During stress, heart rate variability moderates the impact of childhood adversity in women with breast cancer. (4th March 2018)

• Record Type: Journal Article
• Authors: Tell, Dina; Mathews, Herbert L.; Burr, Robert L.; Witek Janusek, Linda
• Is Part Of: Stress. Volume 21:Number 2(2018:Mar.)
• Page Start: 179
• Page End: 187
• Publication Date: 2018-03-04
• Subjects: Childhood adversity -- heart rate variability -- inflammation -- cortisol -- stress -- breast cancer; Stress (Physiology) -- Periodicals; 616.98
• DOI: 10.1080/10253890.2018.1424132
• Languages: English
• ISSNs: 1025-3890

Abstract

Abstract: Childhood adversity has long-lasting neuro-biological effects that can manifest as exaggerated stress responsivity to environmental challenge. These manifestations include a dysregulated hypothalamic-pituitary-adrenocortical (HPA) axis as well as increased levels of inflammatory mediators in response to stress. In this investigation, vagal parasympathetic activity was assessed for its capacity to moderate the relationship between childhood adversity and stress responsivity (cortisol and inflammation) during an acute laboratory challenge (Trier Social Stress Test–TSST). Thirty women recently diagnosed with breast cancer underwent the TSST during which their heart rate was recorded and saliva samples collected for measurement of cortisol and the proinflammatory cytokine, IL-6. Vagal activity during the TSST was calculated as the high-frequency (HF) component of heart rate variability (HRV). Vagal activity during the TSST moderated the effect of childhood adversity on both the cortisol and the IL-6 response. Women who had lower vagal stress-reactivity during the TSST and reported greater childhood adversity showed a larger rise in cortisol and IL-6 when compared to women with lower childhood adversity. The findings demonstrate that women with exposure to childhood adversity and low vagal stress-reactivity (reduced parasympathetic activity) exhibit an elevated stress response characterized by greater cortisol and proinflammatory cytokine release. Inflammatory burden and HPA dysregulation subsequent to stress may impair cancer control.