Pamidronate Affects the Mandibular Cortex of Children with Osteogenesis Imperfecta

Author:

Apolinário A.C.1,Figueiredo P.T.2,Guimarães A.T.3,Acevedo A.C.4,Castro L.C.5,Paula A.P.6,Paula L.M.4,Melo N.S.7,Leite A.F.2

Affiliation:

1. Campus Universitário Darcy Ribeiro, University of Brasília, Brasília, Brazil

2. Oral Radiology, Department of Dentistry, Faculty of Health Science, Campus Universitário Darcy Ribeiro, University of Brasília, Brasília, Brazil

3. Biostatistics, Biological Sciences Department, State University of West Paraná, Cascavel, Paraná, Brazil

4. Oral Care Center for Inherited Diseases, Department of Dentistry, Faculty of Health Science, Campus Universitário Darcy Ribeiro, University of Brasília, Brasília, Brazil

5. Endocrinology, University of Brasília’s Hospital, L2 Norte, Brasília, Brazil

6. Hospital de Base of Federal District, Brasília, Brazil

7. Oral Pathology, Department of Dentistry, Faculty of Health Science, Campus Universitário Darcy Ribeiro, University of Brasília, Brasília, Brazil

Abstract

We hypothesized that mandibular cortical width (MCW) is smaller in children with osteogenesis imperfecta (OI) than in healthy children and that pamidronate can improve the cortical mandibular thickness. The aim of this study was to assess changes in the MCW on dental panoramic radiographs (DPRs) of children with normal bone mineral density (BMD) and with OI. We also compared the MCW of children with different types of OI regarding the number of pamidronate cycles and age at the beginning of treatment. MCW measurements were retrospectively obtained from 197 DPRs of 66 children with OI types I, III, and IV who were in treatment with a comparable dosage of cyclical intravenous pamidronate between 2007 and 2013. The control group had 92 DPRs from normal BMD children. Factorial analysis of variance was used to compare MCW measurements among different age groups and between sexes and also to compare MCW measurements of children with different types of OI among different pamidronate cycles and age at the beginning of treatment. No significant differences in results were found between male and female subjects in both OI and healthy children, so they were evaluated altogether (P > 0.05). There was an increase of MCW values related to aging in all normal BMD and OI children but on a smaller scale in children with OI types I and III. Children with OI presented lower mean MCW values than did children with normal BMD at the beginning of treatment (P < 0.05). A linear model estimated the number of pamidronate cycles necessary to achieve mean MCW values equivalent to those of healthy children. The thinning of the mandibular cortex depended on the number of pamidronate cycles, the type of OI, and the age at the beginning of treatment. DPRs could thus provide a way to identify cyclic pamidronate treatment outcomes in patients with OI.

Publisher

SAGE Publications

Subject

General Dentistry

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