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Recovery of Impaired Endogenous Pain Modulation by Dopaminergic Medication in Parkinson's Disease
[journal article]
Abstract Background: Of patients with Parkinson's disease (PD), 30% to 85% report pain. However, mechanisms underlying this pain remain unclear. In line with known neuroanatomical impairments, we hypothesized that pain in PD is caused by alterations in emotional-motivational as opposed to sensory-discriminat... view more
Background: Of patients with Parkinson's disease (PD), 30% to 85% report pain. However, mechanisms underlying this pain remain unclear. In line with known neuroanatomical impairments, we hypothesized that pain in PD is caused by alterations in emotional-motivational as opposed to sensory-discriminative pain processing and that dopamine recovers the capacity for endogenous emotional-motivational pain modulation in patients with PD. Methods: A total of 20 patients with PD played a random reward paradigm with painful heat stimuli in addition to assessments of pain sensitivity once with and once without levodopa. Results: Levodopa increased endogenous pain inhibition in terms of perceived pain intensity and un/pleasantness compared with a medication off state. Higher clinical pain was associated with higher increases in pain inhibition. Levodopa did not affect heat pain threshold, tolerance, or temporal summation. Conclusion: Patients with PD seem to be predominately impaired in emotional-motivational as opposed to sensory-discriminative pain processing. A differential understanding of pain in PD is urgently needed because effective treatment strategies are lacking.... view less
Keywords
pain; illness; medication; patient
Classification
Medicine, Social Medicine
Free Keywords
Parkinson’s disease; endogenous pain modulation; dopamine; emotional-motivational pain processing; medial pain system; Deutsche Version der Positive and Negative Affect Schedule PANAS (GESIS Panel) (ZIS 242)
Document language
English
Publication Year
2020
Page/Pages
p. 2338-2343
Journal
Movement Disorders, 35 (2020) 12
DOI
https://doi.org/10.1002/mds.28241
ISSN
1531-8257
Status
Published Version; peer reviewed