TY - JOUR
T1 - Toward standardization of hair cortisol measurement
T2 - Results of the first international interlaboratory round robin
AU - Russell, Evan
AU - Kirschbaum, Clemens
AU - Laudenslager, Mark L.
AU - Stalder, Tobias
AU - De Rijke, Yolanda
AU - Van Rossum, Elisabeth F.C.
AU - Van Uum, Stan
AU - Koren, Gideon
N1 - Publisher Copyright:
© 2014 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2015/2/2
Y1 - 2015/2/2
N2 - Background: The importance of hair cortisol as a long-term retrospective measure of systemic cortisol exposure is being increasingly recognized, and over recent years, the field of hair cortisol analysis has seen rapid expansion with laboratories around the globe, integrating hair cortisol analysis into their study designs. These laboratories use different methods of analysis, and presently, no attempt has been made to compare them. To move toward clinical utilization of this novel method, international benchmark reference values must be established. For that end, 4 leading laboratories in hair cortisol testing set up a protocol for comparison of the methods used by them. Methods: Four immunoassay methods and 2 liquid chromatograph-mass spectrometry (LC-MS/MS) methods were compared by analyzing the same hair samples representing the low, intermediate, and high ranges of hair cortisol concentrations (HCC). Results: HCC determined by the 4 immunoassay methods were highly and positively intercorrelated (r between 0.92 and 0.97; all P < 0.0001) in all comparisons of individual laboratories. Additionally, each laboratory's immunoassay HCC had significant positive correlations (r between 0.88 and 0.97; all P < 0.0001) with each of the 2 LC-MS/MS methods, which produced practically identical results. Conclusions: This study indicates that laboratories using immunoassays can use a correction factor that will convert results into standard LC-MS/MS equivalents.
AB - Background: The importance of hair cortisol as a long-term retrospective measure of systemic cortisol exposure is being increasingly recognized, and over recent years, the field of hair cortisol analysis has seen rapid expansion with laboratories around the globe, integrating hair cortisol analysis into their study designs. These laboratories use different methods of analysis, and presently, no attempt has been made to compare them. To move toward clinical utilization of this novel method, international benchmark reference values must be established. For that end, 4 leading laboratories in hair cortisol testing set up a protocol for comparison of the methods used by them. Methods: Four immunoassay methods and 2 liquid chromatograph-mass spectrometry (LC-MS/MS) methods were compared by analyzing the same hair samples representing the low, intermediate, and high ranges of hair cortisol concentrations (HCC). Results: HCC determined by the 4 immunoassay methods were highly and positively intercorrelated (r between 0.92 and 0.97; all P < 0.0001) in all comparisons of individual laboratories. Additionally, each laboratory's immunoassay HCC had significant positive correlations (r between 0.88 and 0.97; all P < 0.0001) with each of the 2 LC-MS/MS methods, which produced practically identical results. Conclusions: This study indicates that laboratories using immunoassays can use a correction factor that will convert results into standard LC-MS/MS equivalents.
KW - Hair
KW - LC-MS/MS
KW - comparison
KW - cortisol
KW - immunoassay
UR - http://www.scopus.com/inward/record.url?scp=84964296827&partnerID=8YFLogxK
U2 - 10.1097/FTD.0000000000000148
DO - 10.1097/FTD.0000000000000148
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C2 - 25387254
AN - SCOPUS:84964296827
SN - 0163-4356
VL - 37
SP - 71
EP - 75
JO - Therapeutic Drug Monitoring
JF - Therapeutic Drug Monitoring
IS - 1
ER -