Extracting Voxel‐Based Cartilage Relaxometry Features in Hip Osteoarthritis Subjects Using Principal Component Analysis

Background MRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability. Purpose First, to incorporate fully automatic voxe...

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Published inJournal of magnetic resonance imaging Vol. 51; no. 6; pp. 1708 - 1719
Main Authors Liao, Tzu‐Chieh, Pedoia, Valentina, Neumann, Jan, Link, Thomas M., Souza, Richard B., Majumdar, Sharmila
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.06.2020
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Abstract Background MRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability. Purpose First, to incorporate fully automatic voxel‐based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities. Study Type Cross‐sectional. Subjects Thirty‐three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years). Sequence A 3.0T scanner using 3D SPGR, combined T1ρ/T2, and fast spin echo sequences. Assessment Pelvic radiographs, patients' self‐reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities. Statistical Tests Chi‐square and independent t‐tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification. Results In T1ρ assessment, OA subjects demonstrated higher T1ρ values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T2 assessment, OA subjects exhibited higher T2 values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009–0.032) when compared with the remaining controls. Data Conclusion The study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively. Level of Evidence: 1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;51:1708–1719.
AbstractList Background MRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability. Purpose First, to incorporate fully automatic voxel‐based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities. Study Type Cross‐sectional. Subjects Thirty‐three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years). Sequence A 3.0T scanner using 3D SPGR, combined T1ρ/T2, and fast spin echo sequences. Assessment Pelvic radiographs, patients' self‐reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities. Statistical Tests Chi‐square and independent t‐tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification. Results In T1ρ assessment, OA subjects demonstrated higher T1ρ values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T2 assessment, OA subjects exhibited higher T2 values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009–0.032) when compared with the remaining controls. Data Conclusion The study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively. Level of Evidence: 1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;51:1708–1719.
BackgroundMRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability.PurposeFirst, to incorporate fully automatic voxel‐based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities.Study TypeCross‐sectional.SubjectsThirty‐three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years).SequenceA 3.0T scanner using 3D SPGR, combined T1ρ/T2, and fast spin echo sequences.AssessmentPelvic radiographs, patients' self‐reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities.Statistical TestsChi‐square and independent t‐tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification.ResultsIn T1ρ assessment, OA subjects demonstrated higher T1ρ values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T2 assessment, OA subjects exhibited higher T2 values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009–0.032) when compared with the remaining controls.Data ConclusionThe study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively.Level of Evidence: 1Technical Efficacy Stage: 2J. Magn. Reson. Imaging 2020;51:1708–1719.
MRI-based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability.BACKGROUNDMRI-based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability.First, to incorporate fully automatic voxel-based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities.PURPOSEFirst, to incorporate fully automatic voxel-based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities.Cross-sectional.STUDY TYPECross-sectional.Thirty-three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years).SUBJECTSThirty-three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years).A 3.0T scanner using 3D SPGR, combined T1ρ /T2 , and fast spin echo sequences.SEQUENCEA 3.0T scanner using 3D SPGR, combined T1ρ /T2 , and fast spin echo sequences.Pelvic radiographs, patients' self-reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities.ASSESSMENTPelvic radiographs, patients' self-reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities.Chi-square and independent t-tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification.STATISTICAL TESTSChi-square and independent t-tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification.In T1ρ assessment, OA subjects demonstrated higher T1ρ values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T2 assessment, OA subjects exhibited higher T2 values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009-0.032) when compared with the remaining controls.RESULTSIn T1ρ assessment, OA subjects demonstrated higher T1ρ values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T2 assessment, OA subjects exhibited higher T2 values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009-0.032) when compared with the remaining controls.The study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively.DATA CONCLUSIONThe study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively.1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;51:1708-1719.LEVEL OF EVIDENCE1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;51:1708-1719.
MRI-based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip osteoarthritis (OA) might provide important information on regional disease variability. First, to incorporate fully automatic voxel-based relaxometry (VBR) with principal component analysis (PCA) to extract distinctive relaxometry features in subjects with radiographic hip OA and nondiseased controls. Second, to use the identified features to further distinguish subjects with cartilage compositional abnormalities. Cross-sectional. Thirty-three subjects with radiographic hip OA (20 males; age, 50.2 ± 13.3 years) and 55 controls participated (28 males; 41.3 ± 12.0 years). A 3.0T scanner using 3D SPGR, combined T /T , and fast spin echo sequences. Pelvic radiographs, patients' self-reported symptoms, physical function, and cartilage morphology were analyzed. Cartilage relaxation times were quantified using traditional regions of interest and VBR approaches. PCA was performed on VBR data to identify distinctive relaxometry features, and were subsequently used to identify a subgroup of subjects from the controls that exhibited compositional abnormalities. Chi-square and independent t-tests were used to compare group characteristics. Logistic regression models were used to identify the possible principal components (PCs) that were able to predict OA vs. control classification. In T assessment, OA subjects demonstrated higher T values in the posterior hip region and deep cartilage layer when compared with controls (P = 0.012 and 0.001, respectively). In T assessment, OA subjects exhibited higher T values in the posterior hip region (P < 0.001). Based on the PC score classification, 16 subjects without radiographic evidence of OA demonstrated relaxometry patterns similar to OA subjects, and exhibited worse physical function (P = 0.003) and cartilage lesions (P = 0.009-0.032) when compared with the remaining controls. The study identified distinctive cartilage relaxometry features that were able to discriminate subjects with and without radiographic hip OA effectively. 1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;51:1708-1719.
Author Liao, Tzu‐Chieh
Majumdar, Sharmila
Pedoia, Valentina
Link, Thomas M.
Neumann, Jan
Souza, Richard B.
AuthorAffiliation 1 Musculoskeletal Quantitative Imaging Research, Department of Radiology and Biomedical Imaging, University of California-San Francisco, San Francisco, CA, USA
2 Department of Physical Therapy and Rehabilitation Science, University of California-San Francisco, San Francisco, CA, USA
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Keywords magnetic resonance imaging
voxel-based relaxometry
hip osteoarthritis
T1ρ and T2
principal component analysis
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Snippet Background MRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in...
MRI-based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip...
BackgroundMRI‐based relaxation time measurements provide quantitative assessment of cartilage biochemistry. Identifying distinctive relaxometry features in hip...
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wiley
SourceType Open Access Repository
Aggregation Database
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StartPage 1708
SubjectTerms Abnormalities
Adult
Arthritis
Biomedical materials
Cartilage
Cartilage diseases
Cartilage, Articular - diagnostic imaging
Classification
Cross-Sectional Studies
Feature extraction
Hip
hip osteoarthritis
Humans
Magnetic Resonance Imaging
Male
Males
Middle Aged
Morphology
Osteoarthritis
Osteoarthritis, Hip - diagnostic imaging
Osteoarthritis, Knee
Principal Component Analysis
Principal components analysis
Radiographs
Radiography
Regression analysis
Regression models
Relaxation time
Sequences
Signs and symptoms
Stability
Statistical analysis
Statistical tests
Subgroups
T1ρ and T2
voxel‐based relaxometry
Title Extracting Voxel‐Based Cartilage Relaxometry Features in Hip Osteoarthritis Subjects Using Principal Component Analysis
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.26955
https://www.ncbi.nlm.nih.gov/pubmed/31614057
https://www.proquest.com/docview/2401716953
https://www.proquest.com/docview/2306213021
https://pubmed.ncbi.nlm.nih.gov/PMC9744136
Volume 51
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