Eruptive Process in Children with Osteogenesis Imperfecta
Clara Sandibel Garcete Delvalle1, M Joaquín De Nova García2, María Rosa Mourelle Martínez2
1Faculty of Dentistry, Complutense University of Madrid, Madrid, Spain. cgarcete@ucm.es.
Insights
Bisphosphonates (BPs) used for Osteogenesis Imperfecta (OI) in children may delay tooth development, root resorption, and permanent molar eruption. These effects, though often subtle, highlight the importance of monitoring dental health in OI patients undergoing BP treatment.
Area of Science:
- Pediatric Dentistry
- Orthodontics
- Genetics and Hereditary Diseases
Background:
- Osteogenesis Imperfecta (OI) is a genetic disorder causing bone fragility.
- Bisphosphonates (BPs) are used to increase bone density in children with OI.
- BPs are antiresorptive agents that can impact physiological processes involving osteoclasts, such as tooth eruption.
Purpose of the Study:
- To investigate the effects of bisphosphonate (BP) treatment on the eruptive process in children with Osteogenesis Imperfecta (OI).
- To compare dental development, primary tooth resorption, and first permanent molar eruption in children with OI on BPs versus a control group.
- To analyze the correlation between cumulative BP dosage and potential delays in dental development.
Main Methods:
- Retrospective analysis of panoramic radiographs from 34 children with OI on BPs and 367 healthy children.
- Utilized the Demirjian method for permanent tooth development assessment and the Haavikko method for primary tooth root resorption.
- Measured alveolar eruption of the first permanent molar and calculated cumulative BP dosage.
Main Results:
- Children with OI on BPs exhibited delayed dental development (0.95 points) and primary tooth exfoliation (1.31–1.66 years).
- A significant delay in primary tooth root resorption was observed (11.8% overall, varying by tooth type).
- Delayed alveolar eruption of the first permanent molar (0.31 years) was noted, with greater delays in those with higher cumulative BP doses (>2000).
Conclusions:
- Bisphosphonate therapy in children with OI can lead to clinically subtle but statistically significant delays in dental development and eruption.
- Primary tooth root resorption is also affected by BP treatment, indicating a broader impact on the dentition.
- Monitoring dental development and eruption is crucial for children with OI receiving bisphosphonate therapy, especially considering cumulative dosage.
Abstract:
Osteogenesis imperfecta (OI) is a hereditary disorder characterized by bone fragility and skeletal abnormalities. The administration of bisphosphonates (BPs) in children with OI increases bone density. This antiresorptive inhibits osteoclast action, thus altering physiological processes, in which osteoclasts play important roles, such as the eruptive process. The aim of this investigation was to study the eruptive process (dental development of permanent dentition, resorption of temporary dentition, and alveolar eruption of the first permanent molar) in children with OI medicated with BPs and to compare the results with those of a control group. In total, 34 panoramic radiographs of children with OI [mean chronological age of 8.43 (± 1.77)] who were medicated with BPs for a period of one year or more were studied and 367 panoramic radiographs of healthy children [mean chronological age of 9.19 (± 1.62)] were used as controls. The Demirjian method was used to study the dental development of the seven permanent teeth in the third quadrant. Alveolar eruption of the first permanent molar was considered when perforation of the alveolar bone was produced. The Haavikko method was used to study the root resorption of the five primary teeth in the third quadrant, and software (PixelStick®) was used to measure the lengths of the mesial and distal roots of the primary molars. The cumulative dose of BPs was obtained by mathematically calculating the total dosage received (mg)/weight (kg) and multiplying the relative potency of the medication. The Mann‒Whitney U test was used for comparisons, and p < 0.05 indicated statistical significance. A delay of 0.95 points in dental development and delayed exfoliation of primary dentition between 1.31 and 1.66 years were described in the study group. A root resorption delay of 11.8% was described among the 5 primary teeth of 23.3% among the single-rooted teeth and of 5.6% among the two-rooted teeth in children with OI medicated with BFs (p < 0.05). Delayed alveolar eruption of the first permanent molar at 0.31 years of age was found in children with OI medicated with BFs. We detected delayed tooth development at one stage of maturation in the study group, which was clinically imperceptible. The dental age (≤ 0.55 years) was greater than the chronological age in both groups. We also reported delayed exfoliation of the primary dentition (from 1.31 to 1.66 years), delayed root resorption of the primary dentition (11.8%), and delayed (from 1 mm to 1.25 mm) root resorption of the primary molars in the study group. Although the degree of dental development of the first permanent molar was similar between the two groups, we found delayed (0.31 years) alveolar eruption in the study group and a greater delay (0.44 years) in children whose cumulative dose of bisphosphonates exceeded 2000.
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