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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Measurement of serum monoclonal components: comparison between densitometry and capillary zone electrophoresis.
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Measurement of serum monoclonal components: comparison between densitometry and capillary zone electrophoresis.

机译:血清单克隆成分的测定:光密度法和毛细管区带电泳的比较。

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Quantitative measurement of serum monoclonal protein (M-protein) is one of the most important tools for monitoring disease activity in monoclonal gammopathies. The aims of this study were to evaluate serum M-protein quantification by capillary zone electrophoresis (CZE) and to compare results with those obtained by densitometric scanning of high-resolution agarose gel electrophoresis (HRE-AGE). The evaluation was carried out on 82 samples from patients with various monoclonal gammopathies. All the suspected M-proteins were confirmed and characterised by immunofixation on agarose gel (IFE). CZE was performed on a Paragon CZE 2000 system (Beckman Coulter). Passing-Bablok regression was: y (CZE)=1.27 x(HRE-AGE)-5.21 g/L. The correlation coefficient was 0.92. Bland-Altman analysis demonstrated a mean difference of -1.83 g/L (95% CI -0.76 to -2.90) with clear evidence of a concentration-related bias. Densitometry gave higher values at low M-spikes (<20 g/L), whereas CZE gave higher values at large M-spikes (>20 g/L). The concentration-related bias was found to be independent of the immunoglobulin isotype. In conclusion, to compare previous results obtained by M-protein densitometric scanning with those obtained by direct measurement of CZE peaks, the calculation of a univocal transforming factor appears to be unreliable.
机译:血清单克隆蛋白(M-蛋白)的定量测​​量是监测单克隆球蛋白病中疾病活动的最重要工具之一。这项研究的目的是评估通过毛细管区带电泳(CZE)进行的血清M蛋白定量,并将结果与​​通过高分辨率琼脂糖凝胶电泳(HRE-AGE)的光密度扫描获得的结果进行比较。对来自患有各种单克隆同性恋症的患者的82个样本进行了评估。通过在琼脂糖凝胶(IFE)上进行免疫固定,确认并鉴定了所有疑似M蛋白。在Paragon CZE 2000系统(Beckman Coulter)上进行CZE。 Passing-Bablok回归为:y(CZE)= 1.27 x(HRE-AGE)-5.21 g / L。相关系数为0.92。 Bland-Altman分析显示平均差异为-1.83 g / L(95%CI -0.76至-2.90),并且有明显的浓度相关偏差证据。在低M峰值(<20 g / L)下,光密度法给出较高的值,而在M峰值(> 20 g / L)下,CZE给出较高的值。发现与浓度相关的偏倚与免疫球蛋白同种型无关。总之,要将以前通过M蛋白光密度扫描获得的结果与通过直接测量CZE峰获得的结果进行比较,单变量转化因子的计算似乎是不可靠的。

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