Significant Association between the T2 Values of Vertebral Cartilage Endplates and Pfirrmann Grading

Objective The T2 value of lumbar cartilage endplates was measured using the T2 mapping imaging technique, aiming to explore the correlation between the T2 value and Pfirrmann grading of intervertebral discs. Methods A total of 130 patients with lumbar spine MR examination due to persistent low back pain were enrolled, including 71 men and 59 women (age: 21–63 years). Lumbar Modic changes and Schmorl nodules were recognized by conventional T1WI and T2WI images in 49 patients, and these patients were excluded from the study. A total of 81 patients were enrolled in this study, including 45 men (45.16 ± 12.20 years) and 36 women (43.33 ± 11.27 years). Pfirrmann (Pm) grading of each lumbar disc was performed based on conventional T2WI median sagittal images and the position of cartilage endplates (CEP) was determined by IDEAL‐SPGR images. Meanwhile, the T2 mapping technique was used to obtain T2 values of cartilage endplates. The T2 values of CEP corresponding to different Pm grade discs were compared, and the correlation between the T2 value and the Pm grade of intervertebral discs was analyzed. Results The T2 values of cephalic and caudal CEP of L1–2 in Pm grades I–II, Pm grades III, and Pm grades IV–V were 61.96 ± 5.89 ms, 54.45 ± 3.29 ms, 42.47 ± 3.69 ms and 64.35 ± 5.93 ms, 55.28 ± 3.97 ms, 44.75 ± 2.12 ms, respectively. For cephalic and caudal CEP of L2–3, the T2 values in Pm grades I–II, Pm grades III, and Pm grades IV–V were 62.96 ± 6.93 ms, 55.19 ± 4.02 ms, 48.67 ± 4.56 ms and 65.51 ± 6.49 ms, 57.16 ± 5.55 ms, 52.05 ± 4.20 ms, respectively. The T2 values of cephalic and caudal CEP from L3–4 to L5–S1 in Pm grades I–II, Pm grades III, and Pm grades IV–V were (63.72 ± 5.76 ms, 53.96 ± 6.52 ms, 48.05 ± 5.00 ms), (65.46 ± 6.37 ms, 55.70 ± 7.50 ms, 48.10 ± 3.27 ms); (66.34 ± 7.68 ms, 56.76 ± 9.48 ms, 47.80 ± 4.33 ms), (64.44 ± 4.65 ms, 59.30 ± 8.80 ms, 47.30 ± 5.78 ms), (65.32 ± 5.11 ms, 55.33 ± 6.65 ms, 48.18 ± 5.37 ms), and (63.47 ± 4.92 ms, 50.32 ± 8.86 ms, 44.77 ± 4.69 ms), respectively. There were significant differences in T2 values of cartilage endplates between the Pm grades I–II, III, and IV–V of intervertebral discs (P = 0.000). T2 values corresponding to Pm I–II grades were higher than those in Pm III grade, while T2 values in Pm grades IV–V were lowest. The T2 value of the L4–5, L5–S1 segment endplates was highly correlated with the Pm grades (r = −0.711, −0.721, −0.796, −0.745; P = 0.000) and that of L1–2, L2–3 endplates were moderately correlated (r = −0.542, −0.562, −0.637, −0.612; P = 0.000). Conclusion The T2 values of cartilage endplates revealed varying degrees of degeneration of intervertebral discs, and more severe degeneration corresponded to lower T2 values. Measurement of changes in the T2 value through cartilage endplates can be useful for the diagnosis of early intervertebral disc degeneration and the prevention of disc degeneration.


