T2‐weighted magnetic resonance imaging texture as predictor of low back pain: A texture analysis‐based classification pipeline to symptomatic and asymptomatic cases
Low back pain is a very common symptom and the leading cause of disability throughout the world. Several degenerative imaging findings seen on magnetic resonance imaging are associated with low back pain but none of them is specific for the presence of low back pain as abnormal findings are prevalen...
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Published in | Journal of orthopaedic research Vol. 39; no. 11; pp. 2428 - 2438 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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01.11.2021
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Abstract | Low back pain is a very common symptom and the leading cause of disability throughout the world. Several degenerative imaging findings seen on magnetic resonance imaging are associated with low back pain but none of them is specific for the presence of low back pain as abnormal findings are prevalent among asymptomatic subjects as well. The purpose of this population‐based study was to investigate if more specific magnetic resonance imaging predictors of low back pain could be found via texture analysis and machine learning. We used this methodology to classify T2‐weighted magnetic resonance images from the Northern Finland Birth Cohort 1966 data to symptomatic and asymptomatic groups. Lumbar spine magnetic resonance imaging was performed using a fast spin‐echo sequence at 1.5 T. Texture analysis pipeline consisting of textural feature extraction, principal component analysis, and logistic regression classifier was applied to the data to classify them into symptomatic (clinically relevant pain with frequency ≥30 days and intensity ≥6/10) and asymptomatic (frequency ≤7 days, intensity ≤3/10, and no previous pain episodes in the follow‐up period) groups. Best classification results were observed applying texture analysis to the two lowest intervertebral discs (L4‐L5 and L5‐S1), with accuracy of 83%, specificity of 83%, sensitivity of 82%, negative predictive value of 94%, precision of 56%, and receiver operating characteristic area‐under‐curve of 0.91. To conclude, textural features from T2‐weighted magnetic resonance images can be applied in low back pain classification. |
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AbstractList | Low back pain is a very common symptom and the leading cause of disability throughout the world. Several degenerative imaging findings seen on magnetic resonance imaging are associated with low back pain but none of them is specific for the presence of low back pain as abnormal findings are prevalent among asymptomatic subjects as well. The purpose of this population-based study was to investigate if more specific magnetic resonance imaging predictors of low back pain could be found via texture analysis and machine learning. We used this methodology to classify T2 -weighted magnetic resonance images from the Northern Finland Birth Cohort 1966 data to symptomatic and asymptomatic groups. Lumbar spine magnetic resonance imaging was performed using a fast spin-echo sequence at 1.5 T. Texture analysis pipeline consisting of textural feature extraction, principal component analysis, and logistic regression classifier was applied to the data to classify them into symptomatic (clinically relevant pain with frequency ≥30 days and intensity ≥6/10) and asymptomatic (frequency ≤7 days, intensity ≤3/10, and no previous pain episodes in the follow-up period) groups. Best classification results were observed applying texture analysis to the two lowest intervertebral discs (L4-L5 and L5-S1), with accuracy of 83%, specificity of 83%, sensitivity of 82%, negative predictive value of 94%, precision of 56%, and receiver operating characteristic area-under-curve of 0.91. To conclude, textural features from T2 -weighted magnetic resonance images can be applied in low back pain classification.Low back pain is a very common symptom and the leading cause of disability throughout the world. Several degenerative imaging findings seen on magnetic resonance imaging are associated with low back pain but none of them is specific for the presence of low back pain as abnormal findings are prevalent among asymptomatic subjects as well. The purpose of this population-based study was to investigate if more specific magnetic resonance imaging predictors of low back pain could be found via texture analysis and machine learning. We used this methodology to classify T2 -weighted magnetic resonance images from the Northern Finland Birth Cohort 1966 data to symptomatic and asymptomatic groups. Lumbar spine magnetic resonance imaging was performed using a fast spin-echo sequence at 1.5 T. Texture analysis pipeline consisting of textural feature extraction, principal component analysis, and logistic regression classifier was applied to the data to classify them into symptomatic (clinically relevant pain with frequency ≥30 days and intensity ≥6/10) and asymptomatic (frequency ≤7 days, intensity ≤3/10, and no previous pain episodes in the follow-up period) groups. Best classification results were observed applying texture analysis to the two lowest intervertebral discs (L4-L5 and L5-S1), with accuracy of 83%, specificity of 83%, sensitivity of 82%, negative predictive value of 94%, precision of 56%, and receiver operating characteristic area-under-curve of 0.91. To conclude, textural features from T2 -weighted magnetic resonance images can be applied in low back pain classification. Low back pain is a very common symptom and the leading cause of disability throughout the world. Several degenerative imaging findings seen on magnetic resonance imaging are associated with low back pain but none of them is specific for the presence of low back pain as abnormal findings are prevalent among asymptomatic subjects as well. The purpose of this population‐based study was to investigate if more specific magnetic resonance imaging predictors of low back pain could be found via texture analysis and machine learning. We used this methodology to classify T2‐weighted magnetic resonance images from the Northern Finland Birth Cohort 1966 data to symptomatic and asymptomatic groups. Lumbar spine magnetic resonance imaging was performed using a fast spin‐echo sequence at 1.5 T. Texture analysis pipeline consisting of textural feature extraction, principal component analysis, and logistic regression classifier was applied to the data to classify them into symptomatic (clinically relevant pain with frequency ≥30 days and intensity ≥6/10) and asymptomatic (frequency ≤7 days, intensity ≤3/10, and no previous pain episodes in the follow‐up period) groups. Best classification results were observed applying texture analysis to the two lowest intervertebral discs (L4‐L5 and L5‐S1), with accuracy of 83%, specificity of 83%, sensitivity of 82%, negative predictive value of 94%, precision of 56%, and receiver operating characteristic area‐under‐curve of 0.91. To conclude, textural features from T2‐weighted magnetic resonance images can be applied in low back pain classification. |
Author | Tervonen, Osmo Niinimäki, Jaakko Inkinen, Satu I. Karppinen, Jaro Nieminen, Miika T. Ketola, Juuso H. J. |
Author_xml | – sequence: 1 givenname: Juuso H. J. orcidid: 0000-0002-7760-6241 surname: Ketola fullname: Ketola, Juuso H. J. email: juuso.ketola@oulu.fi organization: University of Oulu – sequence: 2 givenname: Satu I. orcidid: 0000-0002-9774-8925 surname: Inkinen fullname: Inkinen, Satu I. organization: University of Oulu – sequence: 3 givenname: Jaro orcidid: 0000-0002-2158-6042 surname: Karppinen fullname: Karppinen, Jaro organization: Finnish Institute of Occupational Health – sequence: 4 givenname: Jaakko orcidid: 0000-0002-5591-3726 surname: Niinimäki fullname: Niinimäki, Jaakko organization: Oulu University Hospital – sequence: 5 givenname: Osmo surname: Tervonen fullname: Tervonen, Osmo organization: Oulu University Hospital – sequence: 6 givenname: Miika T. orcidid: 0000-0002-2300-2848 surname: Nieminen fullname: Nieminen, Miika T. organization: Oulu University Hospital |
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Title | T2‐weighted magnetic resonance imaging texture as predictor of low back pain: A texture analysis‐based classification pipeline to symptomatic and asymptomatic cases |
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