A warning machine learning algorithm for early knee osteoarthritis structural progressor patient screening

Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early predict...

Full description

Saved in:
Bibliographic Details
Published inTherapeutic advances in musculoskeletal disease Vol. 13; p. 1759720X21993254
Main Authors Bonakdari, Hossein, Jamshidi, Afshin, Pelletier, Jean-Pierre, Abram, François, Tardif, Ginette, Martel-Pelletier, Johanne
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 2021
SAGE PUBLICATIONS, INC
SAGE Publishing
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time. Methods: The patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients. Results: Feature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men. Conclusion: This is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors. Plain language summary Machine learning model for early knee osteoarthritis structural progression Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life – the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression. We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.
AbstractList Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time. Methods: The patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients. Results: Feature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men. Conclusion: This is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors. Plain language summary Machine learning model for early knee osteoarthritis structural progression Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life – the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression. We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.
In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time.AIMIn osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time.The patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients.METHODSThe patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients.Feature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men.RESULTSFeature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men.This is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors.CONCLUSIONThis is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors.Machine learning model for early knee osteoarthritis structural progression Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life - the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression.We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.PLAIN LANGUAGE SUMMARYMachine learning model for early knee osteoarthritis structural progression Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life - the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression.We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.
Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time. Methods: The patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients. Results: Feature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men. Conclusion: This is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors. Plain language summary Machine learning model for early knee osteoarthritis structural progression Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life – the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression. We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.
In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning (ML) model that bridges major OA risk factors and serum levels of adipokines/related inflammatory factors at baseline for early prediction of at-risk knee OA patient structural progressors over time. The patient- and gender-based model development used baseline serum levels of six adipokines, three related inflammatory factors and their ratios (36), as well as major OA risk factors [age and bone mass index (BMI)]. Subjects (677) were selected from the Osteoarthritis Initiative (OAI) progression subcohort. The probability values of being structural progressors (PVBSP) were generated using our previously published prediction model, including five baseline structural features of the knee, i.e. two X-rays and three magnetic resonance imaging variables. To identify the most important variables amongst the 47 studied in relation to PVBSP, we employed the ML feature classification methodology. Among five supervised ML algorithms, the support vector machine (SVM) demonstrated the best accuracy and use for gender-based classifiers development. Performance and sensitivity of the models were assessed. A reproducibility analysis was performed with clinical trial OA patients. Feature selections revealed that the combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP are the most important variables in predicting OA structural progressors in both genders. Classification accuracies for both genders in the testing stage (OAI) were >80%, with the highest sensitivity of CRP/MCP-1. Reproducibility analysis showed an accuracy ⩾92%; the ratio CRP/MCP-1 demonstrated the highest sensitivity in women and leptin/CRP in men. This is the first time that such a framework was built for predicting knee OA structural progressors. Using this automated ML patient- and gender-based model, early prediction of knee structural OA progression can be performed with high accuracy using only three baseline serum biomarkers and two risk factors. Knee osteoarthritis is a well-known debilitating disease leading to reduced mobility and quality of life - the main causes of chronic invalidity. Disease evolution can be slow and span many years; however, for some individuals, the progression/evolution can be fast. Current treatments are only symptomatic and conventional diagnosis of osteoarthritis is not very effective in early identification of patients who will progress rapidly. To improve therapeutic approaches, we need a robust prediction model to stratify osteoarthritis patients at an early stage according to risk of joint structure disease progression.We hypothesize that a prediction model using a machine learning system would enable such an early identification of individuals for whom osteoarthritis knee structure will degrade rapidly. Data were from the Osteoarthritis Initiative, a National Institute of Health (United States) databank, and the robustness and generalizability of the developed model was further evaluated using osteoarthritis patients from an external cohort. Using the supervised machine learning system (support vector machine), we developed an automated patient- and gender-based model enabling an early clinical prognosis for individuals at high risk of structural progressive osteoarthritis. In brief, this model employed at baseline (when the subject sees a physician) easily obtained features consisting of the two main osteoarthritis risk factors, age and bone mass index (BMI), in addition to the serum levels of three molecules. Two of these molecules belong to a family of factors names adipokines and one to a related inflammatory factor. In brief, the model comprising a combination of age, BMI, and the ratios CRP/MCP-1 and leptin/CRP were found very robust for both genders, and the high accuracy persists when tested with an external cohort conferring the gender-based model generalizability. This study offers a new automated system for identifying early knee osteoarthritis structural progressors, which will significantly improve clinical prognosis with real time patient monitoring.
