Classification of endplate lesions in the lumbar spine and association with risk factors, biochemistry, and genetics
- PMID: 33452926
- DOI: 10.1007/s00586-021-06719-1
Classification of endplate lesions in the lumbar spine and association with risk factors, biochemistry, and genetics
Abstract
Purpose: To detect the associations between the degree of the endplate (EP) lesions with the presence of risk factors, biochemical and genetic markers previously observed in low back pain (LBP) patients with EP defects in comparison with hernia/discopathy patients and healthy controls.
Methods: In this observational retrospective study, T2-weighted sagittal MRI images (n = 223 LBP patients) were scored for EP lesions by two independent observers. Total MRI score and number of affected levels (L1/L2-L5/S1) have been considered for the correlation with demographic, behavioral, clinical, biochemical (25(OH)D, CTx-I and CTx-II levels, n = 69 males) and VDR variables.
Results: Males showed higher BMI and total MRI score than females. Patients bearing TT compared to tt VDR genotypes showed significant higher total MRI scores. Among males (n = 125), TT, bb and aa genotypes showed increased total MRI scores. Higher total MRI score directly correlates with higher levels of CTx-I and CTx-II (n = 69 males).
Conclusions: The markers previously identified as associated with the presence of EP lesions have been confirmed as related to their severity and could be used to follow the pathology progression.
Keywords: Collagen; Endplate lesions; Lumbar spine; Risk factors; Vitamin D receptor polymorphisms.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
Comment in
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Letter to the Editor concerning "Classification of endplate lesions in the lumbar spine and association with risk factors, biochemistry, and genetics" by Alessandra Colombini et al. (Eur Spine J; doi: 10.1007/s00586-021-06719-1).Eur Spine J. 2022 Oct;31(10):2822-2823. doi: 10.1007/s00586-021-06844-x. Epub 2021 Apr 23. Eur Spine J. 2022. PMID: 33891185 No abstract available.
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