Key result
Children with chronic pain had higher early-life stress (P=0.026), psychological distress (P<0.001), and autonomic and immune-inflammatory activation compared to healthy controls.
Why the study?
Psychological and neurophysiological processes interact to activate the stress system and maintain functional somatic symptoms, prompting investigation into stress-system activation in pediatric chronic pain.
Do children and adolescents with chronic pain exhibit greater psychological distress and stress-system activation compared to healthy controls?
Case-Control
Do children and adolescents with chronic pain exhibit greater psychological distress and stress-system activation compared to healthy controls?
Children and adolescents with chronic pain exhibit significant psychological distress and autonomic/immune stress-system activation, highlighting the need for multidisciplinary mind-body interventions.
May support biopsychosocial assessment in pediatric chronic pain; hypothesis-generating and requires longitudinal studies before informing practice.
Accumulating evidence indicates that psychological and neurophysiological processes interconnect and interact to activate the body’s stress system and to trigger and maintain functional somatic symptoms. This study used the Early Life Stress Questionnaire, Depression Anxiety Stress Scales and biological markers (heart rate, heart rate variability, skin conductance, C-reactive protein (CRP) titre, respiratory rate, and accuracy and reaction time in an emotion-face identification task), to examine childhood adversity, psychological distress and stress-system activation in 35 children and adolescents (23 girls and 12 boys, 9–17 years old) disabled by chronic pain (vs two groups of age- and sex-matched healthy controls). Patients reported more early-life stress ( U = 798.5, p = .026) and more psychological distress ( U = 978, p < .001). They showed activation of the autonomic system: elevated heart rate ( U = 862.5, p = .003), elevated electrodermal activity ( U = 804.5, p = .024) and lower heart rate variability in the time domain ( U = 380.5, p = .007) and frequency domain ( U = 409.5, p = .017). The group showed an upward shift of CRP titres (with 75th and 90th CRP percentiles of 4.5 and 10.5 mg/L, respectively), suggesting the activation of the immune–inflammatory system. Elevated CRP titres were associated with elevated heart rate ( p = .028). There were no differences in respiratory rate or in accuracy and reaction time in the emotion-face identification task. The results indicate that interventions for children and adolescents with chronic pain need a multidisciplinary mind–body approach that concurrently addresses psychological distress, physical impairment and stress-system dysregulation.
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McInnis et al. (2019) conducted a case-control in chronic pain. Chronic pain vs. Age- and sex-matched healthy controls was evaluated on Early-life stress, psychological distress, and biological markers of stress-system activation. Children with chronic pain had higher early-life stress (P=0.026), psychological distress (P<0.001), and autonomic and immune-inflammatory activation compared to healthy controls.
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