Author Bonakdari, Hossein
Pelletier, Jean-Pierre
Jamshidi, Afshin
Abram, François
Martel-Pelletier, Johanne
Tardif, Ginette
Author_xml – sequence: 1
  givenname: Hossein
  surname: Bonakdari
  fullname: Bonakdari, Hossein
  organization: Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada
– sequence: 2
  givenname: Afshin
  surname: Jamshidi
  fullname: Jamshidi, Afshin
  organization: Laval University Hospital Research Centre, Quebec, QC, Canada
– sequence: 3
  givenname: Jean-Pierre
  surname: Pelletier
  fullname: Pelletier, Jean-Pierre
  email: jm@martelppelletier.ca
  organization: Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada
– sequence: 4
  givenname: François
  surname: Abram
  fullname: Abram, François
  organization: Medical Imaging Research and Development, ArthroLab Inc., Montreal, QC, Canada
– sequence: 5
  givenname: Ginette
  surname: Tardif
  fullname: Tardif, Ginette
  organization: Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada
– sequence: 6
  givenname: Johanne
  orcidid: 0000-0003-2618-383X
  surname: Martel-Pelletier
  fullname: Martel-Pelletier, Johanne
  organization: Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), 900 Saint-Denis, Suite R11.412, Montreal, QC H2X 0A9, Canada
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33747150$$D View this record in MEDLINE/PubMed
BookMark eNp9Uktv1DAYjFARfcCdE7LEhUvAjt8XpKqCtlIlLiD1Zjn2l6yXJF7spKj_Hi-7LXQlONmab2Y03-O0OpriBFX1muD3hEj5gUiuZYNvG6I1bTh7Vp1soVo2RB09_vHtcXWa8xpjobEmL6pjSiWThOOTan2Ofto0halHo3WrMAEaYA_YoY8pzKsRdTGhgg736PsEgGKeIdo0r0o1ZJTntLh5SXZAmxT7BDkX_sbOAaYZZZcAtn4vq-edHTK82r9n1bfPn75eXNU3Xy6vL85vasc1m2vuWu-xF9zzVisC2BEsrBXCEi-sZ1a3HFqlHQhCGKagW6eo8EppLwkQelZd73x9tGuzSWG06d5EG8xvIKbelOzBDWA8k9QrqUWRso4y3XbMClCuVS22oIrXx53XZmlH8K40VNp8Yvq0MoWV6eOdkRpz2dBi8G5vkOKPBfJsxpAdDIOdIC7ZNBxTIYlWvFDfHlDXcUlTGZVpBKENK-MRhfXm70SPUR5WWghiR3Ap5pygMy7MZRdxGzAMhmCzvR1zeDtFiA-ED97_kdQ7SbY9_In7T_4vtRHVPA
CitedBy_id crossref_primary_10_1302_0301_620X_106B11_BJJ_2024_0453_R1
crossref_primary_10_3390_healthcare11091206
crossref_primary_10_1298_ptr_E10296
crossref_primary_10_1177_1759720X221091359
crossref_primary_10_1016_j_joca_2022_10_014
crossref_primary_10_3390_app14146333
crossref_primary_10_3390_biomedicines10061247
crossref_primary_10_3390_su16083461
crossref_primary_10_1016_j_cpan_2025_02_004
crossref_primary_10_1016_j_joca_2024_11_008
crossref_primary_10_1371_journal_pone_0266964
crossref_primary_10_1186_s12916_022_02491_1
crossref_primary_10_4108_eetiot_5329
crossref_primary_10_1186_s13075_022_02801_1
crossref_primary_10_1136_annrheumdis_2021_221763
crossref_primary_10_1177_1759720X231165560
crossref_primary_10_3233_JCM_215741
crossref_primary_10_1002_jor_25912
crossref_primary_10_3390_app13031658
crossref_primary_10_3390_diagnostics12112679
crossref_primary_10_1007_s00264_022_05628_2
crossref_primary_10_1186_s12891_024_07942_9
crossref_primary_10_3390_bioengineering11080824
crossref_primary_10_1007_s00256_024_04627_1
crossref_primary_10_1038_s41598_023_35832_y
crossref_primary_10_3390_agriculture12070933
crossref_primary_10_1177_1759720X211040300
Cites_doi 10.1016/j.fertnstert.2015.05.007
10.1016/j.joca.2007.02.014
10.1038/s41598-020-66330-0
10.1109/TCSII.2005.857540
10.1177/1759720X12455959
10.1093/rheumatology/kev408
10.1016/j.semarthrit.2017.10.016
10.1186/s40659-015-0057-0
10.1016/j.joca.2018.12.027
10.1002/art.40902
10.1007/s13721-020-00237-8
10.1002/art.20000
10.1061/(ASCE)0733-947X(1991)117:2(178)
10.2337/diacare.27.10.2488
10.1016/j.humov.2019.05.006
10.1093/rheumatology/kes422
10.1002/art.40898
10.1016/j.cyto.2012.06.018
10.1093/rheumatology/key305
10.1007/978-1-4757-3264-1
10.1016/j.joca.2006.10.010
10.1017/S0007114507853347
10.1016/j.joca.2012.05.002
10.1016/j.metabol.2007.09.011
10.1016/j.joca.2012.02.636
10.5958/0974-360X.2020.00458.8
10.1016/j.cyto.2018.06.019
10.1136/annrheumdis-2013-204189
10.1016/j.joca.2005.04.014
10.1093/rheumatology/key181
10.1007/s10067-010-1429-z
10.1177/1759720X20933468
10.1016/j.joca.2006.01.009
10.1097/00075197-200111000-00006
10.1016/j.joca.2019.04.016
10.1155/2017/5468023
10.1016/j.obmed.2019.100152
10.1016/j.joca.2006.11.009
10.1046/j.1365-2796.2000.00678.x
10.1161/STROKEAHA.107.485540
10.1007/s10278-019-00238-8
10.1186/s13075-016-1103-1
10.1186/s12891-019-2624-y
10.1023/A:1010933404324
10.1136/ard.2008.088732
10.1007/s001250050804
10.5312/wjo.v5.i3.319
10.1016/j.cmpb.2020.105464
10.1038/sj.ijo.0803259
10.1002/jor.24201
10.1002/acr.21922
ContentType Journal Article
Copyright The Author(s), 2021
The Author(s), 2021.
The Author(s), 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s), 2021 2021 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses
Copyright_xml – notice: The Author(s), 2021
– notice: The Author(s), 2021.
– notice: The Author(s), 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s), 2021 2021 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses
DBID AFRWT
AAYXX
CITATION
NPM
3V.
7RV
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
K9.
