种族与化疗期间易怒、炎症和抑郁的关系

Amy Zhang, Keming Gao, Zhengyi Chen Chen
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摘要

目的:本研究旨在评估种族是否会改变化疗期间的易怒和免疫炎症,以及它们与加重抑郁的相互作用。方法:对25例非裔美国人和19例白人非转移性乳腺癌患者在基线(t1)和化疗3个月(t2)时的烦躁、炎症生物标志物(hsCRP和IL-6)和抑郁进行评估。采用Wilcoxon秩和检验比较不同种族在这些研究变量上的差异。使用抑郁严重程度作为因变量,种族、炎症生物标志物(hsCRP或IL-6)、易怒、这些变量的相互作用和时间作为自变量,控制年龄、基线抑郁严重程度及其种族差异,计算重复测量的广义估计方程(GEE)回归模型。结果:非裔美国癌症患者的hsCRP (p = 0.040)和IL-6 (p = 0.018)水平在t2时显著高于白人患者,无显著基线差异。在这两个回归模型中,经历更大易怒的非裔美国患者在t2时报告的抑郁程度明显更严重(p = 0.0002;.0048)。在包含hsCRP的回归模型中,易怒和hsCRP水平之间的负交互作用与t2时更严重的抑郁显著相关(p <。)。在包含IL-6的回归模型中,非裔美国患者(p = .03),大多数患者IL-6水平较高(p <0.0001),在t2时报告了更严重的抑郁,而白细胞介素-6水平较高的White患者在t2时也有更严重的抑郁(p = 0.016)。结论:在本研究中,非裔美国人易怒与抑郁的相关性显著强于白人,且hsCRP水平影响易怒及其与抑郁的相关性。确定易怒的因素,特别是非洲裔美国人,对于减少化疗癌症患者的易怒和抑郁非常重要。此外,研究中在化疗期间经历更高IL-6水平的白人癌症患者也有更高的抑郁恶化风险,需要就医。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between Race and Irritability, Inflammation, and Depression During Chemotherapy
Objectives: This study aimed to assess whether race modifies irritability and immunological inflammation, and their interaction to worsen depression during chemotherapy. Methods: 25 African American and 19 White nonmetastasized breast cancer patients were assessed on irritability, inflammation biomarker (hsCRP and IL-6), and depression at baseline (T 1 ) and after 3 months of chemotherapy (T 2 ). Wilcoxon rank sum test was performed to compare racial groups on these study variables. Generalized estimating equations (GEE) regression models for repeated measures were computed, using the severity of depression as the dependent variable, race, an inflammation biomarker (hsCRP or IL-6), irritability, interactions of these variables, and time as independent variables, controlling for age, baseline depression severity level and its racial difference. Results: The African American cancer patients had significantly higher levels of hsCRP (p = .040) and IL-6 (p = .018) than the White patients at T 2, without a significant baseline difference. In both regression models, the African American patients experiencing greater irritability reported significantly more severe depression at T 2 (p = .0002; .0048). In the regression model containing hsCRP, a negative interaction between irritability and hsCRP level was significantly associated with more severe depression at T 2 (p < .0001). In the regression model containing IL- 6, the African American patients (p = .03), most of whom had higher IL-6 (p < .0001), reported significantly more severe depression at T 2 , while White patients who had higher IL-6 levels also had more severe depression at T 2 (p = .016). Conclusion: Association between irritability and depression was significantly stronger for the African American patients than the White patients in this study, and the level of hsCRP influenced irritability and its association with depression. Identification of contributors to irritability, particularly for African Americans, is important for reducing irritability and depression in cancer patients undergoing chemotherapy. Moreover, the White cancer patients in the study who experienced higher IL-6 levels during chemotherapy were also at a higher risk of worsening depression and required medical attention.
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