2002
DOI: 10.1097/00006842-200207000-00010
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Fatigue and Proinflammatory Cytokine Activity in Breast Cancer Survivors

Abstract: Fatigued breast cancer survivors showed elevations in serum markers associated with proinflammatory cytokine activity an average of 5 years after diagnosis. Results suggest mechanisms through which enduring immune activation may occur, including alterations in cortisol and in lymphocyte subsets.

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Cited by 481 publications
(387 citation statements)
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“…However, in the present study, items of the CES-D and the FAS loaded on two different factors (data not shown), as in the development phase of the FAS [19]. This is in line with a study on BC survivors [5], in which fatigue, instead of being secondary to depression, cooccurred with depression as part of a coordinated response elicited by cytokine actions of the central nervous system.…”
Section: Discussionsupporting
confidence: 90%
“…However, in the present study, items of the CES-D and the FAS loaded on two different factors (data not shown), as in the development phase of the FAS [19]. This is in line with a study on BC survivors [5], in which fatigue, instead of being secondary to depression, cooccurred with depression as part of a coordinated response elicited by cytokine actions of the central nervous system.…”
Section: Discussionsupporting
confidence: 90%
“…We have documented elevations in soluble markers of inflammation in two separate cohorts of breast cancer survivors that are suggestive of a chronic inflammatory state (Bower et al, 2002;Collado-Hidalgo et al, 2006). Our recent work extends these findings to the acute treatment setting and suggests that activation of proinflammatory cytokines may also play a role in fatigue onset during radiation therapy among both breast and prostate cancer patients .…”
Section: Conclusion and Recommendations For Future Researchsupporting
confidence: 59%
“…There are two potential pathways for impaired control of proinflammatory cytokines by the HPA axis: decreased glucocorticoid production, and decreased response of the glucocorticoid receptor to hormone ligation (Raison and Miller, 2003). In an initial study, we found that fatigued breast cancer survivors had lower levels of morning serum cortisol than nonfatigued controls, supporting decreased production as a potential mechanism for enhanced inflammation (Bower et al, 2002). Because a single measure of cortisol provides little information about this system, we have also examined two dynamic measures of HPA axis activity, diurnal cortisol secretion and cortisol response to challenge, as well as glucocorticoid receptor sensitivity, in relation to cancer-related fatigue.…”
Section: Mechanisms For Persistent Inflammation and Fatiguementioning
confidence: 83%
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“…In the past few years, IL-1ra has attracted considerable clinical attention because its serum levels are elevated in pathologies as diverse as sepsis, cancer, metabolic diseases and auto-immune diseases [24] whereas the plasma IL-1ra/IL-1 ratio in a healthy population is close to 1 and exhibits minimal variation [25]. A significant increase of plasma IL-1ra is associated with post-treatment fatigue in breast cancer survivors [26].…”
Section: Il-1 Family: Generalitiesmentioning
confidence: 99%