Introduction
L ow back pain and osteoarthritis contribute to disability worldwide and the consequent impacts, including absence at work and on healthcare, have a serious socioeconomic burden [1][2][3] . Intervertebral disc degeneration disease (IDDD) is a common reason for these two diseases 4 . The vertebral endplates have a critical role in the prevention and early diagnosis of IDDD; therefore, it is significant to shed light on the pathogenesis of the degeneration of vertebral endplates.
The cartilage endplate (CEP) is one of the main components of the intervertebral disc, combining the annulus fibrosus and the nucleus pulposus and ensuring the structural and mechanical integrity of the organ. The vertebral endplates are the strongest part of the disc, located at the top and bottom of each intervertebral disc. They transport the cells and other required nutrients in and out of the disc, to keep the disc alive and to prevent degeneration 5,6 . Degeneration of intervertebral discs is mainly due to the degeneration of CEP, which obstructs the nutrition supply to the disc 7 .
Using a noninvasive imaging technique for evaluating CEP is necessary because of its clinical correlation with disc degeneration 8 . Disc degeneration is often measured with the semiquantitative Pfirrmann grading method using T2weighted images with five grades based on morphology and signal intensity 9 . Prior to structural changes in vertebral endplates with degeneration, the cartilage tissue is subjected to biochemical alterations, including a loss of proteoglycans and a concomitant decrease of hydration 10,11 . Hence, the diagnosis of early CEP degeneration requires a high-resolution technique for morphological evaluation and physiologic techniques to detect biochemical abnormalities.
The CEP is an extremely thin and delicate anatomical structure, and most research studies focus on cadaver specimen measurement 12,13 . To be clinically practical, the imaging identification of CEP needs to satisfy high resolution, high signal-to-noise ratio (SNR), and a short time of echo (ET) with optimal sequence parameter 14 . Conventional MRI using T2-weighted imaging takes a long time when multiple images are required, is not sensitive to early morphological changes, and provides no predictive quantitative biomarker profile of early degeneration 15,16 . IDEAL (iterative decomposition of water and fat with echo asymmetry and leastsquares estimation) with highly SNR-efficient and fat-saturated SPGR (spoiled gradient echo), has been considered the clinical reference standard for morphologic quantification and volumetric assessment of cartilage because of its high resolution 14,17,18 .
A previous study performed SPGR imaging on lumbar CEP of cadavers, and the CEP of all lumbar spine specimens were clearly displayed by the SPGR sequence. Importantly, the CEP on the MR images had morphological abnormalities, including thinner height, irregular, erosion, and defects, which were confirmed by anatomical examination 19 . Hence, the IDEAL-SPGR sequence can provide steady water-fat separation with high SNR and resolution with significantly shorter scanning time.
This study applies the IDEAL-SPGR sequence to investigate the lumbar cartilaginous endplate in vivo, which can accurately display the morphology and location of endplates. In addition, T2 mapping is sensitive to changes in collagen (content/alignment) and water, and it can quantitatively reveal the variation of biochemical material 20 . T2 values (i.e. voxel-specific T2-relaxation times) are determined from a series of continually increasing echo times by evaluating the inherent property of the macromolecular environment, including water, protein, collagen, fat, and other solutes. To be more specifically, T2 values correlate to the concentration of water molecules and their interaction with collagenous fibers (amount and orientation), in which the dipole interaction caused by anisotropic motion of water molecules plays a key role 21 . T2 values have been shown to inversely correlate with degeneration grade and were first used to assess the biochemical changes in early degeneration of articular cartilage 20 . T2 values also reported to have the capacity to discriminate the nucleus pulposus from the annulus fibrosus 22 . T2 mapping technology has the characteristics of non-invasiveness and reproducibility. It can be used to quantitatively analyze the changes in the articular cartilage and intervertebral disc matrix composition by measuring the T2 relaxation time. Watanabe et al. describe the potential benefits of standard axial T2 mapping in the lumbar spine and suggest that T2 mapping is a reliable and valid method in biochemical cartilage imaging 23 .
Therefore, this study aims to investigate the correlation between Pfirrmann grading and T2 values, where IDEAL-SPGR provides the precise position for T2 component measurement. Specifically, this research addresses three main points as follows. First, we analyze the difference in T2 values between adjacent cephalic and caudal CEP of the intervertebral disc in different Pm grades. Second, we explore the relationship of the T2 value and the Pm grade through correlation analysis. Finally, based on the results of the above, using T2 mapping technology, we attempt to provide a quantitative evaluation method for early degeneration of lumbar cartilage endplates using T2 mapping technology. Inclusion criteria were as follows. First, clinical symptoms were sustained or the patient had recurrent chronic low back pain, with or without lower extremity radiation pain. Second, patients could cooperate to complete the magnetic resonance examination and measure the T2 value of the lumbar cartilage endplate using the T2 mapping technique. Third, according to the semi-quantitative visual grading system proposed by Pfirrmann in 2001 9 , intervertebral discs from L 1 to S 1 were graded using the T2WI median sagittal images. Takashima et al. 24 report there is no significant difference in the T2 values of the nucleus pulposus between Pfirrmann (Pm) IV and PmV, and it is difficult to distinguish between PmIV and PmV. Here, we divided patients into three groups, G1: Pm I-II (for apparently healthy discs of children and young adults); G2: Pm III (for discs with reduced T2 signal intensity); and G3: Pm IV-V (for discs with progressively decreased height and T2 signal) 9,25 . Fourth, correlation analysis was performed to explore the relationship between T2 values and Pm grades. Finally, the study design used the prospective research method.