KB0
M0S
NAPCQ
PHGZM
PHGZT
PIMPY
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1177/1759720X21993254
DatabaseName Sage Journals GOLD Open Access 2024
CrossRef
PubMed
ProQuest Central (Corporate)
Nursing & Allied Health Database
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
Health & Medical Collection (Alumni Edition)
Nursing & Allied Health Premium
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central China
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Central (New)
ProQuest One Academic Eastern Edition
ProQuest Nursing & Allied Health Source
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest Nursing & Allied Health Source (Alumni)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
Publicly Available Content Database
PubMed

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: AFRWT
  name: Sage Journals GOLD Open Access 2024
  url: http://journals.sagepub.com/
  sourceTypes: Publisher
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1759-7218
ExternalDocumentID oai_doaj_org_article_d473d87969d74f349bf4a6e8cb8b0ae8
PMC7905723
33747150
10_1177_1759720X21993254
10.1177_1759720X21993254
Genre Journal Article
GrantInformation_xml – fundername: Canada First Research Excellence Fund, TransMedTech Institute
– fundername: centre for research on intermediality, university of montreal
  funderid: https://doi.org/10.13039/501100000077
– fundername: ;
GroupedDBID ---
-TM
.WF
01A
0R~
4.4
53G
54M
7RV
7X7
8FI
8FJ
AABMB
AADUE
AAKDD
AAQDB
AARDL
AARIX
AASGM
ABAWP
ABEIX
ABFWQ
ABJIS
ABKRH
ABQXT
ABRHV
ABUWG
ABVFX
ACARO
ACDSZ
ACDXX
ACGFS
ACOFE
ACROE
ACRPL
ADBBV
ADEBD
ADNMO
ADOGD
ADYCS
ADZZY
AEFTW
AEQLS
AERKM
AEUHG
AEWDL
AEXNY
AFCOW
AFEET
AFKRA
AFKRG
AFRWT
AFUIA
AFWMB
AGNHF
AGQPQ
AHHFK
AJUZI
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
ARTOV
ASPBG
AUTPY
AVWKF
AYAKG
AZFZN
B8M
BAWUL
BDDNI
BENPR
BKEYQ
BKSCU
BPHCQ
BSEHC
BVXVI
CAG
CCPQU
CDWPY
CFDXU
COF
DC-
DC.
DIK
DOPDO
EBS
EJD
EMOBN
F5P
FEDTE
FYUFA
GROUPED_DOAJ
GROUPED_SAGE_PREMIER_JOURNAL_COLLECTION
GX1
H13
HF~
HMCUK
HVGLF
HYE
HZ~
J8X
K.F
N9A
NAPCQ
O9-
OK1
P.B
PHGZM
PHGZT
PIMPY
PQQKQ
ROL
RPM
S01
SAUOL
SCDPB
SCNPE
SFC
UKHRP
ZONMY
ZPPRI
ZRKOI
ZSSAH
AAYXX
ACHEB
CITATION
NPM
PPXIY
3V.
7XB
8FK
AZQEC
DWQXO
K9.
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c594t-5cbdd0d65d5b981e0c106aa66a1d6ad4a9b5eb89ce611403e9bc836d889d71e13
IEDL.DBID AFRWT
ISSN 1759-720X
IngestDate Wed Aug 27 01:00:41 EDT 2025
Thu Aug 21 14:34:50 EDT 2025
Fri Jul 11 16:25:08 EDT 2025
Fri Jul 25 04:16:08 EDT 2025
Mon Jul 21 05:18:35 EDT 2025
Tue Jul 01 05:27:26 EDT 2025
Thu Apr 24 23:10:08 EDT 2025
Tue Jun 17 22:28:07 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords early prediction
adipokines
machine learning
structural progressor
biomarkers
knee osteoarthritis
Language English
License This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
The Author(s), 2021.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c594t-5cbdd0d65d5b981e0c106aa66a1d6ad4a9b5eb89ce611403e9bc836d889d71e13
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0003-2618-383X
OpenAccessLink https://journals.sagepub.com/doi/full/10.1177/1759720X21993254?utm_source=summon&utm_medium=discovery-provider
PMID 33747150
PQID 2613245946
PQPubID 4450846
ParticipantIDs doaj_primary_oai_doaj_org_article_d473d87969d74f349bf4a6e8cb8b0ae8
pubmedcentral_primary_oai_pubmedcentral_nih_gov_7905723
proquest_miscellaneous_2503671985
proquest_journals_2613245946
pubmed_primary_33747150
crossref_citationtrail_10_1177_1759720X21993254
crossref_primary_10_1177_1759720X21993254
sage_journals_10_1177_1759720X21993254
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2021-00-00
PublicationDateYYYYMMDD 2021-01-01
PublicationDate_xml – year: 2021
  text: 2021-00-00
PublicationDecade 2020
PublicationPlace London, England
PublicationPlace_xml – name: London, England
– name: England
– name: London
– name: Sage UK: London, England
PublicationTitle Therapeutic advances in musculoskeletal disease
PublicationTitleAlternate Ther Adv Musculoskelet Dis
PublicationYear 2021
Publisher SAGE Publications
SAGE PUBLICATIONS, INC
SAGE Publishing
Publisher_xml – name: SAGE Publications
– name: SAGE PUBLICATIONS, INC
– name: SAGE Publishing
References Srikanth, Fryer, Zhai 2005; 13
Conde, Scotece, Lopez 2014; 73
Pearle, Scanzello, George 2007; 15
Hellstrom, Wahrenberg, Hruska 2000; 247
Breiman 2001; 45
Raynauld, Martel-Pelletier, Berthiaume 2004; 50
Davis, Nihan 1991; 117
Power, Schulkin 2008; 99
Poonpet, Honsawek 2014; 5
de Boer, van Spil, Huisman 2012; 20
Satoh, Naruse, Usui 2004; 27
Ganesan, Sathish, Elamaran 2020; 13
Zhang, Zhong, Yu 2015; 10
Huang, Zhu, Mao 2006; 53
Oda, Imamura, Fujita 2008; 57
Tu, He, Wu 2019; 113
Panee 2012; 60
Presle, Pottie, Dumond 2006; 14
Sarray, Madan, Saleh 2015; 104
Xu, Ke, Wang 2015; 48
