78
Views
6
CrossRef citations to date
0
Altmetric
Original Research

Functional and Structural Changes in Postherpetic Neuralgia Brain Before and Six Months After Pain Relieving

, , , , &
Pages 909-918 | Published online: 04 May 2020

References

  • Cohen JI, Solomon CG. Clinical practice: herpes zoster. N Engl J Med. 2013;369(3):255–263. doi:10.1056/NEJMcp1302674
  • Schmader K. Postherpetic neuralgia in immunocompetent elderly people. Vaccine. 1998;16(18):1768–1770. doi:10.1016/S0264-410X(98)00137-6
  • Keating GM. Shingles (Herpes Zoster) vaccine (Zostavax®): a review in the prevention of herpes zoster and postherpetic neuralgia. Biodrugs. 2016;30(3):243–254. doi:10.1007/s40259-016-0180-7
  • Friesen KJ, Falk J, Alessi-Severini S, Chateau D, Bugden S. Price of pain: population-based cohort burden of disease analysis of medication cost of herpes zoster and postherpetic neuralgia. J Pain Res. 2016;9:543. doi:10.2147/JPR.S107944
  • Yang F, Yu S, Fan B, et al. The epidemiology of herpes zoster and postherpetic neuralgia in China: results from a cross-sectional study. Pain Ther. 2019;8(2):249–259. doi:10.1007/s40122-019-0127-z
  • Pickering G, Gavazzi G, Gaillat J, Paccalin M, Bloch K, Bouhassira D. Is herpes zoster an additional complication in old age alongside comorbidity and multiple medications? Results of the post hoc analysis of the 12-month longitudinal prospective observational ARIZONA cohort study. BMJ Open. 2016;6(2):e009689. doi:10.1136/bmjopen-2015-009689
  • Sah DWY, Ossipo MH, Frank P. Neurotrophic factors as novel therapeutics for neuropathic pain. Nat Rev Drug Discov. 2003;2(6):460–472. doi:10.1038/nrd1107
  • Denkinger MD, Lukas A, Nikolaus T, Peter R, Franke S, Group AS. Multisite pain, pain frequency and pain severity are associated with depression in older adults: results from the ActiFE Ulm study. Age Ageing. 2014;43(4):510–514. doi:10.1093/ageing/afu013
  • Cao S, Zhang D, Yuan J, et al. MicroRNA and circular RNA expression in affected skin of patients with postherpetic neuralgia. J Pain Res. 2019;12:2905–2913. doi:10.2147/JPR.S221615
  • Geha PY, Baliki MN, Chialvo DR, Harden RN, Paice JA, Apkarian AV. Brain activity for spontaneous pain of postherpetic neuralgia and its modulation by lidocaine patch therapy. Pain. 2007;128(1):88–100. doi:10.1016/j.pain.2006.09.014
  • Geha PY, Baliki MN, Wang X, Harden RN, Paice JA, Apkarian AV. Brain dynamics for perception of tactile allodynia (touch-induced pain) in postherpetic neuralgia. Pain. 2008;138(3):641–656. doi:10.1016/j.pain.2008.02.021
  • Zhang Y, Liu J, Li L, et al. A study on small-world brain functional networks altered by postherpetic neuralgia. Magn Reson Imaging. 2014;32(4):359–365. doi:10.1016/j.mri.2013.12.016
  • Gu L, Hong S, Jiang J, et al. Bidirectional alterations in ALFF across slow-5 and slow-4 frequencies in the brains of postherpetic neuralgia patients. J Pain Res. 2019;12:39–47. doi:10.2147/JPR.S179077
  • Li J, Huang X, Sang K, Bodner M, Ma K, Dong XW. Modulation of prefrontal connectivity in postherpetic neuralgia patients with chronic pain: a resting-state functional magnetic resonance-imaging study. J Pain Res. 2018;11:2131–2144. doi:10.2147/JPR.S166571
  • Cao S, Li Y, Deng W, et al. Local brain activity differences between herpes zoster and postherpetic neuralgia patients: a resting-state functional MRI study. Pain Physician. 2017;20(5):E687–E699.
  • Cao S, Song G, Zhang Y, et al. Abnormal local brain activity beyond the pain matrix in postherpetic neuralgia patients: a resting-state functional MRI study. Pain Physician. 2017;20(2):E303–E314.
  • Cao S, Qin B, Zhang Y, et al. Herpes zoster chronification to postherpetic neuralgia induces brain activity and grey matter volume change. Am J Transl Res. 2018;10(1):184–199.
  • Bliss TV, Collingridge GL, Kaang BK, Zhuo M. Synaptic plasticity in the anterior cingulate cortex in acute and chronic pain. Nat Rev Neurosci. 2016;17(8):485–496.
