44.88±7.05,P=0.019;PAD vs control 34.72±5.41 vs 53.74±7.38,P<0.001).In addition, we found that N-PVD group had higher level in hsCRP and Ps than control group(the hsCRP level: N-PVD vs control 61.16±9.41 vs 44.48±6.15,P=0.002;the Ps level: N-PVD vs control 117.87±14.27 vs 90.91±8.09, P=0.001), yet the KLF4 level was decreased markedly in N-PVD group compared with the control group(N-PVD vs control 44.88±7.05 vs 53.74±7.38, P=0.04). Conclusion: hsCRP, Ps as well as KLF4 have the simil

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