Harkey, Davis, Lu 2019; 20
Mohr, von Tscharner, Emery 2019; 66
Smith, Martins, Gopez 2012; 4
Luo, Gao, Zhu 2020; 193
Calders, Van Ginckel 2018; 47
Platt 1998
Martel-Pelletier, Tardif, Rousseau Trépanier 2019; 27
Kim, Park, Kawada 2006; 30
Gao, Tian, Li 2020; 33
Couillard, Mauriège, Prud’homme 1997; 40
Azamar-Llamas, Hernández-Molina, Ramos-Ávalos 2017; 2017
Martel-Pelletier, Raynauld, Dorais 2016; 55
Devi, Bai, Nagarajan 2020; 17
Karvonen-Gutierrez, Harlow, Mancuso 2013; 65
Ed-daoudy, Maalmi 2020; 9
Nelson, Fang, Arbeeva 2019; 27
Masaki, Takahashi, Hashimoto 2019; 37
Culliford, Maskell, Kiran 2012; 20
Davis, Ward, MacKay 2019; 58
Kraus, Stabler, Luta 2007; 15
Blaak 2001; 4
Calvet, Orellana, Gratacos 2016; 18
Norata, Raselli, Grigore 2007; 38
Bonakdari, Tardif, Abram 2020; 10
Valverde-Franco, Tardif, Mineau 2018; 57
Gandhi, Takahashi, Smith 2010; 29
Staikos, Ververidis, Drosos 2013; 52
Jamshidi, Leclercq, Labbe 2020; 12
Tao, Radstake, Pandit 2019; 71
Lin, Chai, Li 2020; 27
Raynauld, Martel-Pelletier, Bias 2009; 68
Altman, Gold 2007; 15
Franks, Martyanov, Cai 2019; 71
bibr44-1759720X21993254
Platt J. (bibr29-1759720X21993254) 1998
bibr19-1759720X21993254
bibr36-1759720X21993254
bibr45-1759720X21993254
bibr52-1759720X21993254
bibr6-1759720X21993254
bibr28-1759720X21993254
bibr43-1759720X21993254
bibr51-1759720X21993254
Kecman V (bibr30-1759720X21993254)
bibr46-1759720X21993254
bibr42-1759720X21993254
bibr7-1759720X21993254
bibr33-1759720X21993254
Zhang P (bibr37-1759720X21993254) 2015; 10
bibr20-1759720X21993254
bibr34-1759720X21993254
bibr47-1759720X21993254
bibr39-1759720X21993254
bibr8-1759720X21993254
bibr26-1759720X21993254
bibr54-1759720X21993254
bibr13-1759720X21993254
bibr41-1759720X21993254
bibr18-1759720X21993254
bibr10-1759720X21993254
bibr5-1759720X21993254
bibr31-1759720X21993254
bibr1-1759720X21993254
bibr23-1759720X21993254
bibr15-1759720X21993254
bibr22-1759720X21993254
bibr2-1759720X21993254
bibr24-1759720X21993254
bibr21-1759720X21993254
bibr3-1759720X21993254
bibr16-1759720X21993254
Breiman L (bibr25-1759720X21993254) 1993
bibr55-1759720X21993254
bibr12-1759720X21993254
bibr50-1759720X21993254
bibr17-1759720X21993254
bibr38-1759720X21993254
Lin G-S (bibr49-1759720X21993254) 2020; 27
bibr4-1759720X21993254
bibr11-1759720X21993254
bibr56-1759720X21993254
bibr32-1759720X21993254
bibr48-1759720X21993254
bibr35-1759720X21993254
bibr27-1759720X21993254
bibr53-1759720X21993254
bibr9-1759720X21993254
bibr14-1759720X21993254
bibr40-1759720X21993254
References_xml – volume: 38
  start-page: 2844
  year: 2007
  end-page: 2846
  article-title: Leptin:adiponectin ratio is an independent predictor of intima media thickness of the common carotid artery
  publication-title: Stroke
– volume: 47
  start-page: 805
  year: 2018
  end-page: 813
  article-title: Presence of comorbidities and prognosis of clinical symptoms in knee and/or hip osteoarthritis: a systematic review and meta-analysis
  publication-title: Semin Arthritis Rheum
– volume: 29
  start-page: 1223
  year: 2010
  end-page: 1228
  article-title: The synovial fluid adiponectin-leptin ratio predicts pain with knee osteoarthritis
  publication-title: Clin Rheumatol
– volume: 104
  start-page: 460
  year: 2015
  end-page: 466
  article-title: Validity of adiponectin-to-leptin and adiponectin-to-resistin ratios as predictors of polycystic ovary syndrome
  publication-title: Fertil Steril
– volume: 30
  start-page: 1347
  year: 2006
  end-page: 1355
  article-title: Circulating levels of MCP-1 and IL-8 are elevated in human obese subjects and associated with obesity-related parameters
  publication-title: Int J Obes (Lond)
– volume: 73
  start-page: 631
  year: 2014
  end-page: 633
  article-title: Differential expression of adipokines in infrapatellar fat pad (IPFP) and synovium of osteoarthritis patients and healthy individuals
  publication-title: Ann Rheum Dis
– volume: 193
  start-page: 105464
  year: 2020
  article-title: Motor imagery EEG classification based on ensemble support vector learning
  publication-title: Comput Methods Programs Biomed
– volume: 20
  start-page: 519
  year: 2012
  end-page: 524
  article-title: The lifetime risk of total hip and knee arthroplasty: results from the UK general practice research database
  publication-title: Osteoarthritis Cartilage
– volume: 66
  start-page: 335
  year: 2019
  end-page: 346
  article-title: Classification of gait muscle activation patterns according to knee injury history using a support vector machine approach
  publication-title: Hum Mov Sci
– volume: 27
  start-page: 1163
  year: 2019
  end-page: 1173
  article-title: The ratio adipsin/MCP-1 is strongly associated with structural changes and CRP/MCP-1 with symptoms in obese knee osteoarthritis subjects: data from the osteoarthritis initiative
