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The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain

PURPOSE: The composition of the subchondral bone marrow and cartilage endplate (CEP) could affect intervertebral disc health by influencing vertebral perfusion and nutrient diffusion. However, the relative contributions of these factors to disc degeneration in patients with chronic low back pain (cL...

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Autores principales: Bonnheim, Noah B., Wang, Linshanshan, Lazar, Ann A., Zhou, Jiamin, Chachad, Ravi, Sollmann, Nico, Guo, Xiaojie, Iriondo, Claudia, O’Neill, Conor, Lotz, Jeffrey C., Link, Thomas M., Krug, Roland, Fields, Aaron J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252939/
https://www.ncbi.nlm.nih.gov/pubmed/35441890
http://dx.doi.org/10.1007/s00586-022-07206-x
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author Bonnheim, Noah B.
Wang, Linshanshan
Lazar, Ann A.
Zhou, Jiamin
Chachad, Ravi
Sollmann, Nico
Guo, Xiaojie
Iriondo, Claudia
O’Neill, Conor
Lotz, Jeffrey C.
Link, Thomas M.
Krug, Roland
Fields, Aaron J.
author_facet Bonnheim, Noah B.
Wang, Linshanshan
Lazar, Ann A.
Zhou, Jiamin
Chachad, Ravi
Sollmann, Nico
Guo, Xiaojie
Iriondo, Claudia
O’Neill, Conor
Lotz, Jeffrey C.
Link, Thomas M.
Krug, Roland
Fields, Aaron J.
author_sort Bonnheim, Noah B.
collection PubMed
description PURPOSE: The composition of the subchondral bone marrow and cartilage endplate (CEP) could affect intervertebral disc health by influencing vertebral perfusion and nutrient diffusion. However, the relative contributions of these factors to disc degeneration in patients with chronic low back pain (cLBP) have not been quantified. The goal of this study was to use compositional biomarkers derived from quantitative MRI to establish how CEP composition (surrogate for permeability) and vertebral bone marrow fat fraction (BMFF, surrogate for perfusion) relate to disc degeneration. METHODS: MRI data from 60 patients with cLBP were included in this prospective observational study (28 female, 32 male; age = 40.0 ± 11.9 years, 19–65 [mean ± SD, min–max]). Ultra-short echo-time MRI was used to calculate CEP T2* relaxation times (reflecting biochemical composition), water-fat MRI was used to calculate vertebral BMFF, and T1ρ MRI was used to calculate T1ρ relaxation times in the nucleus pulposus (NP T1ρ, reflecting proteoglycan content and degenerative grade). Univariate linear regression was used to assess the independent effects of CEP T2* and vertebral BMFF on NP T1ρ. Mixed effects multivariable linear regression accounting for age, sex, and BMI was used to assess the combined relationship between variables. RESULTS: CEP T2* and vertebral BMFF were independently associated with NP T1ρ (p = 0.003 and 0.0001, respectively). After adjusting for age, sex, and BMI, NP T1ρ remained significantly associated with CEP T2* (p = 0.0001) but not vertebral BMFF (p = 0.43). CONCLUSION: Poor CEP composition plays a significant role in disc degeneration severity and can affect disc health both with and without deficits in vertebral perfusion. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00586-022-07206-x.
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spelling pubmed-92529392022-07-06 The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain Bonnheim, Noah B. Wang, Linshanshan Lazar, Ann A. Zhou, Jiamin Chachad, Ravi Sollmann, Nico Guo, Xiaojie Iriondo, Claudia O’Neill, Conor Lotz, Jeffrey C. Link, Thomas M. Krug, Roland Fields, Aaron J. Eur Spine J Original Article PURPOSE: The composition of the subchondral bone marrow and cartilage endplate (CEP) could affect intervertebral disc health by influencing vertebral perfusion and nutrient diffusion. However, the relative contributions of these factors to disc degeneration in patients with chronic low back pain (cLBP) have not been quantified. The goal of this study was to use compositional biomarkers derived from quantitative MRI to establish how CEP composition (surrogate for permeability) and vertebral bone marrow fat fraction (BMFF, surrogate for perfusion) relate to disc degeneration. METHODS: MRI data from 60 patients with cLBP were included in this prospective observational study (28 female, 32 male; age = 40.0 ± 11.9 years, 19–65 [mean ± SD, min–max]). Ultra-short echo-time MRI was used to calculate CEP T2* relaxation times (reflecting biochemical composition), water-fat MRI was used to calculate vertebral BMFF, and T1ρ MRI was used to calculate T1ρ relaxation times in the nucleus pulposus (NP T1ρ, reflecting proteoglycan content and degenerative grade). Univariate linear regression was used to assess the independent effects of CEP T2* and vertebral BMFF on NP T1ρ. Mixed effects multivariable linear regression accounting for age, sex, and BMI was used to assess the combined relationship between variables. RESULTS: CEP T2* and vertebral BMFF were independently associated with NP T1ρ (p = 0.003 and 0.0001, respectively). After adjusting for age, sex, and BMI, NP T1ρ remained significantly associated with CEP T2* (p = 0.0001) but not vertebral BMFF (p = 0.43). CONCLUSION: Poor CEP composition plays a significant role in disc degeneration severity and can affect disc health both with and without deficits in vertebral perfusion. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00586-022-07206-x. Springer Berlin Heidelberg 2022-04-20 2022-07 /pmc/articles/PMC9252939/ /pubmed/35441890 http://dx.doi.org/10.1007/s00586-022-07206-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Bonnheim, Noah B.
Wang, Linshanshan
Lazar, Ann A.
Zhou, Jiamin
Chachad, Ravi
Sollmann, Nico
Guo, Xiaojie
Iriondo, Claudia
O’Neill, Conor
Lotz, Jeffrey C.
Link, Thomas M.
Krug, Roland
Fields, Aaron J.
The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title_full The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title_fullStr The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title_full_unstemmed The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title_short The contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
title_sort contributions of cartilage endplate composition and vertebral bone marrow fat to intervertebral disc degeneration in patients with chronic low back pain
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252939/
https://www.ncbi.nlm.nih.gov/pubmed/35441890
http://dx.doi.org/10.1007/s00586-022-07206-x
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