检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王金行[1] 周雯雯[1] 满冬亮[1] 杨志东[1] 刘柏新[1] 宋鉴清[1]
机构地区:[1]中国医科大学附属第一医院检验科,辽宁沈阳110001
出 处:《现代肿瘤医学》2013年第2期412-414,共3页Journal of Modern Oncology
基 金:辽宁省教育厅科研项目计划(编号:201102291)
摘 要:目的:探讨血清胱抑素C(Cys-C)和血清肌酐与多发性骨髓瘤的关系。方法:选择42例初发多发性骨髓瘤患者和40例健康体检者,分别测定其血清Cys-C、尿素(Urea)、肌酐(Scr)及β2-微球蛋白(β2-microglobulin,β2-MG)水平含量。结果:多发性骨髓瘤组血清Cys-C和β2-MG水平较对照组明显升高,差异有统计学意义(P<0.01);血清Scr水平较对照组明显升高(P<0.05)。多发性骨髓瘤患者Ⅲ期中Cys-C水平较Ⅰ期和Ⅱ期明显升高(P<0.01);Ⅲ期中Scr和β2-MG水平较Ⅰ期和Ⅱ期明显升高(P<0.05)。而Ⅰ期和Ⅱ期血清Cys-C、Scr和β2-MG水平之间没有明显差别,差异无统计学意义(P>0.05)。Cys-C与β2-MG呈正相关(r=0.474,P<0.05)。结论:Cys-C可以作为诊断多发性骨髓瘤患者肾功能损害的敏感内源性标志之一,而且优于Urea、Scr和β2-MG,在多发性骨髓瘤分期和判断预后中也有重要的临床意义。Objective:To explore the relationship between serum cystain c and serum ereatinine in multiple myelo- ma. Methods:To select 42 patients with multiple myeloma and 40 healthy subjects ,which and measure serum Cys - C, level of urea ( Urea), creatinine ( Scr ) and β2 - microglobulin ( β2 - MG). Results : The levels of serum Cys - C and 62 - MG in multiple myeloma group were significantly higher than that in control group, which was statistically significant (P 〈 0.01 ) ;The level of serum Scr increased markedly( P 〈 0.05 ) , the level of Cys -C in patients with muhiple myeloma III was significantly higher than that in stage I and II( P 〈 0.01 ) ; so were the level of Scr and β2 - MG( P 〈 0.05 ). However there were no significant differences among the levels of Cys - C, Scr and β2 - MG in phase I and phase II patients( P 〉 0.05 ). Cys - C and β2 - MG had a positive correlation( r = 0. 474 ,P 〈 0.05 ). Conclusion : Cys - C can be used as one of the sensitive endogenous hallmarks of the diagnosis of multiple myeloma patients with impaired renal function, and superior to Urea, Scr and β2 - MG in multiple myeloma also has important clinical significance in the prognosis.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.145