Evaluation of impaired growth plate development of long bones in skeletally immature mice by antirheumatic agents

• DOI: 10.1002/jor.24819
• Publication Date: 2020-08-02T08:20:19Z
• Authors: Marjolein M. J. C...; Bert van Rietbergen; Tessy M. R. Caste...; Mirella J. J. Haa...; Lodewijk W. van R...; Tim J. M. Welting; Adhiambo M. A. Wi...
• Keywords: FOLINIC ACID; ENDOCHONDRAL BONE; MTX; MESENCHYMAL STEM-CELLS; Cell Line; Mice; 03 medical and health sciences; Naproxen; Osteogenesis; growth plate; naproxen; Animals; Cyclooxygenase Inhibitors; Growth Plate; JUVENILE IDIOPATHIC ARTHRITIS; JIA; Research Articles; 0303 health sciences; Cell Differentiation; COLLAGEN; Arthritis, Juvenile; Mice, Inbred C57BL; DIFFERENTIATION; endochondral ossification; Methotrexate; FINAL HEIGHT; Antirheumatic Agents; HIGH-DOSE METHOTREXATE; SHORT-TERM; Female; Chondrogenesis; NAPROXEN

AbstractRestriction of physical growth and development is a known problem in patients with juvenile idiopathic arthritis (JIA). However, the effect of medical treatment for JIA on skeletal growth in affected children has not been properly investigated. We, therefore, hypothesize that naproxen and methotrexate (MTX) affect endochondral ossification and will lead to reduced skeletal development. Treatment of ATDC5 cells, an in vitro model for endochondral ossification, with naproxen or MTX resulted in increased chondrogenic but decreased hypertrophic differentiation. In vivo, healthy growing C57BL/6 mice were treated with naproxen, MTX, or placebo for 10 weeks. At 15 weeks postnatal, both the length of the tibia and the length of the femur were significantly reduced in the naproxen‐ and MTX‐treated mice compared to their controls. Growth plate analysis revealed a significantly thicker proliferative zone, while the hypertrophic zone was significantly thinner in both experimental groups compared to their controls, comparable to the in vitro results. Micro‐computed tomography analysis of the subchondral bone region directly below the growth disc showed significantly altered bone microarchitecture in naproxen and MTX groups. In addition, the involvement of the PTHrP‐Ihh loop in naproxen‐ and MTX‐treated cells was shown. Overall, these results demonstrate that naproxen and MTX have a profound effect on endochondral ossification during growth plate development, abnormal subchondral bone morphology, and reduced bone length. A better understanding of how medication influences the development of the growth plate will improve understanding of endochondral ossification and reveal possibilities to improve the treatment of pediatric patients.