骨关节炎和正常股骨远端区域深度特异性软骨下骨密度:精度和初步比较

J.D. Johnston , A.E. Sacher , C.E. McLennan , J.A. Lynch , T. Neogi , D.J. Hunter , D.R. Wilson , S.A. Kontulainen
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引用次数: 0

摘要

软骨下骨改变在OA发病机制和疼痛中的确切作用尚不清楚。临床定量CT (QCT)结合深度特异性图像处理已被用于研究胫骨和髌骨近端软骨下骨矿物质密度(BMD)。有限的深度特异性QCT研究已在OA股骨远端完成。目的:1)评估股骨远端自动化、区域性、深度特异性软骨下骨密度测量的短期精度;2)确定区域和局灶骨密度指标是否能够区分正常和OA股骨远端软骨下骨密度模式的差异。方法14例受试者(3M:11F;平均年龄:49.9 (SD: 11.9)岁),分为正常(n=7)和OA (n=7)。每个参与者在两天内使用临床QCT扫描三次。在股骨远端进行两项BMD评估:平均区域密度和峰值病灶密度。根据MOAKS入路,评估三个深度(0-2.5、2.5-5、5-7.5 mm)和股骨远端六个亚区域(内侧/外侧、前/中央/后)的骨密度(图1)。我们使用均方根变异系数(CV%RMS)评估精度。为了探讨骨性关节炎与正常股骨远端之间的潜在差异,我们进行了参数t检验和非参数Mann-Whitney统计分析,并确定了Cohen 's d效应大小,其绝对值为d >;0.8认为有临床意义。结果区域性骨密度测量的scv %RMS范围为1.6% ~ 3.6%(平均为2.2%),局点骨密度测量的CV%RMS范围为1.6% ~ 6.9%(平均为2.7%)。统计比较表明,股骨远端OA在2.5- 5mm深度的中前区骨密度较低(区域:-17%;焦点:-19%)和5-7.5 mm(区域:-21%;focal: -25%)(图2)。所有其他骨密度测量在正常和OA股骨远端之间相似(p >;0.05)。科恩效应值范围从-1.7到0.76。结论:该自动化技术提供了股骨远端软骨下骨密度的精确测量。这种方法有可能量化和区分股骨远端软骨下骨密度的oa相关改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
REGIONAL DEPTH-SPECIFIC SUBCHONDRAL BONE DENSITY IN OA AND NORMAL DISTAL FEMORA: PRECISION AND PRELIMINARY COMPARISONS

INTRODUCTION

The exact role of altered subchondral bone in OA pathogenesis and pain is unclear. Clinical quantitative CT (QCT) combined with depth-specific image processing has been previously used to study subchondral bone mineral density (BMD) at the proximal tibia and patella. Limited depth-specific QCT research has been completed at the OA distal femur.

OBJECTIVES

To 1) assess the short-term precision of automated, regional, depth-specific subchondral BMD measures at the distal femur in individuals with and without OA; and 2) determine whether regional and focal BMD metrics were able to discriminate differences in subchondral bone density patterns between normal and OA distal femora.

METHODS

Fourteen participants (3M:11F; mean age: 49.9 (SD: 11.9) years) were recruited and classified as normal (n=7) or OA (n=7). Each participant was scanned three times over two days using clinical QCT. Two BMD assessments were evaluated at the distal femur: mean regional density and peak focal density. BMD measures were assessed across three depths (0-2.5, 2.5-5, 5-7.5 mm) and six sub-regions of the distal femur (medial/lateral, anterior/central/posterior), as per the MOAKS approach (Fig.1). We assessed precision using root mean square coefficients of variation (CV%RMS). To explore potential differences between OA and normal distal femora, we performed parametric t-tests and non-parametric Mann-Whitney statistical analyses and also determined Cohen’s d effect sizes, with an absolute d > 0.8 considered clinically significant.

RESULTS

CV%RMS ranged from 1.6% to 3.6% (average: 2.2%) for measures of regional BMD while CV%RMS ranged from 1.6% to 6.9% (average: 2.7%) for measures of focal BMD. Statistical comparisons indicated lower BMD in OA distal femoral in the medial-anterior region at depths of 2.5-5 mm (regional: -17%; focal: -19%) and 5-7.5 mm (regional: -21%; focal: -25%) (Fig. 2). All other BMD measures were similar between normal and OA distal femora (p > 0.05). Cohen's d effect sizes ranged from -1.7 to 0.76.

CONCLUSION

This automated technique offers precise measures of subchondral BMD at the distal femur. This approach has potential to quantify and distinguish OA-related alterations in subchondral BMD at the distal femur.
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来源期刊
Osteoarthritis imaging
Osteoarthritis imaging Radiology and Imaging
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