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Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study

BACKGROUND: HBV DNA is the most important molecular marker in hepatitis B, used to determine treatment indication and monitoring. Most patients require lifelong hepatitis B virus (HBV) management, thus viral load (VL) monitoring may be performed at different laboratories, with different HBV assays,...

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Autores principales: Maasoumy, Benjamin, Bremer, Birgit, Lehmann, Patrick, Marins, Ed G., Michel-Treil, Véronique, Simon, Christian O., Njoya, Merlin, Cornberg, Markus, Paxinos, Ellen, Manns, Michael P., Vermehren, Johannes, Sarrazin, Christoph, Sohn, Ji Yeon, Cho, Yunjung, Wedemeyer, Heiner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557192/
https://www.ncbi.nlm.nih.gov/pubmed/28835775
http://dx.doi.org/10.1177/1756283X17722745
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author Maasoumy, Benjamin
Bremer, Birgit
Lehmann, Patrick
Marins, Ed G.
Michel-Treil, Véronique
Simon, Christian O.
Njoya, Merlin
Cornberg, Markus
Paxinos, Ellen
Manns, Michael P.
Vermehren, Johannes
Sarrazin, Christoph
Sohn, Ji Yeon
Cho, Yunjung
Wedemeyer, Heiner
author_facet Maasoumy, Benjamin
Bremer, Birgit
Lehmann, Patrick
Marins, Ed G.
Michel-Treil, Véronique
Simon, Christian O.
Njoya, Merlin
Cornberg, Markus
Paxinos, Ellen
Manns, Michael P.
Vermehren, Johannes
Sarrazin, Christoph
Sohn, Ji Yeon
Cho, Yunjung
Wedemeyer, Heiner
author_sort Maasoumy, Benjamin
collection PubMed
description BACKGROUND: HBV DNA is the most important molecular marker in hepatitis B, used to determine treatment indication and monitoring. Most patients require lifelong hepatitis B virus (HBV) management, thus viral load (VL) monitoring may be performed at different laboratories, with different HBV assays, which may result in different VL results. This multicenter study compares the commutability and concordance of results from four different HBV DNA assays: CAP/CTM HBVv2, HPS/CTM HBVv2 and the new cobas 6800/8800 HBV and cobas 4800 HBV assays. METHODS: Across all four assays, HBV limit of detection (LoD) and linearity at lower concentrations were assessed using panels traceable to the World Health Organization international standard, and concordance was investigated at the important medical decision cutoffs 2000 and 20,000 IU/ml, using specimens from HBV-positive patients. RESULTS: The calculated LoD via a probit curve was 2.7 IU/ml for cobas 6800/8800 HBV, 2.8 IU/ml for cobas 4800 HBV, 9.6 IU/ml for CAP/CTM HBVv2, and 6.2 IU/ml for HPS/CTM HBVv2. The average accuracy was comparable between cobas 6800/8800 HBV, cobas 4800 HBV and CAP/CTM HBVv2 (0.04–0.05 log(10) IU/ml), while a slightly lower accuracy was documented for HPS/CTM HBVv2 (−0.16 log(10) IU/ml). A total of 211–245 clinical samples were used for a pairwise comparison. Mean paired log differences ranged from −0.17 log(10) IU/ml to −0.01 log(10) IU/ml. Coefficient of determination was over 98% for all pairs with high overall percent agreement at the 2000 and 20,000 IU/ml cutoffs (from 91.7% to 96.3%). In a subset of samples with VL±0.5 log(10) to the 2000 and 20,000 IU/ml thresholds, concordance was still 72% and 82%, respectively. CONCLUSIONS: The new cobas 6800/8800 HBV and 4800 HBV assays show high accuracy in samples with low-level viremia and a high concordance with the established HBV tests, CAP/CTM HBVv2 and HPS/CTM HBVv2, at 2000 and 20,000 IU/ml. Thus, all four HBV assays have high commutability and may be used interchangeably in routine clinical practice.
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spelling pubmed-55571922017-08-23 Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study Maasoumy, Benjamin Bremer, Birgit Lehmann, Patrick Marins, Ed G. Michel-Treil, Véronique Simon, Christian O. Njoya, Merlin Cornberg, Markus Paxinos, Ellen Manns, Michael P. Vermehren, Johannes Sarrazin, Christoph Sohn, Ji Yeon Cho, Yunjung Wedemeyer, Heiner Therap Adv Gastroenterol Original Research BACKGROUND: HBV DNA is the most important molecular marker in hepatitis B, used to determine treatment indication and monitoring. Most patients require lifelong hepatitis B virus (HBV) management, thus viral load (VL) monitoring may be performed at different laboratories, with different HBV assays, which may result in different VL results. This multicenter study compares the commutability and concordance of results from four different HBV DNA assays: CAP/CTM HBVv2, HPS/CTM HBVv2 and the new cobas 6800/8800 HBV and cobas 4800 HBV assays. METHODS: Across all four assays, HBV limit of detection (LoD) and linearity at lower concentrations were assessed using panels traceable to the World Health Organization international standard, and concordance was investigated at the important medical decision cutoffs 2000 and 20,000 IU/ml, using specimens from HBV-positive patients. RESULTS: The calculated LoD via a probit curve was 2.7 IU/ml for cobas 6800/8800 HBV, 2.8 IU/ml for cobas 4800 HBV, 9.6 IU/ml for CAP/CTM HBVv2, and 6.2 IU/ml for HPS/CTM HBVv2. The average accuracy was comparable between cobas 6800/8800 HBV, cobas 4800 HBV and CAP/CTM HBVv2 (0.04–0.05 log(10) IU/ml), while a slightly lower accuracy was documented for HPS/CTM HBVv2 (−0.16 log(10) IU/ml). A total of 211–245 clinical samples were used for a pairwise comparison. Mean paired log differences ranged from −0.17 log(10) IU/ml to −0.01 log(10) IU/ml. Coefficient of determination was over 98% for all pairs with high overall percent agreement at the 2000 and 20,000 IU/ml cutoffs (from 91.7% to 96.3%). In a subset of samples with VL±0.5 log(10) to the 2000 and 20,000 IU/ml thresholds, concordance was still 72% and 82%, respectively. CONCLUSIONS: The new cobas 6800/8800 HBV and 4800 HBV assays show high accuracy in samples with low-level viremia and a high concordance with the established HBV tests, CAP/CTM HBVv2 and HPS/CTM HBVv2, at 2000 and 20,000 IU/ml. Thus, all four HBV assays have high commutability and may be used interchangeably in routine clinical practice. SAGE Publications 2017-08-07 2017-08 /pmc/articles/PMC5557192/ /pubmed/28835775 http://dx.doi.org/10.1177/1756283X17722745 Text en © The Author(s), 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Maasoumy, Benjamin
Bremer, Birgit
Lehmann, Patrick
Marins, Ed G.
Michel-Treil, Véronique
Simon, Christian O.
Njoya, Merlin
Cornberg, Markus
Paxinos, Ellen
Manns, Michael P.
Vermehren, Johannes
Sarrazin, Christoph
Sohn, Ji Yeon
Cho, Yunjung
Wedemeyer, Heiner
Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title_full Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title_fullStr Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title_full_unstemmed Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title_short Commutability and concordance of four hepatitis B virus DNA assays in an international multicenter study
title_sort commutability and concordance of four hepatitis b virus dna assays in an international multicenter study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557192/
https://www.ncbi.nlm.nih.gov/pubmed/28835775
http://dx.doi.org/10.1177/1756283X17722745
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