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Reward responsiveness in patients with chronic pain
Author(s) -
Elvemo N.A.,
Landrø N.I.,
Borchgrevink P.C.,
Håberg A.K.
Publication year - 2015
Publication title -
european journal of pain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.305
H-Index - 109
eISSN - 1532-2149
pISSN - 1090-3801
DOI - 10.1002/ejp.687
Subject(s) - nucleus accumbens , anhedonia , reward system , psychology , brain stimulation reward , beck depression inventory , mesolimbic pathway , medicine , chronic pain , neuroscience , ventral tegmental area , psychiatry , central nervous system , dopamine , anxiety , dopaminergic
Abstract Background It is proposed that changes in reward processing in the brain are involved in the pathophysiology of pain based on experimental studies. The first aim of the present study was to investigate if reward drive and/or reward responsiveness was altered in patients with chronic pain ( PCP ) compared to controls matched for education, age and sex. The second aim was to investigate the relationship between reward processing and nucleus accumbens volume in PCP and controls. Nucleus accumbens is central in reward processing and its structure has been shown to be affected by chronic pain conditions in previous studies. Methods Reward drive and responsiveness were assessed with the Behavioral Inhibition Scale/Behavioral Activation Scale, and nucleus accumbens volumes obtained from T1‐weighted brain MRI s obtained at 3T in 19 PCP of heterogeneous aetiologies and 20 age‐, sex‐ and education‐matched healthy controls. Anhedonia was assessed with Beck's Depression Inventory II . Results The PCP group had significantly reduced scores on the reward responsiveness, but not reward drive. There was a trend towards smaller nucleus accumbens volume in the PCP compared to control group. There was a significant positive partial correlation between reward responsiveness and nucleus accumbens volume in the PCP group adjusted for anhedonia, which was significantly different from the same relationship in the control group. Conclusions Reward responsiveness is reduced in chronic pain patients of heterogeneous aetiology, and this reduction was associated with nucleus accumbens volume. Reduced reward responsiveness could be a marker of chronic pain vulnerability, and may indicate reduced opioid function.