Abnormality of spontaneous brain activities in patients with chronic neck and shoulder pain: A resting-state fMRI study

Cheng-Xin Yu, Ting-Ting Ji, Hao Song, Bo Li, Qiang Han, Liang Li, Zhi-Zheng Zhuo, Cheng-Xin Yu, Ting-Ting Ji, Hao Song, Bo Li, Qiang Han, Liang Li, Zhi-Zheng Zhuo

Abstract

Objectives Chronic gneck and shoulder pain (CNSP) is a common clinical symptom of cervical spondylotic radiculopathy. Several studies using resting-state functional magnetic resonance imaging (rs-fMRI) have reported that most chronic pain diseases are accompanied by structural and functional changes in the brain. However, few rs-fMRI studies have examined CNSP. The current study investigated cerebral structural and functional changes in CNSP patients. Methods In total, 25 CNSP patients and 20 healthy volunteers participated in the study. 3D-T1W and rs-fMRI images were acquired. Voxel-based morphometry analysis was applied to structural images, and regional homogeneity (ReHo) was extracted from rs-fMRI. Statistical analysis was performed on post-processing images and ReHo parameter maps. Results The results revealed no significant differences in brain structure between the two groups. In the patient group, ReHo values were significantly increased in the bilateral middle frontal gyrus and decreased in the left insula, superior frontal gyrus, middle cingulate gyrus, supplementary motor area, right postcentral gyrus, and superior parietal lobule. Conclusions This initial structural and rs-fMRI study of CNSP revealed characteristic features of spontaneous brain activity of CNSP patients. These findings may be helpful for increasing our understanding of the neuropathology of CNSP.

Keywords: Chronic neck and shoulder pain; fasting; regional homogeneity; resting-state functional magnetic resonance imaging; spontaneous brain activity; voxel-based morphometry.

Figures

Figure 1.
Figure 1.
One-sample t test of ReHo maps within-groups. (a) and (b) represent the control and patient groups, respectively. In both groups, the standardized ReHo values in the posterior cingulate cortex, precuneus, inferior parietal lobule, and medial prefrontal cortex were significantly higher than the global mean values. The colour bar indicates the t-value of the brain regions exhibiting ReHo changes (p 

Figure 2.

Differences in ReHo values between-groups.…

Figure 2.

Differences in ReHo values between-groups. (a) and (b) show the axial and coronal…

Figure 2.
Differences in ReHo values between-groups. (a) and (b) show the axial and coronal views, respectively. Blue brain regions represent decreased ReHo values, and red regions indicate increased ReHo values in CNSP patients relative to the control group. The right colour bar represents the t value of brain regions with ReHo changes. (two-tailed two-sample t-test; p 
Similar articles
Cited by
References
    1. Thoomes EJ, Scholten-Peeters GG, de Boer AJ, et al. Lack of uniform diagnostic criteria for cervical radiculopathy in conservative intervention studies: a systematic review. Eur Spine J 2012; 21: 1459–1470. - PMC - PubMed
    1. Zhao L, Liu J, Dong X, et al. Alterations in regional homogeneity assessed by fMRI in patients with migraine without aura stratified by disease duration. J Headache Pain 2013; 14: 85–85. - PMC - PubMed
    1. Denkinger MD, Lukas A, Nikolaus T, et al. Multisite pain, pain frequency and pain severity are associated with depression in older adults: results from the ActiFE Ulm study. Age Ageing 2014; 43: 510–514. - PubMed
    1. Linton SJ. A transdiagnostic approach to pain and emotion. J Appl Biobehav Res 2013; 18: 82–103. - PMC - PubMed
    1. Montero-Homs J. Nocioceptive pain, neuropathic pain and pain memory. Neurologia 2009; 24: 419–422. [in Spanish, English Abstract]. - PubMed
Show all 51 references
MeSH terms
Related information
Full text links [x]
[x]
Cite
Copy Download .nbib
Format: AMA APA MLA NLM
Figure 2.
Figure 2.
Differences in ReHo values between-groups. (a) and (b) show the axial and coronal views, respectively. Blue brain regions represent decreased ReHo values, and red regions indicate increased ReHo values in CNSP patients relative to the control group. The right colour bar represents the t value of brain regions with ReHo changes. (two-tailed two-sample t-test; p 

