Standardization of C-peptide measurements

被引:75
|
作者
Little, Randie R. [1 ]
Rohlfing, Curt L.
Tennill, Alethea L.
Madsen, Richard W. [2 ]
Polonsky, Kenneth S. [3 ]
Myers, Gary L. [4 ]
Greenbaum, Carla J. [5 ]
Palmer, Jerry P. [6 ,7 ]
Rogatsky, Eduard [8 ,9 ]
Stein, Daniel T. [8 ,9 ]
机构
[1] Univ Missouri, Sch Med, Dept Pathol & Anat Sci, Diagnost Lab, Columbia, MO 65212 USA
[2] Univ Missouri, Sch Med, Dept Stat, Columbia, MO 65212 USA
[3] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[4] Ctr Dis Control & Prevent, Div Environm Hlth Lab Sci, Ctr Environm Hlth, Chamblee, GA USA
[5] Benaroya Res Inst, Seattle, WA USA
[6] Univ Washington, Seattle, WA 98195 USA
[7] VA Med Ctr, Seattle, WA USA
[8] Yeshiva Univ, Albert Einstein Coll Med, Dept Med, Bronx, NY USA
[9] Yeshiva Univ, Albert Einstein Coll Med, GCRC Analyt Core Lab, Bronx, NY USA
关键词
D O I
10.1373/clinchem.2007.101287
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: C-peptide is a marker of insulin secretion in diabetic patients. We assessed within- and between-laboratory imprecision of C-peptide assays and determined whether serum calibrators with values assigned by mass spectrometry could be used to harmonize C-peptide results. METHODS: We sent 40 different serum samples to 15 laboratories, which used 9 different routine C-peptide assay methods. We also sent matched plasma samples to another laboratory for C-peptide analysis with a reference mass spectrometry method. Each laboratory analyzed 8 of these samples in duplicate on each of 4 days to evaluate within- and between-day imprecision. The same 8 samples were also used to normalize the results for the remaining samples to the mass spectrometry reference method. RESULTS: Within- and between-run CVs ranged from < 2% to > 10% and from < 2% to > 18%, respectively. Normalizing the results with serum samples significantly improved the comparability among laboratories and methods. After normalization, the differences among laboratories in mean response were no longer statistically significant (P = 0.24), with least-squares means of 0.93-1.02. CONCLUSIONS: C-peptide results generated by different methods and laboratories do not always agree, especially at higher C-peptide concentrations. Within-laboratory imprecision also varied, with some methods giving much more consistent results than others. These data show that calibrating C-peptide measurement to a reference method can increase comparability between laboratories. (c) 2008 American Association for Clinical Chemistry.
引用
收藏
页码:1023 / 1026
页数:4
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