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The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain

Facet tropism has been investigated as a predisposing factor for degenerative changes in the lumbar spine; however, no prior study has evaluated the relationship between disc bulge and facet tropism. In this study, we used kinetic magnetic resonance imaging (kMRI) to investigate the association betw...

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Autores principales: Do, Duc H., Taghavi, Cyrus E., Fong, Winston, Kong, Min Ho, Morishita, Yuichiro, Wang, Jeffrey C.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036031/
https://www.ncbi.nlm.nih.gov/pubmed/20734211
http://dx.doi.org/10.1007/s00586-010-1558-8
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author Do, Duc H.
Taghavi, Cyrus E.
Fong, Winston
Kong, Min Ho
Morishita, Yuichiro
Wang, Jeffrey C.
author_facet Do, Duc H.
Taghavi, Cyrus E.
Fong, Winston
Kong, Min Ho
Morishita, Yuichiro
Wang, Jeffrey C.
author_sort Do, Duc H.
collection PubMed
description Facet tropism has been investigated as a predisposing factor for degenerative changes in the lumbar spine; however, no prior study has evaluated the relationship between disc bulge and facet tropism. In this study, we used kinetic magnetic resonance imaging (kMRI) to investigate the association between degree of facet tropism and amount of disc bulge in the lumbar spine in relation to age. kMRIs in the flexion, neutral, and extension positions were performed on 410 consecutive patients with low back pain. T2-weighted midsagittal and axial mid-disc cuts were analyzed to measure disc bulge and facet angle. Facet asymmetry was calculated and classified as: no facet tropism, <6°; mild facet tropism, 6–11°; or severe facet tropism, ≥11°. Maximal static bulge (MSB), maximal dynamic bulge (MDB), and age in the facet tropism groups were compared by age subpopulations and MDB categories, defined by the positions between which the largest change in disc bulge occurs. We found the severe facet tropism group to be associated with a nearly significant increase in MSB and MDB over the no facet tropism group in the older subpopulation at the L4–L5 level only, and a larger MDB in the L4–L5 MDB category [E–N], where the greatest change in disc bulge occurs between neutral and extension positions (p = 0.013). Our findings suggest that severe facet tropism is associated with increased disc bulge at L4–L5 in only a subset of older age patients, but may in large part be due to biomechanical factors that define the [E–N] category.
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spelling pubmed-30360312011-04-05 The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain Do, Duc H. Taghavi, Cyrus E. Fong, Winston Kong, Min Ho Morishita, Yuichiro Wang, Jeffrey C. Eur Spine J Original Article Facet tropism has been investigated as a predisposing factor for degenerative changes in the lumbar spine; however, no prior study has evaluated the relationship between disc bulge and facet tropism. In this study, we used kinetic magnetic resonance imaging (kMRI) to investigate the association between degree of facet tropism and amount of disc bulge in the lumbar spine in relation to age. kMRIs in the flexion, neutral, and extension positions were performed on 410 consecutive patients with low back pain. T2-weighted midsagittal and axial mid-disc cuts were analyzed to measure disc bulge and facet angle. Facet asymmetry was calculated and classified as: no facet tropism, <6°; mild facet tropism, 6–11°; or severe facet tropism, ≥11°. Maximal static bulge (MSB), maximal dynamic bulge (MDB), and age in the facet tropism groups were compared by age subpopulations and MDB categories, defined by the positions between which the largest change in disc bulge occurs. We found the severe facet tropism group to be associated with a nearly significant increase in MSB and MDB over the no facet tropism group in the older subpopulation at the L4–L5 level only, and a larger MDB in the L4–L5 MDB category [E–N], where the greatest change in disc bulge occurs between neutral and extension positions (p = 0.013). Our findings suggest that severe facet tropism is associated with increased disc bulge at L4–L5 in only a subset of older age patients, but may in large part be due to biomechanical factors that define the [E–N] category. Springer-Verlag 2010-08-25 2011-01 /pmc/articles/PMC3036031/ /pubmed/20734211 http://dx.doi.org/10.1007/s00586-010-1558-8 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Do, Duc H.
Taghavi, Cyrus E.
Fong, Winston
Kong, Min Ho
Morishita, Yuichiro
Wang, Jeffrey C.
The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title_full The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title_fullStr The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title_full_unstemmed The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title_short The relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
title_sort relationship between degree of facet tropism and amount of dynamic disc bulge in lumbar spine of patients symptomatic for low back pain
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036031/
https://www.ncbi.nlm.nih.gov/pubmed/20734211
http://dx.doi.org/10.1007/s00586-010-1558-8
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