BONEMATCH · Bone Multi-modal Automated Trabecular Histomorphometry
FP7 — People (Marie Curie Actions)
- Duration
- 2012-05-15 → 2014-05-14
- EU contribution
- €183,606
- Participants
- 1
- Scheme
- MC-IEF
Lines connect the coordinator with its partners.
Results in brief
Bone Multi-modal Automated Trabecular Histomorphometry
Bone Multi-modal Automated Trabecular Histomorphometry (BoneMATCH) aimed atinvestigating bone microarchitecture changes using high-resolution peripheral quantitative computed tomography (HRpQCT), and at discovering relationships between patterns of change and clinical factors such as aging, disease and organ transplantation. The project was motivated by the long-term goal of developing a non-invasion “virtual bone biopsy” which enables clinical evaluation of bone microarchitecture through in-vivo imaging. BoneMATCH serves as a platform for developing clinical image analysis algorithms using state-of-the-art research imaging techniques such microCT and HRpQCT, and then migrating those techniques into clinical imaging such as MDCT through validation on patient cohorts. In this context, BoneMATCH made significant advances in serveral directions. 1. Data acquisition towards a multi-scale parallel corpus of bone microarchitecture Data used for BoneMATCH was sourced using a combination of HRpQCT images from patient cohorts, healthy volunteers, and cadaver specimens. Additionally, we imaged cadaver specimens using micro CT (µCT), HR-pQCT as well as clinical multi-detector CT (MDCT). We implemented highly-accurate registration methods to align these data, and the resulting parallel corpus of imaging data covers bone microarchitecture from the scale of 4 microns to corresponding clinical imaging data. This corpus is the basis for multi-scale, multi-modal image analysis, and algorithm development and validation. 2. Algorithm development to capture changing bone microarchitecture Following data acquisition, the focus of BoneMATCH was on algorithm development and integration for the purpose of developing and validating advanced clinical analysis methods in bone imaging. These methods included 3D texture-based trabecular bone quality assessment, localized longitudinal assessment of bone microarchitecture changes, dictionary learning for denoising and super resolution of HRpQCT images, and spatio-temporal mapping of clinical and microstructural parameters to localized bone microarchitectural changes. Results from BoneMATCH include clinical validation of 3D texture-based trabecular bone quality maps (BQMs) in a cohort of lung transplant recipients. The BQM has been developed to provide radiologists and clinicians with information about bone microarchitecture which goes beyond bone mineral density (BMD), the gold standard for bone health, particularly in cases where images with similar BMD scores have a noticeably different structural appearance. 3. Super-resolution and denoising: briding scales and modalities As a specific focus the BoneMATCH project has explored the use of compressed sensing and sparse signal reconstruction to apply denoising and super-resolution in HRpQCT imaging. 4. Clinically applicable algorithms and concise visualization of bone microarchitecture change Finally, in order to enable the use of BoneMATCH methods in a research- and clinical context it has introduced the concept of the “bone morphogram”, a method for quantifying and visualizing bone microstructural changes which goes beyond the clinical gold standard of comparing BMD, cortical porosity and other summary values between time points. BoneMATCH has produced a collection of software tools for continued research into bone microarchitectural assessment, as well as for establishing standards for advanced clinical quantitative imaging for bone health. The CIR lab at the Medical University of Vienna is actively working with internal and external collaborators to validate and expand on BoneMATCH algorithms on various patient cohorts, and to facilitate the continued use of the tools by the research community. Through these follow-on studies to correlate our techniques with clinical and biomechanical parameters, the research conducted during BoneMATCH should lead to better fracture risk assessment, more detailed analysis of drug therapy response in osteoporosis and other bone diseases, as well as a reduction in radiation exposure to patients through image enhancement and advanced quantitative assessment.
Data: CORDIS, © European Union
Project objective
Osteoporosis is defined as a state of low bone density with underlying alterations in bone microarchitecture leading to an increased fracture risk. The incidence of osteoporosis is rising globally and produces increasing costs to national health care systems since osteoporotic patients are prone to low trauma fractures. Osteoporotic fractures are not only a matter of decreased bone density, but are also associated with alterations in the microarchitecture of the trabecular structure within the bone due to dynamic processes of bone rebuilding and resorption. In clinical practice, histomorphometric analysis of iliac crest biopsies is the current method of reference in the assessment of bone microarchitecture. Bone biopsy, however, is an invasive procedure which allows a limited number of follow-ups while providing limited information about the larger scale bone micro-architecture. Micro computed tomography (microCT) and very recently High-resolution peripheral quantitative computed tomography (HR-pQCT) have enriched bone research by enabling a three-dimensional approach to bone imaging. A particular feature of HR-pQCT is the possibility to acquire high resolution in vivo images, thereby allowing for follow-up observations. At present, however, the resolution of HR-pQCT does not allow for direct inference of the cellular and re-modeling processes within the bone. The goal of this project is to bridge the gap between bone microarchitecture and local re-modeling processes of bone resorption and rebuilding by developing methods for detection of osteoclastic sites and eroded trabecular surfaces in microCT, and ultimately HR-pQCT images through multi-modal analysis using to bone histology images. Such detection will have a clinical impact by improving the ability to target therapy and drugs based on the underlying nature of the disease. In addition, localization of these sites could be used to improve biological bone models at the cellular, tissue, and structural levels.""
Original text from CORDIS.
Participants
- MEDIZINISCHE UNIVERSITAET WIEN · WienCoordinatorAustria
Links
Data: CORDIS, © European Union
