An exploration into the cortical reorganisation of the healthy hand in upper-limb complex regional pain syndrome

Scandinavian Journal of Pain - Tập 13 - Trang 18-24 - 2016
Flavia Di Pietro1,2,3, Tasha R. Stanton1,4, G. Lorimer Moseley1,4, Martin Lotze5, James H. McAuley1,2
1Neuroscience Research Australia, Sydney, NSW 2031, Australia
2Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia
3Department of Anatomy and Histology, Sydney Medical School, University of Sydney, Sydney, NSW 2006, Australia
4Sansom Institute for Health Research, University of South Australia & PainAdelaide, Adelaide, SA 5000, Australia
5Institute for Diagnostic Radiology and Neuroradiology, University of Greifswald, Greifswald 17475, Germany

Tóm tắt

Abstract Background and aims Recent evidence demonstrated that complex regional pain syndrome (CRPS) is associated with a larger than normal somatosensory (S1) representation of the healthy hand. The most intuitive mechanism for this apparent enlargement is increased, i.e. compensatory, use of the healthy hand. We investigated whether enlargement of the S1 representation of the healthy hand is associated with compensatory use in response to CRPS. Specifically, we were interested in whether the size of the S1 representation of the healthy hand is associated with the severity of functional impairment of the CRPS-affected hand. We were also interested in whether CRPS duration might be positively associated with the size of the representation of the healthy hand in S1. Methods Using functional magnetic resonance imaging (fMRI) data from our previous investigation, the size of the S1 representation of the healthy hand in CRPS patients (n = 12) was standardised to that of a healthy control sample (n = 10), according to hand dominance. Responses to questionnaires on hand function, overall function and self-efficacy were used to gather information on hand use in participants. Multiple regression analyses investigated whether the S1 representation was associated with compensatory use. We inferred compensatory use with the interaction between reported use of the CRPS-affected hand and (a) reported overall function, and (b) self-efficacy. We tested the correlation between pain duration and the size of the S1 representation of the healthy hand with Spearman’s rho. Results The relationship between the size of the S1 representation of the healthyh and and the interaction between use of the affected hand and overall function was small and non-significant ( β =-5.488×10-5, 95% C.I. –0.001, 0.001). The relationship between the size of the S1 representation of the healthy hand and the interaction between use of the affected hand and self-efficacy was also small and non-significant (β =-6.027×10-6, 95% C.I. –0.001, 0.001). The S1 enlargement of the healthy hand was not associated with pain duration (Spearman’s rho = –0.14, p = 0.67). Conclusion Our exploration did not yield evidence of any relationship between the size of the healthy hand representation in S1 and the severity of functional impairment of the CRPS-affected hand, relative to overall hand use or to self-efficacy. There was also no evidence of an association between the size of the healthy hand representation in S1 and pain duration. The enlarged S1 representation of the healthy hand does not relate to self-reported function and impairment in CRPS. Implications While this study had a hypothesis-generating nature and the sample was small, there were no trends to suggest compensatory use as the mechanism underlying the apparent enlargement of the healthy hand in S1. Further studies are needed to investigate the possibility that inter-hemispheric differences seen in S1 in CRPS may be present prior to the development of the disorder.