Patients and Methods
Exclusion criteria: long-term heavy physical work; BMI ≥28 kg/m 2 ; having a history of spinal trauma, surgery, congenital malformations of the spine, and various diseases involving the spine, such as inflammation, tumors, blood system diseases, and metabolic bone diseases; claustrophobia, metal implants, or other MR contraindications; and scoliosis >15 .

Image Acquisition
All imaging was performed with the approval of the Regional Committee for Ethics of Tianjin Hospital. MRI was conducted using a Discovery MR 750W 3T scanner (GE Healthcare, Waukesha, WI) employing a CTL surface coil with full coverage of the neck, chest, and waist. Subjects lay in a supine position on the CTL coil, and the positioning line was set at the level of the third lumbar vertebra. Scanning sequences included regular T1WI, T2WI, IDEAL-SPGR, and T2 mapping and imaging was performed in the sagittal plane for all sequences.

Image Data Measurement and Processing
Images were interpreted independently by two MRI diagnosticians of different levels using the double-blind method. T1WI, T2WI images showing the existence of lumbar Modic changes or Schmorl nodules were excluded in this study. The Pm grading was determined by two diagnosticians based on T2WI median sagittal images; when the opinions were inconsistent, the grade was based on the assessment of the senior medical diagnostician.
The nutrition diffusion between intervertebral discs is largely dependent on the central section of the CEP. From the perspective of biomechanics, the reassignment from the loading of the intervertebral disc and the stress conduction also mainly relies on CEP and most of the stress acts on the weakest area, the central region [26][27][28] . Therefore, the Region of Interest (ROI) was set at the center of the CEP in this study, which shows the most prominent and representative characteristics of degeneration of intervertebral discs.
IDEAL-SPGR images are capable of displaying the profile of CEP clearly, based on which the ROI was drawn on IDEAL-SPGR images. Then, the ROI was co-registered on the corresponding T2 mapping slice to calculate the T2 values. First, the midpoint of the anterior and posterior margins of each vertebral body was connected on the maximum amplification of the IDEAL-SPGR median sagittal image to make a line, named "a" (Fig. 1A). Line "b" was perpendicular to line "a," based on which the distance between the upper and lower CEP was recorded as AB, shown in Fig. 1A. The lower and upper CEP of each intervertebral disc were defined as the cephalic endplate and the caudal endplate, respectively.
In the post-processing workstation, the T2 map module was selected using the FuncTool software and the confidence interval was set to 95% on both sides with a color threshold of 20 ms. The color scale which controls the T2 values in the range of 25-75 ms was adjusted, and the T2 mapping pseudo-color map that was obtained was automatically corrected. Similar to the processing of IDEAL-SPGR images, a 0 was a line connecting the midpoints of the anterior and posterior margins of each vertebral body, while b 0 was the midperpendicular of a 0 . We overlapped line a 0 and b 0 with a and b, respectively, then pointed A 0 and B 0 on the T2 map raw images according to point A and B to obtain the position of CEP (Fig. 1B). The nutrition of the intervertebral disc is mainly diffused through the center of the cartilage endplate. Biomechanical studies have shown that CEP plays an important role in the redistribution of disc load and stress transmission, while the stress transmitted by the normal disc mainly affects the weakest area in the center of the endplate 26 . In this study, the position of the T2 value area of interest was selected and set in the center of CEP, which is most closely related to discs. A total of 10 CEP of each subject were enrolled from the lower CEP of L 1 to the upper CEP of S 1 and the corresponding ROI was located at A 0 and B 0 . Considering the thinning trend of CEP in adults, the ROI was limited to 4 mm 2 and the selection of the ROI should avoid the vertebral cortex or disc area. Based on this criterion, the measurement was performed twice for each CEP and took the average value. The schematic diagram of ROI selection is shown in Fig. 1C and the practical measurement is displayed in Fig. 1D.

