Characterization of Bone Perfusion by Dynamic Contrast-Enhanced Magnetic Resonance Imaging and Positron Emission Tomography in the Dunkin-Hartley Guinea Pig Model of Advanced Osteoarthritis

被引:26
作者
Dyke, Jonathan P. [1 ,2 ]
Synan, Michael [2 ]
Ezell, Paula [3 ]
Ballon, Douglas [1 ,2 ]
Racine, Jennifer [4 ]
Aaron, Roy K. [4 ]
机构
[1] Weill Cornell Med Coll, Dept Radiol, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Citigrp Biomed Imaging Ctr, New York, NY USA
[3] Med Univ S Carolina, Dept Comparat Med, Charleston, SC 29425 USA
[4] Brown Univ, Warren Alpert Med Sch, Dept Orthoped, Providence, RI 02912 USA
关键词
Osteoarthritis; PET; MRI; subchondral bone; perfusion; F-18; FLUORIDE-ION; SUBCHONDRAL BONE; ARTICULAR-CARTILAGE; INTRAOSSEOUS PRESSURE; AVASCULAR NECROSIS; BLOOD-FLOW; PET; HIP; HISTOMORPHOMETRY; ABNORMALITIES;
D O I
10.1002/jor.22768
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
This study characterizes changes in subchondral bone circulation in OA and examines relationships to bone structure and cartilage degeneration in Dunkin-Hartley guinea pigs. We have used dynamic contrast-enhanced MRI (DCE-MRI) and PET, with pharmacokinetic modeling, to characterize subchondral bone perfusion. Assessments are made of perfusion kinetics and vascular permeability by MRI, and blood volume and flow, and radionuclide incorporation into bone, by PET. These parameters are compared to cartilage lesion severity and bone histomorphometry. Assessments of intraosseous thrombi are made morphologically. Prolonged signal enhancement during the clearance phase of MRI correlated with OA severity and suggested venous stasis. Vascular permeability was not increased indicating that transvascular migration of contrast agent was not responsible for signal enhancement. Intraosseous thrombi were not observed. Decreased perfusion associated with severe OA was confirmed by PET and was associated with reduced radionuclide incorporation and osteoporosis. MRI and PET can be used to characterize kinetic parameters of circulation in OA and correlate them with subchondral bone metabolism of interest to the pathophysiology of OA. The significance of these observations may lie in alterations induced in the expression of cytokines by OA osteoblasts that are related to bone remodeling and cartilage breakdown. (c) 2014 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 33:???-???, 2015.
引用
收藏
页码:366 / 372
页数:7
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