  • Kuner R, Flor H. Structural plasticity and reorganisation in chronic pain. Nat Rev Neurosci. 2016;18(1):20–30. doi:10.1038/nrn.2016.162
  • Zhang Y, Yu T, Qin B, Li Y, Song G, Yu B. Microstructural abnormalities in gray matter of patients with postherpetic neuralgia: a diffusional kurtosis imaging study. Pain Physician. 2016;19(4):E601–E611.
  • Chen F, Chen F, Shang Z, et al. White matter microstructure degenerates in patients with postherpetic neuralgia. Neurosci Lett. 2017;656:152–157. doi:10.1016/j.neulet.2017.07.023
  • Liu J, Gu L, Huang Q, et al. Altered gray matter volume in patients with herpes zoster and postherpetic neuralgia. J Pain Res. 2019;12:605–616. doi:10.2147/JPR.S183561
  • Ceko M, Shir Y, Ouellet JA, Ware MA, Stone LS, Seminowicz DA. Partial recovery of abnormal insula and dorsolateral prefrontal connectivity to cognitive networks in chronic low back pain after treatment. Hum Brain Mapp. 2015;36(6):2075–2092. doi:10.1002/hbm.22757
  • Seminowicz DA, Wideman TH, Naso L, et al. Effective treatment of chronic low back pain in humans reverses abnormal brain anatomy and function. J Neurosci. 2011;31(20):7540–7550. doi:10.1523/JNEUROSCI.5280-10.2011
  • Gwilym SE, Filippini N, Douaud G, Carr AJ, Tracey I. Thalamic atrophy associated with painful osteoarthritis of the hip is reversible after arthroplasty: a longitudinal voxel-based morphometric study. Arthritis Rheum. 2010;62(10):2930–2940. doi:10.1002/art.27585
  • Rodriguez-Raecke R, Niemeier A, Ihle K, Ruether W, May A, Langguth B. Structural brain changes in chronic pain reflect probably neither damage nor atrophy. PLoS One. 2013;8(2):e54475. doi:10.1371/journal.pone.0054475
  • Merskey H, Bogduk N. Classification of Chronic Pain: Descriptions of Chronic Pain Syndromes and Definitions of Pain Terms. 2nd ed. Seattle: International Association for the Study of Pain; 1994.
  • Mallick-Searle T, Snodgrass B, Brant JM. Postherpetic neuralgia: epidemiology, pathophysiology, and pain management pharmacology. J Multidiscip Healthc. 2016;9:447–454. doi:10.2147/JMDH.S106340
  • Yan C, Zang Y. DPARSF: a MATLAB toolbox for ”pipeline” data analysis of resting-state fMRI. Front Syst Neurosci. 2010;4:13. doi:10.3389/fnsys.2010.00009
  • Greicius MD, Ben K, Reiss AL, Vinod M. Functional connectivity in the resting brain: a network analysis of the default mode hypothesis. Proc Natl Acad Sci U S A. 2003;100(1):253–258. doi:10.1073/pnas.0135058100
  • Song XW, Dong ZY, Long XY, et al. REST: a toolkit for resting-state functional magnetic resonance imaging data processing. PLoS One. 2011;6(9):e25031. doi:10.1371/journal.pone.0025031
  • Zang Y, Jiang T, Lu Y, He Y, Tian L. Regional homogeneity approach to fMRI data analysis. Neuroimage. 2004;22(1):394–400. doi:10.1016/j.neuroimage.2003.12.030
  • Li Z, Kadivar A, Pluta J, Dunlop J, Wang Z. Test–retest stability analysis of resting brain activity revealed by blood oxygen level‐dependent functional MRI. J Magn Reson Imaging. 2012;36(2):344–354. doi:10.1002/jmri.23670
  • Wang L, Li K, Zhang Q, et al. Short-term effects of escitalopram on regional brain function in first-episode drug-naive patients with major depressive disorder assessed by resting-state functional magnetic resonance imaging. Psychol Med. 2014;44(7):1417–1426. doi:10.1017/S0033291713002031
  • Zou QH, Zhu CZ, Yang Y, et al. An improved approach to detection of amplitude of low-frequency fluctuation (ALFF) for resting-state fMRI: fractional ALFF. J Neurosci Methods. 2008;172(1):137–141. doi:10.1016/j.jneumeth.2008.04.012
  • Haag LM, Heba S, Lenz M, et al. Resting BOLD fluctuations in the primary somatosensory cortex correlate with tactile acuity. Cortex. 2015;64:20–28. doi:10.1016/j.cortex.2014.09.018
