Huynh Aaron N, Williams AnnaLynn M, Belcher Elizabeth K, Van Haute Paige, Lotta Louis T, Thompson Bryan, Netherby-Winslow Colleen, Curtis Amarinthia, Esparaz Benjamin T, Jorgensen Carla, Alberti Sara, Bentley Emma, Sun Hongying, Culakova Eva, Janelsins Michelle C
University of Rochester Medical Center, Department of Surgery, Division of Supportive Care in Cancer, Rochester, NY, 14642, USA.
University of Rochester Medical Center, Department of Neuroscience, Rochester, NY, 14642, USA.
Brain Behav Immun Health. 2024 Sep 8;41:100860. doi: 10.1016/j.bbih.2024.100860. eCollection 2024 Nov.
Many patients with cancer experience cancer-related cognitive decline (CRCD). Previous studies have shown that elevated S100β, a calcium-binding protein commonly found in glial cells, can exhibit neurotoxic effects, including disruption of the blood-brain barrier (BBB). We studied changes in S100β levels in patients with breast cancer receiving chemotherapy, and the relationship to changes in cognitive function. A total of 505 women with breast cancer (mean (sd) age; 53.4 (53.6)) and 336 age-matched controls without cancer (52.8 (10.3)) were included from a nationwide study as part of the National Cancer Institute Community Oncology Research Program (NCORP). Both groups provided blood samples and completed neurocognitive assessments within 7 days before the patients with breast cancer received their first chemotherapy dose (pre-chemotherapy; T1) and within 1 month of their last chemotherapy administration (post-chemotherapy; T2). Utilizing a linear mixed model, multivariate linear regressions, and Spearman rank correlations (r), we investigated longitudinal changes in serum S100β concentrations and their relationships to changes in neurocognitive outcomes over time. We observed an increase in S100β for patients with breast cancer (p = 0.002), but not for controls without cancer over time (p = 0.683). Additionally, we identified subtle relationships between increases in serum S100β and worsening in cognitive performance on the Backward Counting test (r = 0.11, p = 0.041) and self-reported FACT-Cog Perceived Cognitive Abilities (r = -0.10, p = 0.025). Regression analyses adjusted for age, race, body-mass index (BMI), education, menopausal status, anxiety, and depression revealed a trend remained for the relationship of S100β with Backward Counting. In conclusion, we found that patients with breast cancer experience a significant increase in concentration of serum S100β over the course of chemotherapy. This increase is correlated with worsening in some neurocognitive outcomes from pre-to post-chemotherapy, with trending results remaining following adjustment for covariates.
许多癌症患者会经历癌症相关的认知衰退(CRCD)。先前的研究表明,S100β水平升高,S100β是一种在神经胶质细胞中常见的钙结合蛋白,可表现出神经毒性作用,包括破坏血脑屏障(BBB)。我们研究了接受化疗的乳腺癌患者S100β水平的变化,以及与认知功能变化的关系。作为美国国立癌症研究所社区肿瘤研究项目(NCORP)的一部分,一项全国性研究纳入了505名乳腺癌女性患者(平均(标准差)年龄;53.4(53.6)岁)和336名年龄匹配的无癌对照者(52.8(10.3)岁)。两组均在乳腺癌患者接受首次化疗剂量前7天内(化疗前;T1)以及末次化疗给药后1个月内(化疗后;T2)提供血样并完成神经认知评估。利用线性混合模型、多变量线性回归和Spearman等级相关性(r),我们研究了血清S100β浓度的纵向变化及其与随时间变化的神经认知结果的关系。我们观察到乳腺癌患者的S100β升高(p = 0.002),但随时间推移无癌对照者未出现这种情况(p = 0.683)。此外,我们发现血清S100β升高与倒背计数测试中的认知表现恶化(r = 0.11,p = 0.041)以及自我报告的FACT - Cog感知认知能力(r = -0.10,p = 0.025)之间存在细微关系。对年龄、种族、体重指数(BMI)教育程度、绝经状态、焦虑和抑郁进行校正的回归分析显示,S100β与倒背计数之间仍存在趋势关系。总之,我们发现乳腺癌患者在化疗过程中血清S100β浓度显著升高。这种升高与化疗前后某些神经认知结果的恶化相关,在对协变量进行校正后仍有趋势性结果。