Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia

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Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia. / Manon-Jensen, T.; Karsdal, M. A.; Nielsen, L. N.; Kjelgaard-Hansen, M.; Vandahl, B.; Olsen, E. H.N.; Enoksson, M.; Roepstorff, K.

I: Journal of Thrombosis and Haemostasis, Bind 14, Nr. 12, 01.12.2016, s. 2419-2429.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Manon-Jensen, T, Karsdal, MA, Nielsen, LN, Kjelgaard-Hansen, M, Vandahl, B, Olsen, EHN, Enoksson, M & Roepstorff, K 2016, 'Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia', Journal of Thrombosis and Haemostasis, bind 14, nr. 12, s. 2419-2429. https://doi.org/10.1111/jth.13518

APA

Manon-Jensen, T., Karsdal, M. A., Nielsen, L. N., Kjelgaard-Hansen, M., Vandahl, B., Olsen, E. H. N., Enoksson, M., & Roepstorff, K. (2016). Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia. Journal of Thrombosis and Haemostasis, 14(12), 2419-2429. https://doi.org/10.1111/jth.13518

Vancouver

Manon-Jensen T, Karsdal MA, Nielsen LN, Kjelgaard-Hansen M, Vandahl B, Olsen EHN o.a. Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia. Journal of Thrombosis and Haemostasis. 2016 dec. 1;14(12):2419-2429. https://doi.org/10.1111/jth.13518

Author

Manon-Jensen, T. ; Karsdal, M. A. ; Nielsen, L. N. ; Kjelgaard-Hansen, M. ; Vandahl, B. ; Olsen, E. H.N. ; Enoksson, M. ; Roepstorff, K. / Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia. I: Journal of Thrombosis and Haemostasis. 2016 ; Bind 14, Nr. 12. s. 2419-2429.

Bibtex

@article{6fa53ee7276e40e49490392d0a1b431a,
title = "Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia",
abstract = "Essentials Joint bleeding in hemophilia may induce significant remodeling of the extracellular matrix. Biomarkers of collagen turnover were investigated in a F8−/− rat model of hemophilic arthropathy. Biomarkers of cartilage degradation increased significantly during development of arthropathy. Basement membrane and interstitial matrix turnover changed significantly following hemarthrosis. Summary: Background Hemophilic arthropathy is a severe complication of hemophilia. It is caused by recurrent bleeding into joint cavities, which leads to synovial inflammation, fibrosis, cartilage degradation and bone remodeling. Extracellular matrix remodeling of affected tissues is a hallmark of these pathological processes. Objectives The aim of this study was to use serological biomarkers of collagen turnover to evaluate extracellular matrix remodeling in a factor VIII-deficient rat model of hemophilic arthropathy. Methods F8−/− rats and wild-type littermate controls were subjected to repeated knee bleeds induced by needle puncture on days 0 and 14. Development of arthropathy was confirmed by histology after termination on day 28. Serum samples were collected at baseline and throughout the study and analyzed for biomarkers of collagen turnover, including collagens of the basement membrane (type IV collagen), the interstitial matrix (collagen types III, V and VI) and cartilage (type II collagen). Results In F8−/− rats, induced knee bleeding and subsequent development of arthropathy caused significant alterations in collagen turnover, measured as changes in serological biomarkers of basement membrane turnover, interstitial matrix turnover and cartilage degradation. Biomarkers of type II collagen degradation correlated significantly with cartilage degradation and degree of arthropathy. Hemophilic rats had a 50% higher turnover of the basement membrane than wild-type littermates at baseline. Conclusions Joint bleeding and hemophilic arthropathy cause changes in turnover of extracellular matrix collagens in hemophilic rats. Biomarkers of collagen turnover may be used to monitor joint bleeding and development of blood-induced joint disease in hemophilia.",
keywords = "basement membrane, cartilage, extracellular matrix, hemarthrosis, matrix metalloproteinases",
author = "T. Manon-Jensen and Karsdal, {M. A.} and Nielsen, {L. N.} and M. Kjelgaard-Hansen and B. Vandahl and Olsen, {E. H.N.} and M. Enoksson and K. Roepstorff",
note = "Publisher Copyright: {\textcopyright} 2016 International Society on Thrombosis and Haemostasis",
year = "2016",
month = dec,
day = "1",
doi = "10.1111/jth.13518",
language = "English",
volume = "14",
pages = "2419--2429",
journal = "Journal of Thrombosis and Haemostasis",
issn = "1538-7933",
publisher = "Wiley-Blackwell",
number = "12",

}

RIS

TY - JOUR

T1 - Altered collagen turnover in factor VIII-deficient rats with hemophilic arthropathy identifies potential novel serological biomarkers in hemophilia

AU - Manon-Jensen, T.

