TY - JOUR
T1 - Within-person changes in cancer-related distress predict breast cancer survivors’ inflammation across treatment
AU - Renna, Megan E.
AU - Shrout, M. Rosie
AU - Madison, Annelise A.
AU - Alfano, Catherine M.
AU - Povoski, Stephen P.
AU - Lipari, Adele M.
AU - Agnese, Doreen M.
AU - Carson, William E.
AU - Kiecolt-Glaser, Janice K.
N1 - Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/11
Y1 - 2020/11
N2 - Background: Among breast cancer survivors, elevated inflammation has been linked to greater recurrence risk. Psychological processes, such as cancer-related distress, can pose threats to a survivor's longevity and wellbeing. Although distress can heighten inflammation, little is known about how fluctuations in distress during and after treatment impact a woman's own inflammation – the primary question of this study. Methods: Breast cancer survivors (n = 165, stages 0-III) completed a baseline visit before treatment and two follow-up visits 6 and 18 months after. At each visit, women completed the Impact of Events Scale to assess cancer-related distress, and a blood sample was collected to measure proinflammatory cytokines IL-6, TNF-α, IL-1β, and IL-8. This longitudinal study related fluctuations in survivor's own cancer-related distress (i.e., within-person effects), as well as average effects of cancer-related distress between survivors (i.e., between-person effects) to inflammatory changes across visits. Results: Women had elevated inflammation at visits where they expressed more cancer-related distress than what was typical. In contrast, the average cancer-related distress was not associated with inflammation. Conclusion: Larger increases in a women's cancer-related distress was linked with higher inflammation across visits. Comparing a survivor's own cancer-related distress to her average levels may prove useful in identifying links between distress and inflammation.
AB - Background: Among breast cancer survivors, elevated inflammation has been linked to greater recurrence risk. Psychological processes, such as cancer-related distress, can pose threats to a survivor's longevity and wellbeing. Although distress can heighten inflammation, little is known about how fluctuations in distress during and after treatment impact a woman's own inflammation – the primary question of this study. Methods: Breast cancer survivors (n = 165, stages 0-III) completed a baseline visit before treatment and two follow-up visits 6 and 18 months after. At each visit, women completed the Impact of Events Scale to assess cancer-related distress, and a blood sample was collected to measure proinflammatory cytokines IL-6, TNF-α, IL-1β, and IL-8. This longitudinal study related fluctuations in survivor's own cancer-related distress (i.e., within-person effects), as well as average effects of cancer-related distress between survivors (i.e., between-person effects) to inflammatory changes across visits. Results: Women had elevated inflammation at visits where they expressed more cancer-related distress than what was typical. In contrast, the average cancer-related distress was not associated with inflammation. Conclusion: Larger increases in a women's cancer-related distress was linked with higher inflammation across visits. Comparing a survivor's own cancer-related distress to her average levels may prove useful in identifying links between distress and inflammation.
KW - Avoidance
KW - Cancer survivors
KW - Cancer-related distress
KW - Inflammation
KW - Intrusive thoughts
UR - http://www.scopus.com/inward/record.url?scp=85091249193&partnerID=8YFLogxK
U2 - 10.1016/j.psyneuen.2020.104866
DO - 10.1016/j.psyneuen.2020.104866
M3 - Article
C2 - 32947247
AN - SCOPUS:85091249193
SN - 0306-4530
VL - 121
JO - Psychoneuroendocrinology
JF - Psychoneuroendocrinology
M1 - 104866
ER -