Visualizing Cortical Pore Space Constituents

可视化皮质孔隙空间成分

• 批准号: 8585475
• 负责人: GALATEIA J KAZAKIA
• 金额: $ 6.21万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-16 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8585475
• 关键词: Accounting; Address; Age; Automobile Driving; Biological; Biomechanics; Blood Vessels; Chronic; Data; Data Set; Development; Discrimination; Disease; Elderly; Endothelial Cells; Fatty acid glycerol esters; Fracture; Future; Goals; Hematopoietic; Hip Fractures; Histology; Hormones; Image; Imagery; Imaging Techniques; Immobilization; Incidence; Individual; Infiltration; Intervention; Investigation; Kidney; Longitudinal Studies; Magnetic Resonance; Magnetic Resonance Imaging; Marrow; Mechanics; Mesenchymal Stem Cells; Metabolic; Neck; Nutrient Canals; Osteon; Parathyroid gland; Patients; Peripheral; Populations at Risk; Porosity; Postmenopause; Process; Property; Reproducibility; Research; Resolution; Site; Skeleton; Stimulus; Techniques; Time; Vascularization; Water; Woman; Work; X-Ray Computed Tomography; age related; bone; bone quality; bone strength; bone turnover; cohort; combat; experience; follow-up; improved; in vivo; osteoporosis with pathological fracture; prevent; public health relevance; response; skeletal; stem cell differentiation; tibia

DESCRIPTION (provided by applicant): Cortical bone strength is critical to skeletal integrity. Cortical microstructure, in particular porosity, has a significant impact on mechanical properties of the cortex. Additionally, cortical bone microstructure is responsive to disease, therapy, and metabolic alterations. Therefore the investigation of cortical microstructure is an important aspect of understanding biological, pathoetiological, and biomechanical processes occurring within the skeleton. The mechanisms driving increased cortical porosity are unknown. Our central hypothesis is that cortical pore space contents may be an indicator of pore expansion mechanisms. Marrow within a pore may indicate endocortical 'trabecularization', or an expansion of the marrow cavity into the cortical envelope. Vessel and hematopoietic components within pore space may indicate the formation of large pores via merging or expansion of the vascular network. In the long term, characterizing pore space constituents and understanding pore expansion mechanisms may aid in the development of strategies to prevent or reverse increased porosity and the associated bone fragility. The overall goal of this research is to develop a technique for in vivo visualization and quantification of cortical porosity and por content, and to apply this technique to a longitudinal data set. We will characterize pore content using in vivo imaging techniques, specifically high resolution peripheral quantitative computed tomography (HR-pQCT) and magnetic resonance (MR) imaging. HR-pQCT enables 3D visualization of cortical microstructure. MR provides 3D visualization and discrimination of fat and water components. The specific aims are to: I) develop and verify pore space content characterization by combined HR-pQCT and MR imaging and II) quantify longitudinal changes in porosity and pore space content by combined HR-pQCT and MR imaging. To address Aim I, combined HR-pQCT and MR analysis will be applied using both conventional and advanced MR techniques in cadaveric tibiae. Histological analysis will be performed to confirm the composition of pore space contents in regions determined by imaging to contain marrow fat and vascular components. To address Aim II, an existing longitudinal data set will be analyzed and longitudinal changes in porosity and distribution of marrow fat and vascular components within the cortical pore space will be quantified. This work will develop in vivo characterization of cortical pore constituents in a longitudinal setting, and will provide pilot data on advanced imaging techniques for future in vivo studies investigating mechanisms of increased cortical porosity. The identification of mechanisms of increased cortical porosity will direct the development of targeted treatments, possibly through osteoblastogenic or anti-angiogenic therapy.

描述（由申请人提供）：皮质骨强度对骨骼完整性至关重要。皮质微观结构，特别是孔隙率，对皮质的机械性能有显著影响。此外，皮质骨微结构对疾病、治疗和代谢改变有反应。因此，皮质微结构的研究是了解骨骼内发生的生物学、病理学和生物力学过程的一个重要方面。导致皮质孔隙率增加的机制尚不清楚。我们的中心假设是，皮质孔隙内容物可能是孔隙扩张机制的一个指标。孔内的骨髓可能表明皮质内“小梁化”，或骨髓腔扩张到皮质包膜内。孔隙空间内的血管和造血成分可指示通过血管网络的合并或扩张形成大孔隙。从长远来看，表征孔隙空间成分和理解孔隙扩张机制可能有助于制定预防或逆转孔隙率增加和相关骨脆性的策略。本研究的总体目标是开发一种技术，在体内可视化和定量的皮质孔隙度和por含量，并将此技术应用于纵向数据集。我们将使用体内成像技术，特别是高分辨率外周定量计算机断层扫描（HR-pQCT）和磁共振（MR）成像来表征孔隙含量。HR-pQCT能够实现皮质微结构的3D可视化。MR提供脂肪和水成分的3D可视化和辨别。具体目标是：I）通过组合HR-pQCT和MR成像开发和验证孔隙含量表征，和II）通过组合HR-pQCT和MR成像量化孔隙率和孔隙含量的纵向变化。为了解决目标I，将使用传统和先进的MR技术对尸体胫骨进行HR-pQCT和MR联合分析。将进行组织学分析，以确认通过成像确定含有骨髓脂肪和血管成分的区域中孔隙内容物的组成。为了解决目标II，将分析现有的纵向数据集，并量化皮质孔隙空间内骨髓脂肪和血管成分的孔隙率和分布的纵向变化。这项工作将开发在体内表征的皮质孔成分在纵向设置，并将提供先进的成像技术，为未来的体内研究调查机制增加皮质孔隙度的试点数据。皮质孔隙率增加的机制的确定将指导靶向治疗的发展，可能通过成骨细胞或抗血管生成治疗。