Tài liệu tham khảo

Bruehl SP. An update on the pathophysiology of complex regional pain syndrome. Anesthesiology 2010;113:713–25. Marinus J, Moseley GL, Birklein F, Baron R, Maihofner C, Kingery WS, van Hilten JJ. Clinical features and pathophysiology of complex regional pain syndrome. Lancet Neurol 2011;10:637–48. Schwenkreis P, Maier C, Tegenthoff M. Functional imaging of central nervous system involvement in complex regional pain syndrome. Am J Neuroradiol 2009;30:1279–84. Juottonen K, Gockel M, Silen T, Hurri H, Hari R, Forss N. Altered central sensorimotor processing in patients with complex regional pain syndrome. Pain 2002;98:315–23. Maihöfner C, Handwerker HO, Neundörfer B, Birklein F. Patterns of cortical reorganization in complex regional pain syndrome. Neurology 2003;61:1707–15. Pleger B, Tegenthoff M, Schwenkreis P, Janssen F, Ragert P, Dinse HR, Völker B, Zenz M, Maier C. Mean sustained pain levels are linked to hemispherical side-to-side differences of primary somatosensory cortex in the complex regional pain syndrome I. Exp Brain Res 2004;155:115–9. Vartiainen NV, Kirveskari E, Forss N. Central processing of tactile and nociceptive stimuli in complex regional pain syndrome. Clin Neurophysiol 2008;119:2380–8. Di Pietro F, McAuley JH, Parkitny L, Lotze M, Wand BM, Moseley GL, Stanton TR. Primary somatosensory cortex function in complex regional pain syndrome: a systematic review and meta-analysis. J Pain 2013;14:1001–18. Di Pietro F, McAuley JH, Parkitny L, Lotze M, Wand BM, Moseley GL, Stanton TR. Primary motor cortex function in complex regional pain syndrome: a systematic review and meta-analysis. J Pain 2013;14:1270–88. McCabe CS, Haigh RC, Ring EF, Halligan PW, Wall PD, Blake DR. A controlled pilot study of the utility of mirror visual feedback in the treatment of complex regional pain syndrome (type 1). Rheumatology 2003;42:97–101. Moseley GL. Graded motor imagery is effective for long-standing complex regional pain syndrome: a randomised controlled trial. Pain 2004;108:192–8. Di Pietro F, Stanton TR, Moseley GL, Lotze M, McAuley JH. Interhemispheric somatosensory differences in chronic pain reflect abnormality of the Healthy side. Hum Brain Mapp 2015;36:508–18. Elbert T, Pantev C, Wienbruch C, Rockstroh B, Taub E. Increased cortical representation of the fingers of the left hand in string players. Science 1995;270:305–7. Pascual-Leone A, Torres F. Plasticity of the sensorimotor cortex representation of the reading finger in Braille readers. Brain 1993;116:39–52. Merzenich MM, Kaas JH, Wall J, Nelson RJ, Sur M, Felleman D. Topographic reorganization of somatosensory cortical areas 3b and 1 in adult monkeys following restricted deafferentation. Neuroscience 1983;8:33–55. Nelson AJ, Chen R. Digit somatotopy within cortical areas of the postcentral gyrus in humans. Cereb Cortex 2008;18:2341–51. Jones LA, Lederman SJ. Neurophysiology of hand function. In: Human hand function. New York: Oxford University Press; 2006. p. 24–43. Tommerdahl M, Delemos KA, Whitsel BL, Favorov OV, Metz CB. Response of anterior parietal cortex to cutaneous flutter versus vibration. J Neurophysiol 1999;82:16–33. Butterworth S, Francis S, Kelly E, McGlone F, Bowtell R, Sawle GV. Abnormal cortical sensory activation in dystonia: an fMRI study. Mov Disord 2003;18:673–82. Francis ST, Kelly EF, Bowtell R, Dunseath WJR, Folger SE, McGlone F. fMRI of the responses to vibratory stimulation of digit tips. Neuroimage 2000;11:188–202. Nelson AJ, Staines WR, Graham SJ, McIlroy WE. Activation in SI and SII: the influence of vibrotactile amplitude during passive and task-relevant stimulation. Cogn Brain Res 2004;19:174–84. Eickhoff SB, Stephan KE, Mohlberg H, Grefkes C, Fink GR, Amunts K, Zilles K. A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data. Neuroimage 2005;25:1325–35. Weibull