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Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration
STUDY DESIGN: Observational comparative study. PURPOSE: To compare fractional anisotropy (FA) maps with T2 values of the nucleus pulposus (NP) and annulus fibrosus (AF) of intervertebral discs in healthy volunteers and patients to develop a predictive disc health scale. OVERVIEW OF LITERATURE: T2-we...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Spine Surgery
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680034/ https://www.ncbi.nlm.nih.gov/pubmed/30966725 http://dx.doi.org/10.31616/asj.2018.0166 |
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author | Vadapalli, Rammohan Mulukutla, Raghavdutt Vadapalli, Abhinav Sriram Vedula, Rajanikanth Rao |
author_facet | Vadapalli, Rammohan Mulukutla, Raghavdutt Vadapalli, Abhinav Sriram Vedula, Rajanikanth Rao |
author_sort | Vadapalli, Rammohan |
collection | PubMed |
description | STUDY DESIGN: Observational comparative study. PURPOSE: To compare fractional anisotropy (FA) maps with T2 values of the nucleus pulposus (NP) and annulus fibrosus (AF) of intervertebral discs in healthy volunteers and patients to develop a predictive disc health scale. OVERVIEW OF LITERATURE: T2-weighted magnetic resonance imaging (MRI) is not sensitive to early morphological changes and provides no quantitative biomarker profile for early degeneration. METHODS: We examined 59 healthy controls and 59 patients with back pain by MRI using T2 relaxometry and diffusion tensor imaging (DTI). Each group was divided into three age subgroups: A (<30 years, n=12); B (30–50 years, n=26); and C (>50 years, n=21). We obtained FA values for AF and NP and T2 values for NP for each intervertebral disc. Furthermore, we calculated the FA (AF/NP) ratios. RESULTS: We categorized 590 intervertebral discs from 118 participants, 566 of which were analyzed with T2 relaxometry and DTI. The T2 values were as follows: subgroup A, 55.8±4.4 ms; B, 48.5±6.9 ms; C, 45.8±8.7 ms (p<0.050). The T2 values for the healthy controls of the subgroups A, B, and C were >120 ms, 90–100 ms, and 70 ms, respectively (p<0.001). Control subgroup A had higher T2 values and AF/NP ratios than subgroups B and C; the AF values were not significantly different. Control subgroup B had higher T2 values and AF/NP ratios than subgroup C but lower FA (NP). CONCLUSIONS: FA maps of the AF/NP ratio and T2 values of NP are potential microstructure biomarkers of normal and degenerating discs and can help detect early degeneration using a predictive disc health score on a continuous scale. |
format | Online Article Text |
id | pubmed-6680034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society of Spine Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-66800342019-08-05 Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration Vadapalli, Rammohan Mulukutla, Raghavdutt Vadapalli, Abhinav Sriram Vedula, Rajanikanth Rao Asian Spine J Basic Study STUDY DESIGN: Observational comparative study. PURPOSE: To compare fractional anisotropy (FA) maps with T2 values of the nucleus pulposus (NP) and annulus fibrosus (AF) of intervertebral discs in healthy volunteers and patients to develop a predictive disc health scale. OVERVIEW OF LITERATURE: T2-weighted magnetic resonance imaging (MRI) is not sensitive to early morphological changes and provides no quantitative biomarker profile for early degeneration. METHODS: We examined 59 healthy controls and 59 patients with back pain by MRI using T2 relaxometry and diffusion tensor imaging (DTI). Each group was divided into three age subgroups: A (<30 years, n=12); B (30–50 years, n=26); and C (>50 years, n=21). We obtained FA values for AF and NP and T2 values for NP for each intervertebral disc. Furthermore, we calculated the FA (AF/NP) ratios. RESULTS: We categorized 590 intervertebral discs from 118 participants, 566 of which were analyzed with T2 relaxometry and DTI. The T2 values were as follows: subgroup A, 55.8±4.4 ms; B, 48.5±6.9 ms; C, 45.8±8.7 ms (p<0.050). The T2 values for the healthy controls of the subgroups A, B, and C were >120 ms, 90–100 ms, and 70 ms, respectively (p<0.001). Control subgroup A had higher T2 values and AF/NP ratios than subgroups B and C; the AF values were not significantly different. Control subgroup B had higher T2 values and AF/NP ratios than subgroup C but lower FA (NP). CONCLUSIONS: FA maps of the AF/NP ratio and T2 values of NP are potential microstructure biomarkers of normal and degenerating discs and can help detect early degeneration using a predictive disc health score on a continuous scale. Korean Society of Spine Surgery 2019-08 2019-04-02 /pmc/articles/PMC6680034/ /pubmed/30966725 http://dx.doi.org/10.31616/asj.2018.0166 Text en Copyright © 2019 by Korean Society of Spine Surgery This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Study Vadapalli, Rammohan Mulukutla, Raghavdutt Vadapalli, Abhinav Sriram Vedula, Rajanikanth Rao Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title | Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title_full | Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title_fullStr | Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title_full_unstemmed | Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title_short | Quantitative Predictive Imaging Biomarkers of Lumbar Intervertebral Disc Degeneration |
title_sort | quantitative predictive imaging biomarkers of lumbar intervertebral disc degeneration |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680034/ https://www.ncbi.nlm.nih.gov/pubmed/30966725 http://dx.doi.org/10.31616/asj.2018.0166 |
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