A cross-sectional study: serum CCL3/MIP-1α levels may reflect lumbar intervertebral disk degeneration in Han Chinese people.

BACKGROUND: The macrophage inflammatory protein-1α (MIP-1α), also named chemokine cytokine ligand 3 (CCL3), has been detected in nucleus pulposus and increased following cytokine stimulation.
OBJECTIVE: The current study was performed to explore the relationship between serum CCL3/MIP-1α levels with lumbar intervertebral disk degeneration (IDD). PATIENTS AND METHODS: A total of 132 disk degeneration patients confirmed by magnetic resonance imaging and 126 healthy controls were enrolled in the current study. Radiological evaluation of the IDD was conducted using a 3.0-T magnetic resonance imaging scanner for entire lumbar vertebra region. Degeneration of intervertebral disk was assessed by Schneiderman criteria. Serum CCL3/MIP-1α levels were investigated using a sandwich enzyme-linked immunosorbent assay. The Visual Analog Scale scores and Oswestry Disability Index index were recorded for clinical severity.
RESULTS: Elevated concentrations of CCL3 in serum were found in IDD patients compared with asymptomatic volunteers. The case group included 49 IDD patients with grade 1, 42 with grade 2, and 41 with grade 3. Grade 3 and 2 had significantly higher CCL3 concentrations in serum compared with those with grade 1. The serum CCL3 levels were positively related to the degree of disk degeneration. In addition, the serum CCL3 levels also demonstrated a significant correlation with the clinical severity determined by Visual Analog Scale scores and Oswestry Disability Index index.
CONCLUSION: Serum CCL3 may serve as a biomarker of IDD.

Introduction

Low back pain (LBP) has an extremely high incidence. It is estimated that nearly 84% of the worldwide population experience LBP during their lifetime, with 10% being chronically disabled.1 LBP severely influences the work and impairs the quality of life, resulting in significant social and economical burdens.2 The etiological factors of LBP are various, among which, lumbar intervertebral disc degeneration (IDD) is a leading cause of lumbar spine-originated LBP.3

Disk degeneration is characterized by a loss of cellularity and degradation of the extracellular matrix resulting in morphologic changes and alterations in biomechanical properties.4 Several imaging techniques have been utilized to detect IDD. Radiography and conventional computed tomography and magnetic resonance imaging (MRI) are the three common imaging methods for evaluation of disk morphology and reactive bony changes.5–7 However, the biochemical events during early IDD, including the breakdown of large aggregating proteoglycan gels and extracellular matrix degradation, occur before the morphologic changes and alterations in biomechanical properties. In addition, there are currently no definite ways to instantly monitor the condition of disk degeneration.8 Therefore, it is necessary to seek more effective, reliable, and rapid methods to monitor early disk degeneration.

Biomarker is objectively measured and evaluated as an indicator of normal biologic processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention.9 The use of biomarkers in various fields in the past decades has been widely proposed. When referring to disk degeneration, analysis of biomarkers could serve as a clinically relevant method before signs of degeneration are visible by radiology assessment.10

Chemokines consist of a large family of small proteins and generally have a low molecular weight ranging from 7 to 15 kDa and were first described as chemoattractant cytokines synthesized at sites of inflammation and are the regulatory proteins for leukocyte recruitment and trafficking.11 Chemokines are subdivided into four subfamilies, C-, CC-, CXC-, and CX3C-chemokine, based on the number and spacing of the first two cysteines in a conserved cysteine structural motif.12 Chemokines have been reported to participate various inflammation and autoimmune disease including osteoarthritis, rheumatoid arthritis, etc.13 Recently, chemokines have also been detected in tissue and serum in disk degeneration disease,14,15 and may exert a pivotal role in disk degeneration. Macrophage inflammatory protein-1α (MIP-1α, also known as CCL3) is a member of the CC chemokine family. CCL3 has been extensively studied since its initial identification as a macrophage-derived inflammatory mediator.16 In one previous study, CCL3 has been detected in herniated intervertebral discs,17 and the expression and activity was related to fibroblasts, endothelial cells, and infiltrating macrophages in the granulation tissues.17 In another bioinformatic analysis of the microarray data on the gene expression profiles of degenerative intervertebral disc cells after exposure to TNF-α, CCL3 was shown to play a crucial role in the development of the disc degeneration.18

All these studies above suggest that CCL3 may play an important role in disc degeneration. To our knowledge, there were no studies available illustrating the relationship between serum CCL3 concentrations and disease severity in IDD. Therefore, we intended to investigate the serum expressions of CCL3 in IDD patients and their association with clinical severity, to determine whether CCL3 could be used as a rapid and novel biomarker for diagnosis of disc degeneration.

