重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2015年
10期
1374-1377
,共4页
陈同庆%周春%陈文清%李振兴%罗兵%唐倩%张文明
陳同慶%週春%陳文清%李振興%囉兵%唐倩%張文明
진동경%주춘%진문청%리진흥%라병%당천%장문명
酶法%血红蛋白 A,糖基化%方法学%性能评价
酶法%血紅蛋白 A,糖基化%方法學%性能評價
매법%혈홍단백 A,당기화%방법학%성능평개
enzymatic method%hemoglobin A,glycosylated%methodology%performance evaluation
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。
目的:探討酶法測定糖化血紅蛋白(HbA1c)方法學性能及其影響因素。方法採用酶法測定 HbA1c,評價該方法學的精密度、抗榦擾性、迴收率、準確性以及標本前處理(抗凝、保存、離心)對結果的影響,分析與高效液相法(HPLC)相關性及偏倚程度。結果酶法批內高、中、低值變異繫數(CV)為1.04%、1.26%、1.37%,批間為1.83%、2.24%、2.64%,與 HPLC 法呈線性相關(r =0.996,P <0.01);HbA1c 靶值濃度為5.20%、6.40%、7.60%、8.80%、10.00%、11.20%,其迴收率分彆為100.15%、98.91%、98.84%、98.20%、103.62%、99.82%;噹葡萄糖小于15.50 mmol/L、尿痠小于516.00μmol/L、膽紅素小于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、毬蛋白小于50 g/L 時,對結果無明顯榦擾。肝素鈉、乙二胺四乙痠二鉀(EDTA-K2)、枸櫞痠鈉抗凝標本 HbA1c 結果在-20~20℃保存3 d 無明顯改變(P >0.05);標本500、1000 r/min(R=15 cm)離心不同時間(1、2、5、10 min)以及2000 r/min 離心1 min,其檢測結果與3000 r/min 離心5 min 比較,差異有統計學意義(P <0.05)。結論酶法測定 HbA1c 其精密度、抗榦擾性、準確性、線性範圍均符閤臨床要求,與常規方法相比其相關性良好且偏差較小,可完全滿足臨床對 HbA1c 檢測需求。
목적:탐토매법측정당화혈홍단백(HbA1c)방법학성능급기영향인소。방법채용매법측정 HbA1c,평개해방법학적정밀도、항간우성、회수솔、준학성이급표본전처리(항응、보존、리심)대결과적영향,분석여고효액상법(HPLC)상관성급편의정도。결과매법비내고、중、저치변이계수(CV)위1.04%、1.26%、1.37%,비간위1.83%、2.24%、2.64%,여 HPLC 법정선성상관(r =0.996,P <0.01);HbA1c 파치농도위5.20%、6.40%、7.60%、8.80%、10.00%、11.20%,기회수솔분별위100.15%、98.91%、98.84%、98.20%、103.62%、99.82%;당포도당소우15.50 mmol/L、뇨산소우516.00μmol/L、담홍소소우217.00μmol/L、삼선감유소우10.20 mmol/L、뇨소소우11.50 mmol/L、청단백소우50 g/L、구단백소우50 g/L 시,대결과무명현간우。간소납、을이알사을산이갑(EDTA-K2)、구연산납항응표본 HbA1c 결과재-20~20℃보존3 d 무명현개변(P >0.05);표본500、1000 r/min(R=15 cm)리심불동시간(1、2、5、10 min)이급2000 r/min 리심1 min,기검측결과여3000 r/min 리심5 min 비교,차이유통계학의의(P <0.05)。결론매법측정 HbA1c 기정밀도、항간우성、준학성、선성범위균부합림상요구,여상규방법상비기상관성량호차편차교소,가완전만족림상대 HbA1c 검측수구。
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.