Altered Resting-State Connectivity with Pain-Related Expectation Regions in Female Patients with Severe Knee Osteoarthritis

Abstract

Purpose

Expectation affects pain experience in humans. Numerous studies have reported that pre-stimulus activity in the anterior insular cortex (aIC), together with prefrontal and limbic regions, integrated pain intensity and expectations. However, it is unclear whether the resting-state functional connectivity (rs-FC) between the aIC and other brain regions affects chronic pain. The purpose of this study was to examine the rs-FC between the aIC and the whole brain regions in female patients with severe knee osteoarthritis (OA).

Patients and Methods

Nineteen female patients with chronic severe knee OA and 15 matched controls underwent resting-state functional magnetic resonance imaging. We compared the rs-FC from the aIC seed region between the two groups. A disease-specific measurement of knee OA was performed.

Results

The aIC showed stronger rs-FC with the right orbitofrontal cortex (OFC), subcallosal area, and bilateral frontal pole compared with controls. The strength of rs-FC between the left aIC and the right OFC was positively correlated with the knee OA pain score (r = 0.49, p = 0.03). The strength of rs-FC between the right aIC and right OFC was positively correlated with the knee OA total score (r = 0.48, p = 0.036) and pain score (r = 0.46, p = 0.049). The OFC, subcallosal area, and frontal pole, together with the aIC, were activated during anticipation of pain stimulus. These areas have been reported as representative pain-related expectation regions.

Conclusion

This was the first study to show the stronger rs-FCs between the aIC and other pain-related expectation regions in female patients with severe knee OA. Female sex and preoperative pain intensity are risk factors of persistent postoperative pain after total knee arthroplasty. It is suggested that the functional relationship between pain-related expectation regions affects the formation of severe knee OA and persistent postoperative pain following total knee arthroplasty.

Introduction

Expectation strongly modulates pain experience in humans. In our brain, the insular cortex (IC) plays an important role in pain processing. Particularly, the anterior insular cortex (aIC) is involved in pain processing, such as expectation,^1–14 cognitive control (attention, value, reward, decision-making),^3,4,8–11 salience,^10,11 and prediction errors (PEs).^12–14 Recently, magnetic resonance imaging (MRI) studies have revealed that the aIC integrated pain intensity and expectation in healthy subjects. Moreover, the aIC is activated with the prefrontal cortex (PFC) and limbic regions during anticipation of a pain stimulus.^1–13 The IC, PFC, and limbic regions are activated by a pain stimulus even in patients with chronic pain.¹⁵ In addition, the IC activity was correlated with pain intensity in patients with knee osteoarthritis (OA) during anticipation of pain.¹⁶ Therefore, functional coupling between the aIC and the other pain-related expectation regions may be involved in the mechanism of chronic pain and occur even at rest without a pain stimulus. However, thus far, there are no studies examining the relationship of resting-state activity between the aIC and other pain-related expectation regions in patients with chronic pain.

Knee OA is a chronic pain disease, with a predominance in female patients.^17,18 Total knee arthroplasty for patients with severe knee OA is a common procedure applied to improve pain and disability; however, this procedure is occasionally associated with persistent postoperative pain.^19–21 Female sex^19,22 and preoperative pain intensity^19,21,22 are recognized as risk factors of persistent postoperative pain. The pathology of knee OA differs depending on sex and pain severity. Therefore, in this study, we targeted only female patients with severe knee OA. In a resting-state functional MRI (rs-fMRI) study, Baliki et al and Cottam et al^23,24 identified that resting-state functional connectivity (rs-FC) between the aIC and the default mode network was altered in patients with chronic knee OA. These studies focused on the salience role of the aIC. As a result, the region of interest (ROI) of the aIC used by Baliki et al and Cottam et al was involved in the salience network. However, the ROI of the aIC involved in expectation can be larger and close to the anatomical size.^5,12,13

The objective of this study was to examine the characteristics of rs-FC between the anatomically defined aIC and the whole brain regions in female patients with severe knee OA using rs-fMRI. We hypothesized that the rs-FC between the aIC and other pain-related expectation regions would be altered in patients versus healthy controls, and the strength of the rs-FC of aIC would be associated with pain scores in female patients with chronic severe knee OA.

