Improvement of bone properties in children with osteogenesis imperfecta after pamidronate: a bone biopsy study.

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM JBMR Plus Pub Date : 2024-12-11 eCollection Date: 2025-02-01 DOI:10.1093/jbmrpl/ziae161
Delphine Farlay, Mathilde Cornier, Sébastien Rizzo, Valérie Cormier-Daire, Maelle Charpié, Graziella Pinto, Hina Simonnet, Isabelle Badoud, Maude Gerbaix, Pascale Chavassieux, Roland Chapurlat
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Abstract

OI, or bone brittle disease, is characterized by increased mineralization of bone matrix independently of clinical severity. So, a beneficial effect of antiresorptive treatments such as bisphosphonates (BP) is questionable. We aim to compare the bone matrix characteristics before and after BP pamidronate (PAM). Fifty-eight children (9 ± 5 yr-old) with OI (Type I, III, IV, V, VI, XI, or unknown) received intravenous PAM for 2 yr and underwent transiliac bone biopsies before (n = 57) and after (n = 35) treatment. Compared with age-matched controls, untreated OI was characterized by cortical and cancellous rarefaction. Two years of PAM in OI patients significantly decreased bone remodeling activity, increased cortical thickness, improved the maturation of both organic and mineral matrix, and most of the nanomechanical properties, despite further increase in the degree of mineralization. Overall, in addition to a gain in bone mass, our results showed for the first time that PAM is able to increase the maturation of mineral crystals and collagen matrix contributing to its antifracture efficacy in OI patients.

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帕米膦酸钠后成骨不全儿童骨特性的改善:一项骨活检研究。
成骨不全或骨脆性疾病的特征是骨基质矿化增加,与临床严重程度无关。因此,抗吸收治疗如双磷酸盐(BP)的有益效果是值得怀疑的。我们的目的是比较帕米膦酸BP (PAM)前后的骨基质特征。58例(9±5岁)成骨不全(I、III、IV、V、VI、XI或未知型)患儿接受静脉注射PAM治疗2年,治疗前(n = 57)和治疗后(n = 35)分别行经髂骨活检。与年龄匹配的对照组相比,未经治疗的成骨不全以皮质和松质疏松为特征。在成骨不全患者中,尽管矿化程度进一步增加,但两年的PAM显著降低了骨重塑活性,增加了皮质厚度,改善了有机和矿物基质的成熟度,以及大多数纳米力学性能。总的来说,除了增加骨量外,我们的研究结果首次表明,PAM能够促进矿物晶体和胶原基质的成熟,有助于其在成骨不全患者中的抗骨折疗效。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
期刊最新文献
Correction to: Management of multiple vertebral fractures during lactation in a patient with osteogenesis imperfecta type I following twin delivery. Special Collection on Rare Musculoskeletal Diseases 2024. Successful treatment of adult cherubism with a 60 mg denosumab 6-monthly regimen. Unraveling melorheostosis: insights into clinical features, diagnosis, and treatment. Improvement of bone properties in children with osteogenesis imperfecta after pamidronate: a bone biopsy study.
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