In:
Pain Practice, Wiley, Vol. 16, No. 1 ( 2016-01), p. 38-45
Abstract:
Whether psychological factors such as anxiety and pain catastrophizing levels influence the expression of endogenous analgesia in general and, more specifically, the conditioned pain modulation (CPM) response is still under debate. It may be assumed that other psychological characteristics also play a role in the CPM response. The neurotransmitters serotonin, dopamine, and norepinephrine are involved both in CPM, as well as personality traits such as harm avoidance (HA), novelty seeking (NS), and reward dependence (RD), which can be obtained by the Tridimensional Personality Questionnaire (TPQ). However, the associations between these traits (HA, NS, and RD) with endogenous analgesia revealed by CPM have not yet been explored. Methods Healthy middle‐age subjects ( n = 28) completed the TPQ, Spielberger's State Anxiety Inventory, and the Pain Catastrophizing Scale and were assessed for CPM paradigms using thermal phasic temporal summation as the “test stimulus” and hand immersion into hot water bath (CPM water ) or contact heat (CPM contact ) for “conditioning stimulus.” Results Higher levels of HA were associated with less‐efficient CPM responses obtained by both paradigms: CPM water ( r = 0.418, P = 0.027) and CPM contact ( r = 0.374, P = 0.050). However, NS and RD were not associated with the other measurements. No significant relationship was observed between state anxiety and pain catastrophizing levels and the CPM responses. Conclusions The relationship between the capacity of endogenous analgesia and the tendency to avoid aversive experience can be explained by mutual mechanisms involving similar neurotransmitters or brain areas. These findings illuminate the key role of harm avoidance obtained by the TPQ in determining the characteristics of pain modulation profile.
Type of Medium:
Online Resource
ISSN:
1530-7085
,
1533-2500
DOI:
10.1111/papr.2016.16.issue-1
Language:
English
Publisher:
Wiley
Publication Date:
2016
detail.hit.zdb_id:
2046672-9