Patients and Methods

Participants

We recruited 19 female patients diagnosed with chronic knee OA and 15 age- and gender-matched controls. The 19 patients with Kellgren–Lawrence²⁵ grade 3 (N = 6) and grade 4 (N = 13) knee OA underwent knee arthroplasty. Five of the 15 controls had knee pain. Considering that their degree of pain using a visual analog scale (VAS) was <30/100, and the duration of pain was <3 months, these patients were not diagnosed with chronic pain. Two patients and two controls received medication. One patient received tramadol and acetaminophen, while the other patient received tramadol and pregabalin. Two controls received celecoxib, as required.

The exclusion criteria were history of neurological disease, brain injury, psychiatric disorders, rheumatoid arthritis, claustrophobia, and insertion of metal or electronic devices. This study was conducted in accordance with the tenets of the Declaration of Helsinki, and approved by the Hiroshima University Ethics Committee (E-302). Written informed consent was provided by all participants.

Clinical Measurements

Participants underwent the following measurements prior to MRI scans. The VAS was used to measure current pain intensity (range: 0–100). A disease-specific measurement of knee OA was performed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC).²⁶ The WOMAC consists of 24 questions (five for pain, two for stiffness, and 17 for physical function), which are rated using an intensity scale of 0–4. The pain score (range: 0–20), stiffness score (range: 0–8), physical function score (range: 0–68), and the total score (range: 0–96) are determined based on this index. The Pain-DETECT²⁷ was used to measure elements of neuropathic pain (range: 0–35). The Pain Catastrophizing Scale (PCS)²⁸ was used to measure the degree of catastrophic thoughts regarding pain (range: 0–52). High scores indicate worse outcome in all measurements. In patients with bilateral knee OA, the side most affected by pain was evaluated.

Acquisition of Neuroimaging Data

The fMRI procedure was performed using a 3.0-Tesla MRI scanner (Ingenia Elition; Philips, Amsterdam, Netherlands) equipped with a 32-channel head coil. Functional images were captured using a single-shot T2*-weighted echo-planar imaging sequence (time repetition: 2500 ms; time echo: 30 ms; flip angle: 80°; matrix: 64 × 64; field of view: 212 × 212 mm²; 40 slices, slice thickness: 0.8 mm without gap; no oblique axial images; voxel size: 3.3 mm × 3.3 mm × 3.2 mm; 240 volumes; scan time: 10 min). During the functional scan, the patients were requested to keep their eyes open, relax, and look at a cross mark in front of them without moving or falling asleep. A three-dimensional high-resolution anatomical image was captured using a T1-weighted gradient echo pulse sequence (time repetition: 6.8 ms; time echo: 3.1 ms; flip angle: 9°; field of view: 256 × 240 mm²; voxel size: 1 mm × 1 mm × 1.2 mm; scan time: 6 min 58 s).

Statistical Analysis

Statistical analysis was performed using the Stata/MP, version 15.1 (Stata Corporation, College Station, TX, USA). A nonparametric statistic test (Mann–Whitney U-test) was used for the age, VAS, WOMAC, Pain-DETECT, and PCS.

FC Analysis

Rs-fMRI data were analyzed using the SPM12 (Welcome Department of Cognitive Neurology, London, UK; http://www.fil.ion.ucl.ac.uk/spm/software/spm12/), CONN (Functional Connectivity Toolbox; http://www.nitrc.org/projects/conn),²⁹ and Matlab version 8.5 (R2017b; MathWorks, Natick, MA, USA). After discarding the first 10 images to eliminate any signal decay, preprocessing was performed including realignment, slice-timing correction, outlier detection, co-registration to the anatomical image, segmentation of the anatomical image (gray matter, white matter, and cerebrospinal fluid), normalization with the standard Montreal Neurological Institute brain, and smoothing with an 8-mm Gaussian kernel. After preprocessing, signal and motion artefacts (global signal z-value threshold ≥5; composite motion threshold ≥0.9 mm) were removed from the data using a CompCor strategy,³⁰ and the data were band-pass filtered (0.02–0.08 Hz) to reduce the influence of noise.

A seed-to-voxel analysis was performed using the left and right aIC as the region of ROI. The ROIs of the left and right aIC were generated using the Neuromorphometrics atlas in SPM12, provided by Neuromorphometrics, Inc. (http://neuromorphometrics.com) under academic subscription.