  publication-title: Osteoarthritis Cartilage
– volume: 27
  start-page: 994
  year: 2019
  end-page: 1001
  article-title: A machine learning approach to knee osteoarthritis phenotyping: data from the FNIH biomarkers consortium
  publication-title: Osteoarthritis Cartilage
– volume: 12
  start-page: 1
  year: 2020
  end-page: 12
  article-title: Identification of the most important features of knee osteoarthritis structural progressors using machine learning methods
  publication-title: Ther Adv Musculoskelet Dis
– volume: 60
  start-page: 1
  year: 2012
  end-page: 12
  article-title: Monocyte chemoattractant protein 1 (MCP-1) in obesity and diabetes
  publication-title: Cytokine
– volume: 15
  year: 2007
  article-title: Atlas of individual radiographic features in osteoarthritis, revised
  publication-title: Osteoarthritis Cartilage
– volume: 55
  start-page: 680
  year: 2016
  end-page: 688
  article-title: The levels of the adipokines adipsin and leptin are associated with knee osteoarthritis progression as assessed by MRI and incidence of total knee replacement in symptomatic osteoarthritis patients: a post hoc analysis
  publication-title: Rheumatology (Oxford)
– volume: 15
  start-page: 516
  year: 2007
  end-page: 523
  article-title: Elevated high-sensitivity C-reactive protein levels are associated with local inflammatory findings in patients with osteoarthritis
  publication-title: Osteoarthritis Cartilage
– volume: 71
  start-page: 1701
  year: 2019
  end-page: 1710
  article-title: A machine learning classifier for assigning individual patients with systemic sclerosis to intrinsic molecular subsets
  publication-title: Arthritis Rheumatol
– year: 1998
  article-title: Sequential minimal optimization: a fast algorithm for training support vector machines
  publication-title: MSR-TR-98-14, Microsoft Research
– volume: 247
  start-page: 457
  year: 2000
  end-page: 462
  article-title: Mechanisms behind gender differences in circulating leptin levels
  publication-title: J Intern Med
– volume: 99
  start-page: 931
  year: 2008
  end-page: 940
  article-title: Sex differences in fat storage, fat metabolism, and the health risks from obesity: possible evolutionary origins
  publication-title: Br J Nutr
– volume: 27
  start-page: 1
  year: 2020
  end-page: 15
  article-title: Vision-based patient identification recognition based on image content analysis and support vector machine for medical information system
  publication-title: EURASIP J Adv Signal Process
– volume: 58
  start-page: 418
  year: 2019
  end-page: 426
  article-title: Effusion-synovitis and infrapatellar fat pad signal intensity alteration differentiate accelerated knee osteoarthritis
  publication-title: Rheumatology (Oxford)
– volume: 113
  start-page: 1
  year: 2019
  end-page: 12
  article-title: An extensive review regarding the adipokines in the pathogenesis and progression of osteoarthritis
  publication-title: Cytokine
– volume: 9
  start-page: 34
  year: 2020
  article-title: Breast cancer classification with reduced feature set using association rules and support vector machine
  publication-title: Netw Model Anal Health Inform Bioinform
– volume: 13
  start-page: 2573
  year: 2020
  end-page: 2577
  article-title: Brain tumour segmentation and measurement based on threshold and support vector machine classifier
  publication-title: Res J Pharm Technol
– volume: 45
  start-page: 5
  year: 2001
  end-page: 32
  article-title: Random forests
  publication-title: Mach Learn
– volume: 48
  start-page: 64
  year: 2015
  article-title: The role of MCP-1-CCR2 ligand-receptor axis in chondrocyte degradation and disease progress in knee osteoarthritis
  publication-title: Biol Res
– volume: 17
  start-page: 100152
  year: 2020
  article-title: A novel hybrid approach for diagnosing diabetes mellitus using farthest first and support vector machine algorithms
  publication-title: Obes Med
– volume: 68
  start-page: 938
  year: 2009
  end-page: 947
  article-title: Protective effects of licofelone, a 5-lipoxygenase and cyclo-oxygenase inhibitor, versus naproxen on cartilage loss in knee osteoarthritis: a first multicentre clinical trial using quantitative MRI
  publication-title: Ann Rheum Dis
– volume: 65
  start-page: 936
  year: 2013
  end-page: 944
  article-title: Association of leptin levels with radiographic knee osteoarthritis among a cohort of midlife women
  publication-title: Arthritis Care Res (Hoboken)
– volume: 53
  start-page: 187
  year: 2006
  end-page: 191
  article-title: Can threshold networks be trained directly?
  publication-title: IEEE Trans Circuits Syst II: Express Briefs
– volume: 4
  start-page: 315
  year: 2012
  end-page: 325
  article-title: Significance of C-reactive protein in osteoarthritis and total knee arthroplasty outcomes
