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雅培IMx全自动免疫分析法检测前列腺特异性抗原的评估

Evaluation of the Abbott IMx automated immunoassay of prostate-specific antigen.

作者信息

Vessella R L, Noteboom J, Lange P H

机构信息

Department of Urology, University of Washington Medical Center, Seattle 98195.

出版信息

Clin Chem. 1992 Oct;38(10):2044-54.

PMID:1382897
Abstract

We detail the performance characteristics of the new IMx PSA immunoassay developed by Abbott Laboratories, addressing PSA recovery, assay reproducibility, standard curve storage, lower limit of detection, dilution linearity, and correlation with the Hybritech Tandem-R PSA immunoassay. We analyzed 686 sera for PSA retrospectively, testing 555 of these concurrently with the IMx and the Tandem-R immunoassays. The IMx PSA standard curve was linear from 0 to 100 micrograms/L, and curve storage was maintained for 4 weeks. The lower limit of detection of the IMx PSA assay was < or = 0.03 microgram/L; allowing for the assay precision yielded a biological detection limit of 0.06 microgram/L. We conservatively set the clinical threshold at 0.1 microgram/L. Regression analysis of dilution linearity involving 10 samples (0.44-200 micrograms/L) resulted in coefficients of correlation ranging from 0.9972 to 1.000. Reproducibility studies with 18 specimens within the range of 0.39-413.67 micrograms/L gave intra- and interassay CVs < 6.5%. The interassay 95% confidence interval for a specimen containing 0.06 microgram of PSA per liter was 0.03-0.09 microgram/L. Correlation between IMx and Tandem-R PSA assay results was excellent: r = 0.9909 and slope = 0.95. Overall, the IMx PSA immunoassay, with the conveniencies of automation, curve storage, and nonisotopic handling, provided an improved lower limit of PSA detection, which allows for earlier indication of residual or recurrent disease after radical prostatectomy.

摘要

我们详细阐述了雅培实验室研发的新型IMx PSA免疫测定法的性能特征,涉及PSA回收率、测定重现性、标准曲线储存、检测下限、稀释线性以及与Hybritech Tandem-R PSA免疫测定法的相关性。我们回顾性分析了686份血清样本中的PSA,并同时使用IMx和Tandem-R免疫测定法对其中555份样本进行检测。IMx PSA标准曲线在0至100微克/升范围内呈线性,且曲线储存可维持4周。IMx PSA测定法的检测下限≤0.03微克/升;考虑到测定精密度,生物学检测限为0.06微克/升。我们保守地将临床阈值设定为0.1微克/升。对10个样本(0.44 - 200微克/升)进行稀释线性回归分析,相关系数范围为0.9972至1.000。对18个浓度在0.39 - 413.67微克/升范围内的样本进行重现性研究,批内和批间变异系数均<6.5%。对于每升含0.06微克PSA的样本,批间95%置信区间为0.03 - 0.09微克/升。IMx和Tandem-R PSA测定结果之间的相关性极佳:r = 0.9909,斜率 = 0.95。总体而言,IMx PSA免疫测定法具有自动化、曲线储存和非同位素处理等便利性,提供了更低的PSA检测下限,有助于在前列腺癌根治术后更早地发现残留或复发病灶。

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