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作 者:李建英[1] 郭进[1] 谭文芳[1] 余文珊[1]
机构地区:[1]广西壮族自治区人民医院干部综合病房二区,南宁530021
出 处:《中国临床新医学》2014年第9期799-802,共4页CHINESE JOURNAL OF NEW CLINICAL MEDICINE
基 金:广西科学研究与技术开发计划课题(编号:桂科攻11138008)
摘 要:目的观察不同剂量阿托伐他汀对老年早期糖尿病肾病(DN)患者外周血单个核细胞中核因子-κB(NF-κB)P65(ser536)的磷酸化水平、血清炎症因子水平(hs-CRP、TNF-α、IL-6、IL-1β)及尿白蛋白排泄率(UAER)的影响。方法将72例2型糖尿病早期DN老年患者,半随机分为两组,分别给予阿托伐他汀钙片10 mg/d(DN1组,37例)和20 mg/d(DN2组,35例),疗程16周。测定两组患者治疗前和治疗16周后外周血NF-κB P65的磷酸化水平、血清炎症因子水平、UAEA、血脂(TC、TG、DHL-C、LDL-C)。结果两组患者治疗后外周血NF-κB P65水平、血清炎症因子水平、TC及LDL-C均较治疗前降低(P<0.01或P<0.05),以DN2组降低更显著。DN2组治疗后UAER较治疗前显著降低(P<0.01),DN1组无显著下降(P>0.05)。结论阿托伐他汀在降低血脂的同时可降低外周血NF-κB P65的活性、血清炎症因子hs-CRP、TNF-α、IL-6、IL-1β水平,改善患者炎症状态,减少尿蛋白,且呈剂量依赖性。Objective To observe the effects of different doses of atorvastatin on phosphorylation of nuclear factor-kappa B(NF-κB) P65(ser536) in peripheral blood mononuclear cells , on the levels of serum inflammatory factors,including high sensitivity C reactive protein (hs-CRP),tumor necrosis factor-α(TNF-α),interleukin-6(IL-6 ),interleukin-1β(IL1-β), and on urinary albumin excretion rate(UAER) in the elderly patients with early diabetic nephropathy.Methods The patients(n=72) of type 2 diabetes with early nephropathy were randomly divided into two groups ,The patients were given atorvastatin 10 mg/d in DN1 group and atorvastatin 20 mg/d in DN2 group for sixteen weeks.Levels of NF-κB, serum inflammation factors,UAER,Total cholesterol(TC),triglyceride( TG),low density lipoprotein ( LDL-C) and hight density lipoprotein ( HDL-C) were measured before treatment and after treat-ment for sixteen weeks .Results After sixteen weeks of treatment ,the levels of NF -kB, serum inflammation factors , TC and LDL were reduced(P〈0.05 or P〈0.01) in two group.DN2 group decreased more significantly.UAER were reduced(P〈0.01)in DN2 group.There was no significant changes in DN1 group(P〉0.05).Conclusion Atorvastatin can reduce activity of NF-κB, levels of hs-CRP,TNF-α,IL-6,IL-1β,TC, and LDL in the olderly patients with type 2 diabetic pristine nephropathy .Atorvastatin may benefit patients with diabetes mellitus by ameliorating in-flammatory stats, as well as reducing urinary albumin ,in a dose-dependent manner .
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