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酶法测定糖化血红蛋白的方法评价及标本前处理对结果的影响
引用本文:陈同庆,周春,陈文清,李振兴,罗兵,唐倩,张文明.酶法测定糖化血红蛋白的方法评价及标本前处理对结果的影响[J].重庆医学,2015(10):1374-1377.
作者姓名:陈同庆  周春  陈文清  李振兴  罗兵  唐倩  张文明
作者单位:1. 安徽省第二人民医院输血科,安徽合肥,230011;2. 安徽省第二人民医院心内科,安徽合肥,230011;3. 安徽省第二人民医院检验科,安徽合肥,230011;4. 安徽省第二人民医院内分泌科,安徽合肥,230011
基金项目:安徽省高校省级自然科学基金资助项目(KJ2013z157);安徽省立新安医院自然科学基金资助项目(KJ2010Y02)。
摘    要:目的:探讨酶法测定糖化血红蛋白(HbA1c)方法学性能及其影响因素。方法采用酶法测定 HbA1c,评价该方法学的精密度、抗干扰性、回收率、准确性以及标本前处理(抗凝、保存、离心)对结果的影响,分析与高效液相法(HPLC)相关性及偏倚程度。结果酶法批内高、中、低值变异系数(CV)为1.04%、1.26%、1.37%,批间为1.83%、2.24%、2.64%,与 HPLC 法呈线性相关(r =0.996,P <0.01);HbA1c 靶值浓度为5.20%、6.40%、7.60%、8.80%、10.00%、11.20%,其回收率分别为100.15%、98.91%、98.84%、98.20%、103.62%、99.82%;当葡萄糖小于15.50 mmol/L、尿酸小于516.00μmol/L、胆红素小于217.00μmol/L、三酰甘油小于10.20 mmol/L、尿素小于11.50 mmol/L、清蛋白小于50 g/L、球蛋白小于50 g/L 时,对结果无明显干扰。肝素钠、乙二胺四乙酸二钾(EDTA-K2)、枸橼酸钠抗凝标本 HbA1c 结果在-20~20℃保存3 d 无明显改变(P >0.05);标本500、1000 r/min(R=15 cm)离心不同时间(1、2、5、10 min)以及2000 r/min 离心1 min,其检测结果与3000 r/min 离心5 min 比较,差异有统计学意义(P <0.05)。结论酶法测定 HbA1c 其精密度、抗干扰性、准确性、线性范围均符合临床要求,与常规方法相比其相关性良好且偏差较小,可完全满足临床对 HbA1c 检测需求。

关 键 词:酶法  血红蛋白  A  糖基化  方法学  性能评价

Methodological evaluation on enzymatic method for detecting HbA1c and influence of sample pre-processing on detection result
Chen Tongqing,Zhou Chun,Chen Wenqing,Li Zhenxing,Luo Bing,Tang Qian,Zhang Wenming.Methodological evaluation on enzymatic method for detecting HbA1c and influence of sample pre-processing on detection result[J].Chongqing Medical Journal,2015(10):1374-1377.
Authors:Chen Tongqing  Zhou Chun  Chen Wenqing  Li Zhenxing  Luo Bing  Tang Qian  Zhang Wenming
Abstract:Objective To evaluate the methodological performance of the new enzymatic method for detecting glycated hemo-globin(HbAIc)and its influencing factors.Methods HbAIc was detected by the enzymatic method.The precision,anti-interfer-ence,recovery rate,accuracy and the influence of pre-processing(anti-coagulation,preservation,centrifugation)on the detection re-sults were evaluated,its correlation with HPLC and the bias degree were analyzed.Results The within-run coefficients of variation (CVs)for high,middle and low value QC samples in the enzymatic assay were 1.04%,1.26% and 1.37% respectively and the be-tween-run CVs were 1.83%,2.24% and 2.64%,respectively;the enzymatic method showed the linear correlation with HPLC(r=0.996,P <0.01);the HbA1c target value concentrations were 5.20%,6.40%,7.60%,8.80%,10.00% and 11.20% respectively, the recovery rates were 100.15%,98.91%,98.84%,98.20%,103.62% and 99.82% respectively;the interference test showed that this method had no significant interference on the detection results when glucose <15.50 mmol/L,UA<516.00 μmol/L,bili-rubin <217.00 μmol/L,triglyceride<10.20 mmol/L,urea<11.50 mmol/L,albumin<50 g/L and globulin <50 g/L.The HbA1c detection results in the samples with anti-coagulation by heparin sodium,EDTA-2K and sodium citrate stored for 3 d under -20-20 ℃ had no obvious change (P >0.05);the sample was centrifuged at 500,1 000 r/min(R=15 cm)for different time(1,2,5,10 min)and at 2 000 r/min for 1 min,their detection results had statistical differences compared with the sample centrifuged=3 000 r/min for 5 min (P <0.05).Conclusion The precision,anti-interference,accuracy and linearity range of the enzymatic method all conform to the clinical requirement.Compared with the conventional method,its correlation is good with small deviation,which can entirely satisfy the demand of the HbAIc detection in clinic.
Keywords:enzymatic method  hemoglobin A  glycosylated  methodology  performance evaluation
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