Assay validation for left-censored data

被引:12
作者
Barnhart, HX
Song, JL
Lyles, RH
机构
[1] Duke Univ, Duke Clin Res Inst, Dept Biostat & Bioinformat, Durham, NC 27715 USA
[2] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
[3] Emory Univ, Rollins Sch Publ Hlth, Dept Biostat, Atlanta, GA 30322 USA
关键词
agreement; assay validation; left censoring; limit of detection; generalized estimating equations;
D O I
10.1002/sim.2225
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In laboratory validation studies, it is often important to assess agreement between two assays, based on different techniques. Oftentimes, both assays have lower limits of detection and thus measurements are left censored. For example, in studies of Human Immunodeficiency Virus (HIV), the branched DNA (bDNA) assay was developed to quantify HIV-1 RNA concentrations in plasma. Validation of newer assays, such as the RT-PCR (reverse transcriptase polymerase chain reaction) involves assessing agreement of measurements obtained using the two techniques. Both bDNA and RT-PCR assays have lower limits of detection and thus new statistical methods are needed for assessing agreement between two left-censored variables. In this paper, we present maximum likelihood and generalized estimating equations approaches to evaluate agreement between two assays that are subject to lower limits of detection. The concordance correlation coefficient is used as an agreement index. The methodology is illustrated using HIV RNA assay data collected as part of a long-term HIV cohort study. Copyright (C) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:3347 / 3360
页数:14
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