检验医学
檢驗醫學
검험의학
LABORATORY MEDICINE
2014年
8期
835-837
,共3页
查成喜%邢福军%张雪燕%郭鹏%习静%韩跃武
查成喜%邢福軍%張雪燕%郭鵬%習靜%韓躍武
사성희%형복군%장설연%곽붕%습정%한약무
慢性粒细胞白血病%核酸适配子%检测方法%诊断价值
慢性粒細胞白血病%覈痠適配子%檢測方法%診斷價值
만성립세포백혈병%핵산괄배자%검측방법%진단개치
Chronic myeloid leukemia%Aptamer%Detection method%Diagnosis significance
目的:评价K562细胞ssDNA适配子检测方法(简称适配子检测法)对慢性粒细胞白血病(CML)的临床诊断价值。方法采集18例CML患者、22例其他白血病患者、20名健康体检者(正常对照组)的血液标本各5 mL,分离粒细胞,用建立的适配子检测法检测荧光强度,绘制受试者工作特征(ROC)曲线。结果 CML组荧光强度为492.26±41.67,与其它白血病组(466.86±33.23)及正常对照组(469.33±37.13)比较,差异无统计学意义(P值分别为0.078、0.243);其它白血病组和正常对照组比较,差异亦无统计学意义(P=0.835)。适配子检测法诊断CML的ROC曲线下面积为0.702,最佳阳性临界值为475.13,灵敏度为83.33%、特异性为54.76%、阳性预测值为44.11%、阴性预测值为88.46%。结论适配子检测法对CML的诊断具有较低的准确性,实际应用还有一定的局限性。
目的:評價K562細胞ssDNA適配子檢測方法(簡稱適配子檢測法)對慢性粒細胞白血病(CML)的臨床診斷價值。方法採集18例CML患者、22例其他白血病患者、20名健康體檢者(正常對照組)的血液標本各5 mL,分離粒細胞,用建立的適配子檢測法檢測熒光彊度,繪製受試者工作特徵(ROC)麯線。結果 CML組熒光彊度為492.26±41.67,與其它白血病組(466.86±33.23)及正常對照組(469.33±37.13)比較,差異無統計學意義(P值分彆為0.078、0.243);其它白血病組和正常對照組比較,差異亦無統計學意義(P=0.835)。適配子檢測法診斷CML的ROC麯線下麵積為0.702,最佳暘性臨界值為475.13,靈敏度為83.33%、特異性為54.76%、暘性預測值為44.11%、陰性預測值為88.46%。結論適配子檢測法對CML的診斷具有較低的準確性,實際應用還有一定的跼限性。
목적:평개K562세포ssDNA괄배자검측방법(간칭괄배자검측법)대만성립세포백혈병(CML)적림상진단개치。방법채집18례CML환자、22례기타백혈병환자、20명건강체검자(정상대조조)적혈액표본각5 mL,분리립세포,용건립적괄배자검측법검측형광강도,회제수시자공작특정(ROC)곡선。결과 CML조형광강도위492.26±41.67,여기타백혈병조(466.86±33.23)급정상대조조(469.33±37.13)비교,차이무통계학의의(P치분별위0.078、0.243);기타백혈병조화정상대조조비교,차이역무통계학의의(P=0.835)。괄배자검측법진단CML적ROC곡선하면적위0.702,최가양성림계치위475.13,령민도위83.33%、특이성위54.76%、양성예측치위44.11%、음성예측치위88.46%。결론괄배자검측법대CML적진단구유교저적준학성,실제응용환유일정적국한성。
Objective To evaluate the significance of K562 cell ssDNA aptamer detection method for the clinical diagnosis of chronic myeloid leukemia(CML).Methods A total of 5 mL blood samples of 18 patients with CML,22 patients with other leukemia and 20 healthy subjects were collected.The granulocytes were separated,and aptamer detection method was established for the determination of fluorescence intensity.The receiver operating characteristics (ROC)curve was drawn.Results The fluorescence intensities were 492.26 ±41.67 in CML group,466.86 ±33.23 in other leukemia group and 469.33 ±37.13 in healthy control group,and the results showed no statistical significance (P=0.078 and P=0.243).There was no statistical significance between other leukemia group and healthy control group (P=0.835).The area under ROC curve was 0.702,the optimal positive threshold was 475.13,the sensitivity was 83.33%,the specificity was 54.76%,the positive predictive value was 44.11%,and the negative predictive value was 88.46%.Conclusions The aptamer detection method has a low accuracy in the clinical diagnosis of CML,and it has some limitations for clinical application.