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Central sensitization inventory scores correlate with pain at rest in patients with hip osteoarthritis: a retrospective study

BMC Musculoskeletal Disorders volume 21, Article number: 595 (2020) Cite this article

Abstract

Background

Patients with persistent pain due to osteoarthritis (OA) complain of multiple symptoms that cannot be explained solely by structural changes. A poor correlation exists between structural and inflammatory changes in OA and pain levels. Central sensitization (CS) has been identified as a factor that induces chronic pain in patients with OA. Although it is important to identify osteoarthritis patients with CS components, the prevalence and characteristics of CS, especially those in patients with hip OA, are not well understood. Thus, we aimed to determine the prevalence and characteristics of CS in patients with hip OA, in this study.

Methods

The CS Inventory (CSI), used as a non-invasive routine clinical tool to evaluate the presence of CS 1 month before surgery in 100 patients with hip OA, was measured at our outpatient clinic, and the data were retrospectively reviewed. We determined the number of patients with a CSI score of 40 points or higher and assessed the relationships between the CSI score and clinical factors (including age, duration of hip pain, degree pain at rest and on activity, by using the visual analogue scale [VAS] and the Harris Hip Score) using the Spearman’s correlation coefficient.

Results

The mean age of participants was 63.9 ± 11.6 years, and there were 15 men and 85 women. All patients had hip OA, categorised as advanced and terminal stage (Tönnis grade 2–3) on preoperative plain radiography. The mean duration of hip pain was 4.2 ± 4.4 years. The mean CSI score was 19.5 ± 11.3 and 5 (5.0%) of the patients had a score of 40 or more points. CSI scores correlated significantly only with VAS pain at rest (r = 0.348, P < 0.001).

Conclusion

In this study, 1 out of every 20 hip OA patients had CS components. CSI scores were significantly correlated with pain at rest in hip OApatients. CS approaches to hip OA may be one of the treatment options for pain at rest.

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Background

Osteoarthritis (OA) is a heterogeneous disease, characterised by progressive cartilage loss, subchondral bone remodelling, osteophyte formation, and synovial inflammation, with resultant joint pain and increasing functional disability. Patients with persistent pain due to OA complain of multiple symptoms that cannot be explained solely by structural changes. It has been reported that there is a poor correlation between structural and inflammatory changes in OA and pain levels [1]. Although the determinants of pain in OA are poorly understood, they are believed to involve multiple interactive pathways that are best explained by a biopsychosocial framework, which includes biological, psychological, and social factors [2, 3].

In 2011, the International Association for the Study of Pain defined central sensitization (CS) as increased responsiveness of nociceptive neurons in the central nervous system to normal or subthreshold afferent input. CS results from persistent, intense nociceptor stimulation that triggers changes in the central pain transmitting neurons, leading to alterations in pain presentation and perception, and centrally mediated symptoms, such as fatigue and mood disorders [4]. Over the last several decades, many authors have reported CS as one of the mechanisms underlying various chronic pain disorders, including headache, whiplash pain, musculoskeletal pain, low back pain, visceral pain, vulvodynia, prostatitis, etc [5]. CS has also been reported as a chronic pain factor in patients with OA [6, 7]. Patients with chronic pain with CS components have been reported to be resistant to conservative treatment, including traditional physiotherapy and pain medication [8]. In recent years, some treatments have been reported for OA patients with CS components [8,9,10,11]. While it is important to identify OA patients with CS components, the prevalence and characteristics of CS, especially in patients with hip OA, are not well understood.

The CS Inventory (CSI) was developed as a comprehensive screening tool with high reliability and reproducibility to identify the existence of a CS component [12, 13]. The CSI comprises of two parts: part A, designed to evaluate symptoms associated with CS, comprises 25 self-reported items on somatic and emotional symptoms, scored from 0 to 100 points, with 0 and 100 being the best and worst scores, respectively. Each item was graded on a 5-point Likert scale (0: never, 1: rarely, 2: sometimes, 3: often, 4: always). Part B screens for previous diagnoses of one or more specific disorders, including seven separate CS syndromes (CSSs) (e.g., fibromyalgia, chronic fatigue syndrome, temporomandibular joint disorder, irritable bowel syndrome, migraine or tension headaches, multiple chemical sensitivities, and restless leg syndrome). CS involvement is strongly suggested in these seven disorders, and CSS was proposed as a comprehensive disease concept [14, 15]. Although some studies have reported that the CSI revealed the presence of CS components in knee OA [11, 16], such investigations in hip OA were not determined.

