Spierto F W, Gardner F, Smith S J
Division of Laboratory Sciences, National Center for Environmental Health Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Steroids. 2001 Jan;66(1):59-62. doi: 10.1016/s0039-128x(00)00139-2.
Two-hydroxyestrone (2OHE-1) and 16alpha-hydroxyestrone (16OHE-1) are two estrogen metabolites that may play important roles in the development or promotion of breast cancer. Our study assessed the reliability of a newly developed kit procedure for measuring 2OHE-1. Although under certain conditions the assay would not distinguish 2OHE-1 from estriol, or possibly 2-methoxyestrone, steroids such as 17beta-estradiol, estrone and 16OHE-1 should not interfere with the test. Our study evaluated the precision of this enzyme immunoassay (EIA) kit for measuring 2OHE-1 levels in serum obtained from healthy men and women. As a result of several replicate analyses of specimens obtained from 18 men and 20 women, we found that the within-run coefficients of variation (CVs) were approximately 20% and the among run CVs, 30%. Because the SD for the procedure is high, the limit of detection (LOD) was also high (130 ng/l). Nonetheless the assay could distinguish between 2OHE-1 levels in men (128 ng/l) and women (332 ng/l) because we performed a large number of analyses on each specimen. Improving the reproducibility of the assay would reduce the: 1. LOD; number of replicates needed to obtain reliable estimates of 2-OHE-1 levels; amount of time, effort, and cost for each analysis; and greatly improve the reliability of the method. Because the within-run variability is relatively smaller than the total variability (among run + within run), use of the assay for determining differences among groups could be justified only when measurements were made in a single run.
二羟基雌酮(2OHE-1)和16α-羟基雌酮(16OHE-1)是两种雌激素代谢产物,它们可能在乳腺癌的发生或发展过程中发挥重要作用。我们的研究评估了一种新开发的用于测量2OHE-1的试剂盒方法的可靠性。尽管在某些条件下该检测方法无法区分2OHE-1与雌三醇,或者可能无法区分2-甲氧基雌酮,但诸如17β-雌二醇、雌酮和16OHE-1等类固醇不应干扰该检测。我们的研究评估了这种酶免疫分析(EIA)试剂盒在测量从健康男性和女性获取的血清中2OHE-1水平时的精密度。对从18名男性和20名女性获取的标本进行多次重复分析的结果显示,批内变异系数(CVs)约为20%,批间CVs为30%。由于该检测方法的标准差较高,检测限(LOD)也较高(130 ng/l)。尽管如此,该检测方法仍能区分男性(128 ng/l)和女性(332 ng/l)的2OHE-1水平,因为我们对每个标本都进行了大量分析。提高该检测方法的可重复性将降低:1.检测限;获得2-OHE-1水平可靠估计值所需的重复次数;每次分析所需的时间、精力和成本;并极大地提高该方法的可靠性。由于批内变异性相对小于总变异性(批间+批内),仅当在单次检测中进行测量时,使用该检测方法来确定组间差异才是合理的。