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高脂血症肾移植患者外周血MCP-1及其受体CCR2 mRNA表达及辛伐他汀治疗的影响
引用本文:王玉新,史艳玲,李清芹,邹和群,徐琴君,唐孝达.高脂血症肾移植患者外周血MCP-1及其受体CCR2 mRNA表达及辛伐他汀治疗的影响[J].中山大学学报(医学科学版),2005,26(6):672-675.
作者姓名:王玉新  史艳玲  李清芹  邹和群  徐琴君  唐孝达
作者单位:1. 中山大学附属第五医院肾内科,广东,珠海,519000
2. 上海交通大学附属上海第一人民医院器官移植中心,上海,200080
基金项目:中国科学院资助项目,美国中华医学会资助项目,广东省博士启动基金
摘    要:目的]探讨肾移植术后高脂血症患者外周血单核细胞趋化蛋白-1(MCP-1)及其受体CCR2 mRNA的表达及辛伐他汀治疗影响.方法]根据患者肾移植术后6个月的血脂水平,从167例肾移植受者中选择60例作为研究对象,其中30例为血脂正常组(A组),30例为血脂增高组(B组),健康体检者30例作为对照组,逆转录聚合酶链反应检测各组外周血MCP-1及CCR2 mRNA表达水平.血脂增高组给予辛伐他汀治疗,分别于1.5个月、3个月时复查血脂水平及MCP-1、CCR2 mRNA表达水平.结果]肾移植受者外周血MCP-1及其CCR2mRNA表达水平显著高于对照组,B组增高更为显著.辛伐他汀治疗1.5个月时,B组患者血脂水平及外周血MCP-1、CCR2 mRNA表达水平显著降低,3个月时进一步降低.结论]肾移植后高脂血症患者外周血MCP-1及CCR2 mRNA表达水平显著增高,可能参与了移植后心血管疾病及慢性移植肾排斥的发生.辛伐他汀治疗可显著降低肾移植受者外周血MCP-1及其CCR2 mRNA表达水平,此可能有助于减少或延缓移植后心血管疾病及慢性移植肾病的发生.

关 键 词:肾移植  高脂血症  单核细胞趋化蛋白-1  逆转录-聚合酶链反应  辛伐他汀
文章编号:1676-3554(2005)06-0672-04
修稿时间:2005年6月30日

mRNA Expression of MCP-1 and Its Receptor CCR2 in Renal Transplant Recipients with Hyperlipidemia and Influence by Simvastatin Treatment
WANG Yu-xin,SHI Yan-ling,LI Qing-qin,ZOU He-qun,XU Qin-jun,TANG Xiao-da.mRNA Expression of MCP-1 and Its Receptor CCR2 in Renal Transplant Recipients with Hyperlipidemia and Influence by Simvastatin Treatment[J].Journal of Sun Yatsen University(Medical Sciences),2005,26(6):672-675.
Authors:WANG Yu-xin  SHI Yan-ling  LI Qing-qin  ZOU He-qun  XU Qin-jun  TANG Xiao-da
Abstract:Objective] To investigate the mRNA expression of MCP-1 and CCR2 in peripheral blood monocyte cells of renal transplant recipients and the influence by Simvastatin treatment. Methods] Sixty recipients were selected from 167 renal transplant recipients, and were divided into two groups. Patients in Group A were without hyperlipidemia (n=30) and group B were with hyperlipidemia (n=30). Control group consists of 30 healthy volunteers. The patients in group B were treated with Simvastatin for 3 months. The mRNA expressions of MCP-1 and CCR2 were detected with RT-PCR. Results] The mRNA expressions of MCP-1 and CCR2 in post transplant recipients were significantly higher compared to normal controls, which were more evident in group B than those in group A. Serum hpid levels in the patients of group B decreased significantly after Simvastatin treatment. Meanwhile, the mRNA expression of MCP-1 and CCR2 reduced significantly at the 1.5th month of Simvastatin treatment, and reduced to a evidence even significantly lower than those in group A at the 3th month.Conclusions] It is suggested that upregulated expression of MCP-1 and CCR2 mRNA may be involved in the pathogenesis of CAN and CVD in renal transplant recipients with hyperlipidemia. Simvastatin might be used to reduce the mRNA expressions of MCP-1 and CCR2 in renal recipients with hyperhpidemia.
Keywords:kidney transplantation  hyperlipidemia  MCP-1  RT-PCR  simvastatin
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