期刊文献+

T细胞受体保守域α链基因-575A/G多态性与终末期肾病微炎症状态的相关性研究 被引量:2

Study on the relationship between the TCRCα-575A/G polymorphism and microinflammatory state of end-stage renal disease
下载PDF
导出
摘要 目的探讨T细胞受体保守域α链基因(TCRCα)-575A/G多态性与终末期肾病微炎症状态的相关关系。方法利用聚合酶链式反应-限制性片段长度多态性分析法(PCR-RFLP)来鉴定基因型,以检测终末期肾病患者和正常对照组TCRCα基因-575A/G多态性分布规律。并收集临床指标,进行病例对照研究及临床资料分析。结果 1在终末期肾病组和对照组,均检测出A、G两种TCRCα基因-575A/G等位基因,三种基因型AA型、AG型、GG型;2终末期肾病组和正常人对照组相比,基因型和等位基因分布频率均无统计学意义(P>0.05);3临床资料显示:终末期肾病患者的CRP、Lp(a)与AngⅡ的水平均比健康对照组高(P<0.05),差异有统计学意义。终末期肾病组,三种基因型在年龄、性别、Lp(a)、AngⅡ水平方面相比,差异无统计学意义(P>0.05),GG基因型的终末期肾病患者的CRP水平较AG和AA基因型明显升高,差异有统计学意义(P<0.05)。正常对照组中,三种基因型在年龄、性别、CRP、Lp(a)和AngⅡ水平方面相比,差异无统计学意义(P>0.05)。结论终末期肾病普遍存在微炎症状态,TCRCα-575A/G基因多态性可能与CRP的水平相关,与终末期肾病的发病易感性不相关。 [Objective] To investigate the clinical relationship of TCRCα-575MG polymorphism with microin- flammatory state of end-stage renal disease. [ Methods ] The genotypes of TCRCαgene polymorphism (-575A/G) was identified by PCR-RFLP to detect TCRC -575A/G gene polymorphism distribution between ESRD patients and nor- mal control group, and the clinic information was obtained for analysis of case-control study and clinical data. [Result] (1)TCRCαgene (-575A/G) included 3 genotype (AA,AG,GG) and 2 allele gene (A or G) in two groups; (2) There were no statistical significant difference of genotypes distribution and allele frequency between ESRD group and the control (P 〉0.05); (3)The CRP, lp (a) and Ang ]I level of ESRD group were higher than the control, and the difference was statistically significant (P 〈0.05). The CRP level in the GG genotype was higher than the AG OR AA genotypes (P 〈0.05), and no correlation was found in the -575A/G polymorphism of TCRCα with sex, age, lp(a) and Ang Ⅱ level (P 〉0.05) in ESRD group. No correlation was found in the -575A/G polymorphism of TCRCα with CRP, lp(a) and Ang Ⅱ level (P 〉0.05) in the control. [ Conclusion ] Microinflammatory state was common in end stage re- nal disease patients. TCRCα-575A/G polymorphism may be associated with the CRP level. However, this polymor-phism was not associated with susceptibility to ESRD.
出处 《中国现代医学杂志》 CAS 北大核心 2015年第4期37-40,共4页 China Journal of Modern Medicine
关键词 T细胞受体 终末期肾病 基因多态性 微炎症 T cell receptor ESRD polymorphism micro inflamnlatory
  • 相关文献

参考文献14

  • 1MUNTNER P, HAMM LL, KUSEK JW, et al. The prevalence of nontraditional risk factors for coronary heart disease in patients with chronic kidney disease[J]. Ann Intern Med, 2004, 140(1): 9-17.
  • 2OBERG BP, MENAMIN E, LUCAS FL, et al. Increased preva- lence of oxidant stress and inflammation in patients with moder- ate to severe chronic kidney disease[J]. Kidney Int, 2004, 65(3): 1009-1016.
  • 3LANDRAY MJ, WHEELER DC, LIP GY, et al. Inflammation, endothelial dysfunction, and platelet activation in patients with chronic kidney disease: the chronic renal impairment in Birm- ingham(CRIB) study[J]. Am J Kidney Dis, 2004, 43(2): 244-253.
  • 4TSIRPANLIS G, CHATZIPANAGIOTOU S, NICOLAOU C. Mi- croinflammation versus inflammation in chronic renal failure pa- tients[J]. Kidney Int, 2004, 66(5): 2093.
  • 5MSCHEN M, WARSKULAT U, HAUSSINGER D, et al. De- ranged CD95 system in a case of Churg-Strauss vasculitis[J]. Gastroenterology, 1998, 114(6): 1351-1.352.
  • 6赵明辉,章友康,刘玉春,刘娜,王海燕.抗中性粒细胞胞浆抗体相关小血管炎的系统表现[J].中华内科杂志,2000,39(1):50-50. 被引量:44
  • 7DEENITCHINA SS, SHINOZAKI M, HIRANO T, et al. Associa- tion of a T-cell receptor constant alpha chain gene polymorphim with progressian of IgA nephropathy in Japanese patients[J]. Am J Kidney Dis, 1999, 34(2): 279-288.
  • 8ELHASSAN EA, KABALLO B, FEDAIL H, et al. Peritoneal dialysis in the Sudan[J]. Perit Dial Int, 2007, 27(5): 503-510.
  • 9SCHOMIG M, EISENHARDT A, RITZ E. The microinflmnmatory state of uremia[J]. Blood Purification, 2000, 18(4): 327-332.
  • 10MARSHALL TG, LEE FE, MARSHALL FE. Common angioten- sion receptor blockers may directly modulate the immune system via VDR, PPAR and CCR2b[J]. Theor Biol Med Model, 2006, 3(1): 21-33.

二级参考文献25

共引文献81

同被引文献19

二级引证文献49

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部