Synopsis
Multifidus muscles (MF) atrophy are common in patients with Low back
pain (LBP). Degenerative diseases of the lumbar spine, such as disc herniation,
disc degeneration and facet joint osteoarthritis, are leading cause of LBP. Various
studies have previously focused on the relationship between MF atrophy and disc degeneration, disc herniation. However, the results are
inconsistent. Besides, no study for the correlation between MF atrophy and facet joint osteoarthritis has previously been conducted. This
study will investigate the correlation between MF atrophy and
disc degeneration, disc herniation, facet joint osteoarthritis using MRI.
PURPOSE
There is a known, but
not thoroughly evaluated association between fatty degeneration of para-spinal
muscle and low back pain (LBP).1-9
Most prior studies have focused on the
multifidus muscle (MF), because of its contribution to lumbar spine segmental
stability.10
Additionally,
most of the previously studied populations
involves patients with radiculopathy, 1, 3-4, 11 disc
herniation5, 12
Moreover, these prior results are inconsistent.
Hence the aim of this study is to investigate potential correlation between MF atrophy and MR signs of lumbar spine degeneration in patients
with LBP.METHODS
Following
IRB approval, patients who had low back pain and an MRI of lumbar spine between June 2015 and July 2016, were evaluated. Patients with deformity (scoliosis, spondylolisthesis, kyphosis, pars
defects) or history of lumbar spine surgery were excluded. 518
patients (278 females and 240 males; age, 10-92 years; mean, 49.99±17.596 years)
were identified and their MRI studies were retrospectively reviewed by a
radiologist twice with a one-month washout period. MF atrophy was graded at L4-5
and L5-S1 levels (largest diameter at these levels, allowing for a better
evaluation) according to the Goutallier classification (Fig.
1-4).
Disc degeneration was graded according to Pfirrmann classification, and facet
joint osteoarthritis was graded according to Fujiwara classification. Disc
herniation was assessed by NASS criteria. These patients were further
classified into two groups according to clinical presentations. One group was
simple low back pain, the other group with superimposed radiculopathy. Age,
gender, height, and weight were also recorded. Significance level was set at P<0.05. Multinomial
logistic regression was used to evaluate relationship between fatty
degeneration of MF and radiculopathy, age, gender, height, weight, signs of
lumbar spine degeneration. Spearman correlation coefficient was calculated. Intra-observer
agreement was tested as well.RESULTS
At both L4-5 and L5-S1 levels,
significant correlation is demonstrated between MF atrophy with
age, gender, and facet joint osteoarthritis, at L4-L5 level, P<0.001 with correlation coefficients
of 0.652, 0.244, and 0.509 respectively. At L5-S1 level, there
were similar correlations between MF atrophy with age (P<0.001), gender (P<0.001), facet joint osteoarthritis
(P=0.002), with correlation
coefficients were 0.546, 0.368, and 0.354 respectively. Additionally, at the
L5-S1 level, there was a significant correlation between MF atrophy and disc
degeneration (P=0.034) with a
correlation coefficient at 0.348.
No correlation was found between MF atrophy
with height, weight, and disc herniation at both L4-L5 and L5-S1 levels. (At the L4-5
level (p =0.072, 0.233 and 0.603 respectively with at the L5-S1 level p = 0.096, 0.762, and 0.565 respectively)). At L4-L5,
there was also no correlation between MF atrophy and disc
degeneration (P= 0.198).
There is no correlation between MF atrophy and
radiculopathy at both level s of L4-L5 and L5-S1 levels with P values at
0.305 and 0.663 respectively.
For
intra-observer agreement, classification of MF atrophy (Kappa
value=0.626, 0.617), disc degeneration (Kappa value=0.556, 0.553), disc
herniation (Kappa value=0.619, 0.485), and facet joint osteoarthritis (Kappa
value=0.598, 0.677) at L4-5, L5-S1 levels respectively.DISCUSSION
We have demonstrated that increasing age
and female gender are both associated with MF atrophy at both L4-L5
and L5-S1 levels. However,
there is no correlation between heights, weight with MF atrophy. In term of disc degeneration,
correlation with MF atrophy was only found at L5-S1 but not at the L4-5 level. Though, facet
osteoarthritis was found to have significant correlation with MF atrophy at both L4-L5 and L5-S1 levels, surprisingly no correlation was found between
disc herniation and radiculopathy with fatty replacement of MF.
Spine pain is related to the pattern of
spinal innervation. Ventral spinal elements (disc/annulus) are innervated
separately from posterior spinal elements (facet joints, posterior muscles). 13, 14
The facet joints and MF are supplied by median
branch of dorsal ramus which supplies the posterior innervation. This pattern
of spinal innervation may explain the correlation between MF atrophy and facet joint osteoarthritis as well as the lack of correlation between
radiculopathy and disc degeneration with MF atrophy.CONCLUSION
The relationship between MF atrophy and degenerative diseases of lumbar spine is complicated.
However, our large study indicates that MF atrophy positively
correlates with advanced age, female gender and facet osteoarthritis, in the
lower lumbar spine, but not with disc herniation in patients with local back
pain. This data has potential at guiding clinical treatment in certain disease
population. Therefore,
further study will be required to elucidate the role of MF atrophy
in degenerative process of lumbar spine.Acknowledgements
The authors thank Kenneth, Wengler Thomas (Biomedical Engineering,Stony Brook university hospital) for his technical support, Xiaona Xia (Department of radiology,Qilu hospital of Shandong university,Qingdao) for statistical advice, and Wenjian Xu (Department of radiology,Affiliated hospital of Qingdao University) for his writing advice.References
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