女性乳腺癌患者的抑郁和炎症:风险和恢复因素。

Biopsychosocial science and medicine Pub Date : 2025-07-01 Epub Date: 2025-05-09 DOI:10.1097/PSY.0000000000001398
J Richard T Korecki, George M Slavich, Patricia A Ganz, Michael R Irwin, Steve Cole, Catherine M Crespi, Julienne E Bower
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引用次数: 0

摘要

目的:乳腺癌的诊断是一种与抑郁和炎症增加相关的深刻压力源。然而,这些结果的相当大的变异性目前还无法解释。我们研究了可能影响新近诊断的乳腺癌患者抑郁症状和炎症标志物的风险和恢复因素,包括终生压力源暴露和心理和行为资源。我们关注的是可改变的资源——睡眠、体育活动和应对资源——这些可以用来促进女性的康复。方法:180例0-IIIA期乳腺癌患者在放疗、化疗或内分泌治疗前进行评估。应激逆境量表(STRAIN)测量终生应激源的总数和严重程度。血液样本捕获血浆炎症蛋白标志物(TNF-α, IL-6和CRP)组合成复合物。自我报告问卷评估抑郁症状、睡眠、身体活动、社会支持、自尊、乐观和精通。结果:总应激因子计数(β=0.30, P0.20)。结论:终生应激源暴露与乳腺癌患者的抑郁和炎症有关。提高睡眠质量、社会支持、乐观和掌握的干预措施可能会预防这一弱势群体的抑郁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Depression and Inflammation in Women With Breast Cancer: Risk and Resilience Factors.

Objective: Diagnosis with breast cancer is a profound stressor associated with increases in depression and inflammation. However, considerable variability in these outcomes is currently unexplained. We examined risk and resilience factors that may influence depressive symptoms and inflammatory markers in recently diagnosed breast cancer patients, including lifetime stressor exposure and psychological and behavioral resources. We focused on modifiable resources-sleep, physical activity, and coping resources-that can be leveraged to enhance women's recovery.

Methods: Women with stage 0-IIIA breast cancer ( N = 180) were assessed before radiation, chemotherapy, or endocrine therapy. The Stress and Adversity Inventory (STRAIN) was administered to measure total count and severity of lifetime stressors. Blood samples assessed plasma protein markers of inflammation (TNF-α, IL-6, and CRP) that were combined into a composite score. Self-report questionnaires evaluated depressive symptoms, sleep, physical activity, social support, self-esteem, optimism, and mastery.

Results: Total lifetime stressor count (β = 0.30, p < .0001) and severity (β = 0.12, p < .0001) were positively associated with depressive symptoms. Total lifetime stressor count (β = 0.01, p = .04), but not severity (β = 0.001, p = .17), was associated with higher inflammation. Sleep quality, social support, optimism, and mastery buffered the negative effects of lifetime stressor severity on depressive symptoms; social support and optimism also buffered stressor count on depressive symptoms ( p < .04). None of the moderators influenced the stress-inflammation association (all p s > .20).

Conclusions: Lifetime stressor exposure is associated with inflammation and depression in breast cancer patients. Interventions enhancing sleep quality, social support, optimism, and mastery may help prevent depression in this vulnerable group.

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