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Toward consensus in the analysis of urinary 8-oxo-7,8-dihydro-2′- deoxyguanosine as a noninvasive biomarker of oxidative stress

Authors :
Evans, M D
Olinski, R
Loft, S
Cooke, M S
Rossner, Jr P
Sram, R
Henriksen, T
Poulsen, H E
Weimann, Allan
Barbieri, A
Sabatini, L
Violante, F
Kino, S
Ochi, T
Sakai, K
Takeuchi, M
Kasai, H
Meerman, J H N
Gackowski, D
Rozalski, R
Siomek, A
Halliwell, Barry
Jenner, Andrew M
Wang, H
Cerda, C
Saez, G
Haghdoost, S
Svoboda, P
Hu, C-W
Chao, M-R
Peng, K-Y
Shih, W-C
Wu, K-Y
Orhan, H
Istanbullu, N S
Mistry, V
Farmer, P B
Sandhu, J
Singh, R
Cortez, C
Su, Y
Santella, R M
Lambert, P
Smith, R
Evans, M D
Olinski, R
Loft, S
Cooke, M S
Rossner, Jr P
Sram, R
Henriksen, T
Poulsen, H E
Weimann, Allan
Barbieri, A
Sabatini, L
Violante, F
Kino, S
Ochi, T
Sakai, K
Takeuchi, M
Kasai, H
Meerman, J H N
Gackowski, D
Rozalski, R
Siomek, A
Halliwell, Barry
Jenner, Andrew M
Wang, H
Cerda, C
Saez, G
Haghdoost, S
Svoboda, P
Hu, C-W
Chao, M-R
Peng, K-Y
Shih, W-C
Wu, K-Y
Orhan, H
Istanbullu, N S
Mistry, V
Farmer, P B
Sandhu, J
Singh, R
Cortez, C
Su, Y
Santella, R M
Lambert, P
Smith, R
Source :
Illawarra Health and Medical Research Institute
Publication Year :
2010

Abstract

Of the DNA-derived biomarkers of oxidative stress, urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodG) is the most frequently measured. However, there is significant discrepancy between chromatographic and immunoassay approaches, and intratechnique agreement among all available chromatography-based assays and ELISAs is yet to be established. This is a significant obstacle to their use in large molecular epidemiological studies. To evaluate the accuracy of intra/intertechnique and interlaboratory measurements, samples of phosphate buffered saline and urine, spiked with different concentrations of 8-oxoG, together with a series of urine samples from healthy individuals were distributed to ESCULA members. All laboratories received identical samples, including 2 negative controls that contained no added 8-oxodG. Data were returned from 17 laboratories, representing 20 methods, broadly classified as mass spectrometric (MS), electrochemical detection (EC), or enzyme-linked immunosorbant assay (ELISA). Overall, there was good within-technique agreement, with the majority of laboratories' results lying within 1 SD of their consensus mean. However, ELISA showed more within-technique variation than did the chromatographic techniques and, for the urine samples, reported higher values. Bland-Altman plots revealed good agreement between MS and EC methods but concentration-dependent deviation for ELISA. All methods ranked urine samples according to concentration similarly. Creatinine levels are routinely used as a correction factor for urine concentration, and therefore we also conducted an interlaboratory comparison of methods for urinary creatinine determination, in which the vast majority of values lay within 1 SD of the consensus value, irrespective of the analysis procedure. This study reveals greater consensus than previously expected, although concern remains over ELISA. © FASEB.

Details

Database :
OAIster
Journal :
Illawarra Health and Medical Research Institute
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1066715861
Document Type :
Electronic Resource