Central Pain Processing in Early-Stage Parkinson's Disease: A Laser Pain fMRI Study

PLoS One. 2016 Oct 24;11(10):e0164607. doi: 10.1371/journal.pone.0164607. eCollection 2016.

Abstract

Background & objective: Pain is a common non-motor symptom in Parkinson's disease. As dopaminergic dysfunction is suggested to affect intrinsic nociceptive processing, this study was designed to characterize laser-induced pain processing in early-stage Parkinson's disease patients in the dopaminergic OFF state, using a multimodal experimental approach at behavioral, autonomic, imaging levels.

Methods: 13 right-handed early-stage Parkinson's disease patients without cognitive or sensory impairment were investigated OFF medication, along with 13 age-matched healthy control subjects. Measurements included warmth perception thresholds, heat pain thresholds, and central pain processing with event-related functional magnetic resonance imaging (erfMRI) during laser-induced pain stimulation at lower (E = 440 mJ) and higher (E = 640 mJ) target energies. Additionally, electrodermal activity was characterized during delivery of 60 randomized pain stimuli ranging from 440 mJ to 640 mJ, along with evaluation of subjective pain ratings on a visual analogue scale.

Results: No significant differences in warmth perception thresholds, heat pain thresholds, electrodermal activity and subjective pain ratings were found between Parkinson's disease patients and controls, and erfMRI revealed a generally comparable activation pattern induced by laser-pain stimuli in brain areas belonging to the central pain matrix. However, relatively reduced deactivation was found in Parkinson's disease patients in posterior regions of the default mode network, notably the precuneus and the posterior cingulate cortex.

Conclusion: Our data during pain processing extend previous findings suggesting default mode network dysfunction in Parkinson's disease. On the other hand, they argue against a genuine pain-specific processing abnormality in early-stage Parkinson's disease. Future studies are now required using similar multimodal experimental designs to examine pain processing in more advanced stages of Parkinson's disease.

MeSH terms

  • Case-Control Studies
  • Humans
  • Lasers*
  • Magnetic Resonance Imaging / methods*
  • Pain / physiopathology*
  • Pain Threshold
  • Parkinson Disease / physiopathology*
  • Parkinson Disease / psychology
  • Surveys and Questionnaires

Grants and funding

C. Petschow received research support from the BONFOR SciMed-Promotionsstipendium of the university of Bonn. L. Scheef has no relevant financial relationships with commercial interest to disclosure. S. Paus is an employer of the University Clinic of Bonn. He has received research grants from Ipsen Pharma and Merz Pharmaceuticals. He is a member of the Advisory Boards of Allergan, Ipsen Pharma and Merz Pharmaceuticals. He has received lecturer fees from Allergan, Ipsen Pharma and Merz Pharmaceuticals. N. Zimmermann has no relevant financial relationships with commercial interest to disclosure. H. Schild has received funding from the Deutsche Forschungsgemeinschaft and the Bundesministerium für Bildung und Forschung (BMBF). T. Klockgether receives/has received research support from the Deutsche Forschungsgemeinschaft (DFG), the Bundesministerium für Bildung und Forschung (BMBF), the Robert Bosch Foundation and the European Union (EU). He serves on the editorial board of The Cerebellum. He has received a consulting fee from ICON Clinical Research. H. Boecker receives/has received research support from the Deutsche Forschungsgemeinschaft (DFG) and the Bundesministerium für Bildung und Forschung (BMBF). He has received a lecturer fee from the National Paralympic Committee Germany and royalties from Springer, NY.