Assessing cortical bone porosity with MRI in an animal model of chronic kidney disease

被引:2
|
作者
Newman, Christopher L. [1 ]
Surowiec, Rachel K. [2 ]
Swallow, Elizabeth A. [3 ]
Metzger, Corinne E. [4 ]
Kim, Jieun [4 ]
Tomaschke, Andrew A. [2 ]
Chen, Neal X. [6 ]
Allen, Matthew R. [2 ,5 ,6 ]
Wallace, Joseph M. [2 ]
Moe, Sharon M. [6 ]
Wu, Yu -Chien [1 ]
Niziolek, Paul J. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Radiol & Imaging Sci, 705 Riley Hosp Dr,Room 1053, Indianapolis, IN 46202 USA
[2] Indiana Univ Purdue Univ, Dept Biomed Engn, Indianapolis, IN USA
[3] Univ South, Sewanee, TN USA
[4] Stanford Univ, Wu Tsai Neurosci Inst, Stanford, CA USA
[5] Indiana Univ Sch Med, Dept Anat Cell Biol & Physiol, Indianapolis, IN USA
[6] Indiana Univ Sch Med, Dept Med, Div Nephrol, Indianapolis, IN USA
关键词
Chronic kidney disease; MRI; UTE; Porosity index; microCT; HIP FRACTURE; MINERAL DENSITY; INCREASED RISK; PORE-WATER; RAT MODEL; UTE-MRI; MORTALITY; CALCIUM;
D O I
10.1016/j.bone.2023.116808
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic kidney disease (CKD) is characterized by secondary hyperparathyroidism and an increased risk of hip fractures predominantly related to cortical porosity. Unfortunately, bone mineral density measurements and high-resolution peripheral computed tomography (HR-pQCT) imaging have shortcomings that limit their utility in these patients. Ultrashort echo time magnetic resonance imaging (UTE-MRI) has the potential to overcome these limitations by providing an alternative assessment of cortical porosity. The goal of the current study was to determine if UTE-MRI could detect changes in porosity in an established rat model of CKD. Cy/+ rats (n = 11), an established animal model of CKD-MBD, and their normal littermates (n = 12) were imaged using microcomputed tomography (microCT) and UTE-MRI at 30 and 35 weeks of age (which approx-imates late-stage kidney disease in humans). Images were obtained at the distal tibia and the proximal femur. Cortical porosity was assessed using the percent porosity (Pore%) calculated from microCT imaging and the porosity index (PI) calculated from UTE-MRI. Correlations between Pore% and PI were also calculated. Cy/+ rats had higher Pore% than normal rats at both skeletal sites at 35 weeks (tibia = 7.13 % +/-5.59 % vs. 0.51 % +/-0.09 %, femur = 19.99 % +/-7.72 % vs. 2.72 % +/-0.32 %). They also had greater PI at the distal tibia at 30 weeks of age (0.47 +/-0.06 vs. 0.40 +/-0.08). However, Pore% and PI were only correlated in the proximal femur at 35 weeks of age (rho = 0.929, Spearman). These microCT results are consistent with prior studies in this animal model utilizing microCT imaging. The UTE-MRI results were inconsistent, resulting in variable correlations with microCT imaging, which may be related to suboptimal bound and pore water discrimination at higher magnetic field strengths. Nevertheless, UTE-MRI may still provide an additional clinical tool to assess fracture risk without using ionizing radiation in CKD patients.
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页数:9
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