  publication-title: Ther Adv Musculoskelet Dis
– volume: 37
  start-page: 593
  year: 2019
  end-page: 600
  article-title: Volume change in infrapatellar fat pad is associated not with obesity but with cartilage degeneration
  publication-title: J Orthop Res
– volume: 20
  start-page: 846
  year: 2012
  end-page: 853
  article-title: Serum adipokines in osteoarthritis; comparison with controls and relationship with local parameters of synovial inflammation and cartilage damage
  publication-title: Osteoarthritis Cartilage
– volume: 50
  start-page: 476
  year: 2004
  end-page: 487
  article-title: Quantitative magnetic resonance imaging evaluation of knee osteoarthritis progression over two years and correlation with clinical symptoms and radiologic changes
  publication-title: Arthritis Rheum
– volume: 33
  start-page: 414
  year: 2020
  end-page: 422
  article-title: Three-dimensional texture feature analysis of pulmonary nodules in CT Images: lung cancer predictive models based on support vector machine classifier
  publication-title: J Digit Imaging
– volume: 14
  start-page: 690
  year: 2006
  end-page: 695
  article-title: Differential distribution of adipokines between serum and synovial fluid in patients with osteoarthritis. Contribution of joint tissues to their articular production
  publication-title: Osteoarthritis Cartilage
– volume: 117
  start-page: 178
  year: 1991
  end-page: 188
  article-title: Nonparametric regression and short-term freeway traffic forecosting
  publication-title: J Transport Eng
– volume: 18
  start-page: 207
  year: 2016
  article-title: Synovial fluid adipokines are associated with clinical severity in knee osteoarthritis: a cross-sectional study in female patients with joint effusion
  publication-title: Arthritis Res Ther
– volume: 27
  start-page: 2488
  year: 2004
  end-page: 2490
  article-title: Leptin-to-adiponectin ratio as a potential atherogenic index in obese type 2 diabetic patients
  publication-title: Diabetes Care
– volume: 15
  start-page: 966
  year: 2007
  end-page: 971
  article-title: Interpretation of serum C-reactive protein (CRP) levels for cardiovascular disease risk is complicated by race, pulmonary disease, body mass index, gender, and osteoarthritis
  publication-title: Osteoarthritis Cartilage
– volume: 2017
  start-page: 5468023
  year: 2017
  article-title: Adipokine contribution to the pathogenesis of osteoarthritis
  publication-title: Mediators Inflamm
– volume: 57
  start-page: 268
  year: 2008
  end-page: 273
  article-title: The ratio of leptin to adiponectin can be used as an index of insulin resistance
  publication-title: Metabolism
– volume: 10
  start-page: 9993
  year: 2020
  article-title: Serum adipokines/related inflammatory factors and ratios as predictors of infrapatellar fat pad volume in osteoarthritis: applying comprehensive machine learning approaches
  publication-title: Sci Rep
– volume: 57
  start-page: 1851
  year: 2018
  end-page: 1860
  article-title: High in vivo levels of adipsin lead to increased knee tissue degradation in osteoarthritis: data from humans and animal models
  publication-title: Rheumatology (Oxford)
– volume: 4
  start-page: 499
  year: 2001
  end-page: 502
  article-title: Gender differences in fat metabolism
  publication-title: Curr Opin Clin Nutr Metab Care
– volume: 10
  year: 2015
  article-title: Significance of increased leptin expression in osteoarthritis patients
  publication-title: PLoS One
– volume: 40
  start-page: 1178
  year: 1997
  end-page: 1184
  article-title: Plasma leptin concentrations: gender differences and associations with metabolic risk factors for cardiovascular disease
  publication-title: Diabetologia
– volume: 52
  start-page: 1077
  year: 2013
  end-page: 1083
  article-title: The association of adipokine levels in plasma and synovial fluid with the severity of knee osteoarthritis
  publication-title: Rheumatology (Oxford)
– volume: 13
  start-page: 769
  year: 2005
  end-page: 781
  article-title: A meta-analysis of sex differences prevalence, incidence and severity of osteoarthritis
  publication-title: Osteoarthritis Cartilage
– volume: 5
  start-page: 319
  year: 2014
  end-page: 327
  article-title: Adipokines: biomarkers for osteoarthritis?
  publication-title: World J Orthop
– volume: 20
  start-page: 241
  year: 2019
  article-title: Early pre-radiographic structural pathology precedes the onset of accelerated knee osteoarthritis
  publication-title: BMC Musculoskelet Disord
– volume: 71
  start-page: 1595
  year: 2019
  end-page: 1598
  article-title: Using machine learning to molecularly classify systemic sclerosis patients
  publication-title: Arthritis Rheumatol
– volume: 10
  year: 2015
  ident: bibr37-1759720X21993254
