Literature DB >> 28212251

Serum Mast Cell Tryptase as a Marker of Posttraumatic Joint Contracture in a Rabbit Model.

Michaela Kopka1, Michael J Monument, A Dean Befus, Mei Zhang, David A Hart, Paul T Salo, Prism S Schneider, Cun-Yi Fan, Xiangdang Liang, Alexandra Garven, Kevin A Hildebrand.   

Abstract

OBJECTIVES: Mast cells have been identified as key mediators of posttraumatic joint contracture, and stabilizing medications (ketotifen) have been shown to decrease contracture severity. Serum mast cell tryptase (SMCT) levels are used clinically to monitor mast cell-mediated conditions. The goals of this study were to determine if SMCT levels are elevated in the setting of joint contracture, if they can be decreased in association with ketotifen therapy, and if they correlate with contracture severity.
METHODS: This study used a previously developed rabbit model in which 39 animals were divided into 4 groups: operatively created joint contracture (ORC, n = 13), operatively created contracture treated with ketotifen at 2 doses (KF0.5, n = 9; KF1.0, n = 9), and healthy rabbits (NC, n = 8). Range of motion measures were performed at 8 weeks after the surgery. Serum samples were collected on postoperative days 1, 3, 5, 7, 21, 35, and 49. SMCT levels were measured using a rabbit-specific enzyme-linked immunosorbent assay.
RESULTS: Levels of SMCT were highest in the operatively created joint contracture group and were significantly greater compared with both ketotifen groups (P < 0.001). Levels were highest at postoperative day 1 with a trend to decrease over time. A positive correlation between SMCT levels and contracture severity was observed in all operative groups (P < 0.05).
CONCLUSIONS: Levels of SMCT are elevated in the setting of joint contracture, decreased in association with ketotifen therapy, and positively correlated with contracture severity. This is the first study to establish a relationship between SMCT and joint injury. Measurement of SMCT may be valuable in identifying those at risk of posttraumatic joint contracture.

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Year:  2017        PMID: 28212251     DOI: 10.1097/BOT.0000000000000747

Source DB:  PubMed          Journal:  J Orthop Trauma        ISSN: 0890-5339            Impact factor:   2.512


  4 in total

1.  Biomechanical, histological, and molecular characterization of a new posttraumatic model of arthrofibrosis in rats.

Authors:  Aaron R Owen; Louis Dagneaux; Afton K Limberg; Jacob W Bettencourt; Banu Bayram; Brad Bolon; Daniel J Berry; Mark E Morrey; Joaquin Sanchez-Sotelo; Andre J van Wijnen; Matthew P Abdel
Journal:  J Orthop Res       Date:  2021-05-16       Impact factor: 3.494

2.  Post-traumatic stiff elbow.

Authors:  Lars Adolfsson
Journal:  EFORT Open Rev       Date:  2018-05-21

3.  Anti-fibrotic effects of the antihistamine ketotifen in a rabbit model of arthrofibrosis.

Authors:  Meagan E Tibbo; Afton K Limberg; Christopher G Salib; Travis W Turner; Alex R McLaury; Anthony G Jay; Jacob W Bettencourt; Jodi M Carter; Brad Bolon; Daniel J Berry; Mark E Morrey; Joaquin Sanchez-Sotelo; Andre J van Wijnen; Matthew P Abdel
Journal:  Bone Joint Res       Date:  2020-07-23       Impact factor: 5.853

4.  An in vivo rabbit joint injury model to measure trauma-induced coagulopathy and the effect of timing of administration of ketotifen fumarate on posttraumatic joint contracture.

Authors:  Daniel You; Nadia Maarouf; Kevin Hildebrand; Andrea Soo; Prism Schneider
Journal:  OTA Int       Date:  2022-03-10
  4 in total

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