Quantifying Bone Marrow Edema Adjacent to the Lumbar Vertebral Endplate on Magnetic Resonance Imaging: A Cross-Sectional Study of Patients with Degenerative Lumbar Disease.
Bone marrow edema
Contrast ratio
Endplate lesion
Low back pain
Journal
Asian spine journal
ISSN: 1976-1902
Titre abrégé: Asian Spine J
Pays: Korea (South)
ID NLM: 101314177
Informations de publication
Date de publication:
Apr 2022
Apr 2022
Historique:
received:
24
01
2021
accepted:
14
02
2021
pubmed:
19
5
2021
medline:
19
5
2021
entrez:
18
5
2021
Statut:
ppublish
Résumé
Cross-sectional study. We aimed to quantitatively assess bone marrow edema (BME) on magnetic resonance imaging (MRI) for patients with degenerative lumbar diseases. BME adjacent to a sclerotic endplate of the lumbar spine, detected using T2-weighted fat-saturated MRI, is closely associated with low back pain in patients with degenerative lumbar diseases. However, currently, there no quantitative evaluation methods for BME adjacent to the vertebral endplate. Patients with degenerative lumbar diseases, whose MRIs detected BME, were enrolled. On a T2-weighted fat-saturated MRI, BME appeared as a high-intensity region adjacent to the vertebral endplate. We calculated the contrast ratios (CRs) of BME and normal bone marrow using the signal intensities of BME, normal bone marrow, and the spinal cord. On computed tomography, we calculated Hounsfield unit (HU) values in the same area as BME, the sclerotic endplate, and normal bone marrow to assess bone density. There were 16 men and 14 women, with an average age of 73.5 years. The mean CRs of BME and normal bone marrow were -0.015±0.056 and -0.407±0.023, respectively. BME's CR was significantly higher than that of normal bone marrow (p<0.01). The HU values in the same area as BME, the sclerotic endplate, and normal bone marrow were 251.9±24.6, 828.3±35.6, and 98.1±9.3, respectively; these values were significantly different from each other (p<0.01). The CR on MRI is a useful quantitative assessment tool for BME in patients with degenerative lumbar diseases.
Identifiants
pubmed: 34000797
pii: asj.2020.0648
doi: 10.31616/asj.2020.0648
pmc: PMC9066264
doi:
Types de publication
Journal Article
Langues
eng
Pagination
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