Here, we determined the prevalence and characteristics of CS in patients with hip OA using CSI in this study.

Methods

Ethics

Ethical approval was obtained from our Institutional Review Board (approval number: B20–096), and the study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. The requirement for informed consent was waived because of the retrospective study design.

Participants

As accumulating evidence indicates the importance of evaluating the CS components in OA pain, CSI was used as a non-invasive routine clinical tool to evaluate the presence of CS in patients with hip OA, 1 month before surgery, at our outpatient. The data of a total of 100 consecutive patients diagnosed with hip OA who were scheduled to undergo total hip arthroplasty between November 2018 and September 2019 were retrospectively included in this study. Patients who were not diagnosed with hip OA and/or previously underwent a hip surgery on the same laterality were excluded.

Assessment of CS involvement

To determine the existence of CS components, patients were assessed using the CSI. An explanation of the Japanese version of the CSI (both parts A and B) were provided to the patients, and the patients completed the CSI by themselves. Tanaka et al. reported that the Japanese version of the CSI is a useful and psychometrically sound tool, comparable to the English version, for assessing CSSs in Japanese patients with musculoskeletal disorders [17]. The CSI Part A score was divided into five categories with increasing severity: subclinical (0–29), mild (30–39), moderate (40–49), severe (50–59), and extreme (60–100) [18]. We determined the number of patients with a score of 40 points or higher based on previous studies as shown in Fig. 1 [13, 16, 19]. The CSI Part B was also completed to evaluate the prevalence of CSSs in the patients. The prevalence of hip OA patients with one or more CSSs was investigated.

Fig. 1
figure 1

Scheme of study protocol. One hundred hip osteoarthritis (OA) patients were assessed using the Central Sensitization Inventory. The relationship between CSI Parts A and B and clinical characteristics including hip OA score (Harris Hip Score), radiographic OA grade (Tönnis grade), and pain score (visual analogue scale at rest and on activity) were also evaluated. Abbreviations: OA: Osteoarthritis; CSI: Central Sensitization Inventory; CSSs: Central Sensitization Syndromes; HHS: Harris Hip Score; VAS: visual analogue scale

Full size image

Relationship analysis between CSI score and clinical characteristics

To analyse the relationship between clinical scores (CSI score and the Harris Hip Score [HHS]) and clinical characteristics (age, sex, and clinical assessments [the duration of hip pain in years, severity of hip pain at rest and on activity), data were collected preoperatively at an outpatient clinic 1 month before surgery.

Radiographic OA was graded as 0 (no changes); 1 (slight narrowing of the joint space, slight lipping at the joint margin, and slight sclerosis of the femoral head or acetabulum); 2 (the presence of small bony cysts, further narrowing of the joint space, and moderate loss of femoral head sphericity); and 3 (the most severe, and indicates large cysts, severe narrowing of the joint space, severe femoral head deformity, and avascular necrosis) using the Tönnis classification. The severity of OA-related hip pain at rest and on activity was assessed using an 11-point visual analogue scale (VAS: 0 = no pain, 10 = worst possible pain). HHS, with a maximum of 100 points, is used to assesses the hip function [scores range from 0 (worse disability) to 100 (less disability)] and includes the following domains: pain, function, deformity, and motion.

