乳腺癌妇女从化疗前到化疗后 S100 钙结合蛋白 β(S100β)和认知功能的变化

IF 3.7 Q2 IMMUNOLOGY Brain, behavior, & immunity - health Pub Date : 2024-09-08 DOI:10.1016/j.bbih.2024.100860
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引用次数: 0

摘要

许多癌症患者都会出现与癌症相关的认知能力下降(CRCD)。以前的研究表明,神经胶质细胞中常见的钙结合蛋白 S100β 升高会产生神经毒性效应,包括破坏血脑屏障(BBB)。我们研究了接受化疗的乳腺癌患者体内 S100β 水平的变化及其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学研究项目(NCORP)的一部分,我们在全国范围内开展了一项研究,共纳入了 505 名乳腺癌女性患者(平均年龄为 53.4 (53.6))和 336 名年龄匹配的非癌症对照组患者(52.8 (10.3))。两组患者均在乳腺癌患者接受首次化疗前 7 天内(化疗前;T1)和最后一次化疗后 1 个月内(化疗后;T2)提供了血液样本并完成了神经认知评估。利用线性混合模型、多元线性回归和斯皮尔曼等级相关性(rs),我们研究了血清 S100β 浓度的纵向变化及其与神经认知结果随时间变化的关系。我们观察到乳腺癌患者的 S100β 有所增加(p = 0.002),但未患癌症的对照组患者的 S100β 并未随时间推移而增加(p = 0.683)。此外,我们还发现血清 S100β 的增加与倒数测试(rs = 0.11,p = 0.041)和自我报告的 FACT-Cog 感知认知能力(rs = -0.10,p = 0.025)的认知能力恶化之间存在微妙的关系。根据年龄、种族、体重指数 (BMI)、教育程度、绝经状态、焦虑和抑郁等因素进行调整后的回归分析表明,S100β 与倒数计时的关系仍然存在趋势。总之,我们发现乳腺癌患者在化疗过程中血清 S100β 浓度会显著增加。从化疗前到化疗后,这种增加与某些神经认知结果的恶化相关,在调整协变量后,结果仍呈趋势。
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Changes in S100 calcium-binding protein β (S100β) and cognitive function from pre- to post-chemotherapy among women with breast cancer
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 (rs), 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 (rs = 0.11, p = 0.041) and self-reported FACT-Cog Perceived Cognitive Abilities (rs = −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.
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来源期刊
Brain, behavior, & immunity - health
Brain, behavior, & immunity - health Biological Psychiatry, Behavioral Neuroscience
CiteScore
8.50
自引率
0.00%
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0
审稿时长
97 days
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