Biological stress systems, adverse life events and the onset of chronic multisite musculoskeletal pain: a 6-year cohort study

Ann Rheum Dis. 2016 May;75(5):847-54. doi: 10.1136/annrheumdis-2014-206741. Epub 2015 Apr 22.

Abstract

Objectives: Dysregulated biological stress systems and adverse life events, independently and in interaction, have been hypothesised to initiate chronic pain. We examine whether (1) function of biological stress systems, (2) adverse life events, and (3) their combination predict the onset of chronic multisite musculoskeletal pain.

Methods: Subjects (n=2039) of the Netherlands Study of Depression and Anxiety, free from chronic multisite musculoskeletal pain at baseline, were identified using the Chronic Pain Grade Questionnaire and followed up for the onset of chronic multisite musculoskeletal pain over 6 years. Baseline assessment of biological stress systems comprised function of the hypothalamic-pituitary-adrenal axis (1-h cortisol awakening response, evening levels, postdexamethasone levels), the immune system (basal and lipopolysaccharide-stimulated inflammation) and the autonomic nervous system (heart rate, pre-ejection period, SD of the normal-to-normal interval, respiratory sinus arrhythmia). The number of recent adverse life events was assessed at baseline using the List of Threatening Events Questionnaire.

Results: Hypothalamic-pituitary-adrenal axis, immune system and autonomic nervous system functioning was not associated with onset of chronic multisite musculoskeletal pain, either by itself or in interaction with adverse life events. Adverse life events did predict onset of chronic multisite musculoskeletal pain (HR per event=1.14, 95% CI 1.04 to 1.24, p=0.005).

Conclusions: This longitudinal study could not confirm that dysregulated biological stress systems increase the risk of developing chronic multisite musculoskeletal pain. Adverse life events were a risk factor for the onset of chronic multisite musculoskeletal pain, suggesting that psychosocial factors play a role in triggering the development of this condition.

Keywords: Epidemiology; Fibromyalgis/Pain Syndromes; Inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anxiety Disorders / complications
  • Anxiety Disorders / epidemiology
  • Autonomic Nervous System / physiopathology
  • Chronic Pain / epidemiology
  • Chronic Pain / etiology*
  • Chronic Pain / physiopathology
  • Cohort Studies
  • Cytokines / blood
  • Depressive Disorder / complications
  • Depressive Disorder / epidemiology
  • Female
  • Humans
  • Hypothalamo-Hypophyseal System / physiopathology
  • Life Change Events*
  • Life Style
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Musculoskeletal Pain / epidemiology
  • Musculoskeletal Pain / etiology*
  • Musculoskeletal Pain / physiopathology
  • Netherlands / epidemiology
  • Pain Measurement / methods
  • Pituitary-Adrenal System / physiopathology
  • Risk Factors
  • Stress, Physiological / physiology*
  • Young Adult

Substances

  • Cytokines