Statistical analysis

Results are expressed as the mean and the standard deviation of the mean unless otherwise indicated. A sample size calculation was performed based on the study’s main objective, which was to evaluate the correlation between CSI scores and significant variables in all patients. The minimum power level was set at 0.80. It was determined that we needed to include 97 patients to satisfy the expected effect size. Therefore, our sample size of 100 patients was deemed adequate. Continuous variables were calculated using the Mann-Whitney U test and categorical variables were calculated using the chi-square test. Correlations between the CSI score and age, duration of hip pain, VAS pain at rest, VAS pain on activity, and HHS in all patients were evaluated using the Spearman’s correlation coefficient. Correlation coefficient is represented by r. All statistical analyses were performed using Statistical Package for the Social Sciences software (version 25.0, IBM, NY, USA). P values < 0.05 were considered to indicate statistical significance.

Results

Patient demographic information

Patient demographics and clinical assessments are summarised in Table 1. The mean age was 63.9 ± 11.6 years, and there were 15 men and 85 women. All patients had hip OA, categorised as advanced and terminal stage (Tönnis grade 2–3) on preoperative plain radiography. The mean duration of hip pain was 4.2 ± 4.4 years. The mean VAS score was 3.2 ± 2.7 for pain at rest and 6.1 ± 2.5 for pain on activity. The mean HHS was 47.4 ± 13.0. The mean CSI score was 19.5 ± 11.3. The classification of CS severity level according to the scoring in CSI Part A is shown in Table 2. Seventy-nine patients were classified as subclinical (score: 0–29), 16 were classified as mild (score: 30–39), 3 were classified as moderate (score: 40–49), 2 were classified as severe (score: 50–59), and none were classified as extreme (score: 60–100). Five percent of the patients had a score of 40 or more points. Prevalence rates of CSS diagnoses according to CSI Part B are shown in Table 3.

Table 1 Patients’ demographics and clinical assessments (N = 100)
Full size table
Table 2 The classification of CS severity level according to the CSI score
Full size table
Table 3 The prevalence rates of patients with a history of CSSs
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Relationship between radiographic hip OA severity and the CSI score

The CSI score did not differ significantly between patients with Tönnis grades 2 and 3 (P = 0.063) in Table 4. There were also no significant differences in other factors, including patient demographics and clinical scores.

Table 4 Comparison between hip OA severities and patients’ demographics and clinical assessments
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Correlation between characteristics of hip OA patients and CSI score

The CSI score significantly correlated with VAS pain at rest (r = 0.348, P < 0.001) in all patients with hip OA (Fig. 2). Other factors, including age, duration of hip pain, VAS pain on activity, and HHS, were not significantly associated with the CSI score.

Fig. 2
figure 2

Correlation between the CSI score and characteristics of the hip OA patients. Correlations between the Central Sensitization Inventory score and age, duration of hip pain, visual analogue scale (VAS) pain at rest, VAS pain on activity, and Harris Hip Score in 100 patients with hip OA were evaluated using the Spearman’s correlation coefficient. Correlation coefficient is represented by r. P < 0.05 indicates statistical significance. Abbreviations: CSI: Central Sensitization Inventory; OA: Osteoarthritis; VAS: visual analogue scale; HHS: Harris Hip Score

Full size image

The CSI score in hip OA patients with and without CSSs

Fifteen percent of the patients were diagnosed with one or more CSSs. The CSI score was significantly higher in patients with one or more CSSs (30.00 ± 12.50) than in patients without a CSS diagnosis (17.70 ± 10.00; P < 0.001) (Table 5). There were no significant differences in other factors, including patient demographics and clinical scores.

Table 5 Comparison between patients with and without CSSs in patients’ demographics and clinical assessments
Full size table

Discussion

A CSI score of 40 out of 100 was reported as the best distinguishing factor in patients with CSSs [13]. Kim et al. reported that 48% of knee OA patients who underwent total knee arthroplasty had a CSI score of 40 or higher and patients with high CSI scores (> 40) before knee arthroplasty exhibited more severe postsurgical pain intensity [16]. Patients with CSI scores of > 40 before vertebral fusion surgery exhibited higher (i.e. worse) patient-reported disability scores after the surgery [19]. In the present study, 5% of the patients with hip OA had CSI scores of at least 40 points and 15% of the patients had a history of at least one CSS. In addition, hip OA patients with CSSs had a higher CSI score compared to hip OA patients without CSSs. Although the percentage of patients with a score of 40 or more in this study was small compared to those of previous knee OA studies, it may be necessary to consider the presence of CS pathology according to different pain mechanisms in individuals undergoing pain management for hip OA, in particular, those with CSSs.