References

    1. Thoomes EJ, Scholten-Peeters GG, de Boer AJ, et al. Lack of uniform diagnostic criteria for cervical radiculopathy in conservative intervention studies: a systematic review. Eur Spine J 2012; 21: 1459–1470.
    1. Zhao L, Liu J, Dong X, et al. Alterations in regional homogeneity assessed by fMRI in patients with migraine without aura stratified by disease duration. J Headache Pain 2013; 14: 85–85.
    1. Denkinger MD, Lukas A, Nikolaus T, et al. Multisite pain, pain frequency and pain severity are associated with depression in older adults: results from the ActiFE Ulm study. Age Ageing 2014; 43: 510–514.
    1. Linton SJ. A transdiagnostic approach to pain and emotion. J Appl Biobehav Res 2013; 18: 82–103.
    1. Montero-Homs J. Nocioceptive pain, neuropathic pain and pain memory. Neurologia 2009; 24: 419–422. [in Spanish, English Abstract].
    1. May A. Chronic pain may change the structure of the brain. Pain 2008; 137: 7–15.
    1. Seifert F, Maihöfner C. Functional and structural imaging of pain-induced neuroplasticity. Curr Opin Anaesthesiol 2011; 24: 515–523.
    1. Fayed N, Andres E, Rojas G, et al. Brain dysfunction in fibromyalgia and somatization disorder using proton magnetic resonance spectroscopy: a controlled study. Acta Psychiatr Scand 2012; 126: 115–125.
    1. McEwen BS, Kalia M. The role of corticosteroids and stress in chronic pain conditions. Metabolism 2010; 59(Suppl 1): S9–S15.
    1. Otti A, Guendel H, Henningsen P, et al. Functional network connectivity of pain-related resting state networks in somatoform pain disorder: an exploratory fMRI study. J Psychiatry Neurosci 2013; 38: 57–65.
    1. Vartiainen N, Forss N. Imaging of brain changes in chronic pain. Duodecim 2014; 130: 1507–1514. [in Finnish, English Abstract].
    1. Jin C, Yuan K, Zhao L, et al. Structural and functional abnormalities in migraine patients without aura. NMR Biomed 2013; 26: 58–64.
    1. Malinen S, Vartiainen N, Hlushchuk Y, et al. Aberrant temporal and spatial brain activity during rest in patients with chronic pain. Proc Natl Acad Sci USA 2010; 107: 6493–6497.
    1. Barkhof F, Haller S, Rombouts SA. Resting-state functional MR imaging: a new window to the brain. Radiology 2014; 272: 29–49.
    1. Yu D, Yuan K, Zhao L, et al. Regional homogeneity abnormalities in patients with interictal migraine without aura: a resting-state study. NMR Biomed 2012; 25: 806–812.
    1. Yoshino A, Okamoto Y, Kunisato Y, et al. Distinctive spontaneous regional neural activity in patients with somatoform pain disorder: A preliminary resting-state fMRI study. Psychiatry Res 2014; 221: 246–248.
    1. Zhang SS, Wu W, Liu ZP, et al. Altered regional homogeneity in experimentally induced low back pain: a resting-state fMRI study. J Neuroeng Rehabil 2014; 11: 115–115.
    1. Hong JY, Kilpatrick LA, Labus J, et al. Patients with chronic visceral pain show sex-related alterations in intrinsic oscillations of the resting Brain. J Neurosci 2013; 33: 11994–12002.
    1. Napadow V, Harris RE. What has functional connectivity and chemical neuroimaging in fibromyalgia taught us about the mechanisms and management of ‘centralized’ pain? Arthritis Res Ther 2014; 16: 425–433.
    1. Wang P, Du H, Chen N, et al. Regional homogeneity abnormalities in patients with tension-type headache: a resting-state fMRI study. Neurosci Bull 2014; 30: 949–955.
    1. Wang P, Du H, Chen N, et al. Regional homogeneity approach to fMRI data analysis. Neuroimage 2004; 22: 394–400.
    1. Zuo XN, Di Martino A, Kelly C, et al. The oscillating brain: complex and reliable. Neuroimage 2010; 49: 1432–1445.
    1. Zuo XN, Xu T, Jiang L, et al. Toward reliable characterization of functional homogeneity in the human brain: preprocessing, scan duration, imaging resolution and computational space. Neuroimage 2013; 65: 374–386.
    1. Obermann M, Rodriguez-Raecke R, Naegel S, et al. Gray matter volume reduction reflects chronic pain in trigeminal neuralgia. Neuroimage 2013; 74: 352–358.
    1. Ivo R, Nicklas A, Dargel J, et al. Brain structural and psychometric alterations in chronic low back pain. Eur Spine J 2013; 22: 1958–1964.
    1. Rodriguez-Raecke R, Niemeier A, Ihle K, et al. Brain gray matter decrease in chronic pain is the consequence and not the cause of pain. J Neurosci 2009; 29: 13746–13750.
