SH Ho Scoliosis Research Laboratory, Department of Orthopaedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.
Joint Scoliosis Research Center of the Chinese University of Hong Kong and Nanjing University, The Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.
Sci Rep. 2017 Jan 5;7:40265. doi: 10.1038/srep40265.
Adolescent idiopathic scoliosis is a complex disease with unclear etiopathogenesis. Systemic and persistent low bone mineral density is an independent prognostic factor for curve progression. The fundamental question of how bone quality is affected in AIS remains controversy because there is lack of site-matched control for detailed analysis on bone-related parameters. In this case-control study, trabecular bone biopsies from iliac crest were collected intra-operatively from 28 severe AIS patients and 10 matched controls with similar skeletal and sexual maturity, anthropometry and femoral neck BMD Z-score to control confounding effects. In addition to static histomorphometry, micro-computed tomography (μCT) and real time-PCR (qPCR) analyses, individual trabecula segmentation (ITS)-based analysis, finite element analysis (FEA), energy dispersive X-ray spectroscopy (EDX) were conducted to provide advanced analysis of structural, mechanical and mineralization features. μCT and histomorphometry showed consistently reduced trabecular number and connectivity. ITS revealed predominant change in trabecular rods, and EDX confirmed less mineralization. The structural and mineralization abnormality led to slight reduction in apparent modulus, which could be attributed to differential down-regulation of Runx2, and up-regulation of Spp1 and TRAP. In conclusion, this is the first comprehensive study providing direct evidence of undefined unique pathological changes at different bone hierarchical levels in AIS.
青少年特发性脊柱侧凸是一种病因不明的复杂疾病。系统性和持续性低骨密度是脊柱侧凸进展的独立预后因素。骨骼质量如何受到 AIS 影响的根本问题仍然存在争议,因为缺乏针对骨相关参数的详细分析的位点匹配对照。在这项病例对照研究中,我们从 28 名严重 AIS 患者和 10 名具有相似骨骼和性成熟度、人体测量学和股骨颈 BMD Z 评分的匹配对照者的髂嵴术中采集了小梁骨活检。除了静态组织形态计量学外,还进行了微计算机断层扫描(μCT)和实时 PCR(qPCR)分析、基于个体小梁分割(ITS)的分析、有限元分析(FEA)、能谱分析(EDX),以提供结构、力学和矿化特征的高级分析。μCT 和组织形态计量学显示小梁数量和连通性持续减少。ITS 显示小梁杆的主要变化,EDX 证实矿化减少。结构和矿化异常导致表观模量略有降低,这可能归因于 Runx2 的差异下调和 Spp1 和 TRAP 的上调。总之,这是第一项提供 AIS 不同骨层次结构定义不明确的独特病理变化的直接证据的综合研究。