  • Tu Y, Yu T, Wei Y, Sun K, Zhao W, Yu B. Structural brain alterations in hemifacial spasm: a voxel-based morphometry and diffusion tensor imaging study. Clin Neurophysiol. 2016;127(2):1470–1474. doi:10.1016/j.clinph.2015.07.036
  • Tabesh A, Jensen JH, Ardekani BA, Helpern JA. Estimation of tensors and tensor-derived measures in diffusional kurtosis imaging. Magn Reson Med. 2011;65(3):823–836. doi:10.1002/mrm.22655
  • Ledberg A, Åkerman S, Roland PE. Estimation of the probabilities of 3D clusters in functional brain images. Neuroimage. 1998;8(2):113–128. doi:10.1006/nimg.1998.0336
  • Peyron R, Laurent B, García-Larrea L. Functional imaging of brain responses to pain. A review and meta-analysis (2000). Neurophysiol Clin. 2000;30(5):263–288. doi:10.1016/S0987-7053(00)00227-6
  • Jensen KB, Kosek E, Wicksell R, et al. Cognitive behavioral therapy increases pain-evoked activation of the prefrontal cortex in patients with fibromyalgia. Pain. 2012;153(7):1495–1503. doi:10.1016/j.pain.2012.04.010
  • Treede RD, Kenshalo DR, Gracely RH, Jones AK. The cortical representation of pain. Pain. 1999;79(2):105–111. doi:10.1016/S0304-3959(98)00184-5
  • Seifert F, Maihöfner C. Central mechanisms of experimental and chronic neuropathic pain: findings from functional imaging studies. Cell Mol Life Sci. 2009;66(3):375–390. doi:10.1007/s00018-008-8428-0
  • Helmchen C, Mohr C, Erdmann C, Petersen D, Nitschke M. Differential cerebellar activation related to perceived pain intensity during noxious thermal stimulation in humans: a functional magnetic resonance imaging study. Neurosci Lett. 2003;335(3):202–206. doi:10.1016/S0304-3940(02)01164-3
  • Jensen KB, Regenbogen C, Ohse MC, Frasnelli J, Freiherr J, Lundström JN. Brain activations during pain: a neuroimaging meta-analysis of patients with pain and healthy controls. Pain. 2016;157(6):1279–1286. doi:10.1097/j.pain.0000000000000517
  • Kim J, Shin J, Oh J-H, et al. Longitudinal FDG microPET imaging of neuropathic pain: does cerebellar activity correlate with neuropathic pain development in a rat model? Acta Neurochir (Wien). 2015;157(6):1051–1057. doi:10.1007/s00701-015-2415-7
  • Shi H, Yuan C, Dai Z, Ma H, Sheng L. Gray matter abnormalities associated with fibromyalgia: a meta-analysis of voxel-based morphometric studies. Semin Arthritis Rheum. 2016;46(3):330–337. doi:10.1016/j.semarthrit.2016.06.002
  • Naegel S, Holle D, Desmarattes N, et al. Cortical plasticity in episodic and chronic cluster headache. Neuroimage Clin. 2014;6:415–423. doi:10.1016/j.nicl.2014.10.003
  • Li M, Yan J, Li S, et al. Reduced volume of gray matter in patients with trigeminal neuralgia. Brain Imaging Behav. 2016;11(2):486–92.
  • Obermann M, Rodriguez-Raecke R, Naegel S, et al. Gray matter volume reduction reflects chronic pain in trigeminal neuralgia. Neuroimage. 2013;74:352–358. doi:10.1016/j.neuroimage.2013.02.029
  • Sinding C, Gransjoen AM, Schlumberger G, Grushka M, Frasnelli J, Singh PB. Grey matter changes of the pain matrix in patients with burning mouth syndrome. Eur J Neurosci. 2016;43(8):997–1005. doi:10.1111/ejn.13156
  • Bocci T, Santarcangelo E, Vannini B, et al. Cerebellar direct current stimulation modulates pain perception in humans. Restor Neurol Neurosci. 2015;33(5):597–609. doi:10.3233/RNN-140453
  • Rodriguez-Raecke R, Niemeier A, Ihle K, Ruether W, May A. Brain gray matter decrease in chronic pain is the consequence and not the cause of pain. J Neurosci. 2009;29(44):13746–13750. doi:10.1523/JNEUROSCI.3687-09.2009
  • DeSouza DD, Davis KD, Hodaie M. Reversal of insular and microstructural nerve abnormalities following effective surgical treatment for trigeminal neuralgia. Pain. 2015;156(6):1112–1123. doi:10.1097/j.pain.0000000000000156
  • Eklund A, Nichols TE, Knutsson H. Cluster failure: why fMRI inferences for spatial extent have inflated false-positive rates. Proc Natl Acad Sci. 2016;113(28):7900–5.