Weinstein Ali A, Seth Krish, Gordy Shana, Jabbar Kashaf, Noori Nylab, Birerdinc Aybike, Baranova Ancha, Winter Patrice, Gerber Lynn H
Department of Global and Community Health, George Mason University, Fairfax, VA, USA.
School of Systems Biology, George Mason University, Fairfax, VA, USA.
BMC Womens Health. 2025 May 29;25(1):263. doi: 10.1186/s12905-025-03758-4.
This study aims to analyze the changes in inflammatory cytokines and state fatigue after exposure to a mental or physical fatiguing activity in breast cancer survivors (BCS).
A total of 46 BCS women (age: 58.9 ± 9.1) were recruited for this study and randomly assigned to one of three groups: exposure to physical fatigue (n = 16), mental fatigue (n = 15), or control (n = 15). Participants exposed to physical fatigue performed a 6-minute walk/run test. Participants exposed to mental fatigue performed a version of a dual 2-back task on a computer. Participants in the control group watched a video for 6 min. Clinically significant fatigue was defined by the FACIT-F. Analytes in serum were profiled using the Bio-Plex 200 Suspension Array System, specifically IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, eotaxin, TNF-α, TGF-β1, and VEGF.
Changes in inflammatory factors in response to the assigned fatigue-inducing tasks were mainly not statistically significant. The presence of clinically significant fatigue reported at baseline was, however, related to reactions to fatigue-inducing stimuli. Levels of TGF-β and eotaxin were consistently altered in reactions to fatigue-inducing tasks, particularly in those with clinical fatigue.
Clinically significant fatigue is related to increased inflammatory reactions to mentally or physically fatiguing tasks, highlighting the consistent impact that fatigue has across various challenges of daily activities. Acute fatigue challenges, the kind that BCS would be exposed to in everyday circumstances, does increase inflammatory responses, and those with clinically significant levels of fatigue at baseline are more likely to show these effects.
本研究旨在分析乳腺癌幸存者(BCS)在经历精神或身体疲劳活动后炎症细胞因子和状态疲劳的变化。
本研究共招募了46名BCS女性(年龄:58.9±9.1岁),并将她们随机分为三组之一:身体疲劳组(n = 16)、精神疲劳组(n = 15)或对照组(n = 15)。身体疲劳组的参与者进行6分钟的步行/跑步测试。精神疲劳组的参与者在电脑上执行一种双2-back任务。对照组的参与者观看6分钟视频。临床显著疲劳由FACIT-F定义。使用Bio-Plex 200悬浮阵列系统分析血清中的分析物,具体包括白细胞介素-1β(IL-1β)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)、嗜酸性粒细胞趋化因子、肿瘤坏死因子-α(TNF-α)、转化生长因子-β1(TGF-β1)和血管内皮生长因子(VEGF)。
针对指定的疲劳诱导任务,炎症因子的变化主要无统计学意义。然而,基线时报告的临床显著疲劳的存在与对疲劳诱导刺激的反应有关。在对疲劳诱导任务的反应中,尤其是在有临床疲劳的参与者中,TGF-β和嗜酸性粒细胞趋化因子的水平持续改变。
临床显著疲劳与对精神或身体疲劳任务的炎症反应增加有关,突出了疲劳对日常活动各种挑战的持续影响。急性疲劳挑战,即BCS在日常情况下会遇到的那种,确实会增加炎症反应,并且基线时具有临床显著疲劳水平的人更有可能表现出这些影响。