Literature DB >> 30187275

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

Masafumi Kashii1, Sadaaki Kanayama2, Taichi Kitaoka3, Takahiro Makino2, Takashi Kaito2, Motoki Iwasaki2, Takuo Kubota3, Takehisa Yamamoto4, Keiichi Ozono3, Hideki Yoshikawa2.   

Abstract

The purpose of this study was to clarify the prevalence of scoliosis and determine risk factors for the development of scoliosis in young children with osteogenesis imperfecta (OI) who underwent intravenous pamidronate (PAM) therapy. Thirty-four young children with OI who had no scoliosis at the first PAM administration underwent cyclic PAM therapy alone. The medical records and radiographs of these patients were retrospectively reviewed. We examined the relationship between scoliosis (Cobb angle ≥ 10) and type of OI (Sillence classification: types I, III, and IV), physical mobility, Z-scores of bone mineral density in L2-4 of the lumbar spine (L2-4 BMD Z-scores), age of patients at first treatment with PAM, pelvic frontal tilt and leg-length discrepancy. The prevalence of scoliosis was 23.5% in 34 young children with OI who underwent PAM therapy for a mean of 4.2 years. Lower L2-4 BMD Z-scores, the presence of coronal and sagittal vertebral deformities and higher percentage of corrective osteotomy in the lower extremities were significant risk factors for the development of scoliosis. In patients with type III or IV OI, L2-4 BMD Z-scores were significantly lower (p = 0.02) and the percentage of patients who started PAM therapy in early childhood was significantly lower in scoliosis group than in the non-scoliosis group (p = 0.01). Development of scoliosis depends on the severity of OI and has a strong relationship with bone fragility even under PAM therapy. Starting intravenous PAM therapy in infancy or early childhood has a potential to prevent the occurrence and progression of scoliosis associated with bone fragility in young children with severe type III or IV OI.

Entities:  

Keywords:  Bisphosphonate; Osteogenesis imperfecta; Pamidronate; Scoliosis; Sillence classification

Mesh:

Substances:

Year:  2018        PMID: 30187275     DOI: 10.1007/s00774-018-0952-x

Source DB:  PubMed          Journal:  J Bone Miner Metab        ISSN: 0914-8779            Impact factor:   2.626


  3 in total

1.  CORR Insights®: Cardiopulmonary Status in Adults with Osteogenesis Imperfecta: Intrinsic Lung Disease May Contribute More Than Scoliosis.

Authors:  Paul Gerdhem
Journal:  Clin Orthop Relat Res       Date:  2020-12       Impact factor: 4.755

2.  Lumbar Scoliosis in Postmenopausal Women Increases with Age but is not Associated with Osteoporosis.

Authors:  Janet Rubin; Rebecca J Cleveland; Alexander Padovano; David Hu; Maya Styner; James Sanders
Journal:  J Endocr Soc       Date:  2021-02-15

3.  Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen.

Authors:  Peikai Chen; Zhijia Tan; Hiu Tung Shek; Jia-Nan Zhang; Yapeng Zhou; Shijie Yin; Zhongxin Dong; Jichun Xu; Anmei Qiu; Lina Dong; Bo Gao; Michael Kai Tsun To
Journal:  Front Genet       Date:  2022-01-28       Impact factor: 4.599

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.