A, Björkman A, Hall H, Rosén B, Lundborg G, Svensson J. Optimizing the mapping of finger areas in primary somatosensory cortex using functional MRI. Magn Reson Imaging 2008;26:1342–51. Jung P, Baumgärtner U, Magerl W, Treede R-D. Hemispheric asymmetry of hand representation in human primary somatosensory cortex and handedness. Clin Neurophysiol 2008;119:2579–86. MacDermid JC. Development of a scale for patient rating of wrist pain and disability. J Hand Ther 1996;9:178–83. Beaton DE, Wright JG, Katz JN. Development of the QuickDASH: comparison of three item-reduction approaches. J Bone Joint Surg 2005;87:1038–46. Nicholas MK. Self-efficacy and chronic pain. In: Annual conference of the British Psychological Society. 1989. Bandura A. Self-efficacy: toward a unifying theory of behavioral change. Psychol Rev 1977;84:191–215. Arnstein P. The mediation of disability by self efficacy in different samples of chronic pain patients. Disabil Rehabil 2000;22:794–801. van der Pas SC, Verbunt JA, Breukelaar DE, van Woerden R, Seelen HA. Assessment of arm activity using triaxial accelerometry in patients with a stroke. Arch Phys Med Rehabil 2011;92:1437–42. O’Connor D, Kortman B, Smith A, Ahern M, Smith M, Krishnan J. Correlation between objective and subjective measures of hand function in patients with rheumatoid arthritis. J Hand Ther 1999;12:323–9. Jung P, Baumgärtner U, Bauermann T, Magerl W, Gawehn J, Stoeter P, Treede R-D. Asymmetry in the human primary somatosensory cortex and handedness. Neuroimage 2003;19:913–23. Sörös P, Knecht S, Imai T, Gürtler S, Lütkenhöner B, Ringelstein EB, Henningsen H. Cortical asymmetries of the human somatosensory hand representation in right- and left-handers. Neurosci Lett 1999;271:89–92. Weibull A, Flondell M, Rosen B, Bjorkman A. Cerebral and clinical effects of short-term hand immobilisation. Eur J Neurosci 2011;33:699–704. Amunts K, Schlaug G, Schleicher A, Steinmetz H, Dabringhaus A, Roland PE, Zilles K. Asymmetry in the human motor cortex and handedness. Neuroimage 1996;4:216–22. Volkmann J, Schnitzler A, Witte OW, Freund H-J. Handedness and asymmetry of hand representation in human motor cortex. J Neurophysiol 1998;79: 2149–54. Ragert P, Nierhaus T, Cohen LG, Villringer A. Interhemispheric interactions between the human primary somatosensory cortices. PLoS ONE 2011;6:e16150. Schwenkreis P, Scherens A, Rönnau A-K, Höffken O, Tegenthoff M, Maier C. Cortical disinhibition occurs in chronic neuropathic, but not in chronic nociceptive pain. BMC Neurosci 2010;11:1–10. Lenz M, Hoffken O, Stude P, Lissek S, Schwenkreis P, Reinersmann A, Frettloh J, Richter H, Tegenthoff M, Maier C. Bilateral somatosensory cortex disinhibition in complex regional pain syndrome type I. Neurology 2011;77: 1096–101. Moseley GL, Gallace A, Spence C. Space-based, but not arm-based, shift in tactile processing in complex regional pain syndrome and its relationship to cooling of the affected limb. Brain 2009;132:3142–51. Moseley GL, Gallace A, Iannetti GD. Spatially defined modulation of skin temperature and hand ownership of both hands in patients with unilateral complex regional pain syndrome. Brain 2012;135:3676–86. Moseley GL, Gallace A, Di Pietro F, Spence C, Iannetti GD. Limb-specific autonomic dysfunction in complex regional pain syndrome modulated by wearing prism glasses. Pain 2013;154:2463–8. Moseley GL, Gallagher L, Gallace A. Neglect-like tactile dysfunction in chronic back pain. Neurology 2012;79:327–32. Stanton TR, Lin C-WC, Smeets RJEM, Taylor D, Law R, Lorimer Moseley G. Spatially defined disruption of motor imagery performance in people with osteoarthritis. Rheumatology 2012;51:1455–64. Reid E, Wallwork SB, Harvie D, Chalmers KJ, Gallace A, Spence C, Moseley GL. A new kind of spatial inattention associated with chronic limb pain? Ann Neurol 2016;79:701–4.