Pfirrmann Grade
Pfirrmann disc grade is a useful scoring tool for evaluating disc degeneration, which was determined collectively using, for instance, the structure/height of the intervertebral disc, the signal intensity of the nucleus pulposus, and the clarity of boundaries between the nucleus pulposus and the annulus fibrosis. The disc characteristics for each Pm grade are detailed below.
Pm Grade I: Homogeneous structure, bright hyperintense white signal intensity, the nucleus pulposus is clearly demarcated from the annulus fibrosus, normal disc height.
Pm Grade II: Inhomogeneous, normal height, a horizontal gray band could be present, keeping the hyperintense white signal, nucleus and annulus are clearly differentiated.
Pm Grade III: Inhomogeneous, an intermittent gray signal intensity, unclear distinction between nucleus and annulus, normal or slightly declined height.
Pm Grade IV: Inhomogeneous with a hypointense dark gray signal intensity, no more distinction between the nucleus and annulus, slightly or moderately decreased disc height.
Pm Grade V: Inhomogeneous with a hypointense black signal intensity, no more distinction, collapsed disc.

Statistical Analysis
Statistical analysis was performed on the measured values using SPSS 17.0 statistical software. The T2 values of CEP Fig. 2 The workflow of the research design.
from L 1 to S 1 were represented by mean ± standard deviation and all data conform to the normal distribution. The difference is statistically significant at P < 0.05. First, one-way analysis of variance was used to compare the difference in T2 values of each CEP in G1-G3 groups. Second, multiple comparisons (least significant difference test) were conducted and the results between groups were compared. Third, the Spearman rank correlation (Spearman's rho) analysis was used to investigate the correlation between T2 values of CEP and Pm grades, in which r > 0.7, 0.5 < r ≤ 0.7, and r ≤ 0.5 indicate high correlation, moderate correlation, and weak correlation correspondingly. The research design is illustrated in Fig. 2, which is helpful for a comprehensive study the workflow and all methodologies.

Results
A total of 49 cases observed with lumbar Modic changes or Schmorl nodules were excluded. Modic changes or Schmorl nodules are degenerative changes in the lumbar spine where the completeness and consecutiveness are destroyed, and they could impact the accuracy of T2 value measurement. Of the available 81 cases, 45 were men, with an average age of 45.16 ± 12.20 years, and 36 women, with an average age of 43.33 ± 11.27 years. Ultimately, there were 405 intervertebral discs and 810 CEP enrolled in this statistical study. Figure 3 shows the T2WI sagittal image, the IDEAL-SPGR scan, the T2 mapping original image, and the T2 mapping pseudo-color image of 1 subject whose intervertebral discs have different Pm grades. The total 405 intervertebral discs were graded using the Pm grading system according to the disc location and the results are listed in Fig. 4. Moreover, to display the distribution of Pm grading in different groups,  we plotted the sum number of G1, G2, and G3 groups simultaneously.

Comparison of T2 Values for Cartilage Endplates in G1-G3 Group
For each cephalic and caudal CEP, the T2 values in the G1 group were highest, while those in the G2 group were higher than those in the G3 group. The T2 values of each corresponding cartilage endplate among the three groups were all statistically significant (P < 0.05, Table 1). Figure 5 compares the T2 values between each two groups and the Pvalues are represented by different symbols for the three comparisons with different colors (G1 and G2, yellow triangle; G1 and G3, red circle; G2 and G3, rectangle). Meanwhile, nonzero values are denoted with specific values. The results showed that all comparisons had significant differences and G1 and G3 groups had the most significant differences, with all zero P-values. In contrast, the comparison between G2 and G3 groups has the lowest significant difference but the highest P-value (0.049) was still lower than 0.05. For G1 and G2 groups, almost all P-values were zero, except for the cephalic L 5 -S 1 CEP (P = 0.009).

Correlation Analysis between T2 Value and Pfirrmann Grading for Each Cartilage Endplates
The P and r values were calculated for each CEP to analyze the correlation between the T2 value and Pm grading. The results are presented in Fig. 6. It should be noted that all Pvalues equal 0.000 for each CEP. The T2 value of each vertebral endplate was correlated with the Pm grading of the intervertebral disc. The T2 value of higher segment endplates was moderately correlated with the Pm grade of the   intervertebral disc. The T2 value of the lower segment endplates was highly correlated with the Pm grade of the intervertebral disc.

