Short communicationPerceived control moderates the influence of active coping on salivary cortisol response to acute pain among women but not men
Introduction
The role of cognition in shaping neuroendocrine responses to threat and challenge is receiving increasing attention (Ursin, 1998, Ursin and Eriksen, 2004); however, evidence for cognition-related influences on cortisol production following experimental pain stimulation is limited. It is suggested that men and women may demonstrate divergent responses to noxious stimuli, yet studies of sex differences in HPA axis responses following stressful stimulation have revealed inconsistent patterns of results (see Zimmer et al., 2003 for review). Additional studies are needed to examine whether (and which) cognitive processes might modulate neuroendocrine responses to noxious stressors, and whether these relations vary as a function of sex.
A dynamic HPA axis response following acute noxious stimulation should be considered adaptive as the release of cortisol has widespread actions which help restore homeostasis following a stressful event. In addition to the nature of the stressor, individuals’ cognitions during the stress experience may partially determine the HPA axis response. In clinical samples, passive coping, repression, and denial of a stressful event have been shown to be related to hypocortisolism, a condition believed to be implicated in inflammatory processes that promote the development of cardiovascular disease (Heim et al., 2000). Additionally, a relation between hypercortisolism and impaired cognition (attentional and memory deficits) has been reported, particularly for individuals reporting depressive symptoms (O’Brien et al., 2004). There is currently insufficient evidence describing whether adaptive cognitions, such as active coping and sense of control, may be related to adaptive cortisol responses following noxious stimulation in non-clinical samples.
In this study, we examined active-coping strategies, perceived control over pain, and their interaction with cortisol response. Furthermore, we examined whether these relations varied as a function of sex. It was hypothesized that (1) perceived control over the painful stressor would interact with active-coping strategies in relation to an adaptive cortisol response and (2) given previous literature suggesting sex differences in cortisol response to noxious stress, men and women would demonstrate divergent cortisol responses in relation to perceived control and coping.
Section snippets
Participants and procedures
The present study conducted secondary analyses on self-report and neuroendocrine data from a study investigating the relations among cortisol awakening response, stress-induced cortisol reactivity, and pain reports following quantitative sensory testing (see Fabian et al., 2009 for review). A total of 80 participants were recruited from an urban university in the mid-Atlantic United States. Participants completed a screening battery to determine eligibility, and exclusion criteria included: (a)
Differences by sex
The independent-samples t-tests demonstrated significant differences between men and women for several key variables. Compared to women, men reported significantly greater active-coping strategies (Men; M = 4.19, SD = 2.19; Women; M = 3.02, SD = 2.04; t(78) = 2.47, p < .05) and perceived control over pain (Men; M = 22.23, SD = 8.64; Women; M = 17.93, SD = 7.85; t(78) = 2.33, p < .05). Men had significantly greater exposure to the painful stimulus (i.e., CPT immersion time) than women (Men; M = 202.33, SD = 113.44; Women; M
Discussion
Research examining cortisol response differences by sex and adaptive cognitive processes following acute noxious stimulation is scant, with mixed findings. The current study found that perceived control moderates an active coping–adrenocortical relation among women but not men. It seems that active-coping strategies may potentiate the release of cortisol in response to a painful stimulus only in the presence of greater perceived control over pain, and this response is independent of the
Role of the funding sources
Funding for this study was provided by NIH Grant R21AT003250-01A1 (L. McGuire) and by a Special Research Initiative Support from the University of Maryland, Baltimore County (L. McGuire); neither the NIH nor UMBC had any further role in study design; in the collection, analysis, and interpretation of data; in the writing of the report; nor in the decision to submit the manuscript for publication.
Conflict of interest
None declared.
Acknowledgements
We thank Ms. Kate Guilfoyle and Mr. Ray Richinelli who assisted with the data collection and project management.
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