J.D. Johnston , A.E. Sacher , C.E. McLennan , J.A. Lynch , T. Neogi , D.J. Hunter , D.R. Wilson , S.A. Kontulainen
{"title":"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","authors":"J.D. Johnston , A.E. Sacher , C.E. McLennan , J.A. Lynch , T. Neogi , D.J. Hunter , D.R. Wilson , S.A. Kontulainen","doi":"10.1016/j.ostima.2025.100294","DOIUrl":null,"url":null,"abstract":"<div><h3>INTRODUCTION</h3><div>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.</div></div><div><h3>OBJECTIVES</h3><div>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.</div></div><div><h3>METHODS</h3><div>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%<sub>RMS</sub>). 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.</div></div><div><h3>RESULTS</h3><div>CV%<sub>RMS</sub> ranged from 1.6% to 3.6% (average: 2.2%) for measures of regional BMD while CV%<sub>RMS</sub> 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.</div></div><div><h3>CONCLUSION</h3><div>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.</div></div>","PeriodicalId":74378,"journal":{"name":"Osteoarthritis imaging","volume":"5 ","pages":"Article 100294"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"REGIONAL DEPTH-SPECIFIC SUBCHONDRAL BONE DENSITY IN OA AND NORMAL DISTAL FEMORA: PRECISION AND PRELIMINARY COMPARISONS\",\"authors\":\"J.D. Johnston , A.E. Sacher , C.E. McLennan , J.A. Lynch , T. Neogi , D.J. Hunter , D.R. Wilson , S.A. Kontulainen\",\"doi\":\"10.1016/j.ostima.2025.100294\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>INTRODUCTION</h3><div>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.</div></div><div><h3>OBJECTIVES</h3><div>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.</div></div><div><h3>METHODS</h3><div>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%<sub>RMS</sub>). 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.</div></div><div><h3>RESULTS</h3><div>CV%<sub>RMS</sub> ranged from 1.6% to 3.6% (average: 2.2%) for measures of regional BMD while CV%<sub>RMS</sub> 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.</div></div><div><h3>CONCLUSION</h3><div>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.</div></div>\",\"PeriodicalId\":74378,\"journal\":{\"name\":\"Osteoarthritis imaging\",\"volume\":\"5 \",\"pages\":\"Article 100294\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Osteoarthritis imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772654125000340\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Osteoarthritis imaging","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772654125000340","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.