A Multiscale Framework Based on the Physiome Markup Languages for Exploring the Initiation of Osteoarthritis at the Bone-Cartilage Interface

被引:18
作者
Shim, Vickie B. [1 ]
Hunter, Peter J. [1 ]
Pivonka, Peter [2 ]
Fernandez, Justin W. [1 ]
机构
[1] Auckland Bioengn Inst, Auckland 1010, New Zealand
[2] Univ Western Australia, Sch Comp Sci & Software Engn, Perth, WA 6009, Australia
关键词
Cartilage; finite elements (FEs); multiscale; osteoarthritis (OA); INTEGRATION; PROTEINS; SYSTEM; ORGANS; MODEL;
D O I
10.1109/TBME.2011.2165955
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The initiation of osteoarthritis (OA) has been linked to the onset and progression of pathologic mechanisms at the cartilage-bone interface. Most importantly, this degenerative disease involves cross-talk between the cartilage and subchondral bone environments, so an informative model should contain the complete complex. In order to evaluate this process, we have developed a multiscale model using the open-source ontologies developed for the Physiome Project with cartilage and bone descriptions at the cellular, micro, and macro levels. In this way, we can effectively model the influence of whole body loadings at the macro level and the influence of bone organization and architecture at the micro level, and have cell level processes that determine bone and cartilage remodeling. Cell information is then passed up the spatial scales to modify micro architecture and provide a macro spatial characterization of cartilage inflammation. We evaluate the framework by linking a common knee injury (anterior cruciate ligament deficiency) to proinflammatory mediators as a possible pathway to initiate OA. This framework provides a "virtual bone-cartilage" tool for evaluating hypotheses, treatment effects, and disease onset to inform and strengthen clinical studies.
引用
收藏
页码:3532 / 3536
页数:5
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