Periodontal Challenges in Orthodontics:

Bone Loss, Tooth Mobility, and Interdisciplinary Approaches.

Authors

DOI:

https://doi.org/10.36557/2009-3578.2025v11n2p2818-2830

Keywords:

Orthodontics, Periodontal disease, Alveolar bone loss, Tooth mobility, Osteoimmunology

Abstract

Orthodontic treatment in adult patients has become increasingly common, but it remains a clinical challenge when associated with alveolar bone loss and tooth mobility, conditions frequently observed in individuals with a history of periodontitis or systemic impairment. Unlike younger patients, whose bone response is more predictable, adults with reduced periodontal support are at higher risk of resorption, dehiscence, and long-term instability. This review aimed to analyze biological, systemic, and clinical aspects related to orthodontic treatment in patients with alveolar bone loss and tooth mobility, highlighting recent evidence on osteoimmunology, systemic conditions, adjuvant therapies, and regenerative strategies. A narrative literature review was carried out, including experimental and clinical studies published in recent years that investigated periodontal response, systemic influences, biological mediators, and long-term outcomes in orthodontic patients with compromised alveolar bone. Evidence shows that alveolar bone remodeling during orthodontic tooth movement is strongly influenced by immune-mediated mechanisms. Osteoimmunology studies have demonstrated that cytokines, osteocyte necroptosis, and Th17/Treg modulation by periodontal ligament cells are central to bone resorption and formation. Systemic conditions such as aging and diabetes negatively affect periodontal homeostasis, while metabolic influences, such as thermogenic supplements, exacerbate bone loss through the RANK/RANKL/OPG pathway. Adjuvant therapies, including parathyroid hormone, recombinant Irisin, Semaphorin 3A, and natural compounds like Chroogomphus rutilus, have shown protective effects in experimental models. Clinically, regenerative strategies such as autologous dentin matrix grafts and long-term evidence in agenesis cases demonstrate that orthodontic tooth movement can promote stable bone formation, preserving alveolar ridge architecture.Orthodontic treatment in patients with alveolar bone loss and tooth mobility is feasible, provided it is performed under strict periodontal control, light and individualized forces, and interdisciplinary management. Advances in biological knowledge, pharmacological modulation, and regenerative approaches expand the possibilities for safe and predictable orthodontic care in compromised patients.

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References

ALGHAMDI, B. et al. Osteoimmunology in periodontitis and orthodontic tooth movement. Current Osteoporosis Reports, v. 21, n. 2, p. 128-146, abr. 2023. DOI: https://doi.org/10.1007/s11914-023-00774-x.

CAVALCANTE, G. R. G. et al. Thermogenic preworkout supplement induces alveolar bone loss in a rat model of tooth movement via RANK/RANKL/OPG pathway. Brazilian Oral Research, v. 38, p. e131, dez. 2024. DOI: https://doi.org/10.1590/1807-3107bor-2024.vol38.0131.

FERREIRA, C. L. et al. Periodontal response to orthodontic tooth movement in diabetes-induced rats with or without periodontal disease. Journal of Periodontology, v. 89, n. 3, p. 341-350, mar. 2018. DOI: https://doi.org/10.1002/JPER.17-0190.

FIGUEIREDO, N. C. et al. Deletion of kinin receptor B2 enhances orthodontic tooth movement and alveolar bone remodeling. PLoS One, v. 20, n. 2, p. e0318436, fev. 2025. DOI: https://doi.org/10.1371/journal.pone.0318436.

LIN, J. et al. Periodontal ligament cells under mechanical force regulate local immune homeostasis by modulating Th17/Treg cell differentiation. Clinical Oral Investigations, v. 26, n. 4, p. 3747-3764, abr. 2022. DOI: https://doi.org/10.1007/s00784-021-04346-0.

