» Articles » PMID: 32303267

An Exploratory Study of Different Definitions and Thresholds for Lumbar Disc Degeneration Assessed by MRI and Their Associations with Low Back Pain Using Data from a Cohort Study of a General Population

Overview
Publisher Biomed Central
Specialties Orthopedics
Physiology
Date 2020 Apr 19
PMID 32303267
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Lumbar disc degeneration seen on magnetic resonance imaging (MRI) is defined as loss of signal intensity and/or disc height, alone or in combination with other MRI findings. The MRI findings and thresholds used to define disc degeneration vary in the literature, and their associations with low back pain (LBP) remain uncertain.

Objective: To explore how various thresholds of lumbar disc degeneration alter the association between disc degeneration and self-reported LBP.

Methods: An exploratory, cross-sectional cohort study of a general population. Participants in the cohort 'Backs-on-Funen' had MRI scans and completed questionnaires about LBP at ages 41, 45 and 49 years. The MRI variables, signal intensity (Grades 0-3) and disc height (Grades 0-3), were dichotomised at different thresholds. Logistic regression analyses were used to determine associations. Arbitrarily, a difference in odds ratio (OR) of > 0.5 between thresholds was considered clinically relevant. Receiver Operating Characteristic curves were used to investigate differences between diagnostic values at each threshold.

Results: At age 41, the difference in ORs between signal loss and LBP exceeded 0.5 between the thresholds of ≥2 (OR = 2.02) and = 3 (OR = 2.57). Difference in area under the curves (AUC) was statistically significant (p = 0.02). At ages 45 and 49, the difference in ORs exceeded 0.5 between the thresholds of ≥2 and = 3, but the differences between AUC were not statistically significant. At age 41, the difference in ORs between disc height loss and LBP at the thresholds of ≥1 (OR = 1.44) and ≥ 2 (OR = 2.53) exceeded 0.5. Differences in AUC were statistically significant (p = 0.004). At age 49, differences in ORs exceeded 0.5 (OR = 2.49 at the ≥1 threshold, 1.84 at ≥2 and 0.89 at =3). Differences between AUC were not statistically significant.

Conclusion: The results suggest that the thresholds used to define the presence of lumbar disc degeneration influence how strongly it is associated with LBP. Thresholds at more severe grades of disc signal and disc height loss were more strongly associated with LBP at age 41, but thresholds at moderate grades of disc degeneration were most strongly associated with LBP at ages 45 and 49.

Citing Articles

The association of lumbar intervertebral disc degeneration with low back pain is modified by underlying genetic propensity to pain.

Suri P, Naeini M, Heagerty P, Freidin M, Granville Smith I, Elgaeva E Spine J. 2024; 25(1):8-17.

PMID: 38942297 PMC: 11637947. DOI: 10.1016/j.spinee.2024.05.018.


Melatonin alleviates oxidative stress-induced injury to nucleus pulposus-derived mesenchymal stem cells through activating PI3K/Akt pathway.

Huang Z, Wang Z, Cheng X, Huang Z, Han Y, Cui Y J Orthop Translat. 2023; 43:66-84.

PMID: 38089645 PMC: 10711395. DOI: 10.1016/j.jot.2023.10.002.


Intervertebral disc degeneration-Current therapeutic options and challenges.

Samanta A, Lufkin T, Kraus P Front Public Health. 2023; 11:1156749.

PMID: 37483952 PMC: 10359191. DOI: 10.3389/fpubh.2023.1156749.


A protocol for recruiting and analyzing the disease-oriented Russian disc degeneration study (RuDDS) biobank for functional omics studies of lumbar disc degeneration.

Leonova O, Elgaeva E, Golubeva T, Peleganchuk A, Krutko A, Aulchenko Y PLoS One. 2022; 17(5):e0267384.

PMID: 35560143 PMC: 9106166. DOI: 10.1371/journal.pone.0267384.


1,25(OH)D Mitigates Oxidative Stress-Induced Damage to Nucleus Pulposus-Derived Mesenchymal Stem Cells through PI3K/Akt Pathway.

Wang J, Zhu L, Shi P, Wang P, Dai Y, Wang Y Oxid Med Cell Longev. 2022; 2022:1427110.

PMID: 35340208 PMC: 8956384. DOI: 10.1155/2022/1427110.


References
1.
Lee R, Griffith J, Lau Y, Leung J, Ng A, Hung E . Diagnostic capability of low- versus high-field magnetic resonance imaging for lumbar degenerative disease. Spine (Phila Pa 1976). 2015; 40(6):382-91. DOI: 10.1097/BRS.0000000000000774. View

2.
Paajanen H, Erkintalo M, Kuusela T, Dahlstrom S, Kormano M . Magnetic resonance study of disc degeneration in young low-back pain patients. Spine (Phila Pa 1976). 1989; 14(9):982-5. DOI: 10.1097/00007632-198909000-00012. View

3.
Leboeuf-Yde C, Kyvik K . At what age does low back pain become a common problem? A study of 29,424 individuals aged 12-41 years. Spine (Phila Pa 1976). 1998; 23(2):228-34. DOI: 10.1097/00007632-199801150-00015. View

4.
Luoma K, Riihimaki H, Raininko R, Luukkonen R, Lamminen A, Viikari-Juntura E . Lumbar disc degeneration in relation to occupation. Scand J Work Environ Health. 1998; 24(5):358-66. DOI: 10.5271/sjweh.356. View

5.
Boos N, Rieder R, Schade V, Spratt K, Semmer N, Aebi M . 1995 Volvo Award in clinical sciences. The diagnostic accuracy of magnetic resonance imaging, work perception, and psychosocial factors in identifying symptomatic disc herniations. Spine (Phila Pa 1976). 1995; 20(24):2613-25. DOI: 10.1097/00007632-199512150-00002. View