The Spine Journal
Volume 15, Issue 4, 1 April 2015, Pages 622–628
The association of combination of disc degeneration, end plate signal change, and Schmorl node with low back pain in a large population study: the Wakayama Spine Study
Masatoshi Teraguchi, MD, PhD
Abstract
Background context
Disc degeneration (DD) reportedly causes low back pain (LBP) and is often observed concomitantly with end plate signal change (ESC) and/or Schmorl node (SN) on magnetic resonance imaging.
Purpose
The purpose of this study was to examine the association between DD and LBP, considering ESC and/or SN presence, in a large population study.
Study design/setting
Cross-sectional population-based study in two regions of Japan.
Patient sample
Of 1,011 possible participants, data from 975 participants (324 men, 651 women; mean age, 66.4 years; range, 21–97 years) were included.
Outcome measures
Prevalence of DD, ESC, and SN alone and in combination in the lumbar region and the association of these prevalence levels with LBP.
Methods
Sagittal T2-weighted images were used to assess the intervertebral spaces between L1–L2 and L5–S1. Disc degeneration was classified using the Pfirrmann classification system (grades 4 and 5 indicated degeneration); ESC was defined as a diffuse high signal change along either area of the end plate, and SN was defined as a small well-defined herniation pit with a surrounding wall of hypointense signal. Logistic regression analysis was used to determine the odds ratios (ORs) and confidence intervals (CIs) for LBP in the presence of radiographic changes in the lumbar region and at each lumbar intervertebral level, compared with patients without radiographic change, after adjusting for age, body mass index, and sex.
Results
The prevalence of lumbar structural findings was as follows: DD alone, 30.4%; ESC alone, 0.8%; SN alone, 1.5%; DD and ESC, 26.6%; DD and SN, 12.3%; and DD, ESC, and SN, 19.1%. These lumbar structural findings were significantly associated with LBP in the lumbar region overall, as follows: DD, ESC, and SN, OR 2.17, 95% CI 1.2–3.9; L1–L2, OR 6.00, 95% CI 1.9–26.6; L4–L5, OR 2.56, 95% CI 1.4–4.9; and L5–S1, OR 2.81, 95% CI 1.1–2.3. The combination of DD and ESC was significantly associated with LBP as follows: L3–L4, OR 2.43, 95% CI 1.5–4.0; L4–L5, OR 1.82, 95% CI 1.2–2.8; and L5–S1, OR 1.60, 95% CI 1.1–2.3.
Conclusions
Our data suggest that DD alone is not associated with LBP. By contrast, the combination of DD and ESC was highly associated with LBP.