A 2026 animal study published in the Journal of Periodontology investigated how altered testosterone levels affect orthodontic tooth movement (OTM), alveolar bone remodeling, periodontal tissues, and root resorption.
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The study provides experimental evidence that testosterone-related disturbances may influence the tissues involved in orthodontic tooth movement. However, because the research was conducted in rats, the findings cannot be directly applied to human orthodontic treatment.
🔹 Study Design
The researchers used a pubertal male rat model to investigate the effects of testosterone dysfunction during orthodontic tooth movement.
Testosterone deficiency was induced through orchiectomy. The researchers subsequently administered testosterone undecanoate, an anabolic-androgenic steroid (AAS), at replacement and high doses.
Orthodontic tooth movement was produced by applying a closed-coil spring to the maxillary right first molar. The surrounding alveolar bone and periodontal ligament were evaluated at 5 and 10 days after orthodontic force application.
The investigators used several analytical methods, including micro-computed tomography (micro-CT), reverse-transcription quantitative polymerase chain reaction (RT-qPCR), and immunohistochemistry. Root resorption and plasma concentrations of testosterone and adrenocorticotropic hormone were also evaluated.
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Both testosterone deficiency and high-dose AAS exposure produced significant changes in bone microarchitecture.
The researchers reported reductions in trabecular thickness and bone connectivity, together with changes involving bone lacunae.
These findings indicate that altered testosterone conditions affected the alveolar bone response during the experimental orthodontic procedure.
The study also found that testosterone dysfunction was associated with greater rotation and intrusion of the orthodontically moved tooth. These observations were obtained from the animal model and should not be interpreted as evidence that testosterone manipulation produces predictable changes in the rate or direction of orthodontic tooth movement in humans.
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One of the clinically relevant findings involved inflammatory changes and root resorption.
According to the study, high-dose AAS exposure intensified the inflammatory infiltrate and root resorption associated with orthodontic tooth movement.
Root resorption is a biological consequence that can occur during orthodontic tooth movement. In this experimental model, the researchers found that high-dose androgen exposure was associated with a greater resorptive response.
The study therefore identifies a potential relationship between androgen disturbance and orthodontically induced tissue changes. However, it does not establish that anabolic-androgenic steroid use causes clinically significant root resorption in human orthodontic patients.
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The investigators also examined molecular markers associated with bone metabolism.
Testosterone dysfunction altered the expression of several genes, including:
▪️ Runx2
▪️ Bmp2
▪️ Spp1
▪️ Bglap
The study also identified deregulation of the RANK/RANKL/OPG pathway following testosterone disturbances.
These molecular findings provide additional evidence that altered testosterone conditions affected biological pathways involved in bone remodeling during orthodontic tooth movement.
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An important finding was that administration of AAS at replacement doses did not normalize the inflammatory infiltrate, orthodontic tooth movement, or the expression of the studied genes to control levels.
Therefore, the experimental response observed in testosterone-deficient animals was not simply reversed by testosterone administration at the replacement dose used in the study.
This finding suggests that the biological effects associated with testosterone disturbance were not completely restored under the experimental conditions evaluated.
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The study provides evidence that testosterone dysfunction can influence several biological processes associated with orthodontic tooth movement, including:
▪️ alveolar bone microarchitecture;
▪️ periodontal inflammatory response;
▪️ tooth movement characteristics;
▪️ root resorption; and
▪️ expression of genes involved in bone metabolism.
However, the study does not establish a clinical protocol for modifying testosterone levels during orthodontic treatment.
It also does not demonstrate that testosterone supplementation can accelerate orthodontic treatment or that testosterone deficiency necessarily causes slower tooth movement in humans.
The experimental findings should therefore be interpreted as evidence of a biological relationship that requires further investigation.
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The principal limitation is the experimental model.
The study was conducted in pubertal male rats, and orthodontic tooth movement was produced experimentally using a closed-coil spring on a maxillary first molar. The observation periods were limited to 5 and 10 days.
Human orthodontic treatment differs substantially from this experimental model in anatomy, skeletal development, treatment duration, biomechanics, hormonal physiology, and clinical management.
Consequently, the findings cannot currently be used to predict how an individual human patient will respond to orthodontic treatment based on testosterone levels.
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The 2026 study by Reis et al. provides experimental evidence that testosterone dysfunction can modify bone remodeling, periodontal inflammation, orthodontic tooth movement, and root resorption in a pubertal male rat model.
Both testosterone deficiency and high-dose anabolic-androgenic steroid exposure produced alterations in alveolar bone microarchitecture. High-dose AAS exposure was additionally associated with increased inflammatory infiltration and root resorption, while testosterone disturbances affected several genes and signaling pathways involved in bone metabolism.
These findings expand the experimental understanding of systemic hormonal influences on orthodontic tooth movement. Nevertheless, human clinical studies are required before the findings can be translated into orthodontic treatment recommendations.
📚 References
Reis, C. L. B., Galisteu-Luiz, K., Pedroso, G. L., Puls, G. L., Cassaro, L., Vieira, B. B., Lourenço Romano, F., Küchler, E. C., Kirschneck, C., de Oliveira, D. S. B., Stuani, M. B. S., & Matsumoto, M. A. N. (2026). Effects of testosterone and high-dose anabolic steroids on orthodontic-induced bone remodeling and root resorption: An animal study. Journal of Periodontology. Advance online publication. https://doi.org/10.1002/jper.70068
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