Inflammatory biomarkers of low back pain and disc degeneration: a review
Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in human subjects. LBP is the leading cause of disability, caused by various spine‐related disorders, including intervertebral disc degeneration,...
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| Published in: | Annals of the New York Academy of Sciences Vol. 1410; no. 1; pp. 68 - 84 |
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| Main Authors: | , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Wiley Subscription Services, Inc
01.12.2017
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| Subjects: | |
| ISSN: | 0077-8923, 1749-6632, 1749-6632 |
| Online Access: | Get full text |
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| Abstract | Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in human subjects. LBP is the leading cause of disability, caused by various spine‐related disorders, including intervertebral disc degeneration, disc herniation, spinal stenosis, and facet arthritis. The focus of these studies is inflammatory mediators, because inflammation contributes to the pathogenesis of disc degeneration and associated pain mechanisms. Increasingly, studies suggest that the presence of inflammatory mediators can be measured systemically in the blood. These biomarkers may serve as novel tools for directing patient care. Currently, patient response to treatment is unpredictable with a significant rate of recurrence, and, while surgical treatments may provide anatomical correction and pain relief, they are invasive and costly. The review covers studies performed on populations with specific diagnoses and undefined origins of LBP. Since the natural history of LBP is progressive, the temporal nature of studies is categorized by duration of symptomology/disease. Related studies on changes in biomarkers with treatment are also reviewed. Ultimately, diagnostic biomarkers of LBP and spinal degeneration have the potential to shepherd an era of individualized spine medicine for personalized therapeutics in the treatment of LBP. |
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| AbstractList | Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in human subjects. LBP is the leading cause of disability, caused by various spine‐related disorders, including intervertebral disc degeneration, disc herniation, spinal stenosis, and facet arthritis. The focus of these studies is inflammatory mediators, because inflammation contributes to the pathogenesis of disc degeneration and associated pain mechanisms. Increasingly, studies suggest that the presence of inflammatory mediators can be measured systemically in the blood. These biomarkers may serve as novel tools for directing patient care. Currently, patient response to treatment is unpredictable with a significant rate of recurrence, and, while surgical treatments may provide anatomical correction and pain relief, they are invasive and costly. The review covers studies performed on populations with specific diagnoses and undefined origins of LBP. Since the natural history of LBP is progressive, the temporal nature of studies is categorized by duration of symptomology/disease. Related studies on changes in biomarkers with treatment are also reviewed. Ultimately, diagnostic biomarkers of LBP and spinal degeneration have the potential to shepherd an era of individualized spine medicine for personalized therapeutics in the treatment of LBP. Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in human subjects. LBP is the leading cause of disability, caused by various spine-related disorders, including intervertebral disc degeneration, disc herniation, spinal stenosis, and facet arthritis. The focus of these studies is inflammatory mediators, because inflammation contributes to the pathogenesis of disc degeneration and associated pain mechanisms. Increasingly, studies suggest that the presence of inflammatory mediators can be measured systemically in the blood. These biomarkers may serve as novel tools for directing patient care. Currently, patient response to treatment is unpredictable with a significant rate of recurrence, and, while surgical treatments may provide anatomical correction and pain relief, they are invasive and costly. The review covers studies performed on populations with specific diagnoses and undefined origins of LBP. Since the natural history of LBP is progressive, the temporal nature of studies is categorized by duration of symptomology/disease. Related studies on changes in biomarkers with treatment are also reviewed. Ultimately, diagnostic biomarkers of LBP and spinal degeneration have the potential to shepherd an era of individualized spine medicine for personalized therapeutics in the treatment of LBP.Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in human subjects. LBP is the leading cause of disability, caused by various spine-related disorders, including intervertebral disc degeneration, disc herniation, spinal stenosis, and facet arthritis. The focus of these studies is inflammatory mediators, because inflammation contributes to the pathogenesis of disc degeneration and associated pain mechanisms. Increasingly, studies suggest that the presence of inflammatory mediators can be measured systemically in the blood. These biomarkers may serve as novel tools for directing patient care. Currently, patient response to treatment is unpredictable with a significant rate of recurrence, and, while surgical treatments may provide anatomical correction and pain relief, they are invasive and costly. The review covers studies performed on populations with specific diagnoses and undefined origins of LBP. Since the natural history of LBP is progressive, the temporal nature of studies is categorized by duration of symptomology/disease. Related studies on changes in biomarkers with treatment are also reviewed. Ultimately, diagnostic biomarkers of LBP and spinal degeneration have the potential to shepherd an era of individualized spine medicine for personalized therapeutics in the treatment of LBP. |
| Author | Khan, Aysha N. Lenke, Lawrence G. Lehman, Ronald A. Jacobsen, Hayley E. Levine, Mitchell Chahine, Nadeen O. Khan, Jansher Filippi, Christopher G. Riew, K. Daniel |
| AuthorAffiliation | 2 Department of Orthopedic Surgery, Columbia University, New York, New York 1 The Feinstein Institute for Medical Research, Northwell Health, Manhasset, New York 4 New York Presbyterian – Spine Hospital, New York, New York 5 Department of Biomedical Engineering, Columbia University, New York, New York 3 Lenox Hill Hospital, Northwell Health, New York, New York |
| AuthorAffiliation_xml | – name: 3 Lenox Hill Hospital, Northwell Health, New York, New York – name: 4 New York Presbyterian – Spine Hospital, New York, New York – name: 2 Department of Orthopedic Surgery, Columbia University, New York, New York – name: 5 Department of Biomedical Engineering, Columbia University, New York, New York – name: 1 The Feinstein Institute for Medical Research, Northwell Health, Manhasset, New York |
| Author_xml | – sequence: 1 givenname: Aysha N. surname: Khan fullname: Khan, Aysha N. organization: Northwell Health – sequence: 2 givenname: Hayley E. surname: Jacobsen fullname: Jacobsen, Hayley E. organization: Columbia University – sequence: 3 givenname: Jansher surname: Khan fullname: Khan, Jansher organization: Northwell Health – sequence: 4 givenname: Christopher G. surname: Filippi fullname: Filippi, Christopher G. organization: Northwell Health – sequence: 5 givenname: Mitchell surname: Levine fullname: Levine, Mitchell organization: Northwell Health – sequence: 6 givenname: Ronald A. surname: Lehman fullname: Lehman, Ronald A. organization: New York‐Presbyterian–Spine Hospital – sequence: 7 givenname: K. Daniel surname: Riew fullname: Riew, K. Daniel organization: New York‐Presbyterian–Spine Hospital – sequence: 8 givenname: Lawrence G. surname: Lenke fullname: Lenke, Lawrence G. organization: New York‐Presbyterian–Spine Hospital – sequence: 9 givenname: Nadeen O. orcidid: 0000-0002-0478-6042 surname: Chahine fullname: Chahine, Nadeen O. email: noc7@columbia.edu organization: Columbia University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29265416$$D View this record in MEDLINE/PubMed |
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| Copyright | 2017 New York Academy of Sciences. 2017 The New York Academy of Sciences |
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| DOI | 10.1111/nyas.13551 |
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| Keywords | intervertebral disc degeneration spine back pain inflammation biomarkers |
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| Snippet | Biomarkers are biological characteristics that can be used to indicate health or disease. This paper reviews studies on biomarkers of low back pain (LBP) in... |
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| SubjectTerms | Arthritis Back pain Biomarkers Biomarkers - blood Cytokines - blood Degeneration Diagnostic systems Humans Inflammation Inflammation Mediators - blood intervertebral disc degeneration Intervertebral Disc Degeneration - blood Intervertebral Disc Degeneration - diagnosis Intervertebral Disc Degeneration - therapy Intervertebral discs Low back pain Low Back Pain - blood Low Back Pain - diagnosis Low Back Pain - therapy Outcome Assessment (Health Care) - methods Pain Pathogenesis Population studies Sensitivity and Specificity Spinal stenosis Spine Surgical instruments Symptomology |
| Title | Inflammatory biomarkers of low back pain and disc degeneration: a review |
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