Previous studies have reported that a relationship exists between radiographic hip OA and pain severity, but have found no evidence of an association between preoperative pain severity and hip OA grade [20]. In our study, no relationship between hip OA severity and the CSI score was discovered; however, CSI scores were significantly correlated with pain at rest in hip OA patients. Pain on activity might be a common phenomenon, while pain at rest may sometimes occur with a variety of pain complaints (e.g., from a dull ache to a sharp, stabbing pain) [21]. Previous studies have suggested different associations of OA-related pain at rest and during activity in the knee and hip joints [22, 23]. Lundblad et al. reported an association between high preoperative VAS pain at rest and a lower pain threshold [23]. Taken together with previous studies’ results, and our results suggested that higher CSI score in hip OA patients was associated with the pathology of pain at rest.

Recently, some treatments of OA pain related to CS components have been reported [8,9,10,11]. Duloxetine is a potent selective serotonin norepinephrine reuptake inhibitor that potentiates the descending inhibitory pain pathways in the central nervous system [24]. The analgesic effect of duloxetine in patients with centrally mediated pain due to OA is well documented [10, 25]. From the results of this study, approaches to the pathology of CS may be important for hip OA patients with pain, particularly, pain at rest.

This study has a limitation to acknowledge. This study used a cross-sectional study design. The relationship between preoperative CS components and postoperative clinical results remains unclear in patients with hip OA. Therefore, a prospective longitudinal study will be needed to evaluate these relationships.

Conclusions

In this study, 1 out of every 20 hip OA patients had CS components. CSI scores were significantly correlated with pain at rest in hip OA patients. Our results suggest that CS approach to hip OA may be one of the treatment options for pain at rest.

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article. The raw data can be requested from the corresponding author.

Abbreviations

OA:

Osteoarthritis

CS:

Central sensitization

VAS:

Visual analogue scale

HHS:

Harris Hip Score

CSI:

Central Sensitization Inventory

CSS:

Central sensitization syndrome

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Acknowledgements

We would like to thank Editage [http://www.editage.com] for editing and reviewing this manuscript for English language.

Funding

The authors received no specific funding for this work.

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Authors and Affiliations

  1. Department of Orthopedic Surgery, Kitasato University School of Medicine, 1-15-1 Minami-ku, Kitasato, Sagamihara City, Kanagawa, 252-0374, Japan

    Yoshihisa Ohashi, Kensuke Fukushima, Gen Inoue, Kentaro Uchida, Tomohisa Koyama, Maho Tsuchiya, Katsufumi Uchiyama & Masashi Takaso

  2. Department of Rehabilitation, Kitasato University School of Allied Health Sciences, 1-15-1 Minami-ku, Kitasato, Sagamihara City, Kanagawa, 252-0374, Japan

    Naonobu Takahira

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  1. Yoshihisa Ohashi
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  2. Kensuke Fukushima
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Contributions

YO, KF and GI designed the study and analysed the data. YO, KeU and KF wrote the manuscript. YO, TK, MT, KaU and NT participated in the data collection, analysis, and interpretation. MT was supervised the study. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kensuke Fukushima.

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Ethics approval and consent to participate

This study was approved by the Ethics Review Board of Kitasato University Hospital (approval number: B20–096). Written consent to participate was not needed to obtain in this study design.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Ohashi, Y., Fukushima, K., Inoue, G. et al. Central sensitization inventory scores correlate with pain at rest in patients with hip osteoarthritis: a retrospective study. BMC Musculoskelet Disord 21, 595 (2020). https://doi.org/10.1186/s12891-020-03630-6

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Keywords

BMC Musculoskeletal Disorders

ISSN: 1471-2474

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