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成骨不全症患儿早期双膦酸盐治疗后牙齿形成异常。

Abnormalities in Tooth Formation after Early Bisphosphonate Treatment in Children with Osteogenesis Imperfecta.

机构信息

Department of Dental Medicine, Division of Orthodontics and Pediatric Dentistry, Karolinska Institutet, POB 4046, 141 04, Huddinge, Sweden.

Developmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

出版信息

Calcif Tissue Int. 2021 Aug;109(2):121-131. doi: 10.1007/s00223-021-00835-2. Epub 2021 Mar 20.


DOI:10.1007/s00223-021-00835-2
PMID:33743023
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8273054/
Abstract

Treatment with intravenous bisphosphonate (BP) in children and adolescents with osteogenesis imperfecta (OI) started in Sweden in 1991. No human studies on the role of BP therapy in development of disturbances in tooth mineralization or tooth morphology have been published. The study cohort comprised 219 individuals who were divided into four groups: group 1, BP treatment onset before 2 years of age (n = 22); group 2, BP treatment onset between 2 and 6 years of age (n = 20); group 3, BP treatment onset between 6 and 10 years of age (n = 13); and a control group of patients with OI who had not received BP therapy (n = 164). The chi-square test was used in between-group comparisons of the prevalence of tooth agenesis. The prevalence of tooth agenesis was significantly higher in children who began BP treatment before the age of 2 years (group 1; 59%,) compared to the controls (10%; p < 0.001) and to children who had begun BP therapy between ages 2 and 6 years (group 2; 10%; p = 0.009) or between ages 6 and 10 years (group 3; 8%; p = 0.003). Different types of disturbances in the enamel formation were seen in 52 premolars, where 51 were seen in those who began BP treatment before the age of 2 years. To conclude, starting BP treatment before the age of 2 years increases the risk of abnormalities in tooth formation manifesting as morphological aberrations, tooth agenesis, and enamel defects.

摘要

在瑞典,1991 年开始对患有成骨不全症(OI)的儿童和青少年进行静脉用双膦酸盐(BP)治疗。目前尚未发表任何关于 BP 治疗在牙齿矿化或牙齿形态发育障碍中的作用的人体研究。该研究队列包括 219 名个体,他们分为四组:组 1,BP 治疗开始于 2 岁之前(n=22);组 2,BP 治疗开始于 2 至 6 岁之间(n=20);组 3,BP 治疗开始于 6 至 10 岁之间(n=13);和一个未接受 BP 治疗的 OI 患者对照组(n=164)。采用卡方检验比较各组间牙齿缺失的发生率。与对照组(10%)和 2 至 6 岁之间开始 BP 治疗的儿童(组 2;10%)相比,2 岁以下开始 BP 治疗的儿童(组 1;59%)牙齿缺失的发生率显著更高(p<0.001),与 6 至 10 岁之间开始 BP 治疗的儿童(组 3;8%)相比也更高(p=0.003)。在 52 颗前磨牙中观察到不同类型的釉质形成障碍,其中 51 颗在前 2 岁开始接受 BP 治疗的患者中发现。总之,2 岁以下开始 BP 治疗会增加牙齿形成异常的风险,表现为形态异常、牙齿缺失和釉质缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/5800d2a92a20/223_2021_835_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/2738105c3755/223_2021_835_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/56a7f77fa47a/223_2021_835_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/a9302ac8044b/223_2021_835_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/5800d2a92a20/223_2021_835_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/2738105c3755/223_2021_835_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/56a7f77fa47a/223_2021_835_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/a9302ac8044b/223_2021_835_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1de/8273054/5800d2a92a20/223_2021_835_Fig4_HTML.jpg

相似文献

[1]
Abnormalities in Tooth Formation after Early Bisphosphonate Treatment in Children with Osteogenesis Imperfecta.

