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Serological CTX-II does not measure the same as urinary CTX-II

OBJECTIVE: Type II collagen is the most abundant protein of articular cartilage. The urinary cross-linked C-terminal telopeptide of type II collagen (uCTX-II) is a matrix metalloproteinase (MMP) cleaved fragment and may be the most well-validated biomarker in osteoarthritis. The aim was to develop a...

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Autores principales: Luo, Yunyun, He, Yi, Karsdal, Morten, Bay-Jensen, Anne-Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718164/
https://www.ncbi.nlm.nih.gov/pubmed/36474683
http://dx.doi.org/10.1016/j.ocarto.2020.100082
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author Luo, Yunyun
He, Yi
Karsdal, Morten
Bay-Jensen, Anne-Christine
author_facet Luo, Yunyun
He, Yi
Karsdal, Morten
Bay-Jensen, Anne-Christine
author_sort Luo, Yunyun
collection PubMed
description OBJECTIVE: Type II collagen is the most abundant protein of articular cartilage. The urinary cross-linked C-terminal telopeptide of type II collagen (uCTX-II) is a matrix metalloproteinase (MMP) cleaved fragment and may be the most well-validated biomarker in osteoarthritis. The aim was to develop a serological immunoassay of CTX-II (sCTX-II) and evaluated both sCTX-II and uCTX-II levels in a cross-sectional osteoarthritis cohort. METHODS: The biological relevance of sCTX-II was validated in bovine cartilage explants cultured in the presence of Oncostatin M and tumor necrosis factor alpha (OT) or OT supplemented with GM6001 for 3 weeks. Serum and urine samples from an osteoarthritis cohort were assayed using sCTX-II and uCTX-II, respectively. Spearman's correlation was performed to evaluate the correlation between sCTX-II and uCTX-II. The association between the level of biomarkers and clinical variables was also investigated. RESULTS: The supernatant analyzed in sCTX-II showed significant higher CTX-II levels in the end phases of explant culture compared to the vehicle group. The release of CTX-II was completely suppressed by GM6001. The sCTX-II levels in serum were not associated with uCTX-II in urine although sCTX-II levels in urine were significantly correlated with uCTX-II. uCTX-II correlated with age and gender while sCTX-II did not. sCTX-II cannot demonstrate any clinical relevance in a cross-sectional OA cohort as uCTX-II did. CONCLUSION: The sCTX-II assay can reflect the MMP-mediated type II collagen degradation in bovine cartilage explants. However, sCTX-II and uCTX-II assays show different patterns suggesting the presence of CTX-II in blood may be different from that of urine.
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spelling pubmed-97181642022-12-05 Serological CTX-II does not measure the same as urinary CTX-II Luo, Yunyun He, Yi Karsdal, Morten Bay-Jensen, Anne-Christine Osteoarthr Cartil Open ORIGINAL PAPER OBJECTIVE: Type II collagen is the most abundant protein of articular cartilage. The urinary cross-linked C-terminal telopeptide of type II collagen (uCTX-II) is a matrix metalloproteinase (MMP) cleaved fragment and may be the most well-validated biomarker in osteoarthritis. The aim was to develop a serological immunoassay of CTX-II (sCTX-II) and evaluated both sCTX-II and uCTX-II levels in a cross-sectional osteoarthritis cohort. METHODS: The biological relevance of sCTX-II was validated in bovine cartilage explants cultured in the presence of Oncostatin M and tumor necrosis factor alpha (OT) or OT supplemented with GM6001 for 3 weeks. Serum and urine samples from an osteoarthritis cohort were assayed using sCTX-II and uCTX-II, respectively. Spearman's correlation was performed to evaluate the correlation between sCTX-II and uCTX-II. The association between the level of biomarkers and clinical variables was also investigated. RESULTS: The supernatant analyzed in sCTX-II showed significant higher CTX-II levels in the end phases of explant culture compared to the vehicle group. The release of CTX-II was completely suppressed by GM6001. The sCTX-II levels in serum were not associated with uCTX-II in urine although sCTX-II levels in urine were significantly correlated with uCTX-II. uCTX-II correlated with age and gender while sCTX-II did not. sCTX-II cannot demonstrate any clinical relevance in a cross-sectional OA cohort as uCTX-II did. CONCLUSION: The sCTX-II assay can reflect the MMP-mediated type II collagen degradation in bovine cartilage explants. However, sCTX-II and uCTX-II assays show different patterns suggesting the presence of CTX-II in blood may be different from that of urine. Elsevier 2020-06-08 /pmc/articles/PMC9718164/ /pubmed/36474683 http://dx.doi.org/10.1016/j.ocarto.2020.100082 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle ORIGINAL PAPER
Luo, Yunyun
He, Yi
Karsdal, Morten
Bay-Jensen, Anne-Christine
Serological CTX-II does not measure the same as urinary CTX-II
title Serological CTX-II does not measure the same as urinary CTX-II
title_full Serological CTX-II does not measure the same as urinary CTX-II
title_fullStr Serological CTX-II does not measure the same as urinary CTX-II
title_full_unstemmed Serological CTX-II does not measure the same as urinary CTX-II
title_short Serological CTX-II does not measure the same as urinary CTX-II
title_sort serological ctx-ii does not measure the same as urinary ctx-ii
topic ORIGINAL PAPER
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718164/
https://www.ncbi.nlm.nih.gov/pubmed/36474683
http://dx.doi.org/10.1016/j.ocarto.2020.100082
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