The within-group imaging analysis was performed using a one-sample test, with age as a covariate. The threshold for statistical significance was determined at p < 0.001 for the uncorrected peak-level and p < 0.05 for the cluster-level after family-wise error correction.

Spearman’s rank correlation coefficients were calculated to investigate the relationship between the strength of rs-FC with the aIC and clinical measurements in female patients with chronic severe knee OA.

Results

Demographic and Clinical Measurements

The demographic and clinical measurements of the participants are shown in Table 1. Compared with the controls, patients with chronic knee OA exhibited significantly higher scores in the VAS, WOMAC, pain-DETECT, and PCS; however, they did not differ in age.

Table 1.

Demographic and Clinical Measurements of the Participants

Data	Patients with Knee OA	Controls	p
	(N = 19)	(N = 15)
Age, year	73.2 ± 5.1	74.9 ± 4.6	0.25
Duration, month	102.9 ± 88.6
VAS	64.5 ± 15.1	5.1 ± 8.1	< 0.001
WOMAC
total	61.1 ± 12.4	7.9 ± 14.7	< 0.001
pain	12.3 ± 3.0	1.1 ± 1.6	< 0.001
stiffness	5.1 ± 2.5	0.9 ± 1.8	< 0.001
physical activity	43.2 ± 9.9	5.9 ± 11.6	< 0.001
Pain-DETECT	9.2 ± 5.4	2.6 ± 2.9	< 0.001
PCS	26.3 ± 10.8	9.2 ± 13.0	< 0.001

Note: Data are presented as the means ± SD.

Abbreviations: OA, osteoarthritis; PCS, Pain Catastrophizing Scale; SD, standard deviation; VAS, visual analog scale; WOMAC, Western Ontario and McMaster Universities Osteoarthritis Index.

The rs-FC of aIC

In female patients with chronic severe knee OA, the left aIC showed stronger rs-FC with the right orbitofrontal cortex (OFC) and the subcallosal area (SCA) compared with controls (Table 2; Figure 1). The right aIC showed stronger rs-FC with the right OFC, SCA, and the bilateral frontal pole (FP) compared with controls (Table 2; Figure 2).

Table 2.

Brain Regions Showing Increased Functional Connectivity with the Left and Right Anterior Insular Cortex in Patients with Knee Osteoarthritis Relative to Control Subjects

Anatomical Location	MNI Coordinates			Cluster Size	p-FWE
	X	Y	Z
Left
Rt. orbitofrontal cortex	18	14	−30	150	< 0.005
subcallosal area				87
Right
Rt. orbitofrontal cortex	14	20	−22	171	< 0.005
subcallosal area				96
Bil. frontal pole	8	68	20	519	< 0.001

Note: The X, Y, and Z coordinates accord with the MNI atlas.

Abbreviations: Rt, right; Bil, bilateral; MNI, Montreal Neurological Institute; FWE, family-wise error corrected.

Figure 1.

Resting-state functional connectivity of the left anterior insular cortex. Brain regions showing a significant increase in the functional connectivity of the left anterior insular cortex in patients with knee osteoarthritis relative to controls (p < 0.001 uncorrected, peak-level and p < 0.05 cluster-level, after FWE correction).

Abbreviations: FWE, family-wise error; Rt, right; OFC, orbitofrontal cortex; SCA, subcallosal area.

Figure 2.

Resting-state functional connectivity of the right anterior insular cortex. Brain regions showing a significant increase in the functional connectivity of the right anterior insular cortex in patients with knee osteoarthritis relative to controls (p < 0.001 uncorrected, peak-level and p < 0.05 cluster-level, after FWE correction).

Abbreviations: FWE, family-wise error; Rt, right; Bil, bilateral; OFC, orbitofrontal cortex; SCA, subcallosal area; FP, frontal pole.

Correlation Between FC and Clinical Measurements

In female patients with chronic severe knee OA, the correlation analyses revealed that the strength of rs-FC between the left aIC and right OFC was correlated with the WOMAC pain score (r = 0.49, N = 19, p = 0.03; Figure 3A). Moreover, the strength of rs-FC between the right aIC and right OFC was correlated with the WOMAC total score (r = 0.48, N = 19, p = 0.036; Figure 3B) and WOMAC pain score (r = 0.46, N = 19, p = 0.049; Figure 3C). We did not detect any significant relationship between the strength of FC and other clinical measurements (Table 3).