Calcif Tissue Int. 2021-8

[2]
Bisphosphonate Therapy and Tooth Development in Children and Adolescents with Osteogenesis Imperfecta.

Calcif Tissue Int. 2020-8

[3]
Timing of dental development in osteogenesis imperfecta patients with and without bisphosphonate treatment.

Bone. 2017-1

[4]
Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy.

J Bone Miner Metab. 2018-9-5

[5]
Cranial base pathology in pediatric osteogenesis imperfecta patients treated with bisphosphonates.

J Neurosurg Pediatr. 2015-3

[6]
Effects of bisphosphonates on tooth eruption in children with osteogenesis imperfecta.

Eur J Oral Sci. 2008-6

[7]
Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.

Bone. 2016-5

[8]
Pain and quality of life of children and adolescents with osteogenesis imperfecta over a bisphosphonate treatment cycle.

Eur J Pediatr. 2018-4-11

[9]
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Osteoporos Int. 2017-7-9

[10]
Intravenous Bisphosphonate Therapy of Young Children With Osteogenesis Imperfecta: Skeletal Findings During Follow Up Throughout the Growing Years.

J Bone Miner Res. 2015-12

引用本文的文献

[1]
Orthodontics in Pediatric Osteoporosis: A Narrative Literature Review.

Children (Basel). 2025-5-28

[2]
Investigation of oral health findings and genotype correlations in osteogenesis imperfecta.

Odontology. 2024-12-15

[3]
Dental Abnormalities in Osteogenesis Imperfecta: A Systematic Review.

Calcif Tissue Int. 2024-11

[4]
A Narrative Review of the Association between Dental Abnormalities and Chemotherapy.

J Clin Med. 2024-8-22

[5]
A standard set of outcome measures for the comprehensive assessment of oral health and occlusion in individuals with osteogenesis imperfecta.

Orphanet J Rare Dis. 2024-8-13

[6]
Root resorption of primary molars and dental development of premolars in children with Osteogenesis Imperfecta medicated with bisphosphonates, grouped according to age and gender.

BMC Oral Health. 2024-7-28

[7]
Dental anomalies in individuals with osteogenesis imperfecta: a systematic review and meta-analysis of prevalence and comparative studies.

J Appl Oral Sci. 2023

[8]
Effects of antiresorptive medications on tooth root formation and tooth eruption in paediatric patients.

Orthod Craniofac Res. 2023-12

[9]
Pamidronate Therapy Increases Trabecular Bone Complexity of Mandibular Condyles in Individuals with Osteogenesis Imperfecta.

Calcif Tissue Int. 2022-3

[10]
Missing and unerupted teeth in osteogenesis imperfecta.

Bone. 2021-9

本文引用的文献

[1]
Bisphosphonate Therapy and Tooth Development in Children and Adolescents with Osteogenesis Imperfecta.

Calcif Tissue Int. 2020-8

[2]
Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta.

Orphanet J Rare Dis. 2020-3-31

[3]
Prevalence of Premolars with Dens Evaginatus in a Taiwanese and Spanish Population and Related Complications of the Fracture of its Tubercle.

Eur Endod J. 2018-7-19

[4]
Nosology and classification of genetic skeletal disorders: 2019 revision.

Am J Med Genet A. 2019-10-21

[5]
Consensus guidelines on the use of bisphosphonate therapy in children and adolescents.

J Paediatr Child Health. 2018-3

[6]
Osteogenesis imperfecta.

Nat Rev Dis Primers. 2017-8-18

[7]
Health-Related Quality of Life in Adults with Osteogenesis Imperfecta.

Calcif Tissue Int. 2017-7-4

[8]
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.

PLoS One. 2017-5-12

[9]
Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.

Oral Dis. 2017-1

[10]
A Rare Case of Type III Dens Invaginatus in a Mandibular Second Premolar and Its Nonsurgical Endodontic Management by Using Cone-beam Computed Tomography: A Case Report.

J Endod. 2016-4

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