    1. Davis KD, Moayedi M. Central mechanisms of pain revealed through functional and structural MRI. J Neuroimmune Pharmacol 2013; 8: 518–534.
    1. Naegel S, Holle D, Desmarattes N, et al. Cortical plasticity in episodic and chronic cluster headache. Neuroimage Clin 2014; 6: 415–423.
    1. Cui Y, Jiao Y, Chen YC, et al. Altered spontaneous brain activity in type 2 diabetes: a resting-state functional MRI study. Diabetes 2014; 63: 749–760.
    1. An L, Cao QJ, Sui MQ, et al. Local synchronization and amplitude of the fluctuation of spontaneous brain activity in attention-deficit/hyperactivity disorder: a resting-state fMRI study. Neurosci Bull 2013; 29: 603–613.
    1. Schlereth T, Baumgärtner U, Magerl W, et al. Left-hemisphere dominance in early nociceptive processing in the human parasylvian cortex. NeuroImage 2003; 20: 441–454.
    1. Zubieta JK, Ketter TA, Bueller JA, et al. Regulation of human affective responses by anterior cingulated and limbic mu-opioid neurotransmission. Arch Gen Psychiatry 2003; 60: 1145–1153.
    1. Gasquoine PG. Contributions of the insula to cognition and emotion. Neuropsychol Rev 2014; 24: 77–87.
    1. Zhao L, Liu J, Zhang F, et al. Effects of long-term acupuncture treatment on resting state brain activity in migraine patients: a randomized controlled trial on active acupoints and inactive acupoints. Plos One 2014; 9: e99538–e99538.
    1. Duerden EG, Albanese MC. Localization of pain-related brain activation: a meta-analysis of neuroimaging data. Hum Brain Mapp 2013; 34: 109–149.
    1. Taylor KS, Seminowicz DA, Davis KD. Two systems of resting state connectivity between the insula and cingulate cortex. Hum Brain Mapp 2009; 30: 2731–2745.
    1. Favilla S, Huber A, Pagnoni G, et al. Ranking brain areas encoding the perceived level of pain from fMRI data. Neuroimage 2014; 90: 153–162.
    1. Isnard J, Magnin M, Jung J, et al. Does the insula tell our brain that we are in pain? Pain 2011; 152: 946–951.
    1. Abe N, Suzuki M, Mori E, et al. Deceiving others: distinct neural responses of the prefrontal cortex and amygdala in simple fabrication and deception with social interactions. J Cogn Neurosci 2007; 19: 287–295.
    1. Michael J, Zigmond, Joseph T, Coyle, Lewis P. Rowland. Neurobiology of Brain Disorders. In: Pressman P, Howard JR. (eds). Disorders of frontal lobe function, 1st ed USA: Academic Press, 2015, pp. 542–557.
    1. Yang FC, Chou KH, Fu JL, et al. Altered gray matter volume in the frontal pain modulation network in patients with cluster headache. Pain 2013; 154: 801–807.
    1. Absinta M, Rocca MA, Colombo B, et al. Selective decreased grey matter volume of the pain-matrix network in cluster headache. Cephalalgia 2012; 32: 109–115.
    1. Kim JH, Suh SI, Seol HY, et al. Regional grey matter changes in patients with migraine: a voxel-based morphometry study. Cephalalgia 2008; 28: 598–604.
    1. Kanda M, Nagamine T, Ikeda A, et al. Primary somatosensory cortex is actively involved in pain processing in human. Brain Res 2000; 853: 282–289.
    1. Peyron R, Laurent B, Garcia-Larrea L. Functional imaging of brain responses to pain: a review and meta-analysis. Neurophysiol Clin 2000; 30: 263–288.
    1. Aron AR, Poldrack RA. Cortical and subcortical contributions to stop signal response inhibition: role of the subthalamic nucleus. J. Neurosci 2006; 26: 2424–2433.
    1. Roy M, Piché M, Chen JI, et al. Cerebral and spinal modulation of pain by emotions. Proc. Natl. Acad. Sci 2009; 106: 20900–20905.
    1. Geha PY, Baliki MN, Harden RN, et al. The brain in chronic CRPS pain: abnormal gray–white matter interactions in emotional and autonomic regions. Neuron 2008; 60: 570–581.
    1. Otti A, Guendel H, Henningsen P, et al. Functional network connectivity of pain-related resting state networks in somatoform pain disorder: an exploratory fMRI study. J Psychiatry Neurosci 2013; 38: 57–65.
    1. Emmert K, Breimhorst M, Bauermann T, et al. Comparison of anterior cingulate vs. insular cortex as targets for real-time fMRI regulation during pain stimulation. Front Behav Neurosci 2014; 8: 350–350.
    1. Bouwense SA, de Vries M, Schreuder LT, et al. Systematic mechanism-orientated approach to chronic pancreatitis pain. World J Gastroenterol 2015; 21: 47–59.

Source: PubMed

3
Abonneren