Figure 3.

Correlations between the anterior insular cortex-right orbitofrontal cortex functional connectivity and clinical measurements. Scatter plots showing the correlations of functional connectivity with the (A) WOMAC pain score in the Lt. aIC and Rt. OFC; (B) WOMAC total score in the Rt. aIC and Rt. OFC; and (C) WOMAC pain score in the Rt. aIC and Rt. OFC.

Abbreviations: aIC, anterior insular cortex; Lt, left; Rt, right; OFC, orbitofrontal cortex; WOMAC, Western Ontario and McMaster Universities Osteoarthritis Index.

Table 3.

Correlation Between the Anterior Insular Cortex-Right Orbitofrontal Cortex Functional Connectivity and Clinical Measurements

Lt.aIC-Rt.OFC	WOMAC total	WOMAC pain	WOMAC stiffness	WOMAC physical
cc	0.29	0.49*	0.15	0.23
p	0.22	0.03	0.52	0.34
	VAS	Pain-DETECT	PCS
cc	0.26	−0.02	0.05
p	0.28	0.92	0.84
Rt.aIC-Rt.OFC	WOMAC total	WOMAC pain	WOMAC stiffness	WOMAC physical
cc	0.48*	0.46*	0.24	0.37
p	0.04	0.049	0.31	0.12
	VAS	Pain-DETECT	PCS
cc	0.26	−0.01	0.02
p	0.28	0.97	0.94

Note: *p < 0.05 denotes significant correlation.

Abbreviations: Lt, left; Rt, right; aIC, anterior insular cortex; cc, Spearman’s rank correlation coefficients; OFC, orbitofrontal cortex; PCS, Pain Catastrophizing Scale; VAS, visual analog scale; WOMAC, Western Ontario and McMaster Universities Osteoarthritis Index.

Discussion

Using rs-fMRI, we investigated the abnormality of rs-FCs between bilateral aIC and other brain regions in female patients with chronic severe knee OA. We found that the patients exhibited an increased rs-FC of left aIC to right OFC, and SCA. In addition, the rs-FC with the right aIC, SCA, right OFC, and bilateral FP was increased. Furthermore, we showed that the strength of rs-FC between the left aIC and right OFC was significantly associated with the WOMAC pain score. Moreover, the strength of rs-FC between the right aIC and right OFC was significantly associated with the WOMAC total score and WOMAC pain score.

Previous studies suggested that healthy subjects perceived a noxious stimulus as more painful or fearful when they expected aversiveness or experienced a nocebo effect prior to the stimulus. In addition, the FC of the aIC and OFC was increased prior to or during the stimulus.^4,7,31,32 During anticipation of dental treatment and hyperventilation, an increased activation of the aIC and OFC was also found in healthy subjects.^8,33 The OFC represents and retains the affective value of past comfort-discomfort.^34–36 Atlas et al⁴ suggested that the aIC modulates pain perception by integrating aversive expectation from the OFC during anticipation. On the other hand, the expectation of pleasure mediates pain. The FC of the aIC and OFC was decreased when a pain stimulus and monetary wins occurred simultaneously.³⁷ In summary, the OFC is an expectation region of value and reward for pain, and involved in the modulation of pain processing. Our results suggested that the increased rs-FC of the aIC and OFC affect subjective pain by increasing the aversive expectation for pain. In fact, we found that the strength of rs-FC between the aIC and OFC exhibited a positive correlation with the disease-specific measurement of knee OA. Approximately 15–30% of patients experience persistent postoperative pain after undergoing total knee arthroplasty.^19–21 This may be due to the aversive expectation of pain remaining after total knee arthroplasty, which completely removes the sensory aspects of pain.

