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ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy

INTRODUCTION: Osteoarthritis (OA) and haemophilic arthropathy (HA) are clinically similar, but pathologically distinct conditions which result in joint pain and loss of function. Distinguishing their disease mechanisms is therefore a key step in the development of curative therapy, as opposed to cur...

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Autores principales: Kalebota, Natasa, Salai, Grgur, Peric, Porin, Hrkac, Stela, Novak, Rudjer, Durmis, Kristina Kovac, Grgurevic, Lovorka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544250/
https://www.ncbi.nlm.nih.gov/pubmed/35536550
http://dx.doi.org/10.1111/hae.14569
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author Kalebota, Natasa
Salai, Grgur
Peric, Porin
Hrkac, Stela
Novak, Rudjer
Durmis, Kristina Kovac
Grgurevic, Lovorka
author_facet Kalebota, Natasa
Salai, Grgur
Peric, Porin
Hrkac, Stela
Novak, Rudjer
Durmis, Kristina Kovac
Grgurevic, Lovorka
author_sort Kalebota, Natasa
collection PubMed
description INTRODUCTION: Osteoarthritis (OA) and haemophilic arthropathy (HA) are clinically similar, but pathologically distinct conditions which result in joint pain and loss of function. Distinguishing their disease mechanisms is therefore a key step in the development of curative therapy, as opposed to current symptomatic treatments. A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) 4 is a metzincin‐family member proteoglycan with known local involvement in OA pathogenesis. AIM: To investigate the potential differences and discriminatory potential of ADAMTS‐4 between OA and HA patients. METHODS: We determined ADAMTS‐4 plasma concentrations by ELISA in patients with HA and OA. This pilot cross‐sectional study included N = 40 male participants equally divided across four subgroups: haemophilia patients with severe or mild HA and control subjects with severe or mild/no OA. RESULTS: Our study showed a striking elevation in plasma ADAMTS‐4 expression levels in HA patients as compared to OA, as well as an increase in patients with severe as compared to mild HA. By performing the binomial logistical analysis and fitting the receiver–operator curve (ROC) (cut‐off probability .5), ADAMTS‐4 had a sensitivity of 95% and specificity of 50% in discriminating between HA and OA among our study participants. CONCLUSION: Uncovering the marked differences in plasma levels of ADAMTS‐4 in patients with HA versus OA potentially sheds new light on the mechanisms of HA pathogenesis and could foster more research into the roles ADAMTS‐4 and other matrix metalloproteinases (MMPs) play in HA versus OA.
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spelling pubmed-95442502022-10-14 ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy Kalebota, Natasa Salai, Grgur Peric, Porin Hrkac, Stela Novak, Rudjer Durmis, Kristina Kovac Grgurevic, Lovorka Haemophilia Original Articles INTRODUCTION: Osteoarthritis (OA) and haemophilic arthropathy (HA) are clinically similar, but pathologically distinct conditions which result in joint pain and loss of function. Distinguishing their disease mechanisms is therefore a key step in the development of curative therapy, as opposed to current symptomatic treatments. A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) 4 is a metzincin‐family member proteoglycan with known local involvement in OA pathogenesis. AIM: To investigate the potential differences and discriminatory potential of ADAMTS‐4 between OA and HA patients. METHODS: We determined ADAMTS‐4 plasma concentrations by ELISA in patients with HA and OA. This pilot cross‐sectional study included N = 40 male participants equally divided across four subgroups: haemophilia patients with severe or mild HA and control subjects with severe or mild/no OA. RESULTS: Our study showed a striking elevation in plasma ADAMTS‐4 expression levels in HA patients as compared to OA, as well as an increase in patients with severe as compared to mild HA. By performing the binomial logistical analysis and fitting the receiver–operator curve (ROC) (cut‐off probability .5), ADAMTS‐4 had a sensitivity of 95% and specificity of 50% in discriminating between HA and OA among our study participants. CONCLUSION: Uncovering the marked differences in plasma levels of ADAMTS‐4 in patients with HA versus OA potentially sheds new light on the mechanisms of HA pathogenesis and could foster more research into the roles ADAMTS‐4 and other matrix metalloproteinases (MMPs) play in HA versus OA. John Wiley and Sons Inc. 2022-05-10 2022-07 /pmc/articles/PMC9544250/ /pubmed/35536550 http://dx.doi.org/10.1111/hae.14569 Text en © 2022 The Authors. Haemophilia published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Kalebota, Natasa
Salai, Grgur
Peric, Porin
Hrkac, Stela
Novak, Rudjer
Durmis, Kristina Kovac
Grgurevic, Lovorka
ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title_full ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title_fullStr ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title_full_unstemmed ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title_short ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
title_sort adamts‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544250/
https://www.ncbi.nlm.nih.gov/pubmed/35536550
http://dx.doi.org/10.1111/hae.14569
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