Patients and methods

Study patients

From July 2016 to August 2017, a total of 132 patients diagnosed with lumbar IDD were enrolled in the current study. This study was approved by the ethics committee of Southern Medical University. The inclusion criteria of patients were the presence of significant back pain, which was defined as a pain in the low back for >2 weeks and severe enough to require physician consultation or treatment.19 Moreover, inclusion criteria of asymptomatic volunteers were done based on a report by Pfirrmann,20 who observed the process of normal aging in the lumbar disks, as follows: 1) no back pain within the last 3 years; 2) never absent from work because of LBP; 3) no history of consulting a physician because of LBP. One hundred and twenty six sex- and age-matched healthy volunteers receiving body check were recruited as controls. All the patients and healthy control individuals signed the informed consent form approved by the university ethics committee. The study design was in accordance with the Declaration of Helsinki guidelines.

Laboratory investigation

Peripheral venous blood was obtained from the antecubital vein following a 12 hours fasting period. Blood was collected using EDTA as an anticoagulant and centrifuged for 15 minutes at 1,000 g within 30 minutes of collection. Serum samples were aliquoted and stored at −80° until use. CCL3 concentrations in serum were examined using the human CCL3 Quantikine ELISA Kit (R&D Systems, Minneapolis, MN, USA) according to the manufacturer’s instructions. Briefly, standards of recombinant human CCL3 and serum samples were added to 96-well microtiter plates precoated with mouse monoclonal antibody against CCL3 and incubated for 2 hours at room temperature. The wells were then washed four times with washing buffer and incubated for 2 hours at room temperature with a horseradish peroxidase-conjugated goat polyclonal antibody against CCL3. After four washes, substrate solution was added to each well, and the plate was incubated for 30 minutes at room temperature in the dark. Finally, the reaction was stopped with the stop solution and absorbance was measured at 450 nm using an automated microplate reader. Recombinant human CCL3 was used to generate a linear standard calibration curve. All examinations were repeated at least three times.

Radiological evaluation

All participants underwent whole spine T2-weighted sagittal MRI without fat suppression. The MRI protocol was as follows: 5 mm slice thickness, 1 mm slice gap, FOV of 280×240 mm2, and a matrix of 448×336. The degree of discs degeneration of the lumbar spine (L1-S1) was assessed according to the Schneiderman criteria21 for disc degeneration. This grading system scores from level 0 to 3: 0 level means no degeneration denoted by high signal intensity of the disc; 1 level represent mild degeneration with slight decrease in signal intensity of the nucleus pulposus; 2 levels indicate moderate degeneration with generalized hypointensity of the nucleus pulposus (black disc) with normal disc height; and 3 levels suggest severe degeneration (black disc) with disc height narrowing. Based on this classification scheme, each of the five lumbar discs was assigned a grade (potential range: 0–3). The results of MRI evaluation were read by two radiology experts. The reliability of the MRI evaluations was assessed using agreement percentage and Kappa statistics. The agreement was rated as follows: Kappa value = 0–0.2 indicated slight agreement, 0.21–0.4 fair agreement, 0.41–0.60 moderate agreement, 0.61–0.8 substantial agreement, and 0.81 upward excellent agreement.

Evaluation of symptomatic severity

The symptomatic severity was evaluated by Visual Analog Scale (VAS) score to assess degree of pain and Oswestry Disability Index (ODI) index to evaluate functional disability. For VAS score, all the patients were asked to rate their pain intensity on a 10 cm VAS with end points “no pain” and “worst possible pain.” The Oswestry Low Back Pain Disability Index is a 10-item self-assessing questionnaire, and each item contains 6 levels of answers that can be scored from 0 to 5. These items are: pain, personal care, lifting and moving objects, walking, sitting, standing, sleep disorders caused by the LBP, sex life, social life, and traveling. A total score is calculated, and percentage of disability (score obtained divided by 50 and multiplied by 100) ranges from 0 (no disability) to 100 (complete disability). The interpretation of this scale is based on the scores: from 0 to 20: minimal disability; from 20 to 40: moderate disability; from 40 to 60: severe disability; from 60% to 80% crippling LBP; and beyond 80: the person is confined to bed.22

Statistical analysis

Statistical calculations and analysis were carried out using GraphPad Prism 6.0 (GraphPad Software, La Jolla, CA, USA). The basic data were expressed as mean ± SD. The data of CCL3 levels were presented as mean ± standard error of mean. We determined the differences in CCL3 levels between the control and disease groups using Student’s t-test or Mann–Whitney test. The Kolmogorov–Smirnov test was used to examine the normality of the distribution. The Spearman correlation test (nonparametric) was employed to examine the relationship between serum CCL3 concentrations and MRI grade of disc degeneration as well as VAS score and ODI index. P-values less than 0.05 were regarded as significant.

