Diffusion-weighted MR imaging in chronic non-bacterial osteitis: Proof-of-concept of the apparent diffusion coefficient as an outcome measure

被引:0
|
作者
Moller, Jakob M. [1 ,2 ]
Andreasen, Caroline M. [3 ,4 ]
Buus, Thomas W. [5 ,6 ]
Pedersen, Susanne J. [7 ]
ostergaard, Mikkel [2 ,7 ]
Thomsen, Henrik S. [1 ,2 ]
Jurik, Anne G. [5 ,6 ]
机构
[1] Herlev Gentofte Hosp, Dept Radiol, Herlev, Denmark
[2] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[3] Aarhus Univ Hosp, Dept Rheumatol, Aarhus, Denmark
[4] Vejle Hosp, Rheumatol, Dept Med, Vejle, Denmark
[5] Aarhus Univ Hosp, Dept Radiol, Aarhus, Denmark
[6] Aarhus Univ Hosp, Dept Clin Med, Aarhus, Denmark
[7] Rigshosp, Copenhagen Ctr Arthrit Res, Ctr Rheumatol & Spine Dis, Glostrup, Denmark
关键词
Magnetic resonance imaging; diffusion-weighted imaging; apparent diffusion coefficient; chronic; HODGKIN-LYMPHOMA; ROI METHODS; ADC VALUES; CANCER; SAPHO; DIAGNOSIS;
D O I
10.1177/20584601211044478
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: The apparent diffusion coefficient (ADC), as determined by whole-body diffusion-weighted MRI, may be useful as an outcome measure for monitoring response to treatment in chronic non-bacterial osteitis. Purpose: To test and demonstrate the feasibility of ADC-measurement methods for use as outcome measure in chronic non-bacterial osteitis. Materials and Methods: Using data from a randomized pilot study, feasibility of change-score ADC between baseline and second MRI (Delta ADC(12)) and third MRI (Delta ADC(13)) as outcome measure was assessed in three settings: "whole-lesion," "single-slice per lesion," and "index-lesion per patient". Bone marrow edema lesions were depicted on short tau inversion recovery sequence at baseline and copied to ADC maps at the three time-points. Correlations between the three settings were measured as were analysis of variances. Discriminant validity was assessed as inter- and intra-observer reproducibility and smallest detectable change. Results: 12 subjects were enrolled, and MRI was performed at baseline and weeks 12 and 36. Pearson correlation was high (r > 0.86; p <= 0.01) for Delta ADC between single-slice-whole-lesion and whole-lesion-index-lesion and tended to be significant for single-slice-index-lesion settings (p = 0.06). For Delta ADC(12) and Delta ADC(13), Bland-Altman plots showed small differences (0.02, 0.03) and narrow 95% limits-of-agreement (-0.13-0.09, -0.07-0.05 mu m(2)/s) between whole-lesion and single-slice ROI settings. Inter-observer reproducibility measured by intra-class correlation coefficient was poor-to-fair (range: 0.09-0.31), whereas intra-observer reproducibility was good-to-excellent (range: 0.67-0.90). Smallest detectable changes were between 0.21-0.28 mu m(2)/s. Conclusion: ADC change-score as outcome measure was feasible, and the single-slice per lesion ROI setting performed almost equally to whole-lesion setting resulting in reduced assessment time.
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页数:9
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