Discussion
L umbar degenerative osteoarthrosis is a frequently occurring disease in the middle-aged and elderly population, derived from various reasons but with the early degeneration of intervertebral discs considered the principal factor. The most significant reason might be the obstruction of the nutrition supply between intervertebral discs induced by CEP degeneration. Therefore, in-depth study of CEP degeneration is valuable for analyzing the mechanism of disc degeneration, which is of great significance in the prevention and early diagnosis of lumbar degenerative osteoarthropathy. A series of factors may cause CEP degeneration, including apoptosis, abnormal stress, genetic abnormalities, inflammatory factors, and aging.

Role of Cartilage Endplates in the Degeneration of Intervertebral Discs
A great many studies have suggested that CEP degeneration plays an important role in the occurrence and development of degenerative disc disease 29,30 . Ariga et al. 31 show that chondrocyte apoptosis occurs in CEP, and the percentage of apoptotic cells increases with age, followed by tearing and disappearance of CEP, where the mechanical stress may be one of the causes resulting in apoptosis. Antoniou et al. 32 found that during the growth phase, the synthesis and catabolism of type II collagen and proteoglycan are relatively strong, while the degeneration of type II collagen is increased, accompanied by type I collagen synthesis, fibrosis in the endplates, and stagnation of metabolites in the degeneration phase 33 . Moreover, matrix synthesis in cartilage endplates reduces with aging and degeneration, when the amount of proteoglycan, water and collagen of the CEP is decreased, and with the collagen fibers arranged disorderly. Consequently, biochemical components of the cartilage endplate undergo qualitative and quantitative changes 34,35 .
These changes inevitably affect the normal physiological function of CEP, further leading to morphological abnormalities such as cartilage calcification, fission, and loss 36 . It has been supported that the histological changes in CEP always precede the histological abnormalities of the nucleus pulposus and there are often significant histological variations in the cartilage endplates before disc degeneration and failure.
Neidlinger-Wilke et al. 37 indicated that CEP and the nucleus pulposus tissue interact with each other through molecular factors to upregulate matrix-degrading enzymes and inflammatory factors, thus affecting the pathophysiology of intervertebral disc degeneration. Experimental results showed that abnormal high stress can change the content of proteoglycan in CEP, which hinders the diffusion of sulfur ions into the annulus fibrosus through CEP reducing the content of chondroitin sulfate. In contrast, it promotes self-calcification, weakening its ability to transmit loads and impedes nutrients from the nucleus pulposus, leading to degeneration of the intervertebral disc 38,39 . Boos et al. 2 found cracks and microfractures in CEP by investigating the histological changes of CEP in cadaveric and intraoperative intervertebral disc samples, which may lead to the decreased blood supply and degeneration of the intervertebral disc.
T2 Value as a Biomarker for Cartilage Endplate Imaging T2 relaxation time is the attenuation constant of T2 signal intensity in MRI, which is independent of scanner and imaging parameters 16 . It is an inherent property of tissue and reflects the macromolecular environment, including water, protein, collagen, fat, and other solutes. T2 relaxation time is sensitive to water content and the collagen network structure, and is also affected by the dipole interaction caused by the anisotropic movement of water molecules in the collagen matrix 21 . Studies have shown that the T2 value of the nucleus pulposus and fibrous rings of the intervertebral disc is significantly related to the water content and weakly related to the proteoglycan content 16 . The alignment and content of collagen fibers and water content in CEP are the main determinants of the T2 value 20,40 . T2 mapping imaging technology can reflect the tissue macromolecular environment and changes in biochemical components, including water, proteoglycans, and collagen by measuring the T2 relaxation time 36 . This study uses T2 mapping imaging technique to quantitatively measure the T2 value of CEP, and then analyze correlations between CEP degeneration and intervertebral disc degeneration.