Results

Baseline characteristics

All data were obtained from a total of 132 patients including 67 men and 65 women (age ranging from 20 to 57 years) and 126 healthy controls including 63 males and 63 females (age ranging from 21 to 60 years). As shown in Table 1, there were no significant differences in baseline characteristics between IDD patients and healthy controls (P>0.05) including age, sex distribution, height, and body mass index (Table 1). Elevated levels of CCL3 in serum were found in IDD patients compared with healthy controls (277.3±4.3 pg/mL vs 150.2±2.4 pg/mL, P<0.001) (Figure 1).

Table 1

Baseline clinical characteristics

Items	IDD patients (n=132)	Healthy controls (n=126)	P-value
Age (years)	40.3±1.1	41.2±0.6	0.278
Sex (F/M)	65/67	63/63	0.903
BMI (kg/m2)	22.1±0.2	22.3±0.3	0.461
VAS score	3.6±0.1
ODI index	24.1±0.7
Schneiderman grading (1/2/3)	49/42/41
Serum CCL3 levels (pg/mL)	277.3±4.3	150.2±2.4	<0.001

Notes: Basic values and serum CCL3 levels are expressed as the mean value ± SEM.

Abbreviations: IDD, intervertebral disk degeneration; BMI, body mass index; VAS, Visual Analog Scale; ODI, Oswestry Disability Index; SEM, standard error of the mean.

Figure 1

Serum CCL3 levels between IDD patients and healthy controls (mean ± SEM).

Abbreviations: IDD, intervertebral disk degeneration; SEM, standard error of the mean.

Serum CCL3 levels in IDD patients with MRI severity defined by Schneiderman criteria

The κ value for radiographic assessment was 0.77 following evaluation. The CCL3 concentrations in serum of IDD patients with different Schneiderman MRI grades are depicted in Figure 2. With regard to the MRI severity of IDD, the patients were categorized into 3 groups according to the Schneiderman classification. The case group included 49 with grade 1, 42 with grade 2, and 41 with grade 3. IDD patients with grade 3 and grade 2 showed significantly elevated levels of CCL3 in serum compared with those with grade 1 (grade 3 vs grade 1: 300.6±6.6 pg/mL vs 250.7±6.2 pg/mL, P<0.001; grade 2 vs grade 1: 285.5±7.4 pg/mL vs 250.7±6.2 pg/mL, P<0.001). The difference of CCL3 levels between Schneiderman 2 and 3 patients did not reach significance (grade 3 vs grade 2: 300.6±6.6 pg/mL vs 285.5±7.4 pg/mL, P=0.385) (Figure 2A). The serum CCL3 levels were positively associated with Schneiderman grading system (r=0.425, P<0.001) by Spearman’s correlation analysis (Figure 2B).

Figure 2

Correlation of serum CCL3 levels with radiographic severity in IDD patients

Notes: (A) Comparison of serum CCL3 levels among different Schneiderman MRI grades (mean ± SEM). (B) Correlation of serum CCL3 levels with Schneiderman Grading.

Abbreviations: IDD, intervertebral disk degeneration; MRI, magnetic resonance imaging; SEM, standard error of the mean.

Serum CCL3 levels in IDD patients with clinical severity defined by VAS and ODI index

Based on intensity of pain on a VAS (0–10 cm), the patients were divided into two groups, the high- and low-pain group with VAS ≥3 and VAS <3, respectively. There were 76 patients in high-pain group and 56 patients in low-pain group. Serum CCL3 levels were significantly increased in high-pain group compared with low-pain group. (290.1±5.2 pg/mL vs 259.9±6.6 pg/mL, P=0.013) (Figure 3A). In addition, serum CCL3 concentrations were positively related to VAS scores (r=0.395, P<0.001) (Figure 3B). We further explored the relationship between serum CCL3 levels and ODI index to illustrate whether higher levels of CCL3 would affect the functional ability in IDD patients. We found that serum CCL3 concentrations were also related to ODI index (r=0.358, P<0.001) (Figure 3C).

