State-of-the-Art Vitamin D Assays: A Comparison of Automated Immunoassays with Liquid Chromatography-Tandem Mass Spectrometry Methods

被引:309
作者
Farrell, Christopher-John L. [2 ,3 ]
Martin, Steven [3 ]
McWhinney, Brett
Straub, Isabella
Williams, Paul [4 ,5 ]
Herrmann, Markus [1 ,3 ]
机构
[1] Univ Sydney, Dept Biochem, Royal Prince Alfred Hosp, Cent & Nepean Clin Sch, Camperdown, NSW 2050, Australia
[2] Royal N Shore Hosp, PaLMS Pathol, Sydney, NSW, Australia
[3] Laverty Pathol, N Ryde, NSW, Australia
[4] Univ Sydney, Cent Clin Sch, Camperdown, NSW 2050, Australia
[5] Royal Prince Alfred Hosp, Sydney SW Pathol Serv, Sydney, NSW, Australia
关键词
25-HYDROXYVITAMIN D-2; SERUM; INFANTS; HPLC;
D O I
10.1373/clinchem.2011.172155
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Vitamin D testing is increasing worldwide. Recently several diagnostic manufacturers including Abbott and Siemens have launched automated 25-hydroxy vitaminD(25OH-D) immunoassays. Furthermore, preexisting assays from DiaSorin and Roche have recently been modified. We compared the performance of 5 automated immunoassays, an RIA and 2 liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods. METHODS: Aliquots of 170 randomly selected patient samples were prepared and 25OH-D was measured by 2 LC-MS/MS methods, an RIA (DiaSorin), and automated immunoassays from Abbott (Architect), DiaSorin (LIAISON), IDS (ISYS), Roche (E170, monoclonal 25OH-D-3 assay), and Siemens (Centaur). Within-run and between-run imprecision were evaluated by measurement of 5 replicates of 2 serum pools on 5 consecutive days. RESULTS: The LC-MS/MS methods agreed, with a concordance correlation coefficient (CCC) of 0.99 and bias of 0.56 mu g/L (1.4 nmol/L). The RIA assay showed a performance comparable to LC-MS/MS, with a CCC of 0.97 and a mean bias of 1.1 mu g/L (2.7 nmo/L). All immunoassays measured total 25OH-D (including D-3 and D-2), with the exception of the Roche assay (D-3 only). Among the immunoassays detecting total 25OH-D, the CCCs varied between 0.85 (Abbott) to 0.95 (LIAISON). The mean bias ranged between 0.2 mu g/L (0.5 nmol/L) (LIAISON) and 4.56 mu g/L (11.4 nmol/L) (Abbott). The Roche 25OH-D-3 assay demonstrated small mean bias [-2.7 mu g/L (-6.7 nmol/L)] [-2.7 mu g/L (-6.7 nmol/L)] but a low CCC of just 0.66. Most assays demonstrated good intra-and interassay precision, with CV < 10%. CONCLUSIONS: Automated immunoassays demonstrated variable performance and not all tests met our minimum performance goals. It is important that laboratories be aware of the limitations of their assay. (C) 2011 American Association for Clinical Chemistry
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收藏
页码:531 / 542
页数:12
相关论文
共 28 条
[1]  
[Anonymous], 2001, Biological variation: from principles to practice
[2]  
Antoniucci DM, 2005, CLIN CHEM, V51, P258
[3]   Current status of clinical 25-hydroxyvitamin D measurement: An assessment of between-laboratory agreement [J].
Binkley, Neil ;
Krueger, Diane C. ;
Morgan, Sarah ;
Wiebe, Donald .
CLINICA CHIMICA ACTA, 2010, 411 (23-24) :1976-1982
[4]   Use of a common standard improves the performance of liquid chromatography-tandem mass spectrometry methods for serum 25-hydroxyvitamin-D [J].
Carter, Graham D. ;
Jones, Julia C. .
ANNALS OF CLINICAL BIOCHEMISTRY, 2009, 46 :79-81
[5]   Vitamin D: Metabolism [J].
Christakos, Sylvia ;
Ajibade, Dare V. ;
Dhawan, Puneet ;
Fechner, Adam J. ;
Mady, Leila J. .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 2010, 39 (02) :243-+
[6]   SERUM VITAMIN-D2 AND VITAMIN-D3 METABOLITE CONCENTRATIONS AND ABSORPTION OF VITAMIN-D2 IN ELDERLY SUBJECTS [J].
CLEMENS, TL ;
ZHOU, XY ;
MYLES, M ;
ENDRES, D ;
LINDSAY, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (03) :656-660
[7]  
DeLuca HF, 2004, AM J CLIN NUTR, V80, p1689S, DOI 10.1093/ajcn/80.6.1689S
[8]   Current assays overestimate 25-hydroxyvitamin D3 and underestimate 25-hydroxyvitamin D2 compared with HPLC:: need for assay-specific decision limits and metabolite-specific assays [J].
Glendenning, P ;
Taranto, M ;
Noble, JM ;
Musk, AA ;
Hammond, C ;
Goldswain, PR ;
Fraser, WD ;
Vasikaran, SD .
ANNALS OF CLINICAL BIOCHEMISTRY, 2006, 43 :23-30
[9]  
Hart GR, 2006, CLIN LAB, V52, P335
[10]  
Herrmann M, 2011, VITAMINS IN THE PREVENTION OF HUMAN DISEASES, P395