Relationship between the Degree of Disc Degeneration and T2 Value of Cartilage Endplates
Structural and compositional changes in CEP are one reason for the intervertebral disc degeneration 41 . In the period of degeneration or aging, the reduction of water, proteoglycan and collagen of CEP and the degree of disarrangement of the collagen fiber network are proportional to the degree of CEP degeneration 42 . Changes in the biochemical composition of CEP can stimulate the formation of cartilage calcification and further reduce the CEP permeability. Subsequently, the substance transport through intervertebral discs is prevented, thus reducing the synthesis of the intervertebral disc matrix and the water content of the nucleus pulposus. This vicious cycle ultimately leads to the degeneration of intervertebral discs and varies in accordance with biomechanical functions 43 . This study showed that the T2 values of the endplates in the Pm grade I-II and III, I-II and IV-V, and III and IV-V were statistically significant. The T2 value of the cartilage endplate corresponding to degenerative intervertebral discs graded to III and IV-V was significantly lower than that of I-II graded discs. The higher grade of intervertebral disc degeneration and the heavier degeneration degree of CEP result in lower T2 values of adjacent cephalic and caudal cartilage endplates.
It is suggested that when the cartilage endplate degenerates, the cartilage endplate T2 value decreases, the Pm grade increases, and its proteoglycan and water content decrease. Intervertebral disc degeneration has a strong correlation with the T2 value of cartilage endplates, which is consistent with previous studies 7 , indicating that cartilage endplate degeneration is an important factor leading to degeneration of the intervertebral disc.
Muftuler et al. 44 found that the Pm classification was positively correlated with the dynamic MRI enhancement of the CEP and differential enhancement of the cephalic and caudal endplates was also observed. This enhancement increases with increasing Pm classification, and this differential enhancement also depends on the lumbar segment. The subchondral bone that connects the caudal cartilage endplate is thinner than that on the cephalic endplate side. Thinner subchondral bone may be more easily damaged, resulting in more infiltration of contrast media; hence, the enhancement is usually higher in the caudal CEP. In this study, the T2 values of the caudal CEP were higher than for cephalic sides, except L 4-5 and L 5 -S 1 intervertebral discs, which needs further investigation.

Analysis of T2 Values of Cartilage Endplates in Different Lumbar Segments
Shirado et al. 45 applied axial load to the lumbar vertebral body, indicating that the maximum bearing pressure of the vertebral body is concentrated in the center of the endplate and the vertebral cancellous bone below it. In addition, when the bearing load exceeds the limit, it will result in the rupture of the central area of the endplate. The overall load gradually increases from L 1-2 to L 5 -S 1 , so the L 4-5 and L 5 -S 1 intervertebral discs bear the highest load. It has been reported that segmental cartilage defects with disc degeneration have segmental differences, which may reflect the characteristics of the maximum load in the lower lumbar region 46 . The present study shows that the lower lumbar disc has a greater degree of degeneration, which is consistent with previous studies.
The upper lumbar segment has more favorable conditions to achieve the balance and regeneration in vivo, which may alleviate the deleterious effects of degeneration of CEP in the upper lumbar on the degeneration of the intervertebral disc. Moreover, mechanical factors, like the high load, also affect the CEP permeability to a certain extent, resulting in the structural change of the cartilage endplate. Fields et al. 47 reveal that CEP are affected by high tensile strain and are most prone to the earliest degeneration. Hee et al. 48 suggest that pressurization could lead to CEP degeneration and a decrease in the vascular passage of the bony endplate, which, in turn, results in degeneration of intervertebral discs. Different lumbar segments were subjected to different stresses. This study found that the T2 values of CEP of the L 1-2 and L 2-3 segment were moderately correlated with the Pm classification. The T2 values of CEP in the L 4-5 and L 5 -S 1 segments were highly correlated with the Pm classification. This might be the result of the higher load on the L 4-5 and L 5 -S 1 segments and the subsequent greater stress in the CEP and intervertebral discs. These results imply that different levels of stress can affect the biochemical metabolism of CEP and intervertebral discs.

Limitations
The limitations of this study include, first, that the observation of the morphological variation of CEP was limited by imaging data without the support of surgical or pathological verification. Second, the enrolled cases were derived from patients with chronic low back pain, resulting in an unbalanced Pm distribution (i.e. the concentration in the Pm 2-4 group). In addition, due to the studied subjects being clinical patients, the biochemical changes in CEP degeneration were not studied in vitro, which would be necessary in future studies.

Conclusion
T2 values of CEP vary from intervertebral discs with different degeneration levels with a negative correlation, but there is no significant difference between corresponding cephalic and caudal CEP. Measurement of the T2 value of the CEP can be used for the diagnosis of early degeneration of the lumbar intervertebral disc and has important clinical significance for the prevention of disc degeneration.