The SCA is connected to the medial OFC and subgenual anterior cingulate cortex (ACC). Moreover, the amygdala, ventral striatum, and hippocampus are involved in emotion experience and processing.³⁸ The aIC, SCA, OFC, and ACC are composed of agranular visceromotor cortices. These areas contribute to generating predictions for somatosensory inputs, such as pain stimulus, and indirectly enabling the creation of PEs.^39,40 In fact, PEs to a cued pain stimulus have been found in the aIC, PFC, and limbic regions.^12,13 Geuter et al¹² indicated that the predictions and PEs played an important role in our pain perception, and brain processes of the predictions and PEs may contribute to chronic pain. Therefore, it is suggested that the increased rs-FC with the aIC, SCA, and OFC may be involved in our pain perception by increasing the emotional experiences and creating the predictions and PEs without a stimulus.

The SCA, medial FP, and medial OFC are included in medial PFC (mPFC), together with pregenual ACC. In female patients with chronic pelvic pain, the rs-FC between the aIC and mPFC (medial FP) increased, and the increased rs-FC between these regions was positively correlated with pain intensity, anxiety, and depression scale.⁴¹ In nonspecific chronic low back pain patients with a high clinical sign, activation of the aIC and mPFC (medial FP, pregenual ACC) showed a positive covariance in anxiety and depression scales in response to expected pain.⁴² In major depressive disorder, an increased rs-FC of the aIC/ventrolateral PFC and FP with the SCA was associated with remission and treatment failure.⁴³ Although we did not evaluate anxiety and depression scores in this study, it has been reported that chronic pain patients with knee OA have higher scores versus healthy controls.^24,44 Moreover, older knee OA patients with depressive symptoms are at elevated risk for incidental major depression or anxiety disorders.⁴⁵ On the other hand, it was reported that decreased rs-FC between the aIC and mPFC (medial FP) was negatively associated with pain score in females with primary dysmenorrhea during menstruation.⁴⁶ The role of connectivity between the aIC and mPFC in chronic pain is inconsistent. However, our results suggest that the increased rs-FC between the aIC, SCA, and FP may be a neural network change, indicating the psychological aspects of female patients with chronic severe knee OA.

The present study had several limitations. Firstly, owing to the cross-sectional design of this study, we could not determine the causal relationships between chronic pain and cerebral abnormalities. Further longitudinal studies would be necessary to answer this question. In fact, it was reported that structures in the brain were altered following surgery in patients with chronic knee and hip OA.^47,48 Secondly, two subjects received medicines, which could affect the central nervous system. In a sub-analysis excluding those two subjects, the stronger rs-FC between the aIC and pain-related expectation regions remained. However, it is possible that medicines may have influenced the results. Thirdly, the number of participants was small. In this study, we targeted only females and showed a significant correlation between the strength of rs-FC and pain scores. For the generalization of the present findings, it would be important to also examine males and increase the number of participants. Fourthly, we did not directly measure pain expectation. It would be necessary to investigate the effect of expectation on pain and subsequently evaluate its relationship with rs-FC. Recently, pain-free rs-FC has been reported to predict individual pain sensitivity or the placebo effect.^49,50 In fact, Wagner et al⁵⁰ identified that placebo-induced pain reduction (positive expectation effect) was associated with pain-free rs-FC networks, including the aIC. Finally, it has been reported that the activity of the ventral aIC was different from that of the dorsal aIC in the expectation or PEs.^12,13 The ventral aIC contributed to both expectation and PEs, while the dorsal aIC did only to the former.¹³ Future studies should investigate the subdivisions of ROIs in the aIC.

Conclusion

Using rs-fMRI analysis, this was the first study to show that the rs-FC between the aIC and other pain-related expectation regions was already increased in female patients with chronic severe knee OA. The extent of this increase was significantly associated with disease-specific measurement. These findings enhance our understanding of the neuropathology and treatment of female patients with chronic severe knee OA.

Abbreviations

ACC, anterior cingulate cortex; aIC, anterior insular cortex; FP, frontal pole; IC, insular cortex; MRI, magnetic resonance imaging; OA, osteoarthritis; OFC, orbitofrontal cortex; PCS, Pain Catastrophizing Scale; PEs, prediction errors; PFC, prefrontal cortex; ROI, region of interest; rs-FC, resting-state functional connectivity; rs-fMRI, resting-state functional magnetic resonance imaging; VAS, visual analog scale; WOMAC, Western Ontario and McMaster Universities Osteoarthritis Index.

Author Contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.