  publication-title: PLoS One
– ident: bibr9-1759720X21993254
  doi: 10.1016/j.fertnstert.2015.05.007
– ident: bibr46-1759720X21993254
  doi: 10.1016/j.joca.2007.02.014
– ident: bibr13-1759720X21993254
  doi: 10.1038/s41598-020-66330-0
– ident: bibr26-1759720X21993254
  doi: 10.1109/TCSII.2005.857540
– ident: bibr39-1759720X21993254
  doi: 10.1177/1759720X12455959
– ident: bibr3-1759720X21993254
  doi: 10.1093/rheumatology/kev408
– ident: bibr1-1759720X21993254
  doi: 10.1016/j.semarthrit.2017.10.016
– ident: bibr36-1759720X21993254
  doi: 10.1186/s40659-015-0057-0
– ident: bibr16-1759720X21993254
  doi: 10.1016/j.joca.2018.12.027
– ident: bibr31-1759720X21993254
  doi: 10.1002/art.40902
– start-page: 215
  volume-title: Paper presented at 11th European Symposium on Artificial Neural Networks (ESANN)
  ident: bibr30-1759720X21993254
– ident: bibr54-1759720X21993254
  doi: 10.1007/s13721-020-00237-8
– ident: bibr2-1759720X21993254
  doi: 10.1002/art.20000
– ident: bibr23-1759720X21993254
  doi: 10.1061/(ASCE)0733-947X(1991)117:2(178)
– ident: bibr12-1759720X21993254
  doi: 10.2337/diacare.27.10.2488
– ident: bibr28-1759720X21993254
  doi: 10.1016/j.humov.2019.05.006
– ident: bibr7-1759720X21993254
  doi: 10.1093/rheumatology/kes422
– ident: bibr53-1759720X21993254
  doi: 10.1002/art.40898
– ident: bibr41-1759720X21993254
  doi: 10.1016/j.cyto.2012.06.018
– ident: bibr17-1759720X21993254
  doi: 10.1093/rheumatology/key305
– ident: bibr27-1759720X21993254
  doi: 10.1007/978-1-4757-3264-1
– ident: bibr40-1759720X21993254
  doi: 10.1016/j.joca.2006.10.010
– ident: bibr44-1759720X21993254
  doi: 10.1017/S0007114507853347
– ident: bibr8-1759720X21993254
  doi: 10.1016/j.joca.2012.05.002
– ident: bibr10-1759720X21993254
  doi: 10.1016/j.metabol.2007.09.011
– ident: bibr56-1759720X21993254
  doi: 10.1016/j.joca.2012.02.636
– year: 1998
  ident: bibr29-1759720X21993254
  publication-title: MSR-TR-98-14, Microsoft Research
– ident: bibr50-1759720X21993254
  doi: 10.5958/0974-360X.2020.00458.8
– ident: bibr32-1759720X21993254
  doi: 10.1016/j.cyto.2018.06.019
– ident: bibr35-1759720X21993254
  doi: 10.1136/annrheumdis-2013-204189
– ident: bibr43-1759720X21993254
  doi: 10.1016/j.joca.2005.04.014
– ident: bibr33-1759720X21993254
  doi: 10.1093/rheumatology/key181
– ident: bibr15-1759720X21993254
  doi: 10.1007/s10067-010-1429-z
– ident: bibr20-1759720X21993254
  doi: 10.1177/1759720X20933468
– ident: bibr5-1759720X21993254
  doi: 10.1016/j.joca.2006.01.009
– ident: bibr45-1759720X21993254
  doi: 10.1097/00075197-200111000-00006
– ident: bibr14-1759720X21993254
  doi: 10.1016/j.joca.2019.04.016
– ident: bibr34-1759720X21993254
  doi: 10.1155/2017/5468023
– ident: bibr55-1759720X21993254
  doi: 10.1016/j.obmed.2019.100152
– volume: 27
  start-page: 1
  year: 2020
  ident: bibr49-1759720X21993254
  publication-title: EURASIP J Adv Signal Process
– ident: bibr22-1759720X21993254
  doi: 10.1016/j.joca.2006.11.009
– ident: bibr47-1759720X21993254
  doi: 10.1046/j.1365-2796.2000.00678.x
– ident: bibr11-1759720X21993254
  doi: 10.1161/STROKEAHA.107.485540
– ident: bibr51-1759720X21993254
  doi: 10.1007/s10278-019-00238-8
– ident: bibr6-1759720X21993254
  doi: 10.1186/s13075-016-1103-1
– ident: bibr18-1759720X21993254
  doi: 10.1186/s12891-019-2624-y
– ident: bibr24-1759720X21993254
  doi: 10.1023/A:1010933404324
– ident: bibr21-1759720X21993254
  doi: 10.1136/ard.2008.088732
– ident: bibr48-1759720X21993254
  doi: 10.1007/s001250050804
– ident: bibr4-1759720X21993254
  doi: 10.5312/wjo.v5.i3.319
– volume-title: Classification and regression trees
  year: 1993
  ident: bibr25-1759720X21993254
– ident: bibr52-1759720X21993254
  doi: 10.1016/j.cmpb.2020.105464
– ident: bibr42-1759720X21993254
  doi: 10.1038/sj.ijo.0803259
– ident: bibr19-1759720X21993254
  doi: 10.1002/jor.24201
– ident: bibr38-1759720X21993254
  doi: 10.1002/acr.21922
SSID ssj0069091
Score 2.3892725
Snippet Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine...
In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine learning...
Aim: In osteoarthritis (OA) there is a need for automated screening systems for early detection of structural progressors. We built a comprehensive machine...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
sage
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1759720X21993254
SubjectTerms Accuracy
Arthritis
Automation
Gender
Knee
Machine learning
Original Research
Osteoarthritis
Patients
Reproducibility
Risk factors
Support vector machines