MAREK, I.; NOVÁČKOVÁ, S.; KUČERA, J. Agenesis of maxillary lateral incisors: Bone formation by orthodontic tooth movement and long-term stability of the edentulous alveolar ridge at 12–15 years after treatment. American Journal of Orthodontics and Dentofacial Orthopedics, v. 167, n. 4, p. 464-472, abr. 2025. DOI: https://doi.org/10.1016/j.ajodo.2024.11.007.

MIAO, Y. et al. Impact of frontier development of alveolar bone grafting on orthodontic tooth movement. Frontiers in Bioengineering and Biotechnology, v. 10, p. 869191, jun. 2022. DOI: https://doi.org/10.3389/fbioe.2022.869191.

OHORI, F. et al. Osteocyte necroptosis drives osteoclastogenesis and alveolar bone resorption during orthodontic tooth movement. Scientific Reports, v. 15, n. 1, p. 19413, jun. 2025. DOI: https://doi.org/10.1038/s41598-025-04697-8.

OUYANG, L. et al. Comparison of clinical efficacy between autologous partially demineralized dentin matrix and deproteinized bovine bone mineral for bone augmentation in orthodontic patients with alveolar bone deficiency: a randomized controlled clinical trial. BMC Oral Health, v. 24, n. 1, p. 984, ago. 2024. DOI: https://doi.org/10.1186/s12903-024-04730-8.

RAMOS, A. L. et al. Bone dehiscence formation during orthodontic tooth movement through atrophic alveolar ridges. Angle Orthodontist, v. 90, n. 3, p. 321-329, maio 2020. DOI: https://doi.org/10.2319/063019-443.1.

RIZK, M. et al. Periodontal ligament and alveolar bone remodeling during long orthodontic tooth movement analyzed by a novel user-independent 3D-methodology. Scientific Reports, v. 13, n. 1, p. 19919, nov. 2023. DOI: https://doi.org/10.1038/s41598-023-47386-0.

SATOMI, K.; NISHIMURA, K.; IGARASHI, K. Semaphorin 3A protects against alveolar bone loss during orthodontic tooth movement in mice with periodontitis. Journal of Periodontal Research, v. 57, n. 5, p. 991-1002, out. 2022. DOI: https://doi.org/10.1111/jre.13038.

WU, S. et al. Recombinant Irisin protects against alveolar bone destruction during orthodontic tooth movement. Inflammation, v. 46, n. 3, p. 1106-1117, jun. 2023. DOI: https://doi.org/10.1007/s10753-023-01797-3.

ZHANG, C. et al. Parathyroid hormone increases alveolar bone homoeostasis during orthodontic tooth movement in rats with periodontitis via crosstalk between STAT3 and β-catenin. International Journal of Oral Science, v. 12, n. 1, p. 38, dez. 2020. DOI: https://doi.org/10.1038/s41368-020-00104-2.

ZHANG, Y. et al. Age-related alveolar bone maladaptation in adult orthodontics: finding new ways out. International Journal of Oral Science, v. 16, n. 1, p. 52, ago. 2024. DOI: https://doi.org/10.1038/s41368-024-00319-7.

ZHOU, Y. et al. Chroogomphus rutilus regulates bone metabolism to prevent periodontal bone loss during orthodontic tooth movement in osteoporotic rats. Nutrients, v. 15, n. 23, p. 4906, nov. 2023. DOI: https://doi.org/10.3390/nu15234906.

Published

2025-09-13

How to Cite

de Castro e Silva, A. L., Vera Santos Gumert, J., Menezes de Oliveira, K. R., Dias Chaves Campos de Amaral, E., Barbosa da Silva, D., Castro Costa, J., … Nascimento Lemos Cavanha , N. (2025). Periodontal Challenges in Orthodontics:: Bone Loss, Tooth Mobility, and Interdisciplinary Approaches . INTERFERENCE: A JOURNAL OF AUDIO CULTURE, 11(2), 2818–2830. https://doi.org/10.36557/2009-3578.2025v11n2p2818-2830

Issue

Section

Literature Review