File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.jot.2022.12.006
- Scopus: eid_2-s2.0-85146063918
- PMID: 36721766
- WOS: WOS:000923229200001
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: The effect of drug holiday on preventing medication-related osteonecrosis of the jaw in osteoporotic rat model
Title | The effect of drug holiday on preventing medication-related osteonecrosis of the jaw in osteoporotic rat model |
---|---|
Authors | |
Keywords | Bisphosphonate Bone turnover Drug holiday Medication-related osteonecrosis of the jaw Osteoclast Osteoporosis |
Issue Date | 10-Jan-2023 |
Publisher | Elsevier |
Citation | Journal of Orthopaedic Translation, 2023, v. 39, p. 55-62 How to Cite? |
Abstract | Background: Medication-related osteonecrosis of the jaw (MRONJ) is a severe complication associated with antiresorptive medications managing osteoporosis, such as bisphosphonates (BPs). To date, there is very limited evidence from prospective, controlled studies to support or refute the controversial prevention regimen that if a discontinuation of BPs before dentoalveolar surgery, so called "drug holiday", is effective in reducing the risk of MRONJ development in patients with osteoporosis. We proposed an experimental animal study, aiming to investigate the prevention of MRONJ following tooth extractions in osteoporotic condition, with the implementation of a BP drug holiday. Methods: Twenty rats were subjected to bilateral ovariectomy. After establishing the osteoporotic condition, all rats were exposed to weekly injections of zoledronate acid (ZA) for 8 weeks. After ZA treatment, 10 rats were subjected to dental extraction and defined as control group, and the rest 10 rats assigned to the DH group had a drug holiday of 8 weeks prior to dental extraction. Eight weeks after the dentoalveolar surgery, bone turnover biomarker in serum, occurrence of MRONJ-like lesion and histomorphometric assessment of osteonecrosis in mandible, and bone microarchitecture indices in femur, were examined. Results: Eight weeks after dental extraction, the DH group showed a recovered osteoclastic activity, indicated by significantly increased number of osteoclasts in the mandibles and serum level of C-terminal telopeptides of type I collagen, as compared to the control group. No significant differences were observed in the gross-view and histological occurrences of MRONJ-like lesions between the two groups. There was no significant difference in bone microarchitecture in the femur between the control and DH groups before ZA therapy and 8 weeks after dental extraction. Conclusion: Our data provided the first experimental evidence in the osteoporotic animal model that the implementation of a BP holiday in prior to dental extractions could partially recover osteoclastic activity, but could not alleviate the development of MRONJ-like lesion or exacerbate the osteoporotic condition in the femur. Longerterm drug holiday, or combination of drug holiday and other prophylaxes to prevent MRONJ in patients with osteoporosis could be worth exploring in future studies, to pave the way for clinical managements. The translational potential of this article: This in vivo prospective study reported that a recovery of osteoclastic activity by a BP drug holiday for 8 weeks in osteoporosis rats did not alleviate the development of MRONJ-like lesion followed by dental extractions. It contributes to the understanding of regimens to prevent MRONJ. |
Persistent Identifier | http://hdl.handle.net/10722/337599 |
ISSN | 2023 Impact Factor: 5.9 2023 SCImago Journal Rankings: 1.259 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhu, WY | - |
dc.contributor.author | Yang, WF | - |
dc.contributor.author | Wang, LL | - |
dc.contributor.author | Lan, XM | - |
dc.contributor.author | Tao, ZY | - |
dc.contributor.author | Guo, JX | - |
dc.contributor.author | Xu, JK | - |
dc.contributor.author | Qin, L | - |
dc.contributor.author | Su, YX | - |
dc.date.accessioned | 2024-03-11T10:22:25Z | - |
dc.date.available | 2024-03-11T10:22:25Z | - |
dc.date.issued | 2023-01-10 | - |
dc.identifier.citation | Journal of Orthopaedic Translation, 2023, v. 39, p. 55-62 | - |
dc.identifier.issn | 2214-031X | - |
dc.identifier.uri | http://hdl.handle.net/10722/337599 | - |
dc.description.abstract | Background: Medication-related osteonecrosis of the jaw (MRONJ) is a severe complication associated with antiresorptive medications managing osteoporosis, such as bisphosphonates (BPs). To date, there is very limited evidence from prospective, controlled studies to support or refute the controversial prevention regimen that if a discontinuation of BPs before dentoalveolar surgery, so called "drug holiday", is effective in reducing the risk of MRONJ development in patients with osteoporosis. We proposed an experimental animal study, aiming to investigate the prevention of MRONJ following tooth extractions in osteoporotic condition, with the implementation of a BP drug holiday. Methods: Twenty rats were subjected to bilateral ovariectomy. After establishing the osteoporotic condition, all rats were exposed to weekly injections of zoledronate acid (ZA) for 8 weeks. After ZA treatment, 10 rats were subjected to dental extraction and defined as control group, and the rest 10 rats assigned to the DH group had a drug holiday of 8 weeks prior to dental extraction. Eight weeks after the dentoalveolar surgery, bone turnover biomarker in serum, occurrence of MRONJ-like lesion and histomorphometric assessment of osteonecrosis in mandible, and bone microarchitecture indices in femur, were examined. Results: Eight weeks after dental extraction, the DH group showed a recovered osteoclastic activity, indicated by significantly increased number of osteoclasts in the mandibles and serum level of C-terminal telopeptides of type I collagen, as compared to the control group. No significant differences were observed in the gross-view and histological occurrences of MRONJ-like lesions between the two groups. There was no significant difference in bone microarchitecture in the femur between the control and DH groups before ZA therapy and 8 weeks after dental extraction. Conclusion: Our data provided the first experimental evidence in the osteoporotic animal model that the implementation of a BP holiday in prior to dental extractions could partially recover osteoclastic activity, but could not alleviate the development of MRONJ-like lesion or exacerbate the osteoporotic condition in the femur. Longerterm drug holiday, or combination of drug holiday and other prophylaxes to prevent MRONJ in patients with osteoporosis could be worth exploring in future studies, to pave the way for clinical managements. The translational potential of this article: This in vivo prospective study reported that a recovery of osteoclastic activity by a BP drug holiday for 8 weeks in osteoporosis rats did not alleviate the development of MRONJ-like lesion followed by dental extractions. It contributes to the understanding of regimens to prevent MRONJ. | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Journal of Orthopaedic Translation | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Bisphosphonate | - |
dc.subject | Bone turnover | - |
dc.subject | Drug holiday | - |
dc.subject | Medication-related osteonecrosis of the jaw | - |
dc.subject | Osteoclast | - |
dc.subject | Osteoporosis | - |
dc.title | The effect of drug holiday on preventing medication-related osteonecrosis of the jaw in osteoporotic rat model | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.jot.2022.12.006 | - |
dc.identifier.pmid | 36721766 | - |
dc.identifier.scopus | eid_2-s2.0-85146063918 | - |
dc.identifier.volume | 39 | - |
dc.identifier.spage | 55 | - |
dc.identifier.epage | 62 | - |
dc.identifier.eissn | 2214-031X | - |
dc.identifier.isi | WOS:000923229200001 | - |
dc.publisher.place | AMSTERDAM | - |
dc.identifier.issnl | 2214-031X | - |