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwEB6hHiouCMorUJCREBKHaOPEz2OpWlVI5USlvUV-TLqFNlvBIv4-Y8e77fK8kGM8iUbjsefh8TcAr9XQGbSC14PWKVsVY-1l62pN7qtG563LF4VPP6iTM_F-Lue3Wn2lmrAJHngS3CwK3UWjrbJRi6ET1g_CKTTBG984zNd8yeatg6lpD6aQz_KbQ8kZ2Uir22bepnK1VootI5Sx-n_nYP5aJ3mr2Cvbn-P7cK84juxgYvgB3MFxD3ZPy9H4Q_h0wL5PWQ52lQskkZWOEOfMXZ4vv1ysFleMXFSGCdOYfR4RWbrhsSQZLDK0EZvAZBMQB8t1W7QLEn2BXmW0wVDQS_97BGfHRx8PT-rSSKEO0opVLYOPsYlKRumt4dgECgSdU8rxqFwUznqJ3tiAiif8PrQ-mE5FY0joHHn3GHbG5YhPgRklebTktoUhIdG11g3B0dMYlJoi0gpma8n2oaCMp2YXlz0vwOI_z0UFbzdfXE8IG3-hfZcma0OXsLHzC9KYvmhM_y-NqWB_PdV9WbBfewokybUkaakKXm2Gaaml8xM34vIb0Ugy95pbIyt4MmnGhpOuS9G9bCrQWzqzxer2yHixyHDeCSJNt10Fb5J23bD0JyE8-x9CeA5321Sdk5NJ-7BD-oUvyL1a-Zd5Jf0A17sh6Q
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagSIhLxZtAQUZCSByijRM_T6itqCqkcqLS3iK_sgu0SR9b8feZcbxZlkdzdJxk4pmxZ8bjbwh5J7tGR8NZ2SmF0aoQSidqWyowX1W0zth0UPjkizw-5Z_nYp4Dbtc5rXI9J6aJOgweY-QzsPRh7ReGy48XlyVWjcLd1VxC4y65h9BlmNKl5pPDBY5fqpgHK6SBj1fzzTblDNuwqcYEtlrwrWUpoff_y-T8O3Pyt_SvtCIdPSS72ZSk-yPvH5E7sX9M7p_kzfIn5Ps-_TnGPeh5SpmMNNeIWFB7toCfWy3PKRitNCLKMf3Rx0jxzMcA4rRMYEd0hJdFaA6aMrlgXoT-GYyVwpQDbjC87yk5Pfr09fC4zKUVSg9DuCqFdyFUQYognNEsVh5cQ2ultCxIG7g1TkSnjY-SIaJfNM7rRgatTVAssuYZ2emHPr4gVEvBggFDzneITVcb23kLV6WjUOCjFmS2HtnWZ9xxLH9x1rIMNf4nLwryYXriYsTcuKXvATJr6odo2alhuFq0WfnawFUTtDISiOddw43ruJVRe6ddZSOQuLdmdZtV-LrdCFxB3k63QflwR8X2cbiBPgIMAMWMFgV5PkrGREnToL8vqoKoLZnZInX7Tv9tmQC-ETRN1U1B3qN0bUj63yC8vJ3-V-RBjZk4KXC0R3ZAcuJrMKVW7k3Sl19shBq9
  priority: 102
  providerName: ProQuest
Title A warning machine learning algorithm for early knee osteoarthritis structural progressor patient screening
URI https://journals.sagepub.com/doi/full/10.1177/1759720X21993254
https://www.ncbi.nlm.nih.gov/pubmed/33747150
https://www.proquest.com/docview/2613245946
https://www.proquest.com/docview/2503671985
https://pubmed.ncbi.nlm.nih.gov/PMC7905723
https://doaj.org/article/d473d87969d74f349bf4a6e8cb8b0ae8
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3raxNBEF_6APGL-PZqDSuI4Icz99rXJ0mloQgtUlrMt2Nfl7Q2F2kTxP_emb291FgV8-XgbnI3zM7szmt_S8gb3pTSqypPGyEwW-VcalihUwHuq_DaKB02Ch-f8KPz6tOETbZI2--FiRK8eY9tVcBRmKzRujEbPYxFxiGseUoU2aTA9jMIcT6slvO6y3b3h2rgHSxPr-ZY2bbYD_kj7Xe3bZPdQnAGhrw7Gp9-OevnbggVwxl7-P4UP3Bb2LzzzY2FLOD9_8lJvdtr-UvDWFjDxg_Jg-h80lGnLY_Ilm8fk3vHsbz-hFyO6PcuU0LnocnS03iqxJTqq-ni-mI5m1Nwc6lHXGT6tfWe4i6RBSjgLMAj0Q6QFsE8aOj9gpkU6CN8K4VJCgJneN9Tcj4-PPt4lMbDGFLLVLVMmTXOZY4zx4ySuc8sBJNac65zx7WrtDLMG6ms5zliAHplrCy5k1I5kfu8fEZ22kXrXxAqQfJOgetnG0SzK5RurIZfJj0TENUmZNhLtrYRqRwPzLiq8whO_vtYJOTd-h_fOpSOf9Ae4GCt6RBfO9xYXE_raK61q0TppFAcmK-aslKmqTT30hppMu2Bxf1-qOteZWsIRsE9BWnxhLxePwZzxRqMbv1iBTQMXAaRK8kS8rzTjDUnZYkZApYlRGzozAarm0_ai1mABEeYNVGUCXmL2nXL0t-EsPe_hC_J_QK7eELSaZ_sgA75V-CGLc2AbIuJGEQLguvB4cnn00FIavwEhh8xuQ
linkProvider SAGE Publications
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LbxMxEB6VVAIuiDcLBYwESBxW2YefB4RaaJXSJkKolXLb2mtvArSbQoMq_hS_kbF3NyE8euse_dKsPR7PjMffADznVS6domlcCeG9VdbGhmU6Fqi-CqeN0uGh8HDEB4f0_ZiN1-Bn9xbGh1V2MjEIajsrvY-8j5o-nv1MUf7m9Gvss0b529UuhUbDFnvuxzmabGevd9_h-r7Isp3tg7eDuM0qEJfYex6z0libWM4sM0qmLinRKtKac51ari3VyjBnpCodTz2YnVOmlDm3UiorUpfmOO4VWKc5mjI9WN_aHn342Ml-NDVDjj48kxX-bjJeXoz2fZkvynzIXMboykEY8gX8S8n9O1bzt4CzcAbu3IQbrfJKNhtuuwVrrr4NV4ft9fwd-LxJzhtPCzkJQZqOtFkpJkQfT3A659MTgmoycR5XmXypnSP-lckMGXga4JVIA2jrwUBIiB1DSYztW_hXgkIODW8c7y4cXsq034NePavdAyCSs9QqVB3LyqPhZUpXpcYvkY4JtIoj6HczW5Qt0rlPuHFcpC24-Z9rEcGrRY_TBuXjgrZbfrEW7Tw-dyiYfZsU7XYvLBW5lUJxJJ5WOVWmopo7WRppEu2QxI1uqYtWaJwVSxaP4NmiGre7v8PRtZt9xzYMVQ6RKskiuN9wxoKSPPceBpZEIFZ4ZoXU1Zr60zRAinuYNpHlEbz03LUk6X-T8PBi-p_CtcHBcL_Y3x3tPYLrmY8DCm6rDeghF7nHqMjNzZN29xA4uuwN-wusI1nq
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1ZbxQxDLZgK1W8IO4OFAgSQuJh2LlyPS7HqhytEGrFvo2SSWa30M5UZRF_HzuT3bIUEPM4cSLLsRM7dr4APBVtqbyu8rSVkk6rnEstL0wq0X2V3lhtwkXh_QOxd1S9m_FZrM2huzBRgt9eUFkVchQWa7LuM9eOY45xjFuelkU2K6j6DCOcq7BVVbg1jmBrMv30-XC1FGPkF57MI_qUOlzkKS-NsbEvBfj-P_mcl0snf6n_ClvS9AZcj74kmwyTfxOu-O4WbO_HbPlt-DJhP4aDD3YaaiY9i49EzJk5mffnx8vFKUOvlXmCOWZfO-8ZXfroUZ8WAe2IDfiyhM3BQikXLoxIH9FYGa45GAfjeHfgaPrm8NVeGt9WSBuuq2XKG-tc5gR33GqV-6zB2NAYIUzuhHGV0ZZ7q3TjRU6Qfl7bRpXCKaWdzH1e3oVR13d-B5gSPHcaPbmmJXC6Qpu2MfhlynOJQWoC45Vk6yYCj9P7Fyd1HrHGf5-LBJ6ve5wNoBv_oH1Jk7WmI7js8KM_n9fR-mpXydIpqQUyX7VlpW1bGeFVY5XNjEcWd1dTXa80sMbYEr1NlJZI4Mm6Ga2PUiqm8_13pOHoAchcK57AvUEz1pyUJQX8PEtAbujMBqubLd3xIiB8E2qaLMoEnpF2XbD0NyHc_1_Cx7D98fW0_vD24P0DuFZQfU44TtqFEaqTf4gO1tI-imb0E7QRHLw
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+warning+machine+learning+algorithm+for+early+knee+osteoarthritis+structural+progressor+patient+screening&rft.jtitle=Therapeutic+advances+in+musculoskeletal+disease&rft.au=Bonakdari%2C+Hossein&rft.au=Jamshidi%2C+Afshin&rft.au=Pelletier%2C+Jean-Pierre&rft.au=Abram%2C+Fran%C3%A7ois&rft.date=2021&rft.issn=1759-720X&rft.volume=13&rft.spage=1759720X21993254&rft_id=info:doi/10.1177%2F1759720X21993254&rft_id=info%3Apmid%2F33747150&rft.externalDocID=33747150
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1759-720X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1759-720X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1759-720X&client=summon