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成骨不全V型骨中的过度矿化和高骨细胞陷窝密度表明原发性骨形成旺盛。

Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation.

作者信息

Blouin Stéphane, Fratzl-Zelman Nadja, Glorieux Francis H, Roschger Paul, Klaushofer Klaus, Marini Joan C, Rauch Frank

机构信息

Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of WGKK and AUVA Trauma Centre, Meidling, 1st Medical Department Hanusch Hospital, Vienna, Austria.

Shriners Hospital for Children, Montreal, Quebec, Canada.

出版信息

J Bone Miner Res. 2017 Sep;32(9):1884-1892. doi: 10.1002/jbmr.3180. Epub 2017 Jun 26.

Abstract

In contrast to "classical" forms of osteogenesis imperfecta (OI) types I to IV, caused by a mutation in COL1A1/A2, OI type V is due to a gain-of-function mutation in the IFITM5 gene, encoding the interferon-induced transmembrane protein 5, or bone-restricted interferon-inducible transmembrane (IFITM)-like protein (BRIL). Its phenotype distinctly differs from OI types I to IV by absence of blue sclerae and dentinogenesis imperfecta, by the occurrence of ossification disorders such as hyperplastic callus and forearm interosseous membrane ossification. Little is known about the impact of the mutation on bone tissue/material level in untreated and bisphosphonate-treated patients. Therefore, investigations of transiliac bone biopsy samples from a cohort of OI type V children (n = 15, 8.7 ± 4 years old) untreated at baseline and a subset (n = 8) after pamidronate treatment (2.6 years in average) were performed. Quantitative backscattered electron imaging (qBEI) was used to determine bone mineralization density distribution (BMDD) as well as osteocyte lacunar density. The BMDD of type V OI bone was distinctly shifted toward a higher degree of mineralization. The most frequently occurring calcium concentration (CaPeak) in cortical (Ct) and cancellous (Cn) bone was markedly increased (+11.5%, +10.4%, respectively, p < 0.0001) compared to healthy reference values. Treatment with pamidronate resulted in only a slight enhancement of mineralization. The osteocyte lacunar density derived from sectioned bone area was elevated in OI type V Ct and Cn bone (+171%, p < 0.0001; +183.3%, p < 0.01; respectively) versus controls. The high osteocyte density was associated with an overall immature primary bone structure ("mesh-like") as visualized by polarized light microscopy. In summary, the bone material from OI type V patients is hypermineralized, similar to other forms of OI. The elevated osteocyte lacunar density in connection with lack of regular bone lamellation points to an exuberant primary bone formation and an alteration of the bone remodeling process in OI type V. © 2017 American Society for Bone and Mineral Research.

摘要

与由COL1A1/A2基因突变引起的I至IV型“经典”成骨不全症(OI)不同,V型OI是由IFITM5基因的功能获得性突变所致,该基因编码干扰素诱导跨膜蛋白5,即骨限制性干扰素诱导跨膜(IFITM)样蛋白(BRIL)。其表型与I至IV型OI明显不同,表现为无蓝色巩膜和牙本质发育不全,以及出现诸如增生性骨痂和前臂骨间膜骨化等骨化障碍。关于该突变在未经治疗和接受双膦酸盐治疗的患者中对骨组织/材料水平的影响,目前所知甚少。因此,我们对一组V型OI儿童(n = 15,平均年龄8.7±4岁)的髂骨活检样本进行了研究,这些儿童在基线时未接受治疗,其中一部分(n = 8)在接受帕米膦酸盐治疗(平均2.6年)后进行了研究。采用定量背散射电子成像(qBEI)来确定骨矿化密度分布(BMDD)以及骨细胞陷窝密度。V型OI骨的BMDD明显向更高矿化程度偏移。与健康参考值相比,皮质骨(Ct)和松质骨(Cn)中最常出现的钙浓度(CaPeak)显著升高(分别升高11.5%和10.4%,p < 0.0001)。帕米膦酸盐治疗仅导致矿化略有增强。与对照组相比,V型OI的Ct和Cn骨中,源自切片骨面积的骨细胞陷窝密度升高(分别升高171%,p < 0.0001;升高183.3%,p < 0.01)。通过偏光显微镜观察,高骨细胞密度与整体不成熟的初级骨结构(“网状”)相关。总之,V型OI患者的骨材料矿化过度,与其他形式的OI相似。骨细胞陷窝密度升高以及缺乏规则的骨板层,表明V型OI中初级骨形成旺盛且骨重塑过程发生改变。© 2017美国骨与矿物质研究学会。

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