AU - Karsdal, M. A.

AU - Nielsen, L. N.

AU - Kjelgaard-Hansen, M.

AU - Vandahl, B.

AU - Olsen, E. H.N.

AU - Enoksson, M.

AU - Roepstorff, K.

N1 - Publisher Copyright: © 2016 International Society on Thrombosis and Haemostasis

PY - 2016/12/1

Y1 - 2016/12/1

N2 - Essentials Joint bleeding in hemophilia may induce significant remodeling of the extracellular matrix. Biomarkers of collagen turnover were investigated in a F8−/− rat model of hemophilic arthropathy. Biomarkers of cartilage degradation increased significantly during development of arthropathy. Basement membrane and interstitial matrix turnover changed significantly following hemarthrosis. Summary: Background Hemophilic arthropathy is a severe complication of hemophilia. It is caused by recurrent bleeding into joint cavities, which leads to synovial inflammation, fibrosis, cartilage degradation and bone remodeling. Extracellular matrix remodeling of affected tissues is a hallmark of these pathological processes. Objectives The aim of this study was to use serological biomarkers of collagen turnover to evaluate extracellular matrix remodeling in a factor VIII-deficient rat model of hemophilic arthropathy. Methods F8−/− rats and wild-type littermate controls were subjected to repeated knee bleeds induced by needle puncture on days 0 and 14. Development of arthropathy was confirmed by histology after termination on day 28. Serum samples were collected at baseline and throughout the study and analyzed for biomarkers of collagen turnover, including collagens of the basement membrane (type IV collagen), the interstitial matrix (collagen types III, V and VI) and cartilage (type II collagen). Results In F8−/− rats, induced knee bleeding and subsequent development of arthropathy caused significant alterations in collagen turnover, measured as changes in serological biomarkers of basement membrane turnover, interstitial matrix turnover and cartilage degradation. Biomarkers of type II collagen degradation correlated significantly with cartilage degradation and degree of arthropathy. Hemophilic rats had a 50% higher turnover of the basement membrane than wild-type littermates at baseline. Conclusions Joint bleeding and hemophilic arthropathy cause changes in turnover of extracellular matrix collagens in hemophilic rats. Biomarkers of collagen turnover may be used to monitor joint bleeding and development of blood-induced joint disease in hemophilia.

AB - Essentials Joint bleeding in hemophilia may induce significant remodeling of the extracellular matrix. Biomarkers of collagen turnover were investigated in a F8−/− rat model of hemophilic arthropathy. Biomarkers of cartilage degradation increased significantly during development of arthropathy. Basement membrane and interstitial matrix turnover changed significantly following hemarthrosis. Summary: Background Hemophilic arthropathy is a severe complication of hemophilia. It is caused by recurrent bleeding into joint cavities, which leads to synovial inflammation, fibrosis, cartilage degradation and bone remodeling. Extracellular matrix remodeling of affected tissues is a hallmark of these pathological processes. Objectives The aim of this study was to use serological biomarkers of collagen turnover to evaluate extracellular matrix remodeling in a factor VIII-deficient rat model of hemophilic arthropathy. Methods F8−/− rats and wild-type littermate controls were subjected to repeated knee bleeds induced by needle puncture on days 0 and 14. Development of arthropathy was confirmed by histology after termination on day 28. Serum samples were collected at baseline and throughout the study and analyzed for biomarkers of collagen turnover, including collagens of the basement membrane (type IV collagen), the interstitial matrix (collagen types III, V and VI) and cartilage (type II collagen). Results In F8−/− rats, induced knee bleeding and subsequent development of arthropathy caused significant alterations in collagen turnover, measured as changes in serological biomarkers of basement membrane turnover, interstitial matrix turnover and cartilage degradation. Biomarkers of type II collagen degradation correlated significantly with cartilage degradation and degree of arthropathy. Hemophilic rats had a 50% higher turnover of the basement membrane than wild-type littermates at baseline. Conclusions Joint bleeding and hemophilic arthropathy cause changes in turnover of extracellular matrix collagens in hemophilic rats. Biomarkers of collagen turnover may be used to monitor joint bleeding and development of blood-induced joint disease in hemophilia.

KW - basement membrane

KW - cartilage

KW - extracellular matrix

KW - hemarthrosis

KW - matrix metalloproteinases

UR - http://www.scopus.com/inward/record.url?scp=84998673665&partnerID=8YFLogxK

U2 - 10.1111/jth.13518

DO - 10.1111/jth.13518

M3 - Journal article

C2 - 27681457

AN - SCOPUS:84998673665

VL - 14

SP - 2419

EP - 2429

JO - Journal of Thrombosis and Haemostasis

JF - Journal of Thrombosis and Haemostasis

SN - 1538-7933

IS - 12

ER -

ID: 345682904