Zeng qi1, Zhang ziwei1, Nie lisha2, Zhu xia1, Huang zaoshu1, and Song lingling1
1The affiliated hospital of Guizhou mdeical university, Guizhou guiyang, China, 2GE Healthcare,MR Resertch China, Beijing, China
Synopsis
Lumbar disc degeneration is an important
cause of lower back pain, sedentary, prolonged-standing behavior accelerates
its course. In this study we evaluate intervertebral disc degeneration
quantified by T1ρ and T2 mapping magnetic resonance imaging in sedentary and
long standing populations compared with a healthy control group matched for age.
We conclude that prolonged-standing is more likely to affect the L1 / 2 level
discs, while sedentary is more likely to affect the lower segment discs (L4 / 5
and L5/S1).
Introduction
Low back pain is one of the most common clinical diseases, which affects
approximately 637 million people worldwide [1]. Lumbar intervertebral
disc degeneration (IVDD) is an important cause of low back pain. IVDD typically
begins at 20 years of age and excessive mechanical loading (Sedentary, prolonged-standing
behavior and high impact loads) accelerates its course [2]. Magnetic resonance imaging
(MRI) is a non-invasive medical imaging modality that provides excellent
anatomic detail of spinal tissues, and Pfirrmann et al devised
a five grade grading system based on MR signal intensity, disc structure,
nucleus to annulus distinction and disc height [3]. However, this
scoring system is limited in the evaluation of IVDD due to the unsatisfactory
objectivity. Quantitative MRI, such as
T1ρ、T2 mapping technique, can reflect the
molecular environment in early degeneration discs and provide objective
continuous measures[4]. However, there
are limited studies comparing quantitative IVD measures of sedentary and prolonged-
standing behavior individuals. This study aimed to evaluate
the performance of T1ρand T2 mapping in disc
degeneration assessment in sedentary and prolonged-standing
populations. Methods
Subjects: 30 volunteers (14 sedentary,
8 prolonged-standing, 8 healthy volunteer; age range
from 23 to 44 years; BMI range: 21.9-24.8) were included in this study with Institution
Review Broad approval. Inclusion criteria consisted of: (1)no contraindications
for MR examination; (2) no obvious scoliosis or spondylolisthesis; (3)no
history of spine trauma and deformity; (4) no metabolic or autoimmune diseases;
(5)the sedentary group and the prolonged-standing group spent an average of
more than 6 hours per day ; (6)the healthy volunteer have no history of vigorous
exercise for long periods; (7) BMI<25 kg /m2. MR scanning was performed using a GE Discovery 750W 3.0T scanner with a
spine coil. The key protocols were performed in the table1.For measurement,
the disc was divided into five equal areas, the first covering the anterior
annulus fibrosus (AAF), the middle covering the nucleus pulposus (NP), and the
last covering the posterior annulus fibrosus (PAF), mean values of regions of
interest (ROI, 5mm diameter) were measured. In addition, two clinical
radiologist using the system described by Pfirrmann examined and graded
midsagittal sections of MRI T2 weighted images of 5 lumbar discs.
Statistical methods:Statistical analyses were conducted using SPSS
19.0 software. Inter-and intra‑observer reliabilities of Pfirrmann grading were examined using the kappa
concordance test. We compared median T1ρ、T2 values of NPs and AFs of healthy volunteers,
sedentary, and prolonged-standing groups according to the anatomic level of
each disc, using the Kruskal Wallis test. Scatter plots were mapped and the
Spearman rank correlation coefficient were applied to determine the
relationship between NP、AF and Pfirrmann grade, and the decreasing trend
of the relationship between NP、AF and age were evaluated as well. P < 0.05
was considered statistically significant.Results
The T1ρ values of 145 discs, T2
values of 150 discs were successfully obtained eventually. MRI indicated that
the T1ρ values of NP at L1/2 were significantly reduced in the prolonged-standing
group, whereas there was no significant difference between the sedentary group
and the healthy volunteers. The T1ρ values of NP at L4/5 and L5/S1 discs were
significantly and mildly reduced in the sedentary group and the prolonged-standing
group respectively. In addition, the T2 values of NP and PAF at L4/5 and L5/S1
discs were significantly and mildly reduced in the sedentary group and the prolonged-standing
group respectively. For NP and AF, the T1ρ and T2 values were significantly
different between the Pfirrmann grades (P<0.05; with the exception of grade
I and grade II、grades IV and V). The T1ρ and
T2 values decreased with the increase of age, there was no statistically
significant difference between the T1ρ and T2 values.Discussion and Conclusion
This study quantitatively assessed the disc degeneration in sedentary
and prolonged-standing populations with T2 mapping and T1rho. The previous
literatures suggest that behaviors such as spine overload (sedentary, prolonged
standing) may be detrimental to the disc and leading cause of catabolism [2]. Our results
suggest that sedentary behavior and prolonged-standing behavior can affect
different levels of the lumbar disc. Prolonged-standing is more likely to affect
the L1 / 2 level discs, while sedentary is more likely to affect the lower
segment discs (L4 / 5 and L5/S1). The different
target spot in each vertebral level with certain movements may explain why
segment of discs varies between different overload [5]. However, spine
overload factors cannot be considered as the only cause of degeneration. IVDD
is also influenced by the increase of age, and the lower segment discs are inherently
more susceptible to degeneration than upper segments [6]. In addition, we found that significant Pfirrmann grades-related reduction of T1ρ and
T2 values, however, the detection efficacy was roughly comparable between T1ρ and
T2 mapping. The results can be considered as preliminary given the small sample
size. The T1ρ and T2 mapping are promising techniques
for the diagnosis of IVDD, and may be a useful guide to evaluate patients in
future clinical trials of IVD regeneration strategies [7].Acknowledgements
No acknowledgement found.References
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