Figure 3

Relationship between serum CCL3 levels and VAS as well as ODI index in IDD patients

Notes: (A) Comparison of serum CCL3 levels between high-pain and low-pain patients (mean ± SEM). (B) Correlation of serum CCL3 levels with VAS scores. (C) Correlation of serum CCL3 levels with ODI index.

Abbreviations: IDD, intervertebral disk degeneration; VAS, Visual Analog Scale; ODI, Oswestry Disability Index; SEM, standard error of the mean.

Discussion

The current study investigated the relationship between serum CCL3 levels and degree of lumbar IDD. We demonstrated for the first time that increased serum CCL3 levels were observed in IDD patients compared with controls. In addition, CCL3 concentration in serum was independently and positively correlated with radiographic progression and clinical severity. These findings implicate that serum CCL3 may serve as a potential serum biomarker for reflecting lumbar IDD.

The increased number of people with IDD in recent years impelled the need for early diagnosis. Authors looking to embrace a consensus of opinion related to the pathogenesis of IDD in their works have been devoting increasingly more attention to the importance of an inflammatory component.23 The expression of inflammatory mediators in the degenerated/herniated disks as well as their involvement in the process of disk degeneration (ie, in the induction of catabolic processes) has been investigated by both clinical studies as well as by laboratory investigation during the past decade.24,25 Identification of the relevance of these mediators in the development of discogenic back pain has led to an improved understanding of the molecular mechanisms of back pain, thus creating new possibilities of more targeted therapeutic intervention.26

The inflammatory chemokine CCL3 has been investigated in several studies addressing arthritic diseases. Plasma CCL3 could be a potential serum biomarker for knee osteoarthritis with the ability to detect pre-X-ray-defined changes and stage the severity of damage in knee.27 In addition, expression and secretion of CCL3 by synovial fluid neutrophils may be indicative of local and systemic inflammation in rheumatoid arthritis.28 CCL3 could be produced by different type of cells, and its production can be upregulated by the proinflammatory cytokines IL-1 and TNF-α.29,30 More recently, CCL3 has been recognized as a chemotactic mediator produced by intervertebral disc cells.29,30

Pain is the main complain in IDD patients. In previous studies, elevated CCL3 levels have been detected in patients with neck/shoulder pain, migraine, and prostatitis pelvic pain, and these levels significantly correlated with pain intensity.31–33 In addition, in nonspecific patients with LBP, improvements in VAS and ODI scores were closely accompanied by the obvious decline of CCL3 following spinal manipulation.34 All these works implicate that systematic CCL3 levels may participate the pain production in various disease. In our study, we observed that increased CCL3 levels were related to pain determined by VAS scores and functional disability by ODI index, suggesting serum that CCL3 expression plays a major role in the pain formation of disk degeneration through potential mechanisms.

MR imaging can reflect both the macromolecular concentrations and the structural integrity in the intervertebral disk and has been considered as a noninvasive method of characterizing IDD in humans and animal models in vivo.35,36 However, previous studies have also noted that a relationship between disc degeneration and LBP is a coincidental finding and that the predictive capacity of MRI in terms of LBP is questionable.37,38 We found increased serum CCL3 levels were positively related to MR imaging by Schneiderman grading, implicating CCL3 as a diagnosis biomarker in combination with the radiographic changes.

Limitations

Several potential limitations should be taken into account in our study. First, our study was based on a small sample size of Han Chinese people. A further study conducted on a random sample of a larger population will be needed to substantiate our results. Second, only serum CCL3 concentration has been measured in the serum. Additional immunohistochemical investigations of CCL3 expression in lumbar disk annulus fibrosus or nucleus pulposus may provide complete information on the pathogenic role of CCL3 in IDD. Third, we did not investigate the role of other soluble chemokines.

Conclusion

Collectively, in spite of the abovementioned limitations, the study revealed a significant elevation in serum CCL3 levels of IDD subjects compared with healthy controls and illustrated a pronounced positive correlation of serum CCL3 levels with the extent of radiographic and symptomatic severity in IDD patients. This study is the first to show that serum CCL3 is related to the disease progression of IDD. Further investigations are needed to define the mechanisms underlying this correlation. Therapies targeting CCL3 deserve further intensive study.