Depression and Inflammation Predict Depression Trajectory of Non-Small Cell Lung Cancer Patients.

Biopsychosocial science and medicine Pub Date : 2025-07-01 Epub Date: 2025-06-11 DOI:10.1097/PSY.0000000000001379
Kylie R Park, Peter G Shields, John V Myers, Sarah A Reisinger, Barbara L Andersen
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Abstract

Objective: Depression and systemic inflammation at diagnosis are associated with poor oncologic outcomes for lung cancer (LC) patients. Research has not explored the interaction of these biomarkers and potential for subsequent psychological morbidity. The aim determines if the co-occurrence of depression and systemic inflammation predicts a worsened trajectory of depressive symptoms from diagnosis through 8 months.

Methods: An observational longitudinal cohort design was used (ClinicalTrials.gov Identifier: NCT03199651). Individuals ( N =182) with advanced non-small cell lung cancer were enrolled at diagnosis/pretreatment, had blood drawn, and completed a depression assessment and followed with 8 monthly reassessments. Measures were the Advanced Lung Cancer Inflammation Index (ALI) and self-reported depressive symptoms (Patient Health Questionnaire-9). Using validated cutoffs for biomarkers of inflammation (ALI <24 vs. ALI ≥24) and depression (PHQ <8 vs. PHQ ≥8), the sample was subdivided into 4 cohorts: (1) no/low depression and low inflammation (neither); (2) no/low depression but high inflammation (inflammation); (3) high depression but low inflammation (depression); and (4) high depression and high inflammation (depression+inflammation).

Results: Linear mixed models were tested for Group, Time, and Group × Time effects predicting the depression trajectory, adjusting for baseline depression/inflammation, age, partner status, education, smoking history, and cancer treatment. Overall, depressive symptoms did not change across time ( p =0.26), but as predicted, only for Cohort 4 (depression+inflammation) was the interaction significant [ F(24,945) =-0.04, p =0.001], with patients having an elevated depression trajectory.

Conclusions: Novel data contribute to the depression pathophysiology literature, showing that co-occurring depression and inflammation can predict depression. Clinically, data suggest a new biobehavioral metric for the identification of depression maintenance in LC patients.

Trial registration: ClinicalTrials.gov identifier: NCT03199651.

抑郁和炎症预测非小细胞肺癌患者抑郁轨迹。
目的:诊断时的抑郁和全身性炎症与肺癌(LC)患者不良的肿瘤预后相关。研究还没有探索这些生物标志物的相互作用和随后的心理疾病的可能性。目的是确定抑郁症和全身性炎症的共同发生是否预示着抑郁症状从诊断到8个月的恶化轨迹。方法:采用观察性纵向队列设计(ClinicalTrials.gov识别码:NCT03199651)。晚期非小细胞肺癌患者(N=182)在诊断/预处理时入组,抽血,完成抑郁评估,随后进行8个月的重新评估。测量方法是晚期肺癌炎症指数(ALI)和自我报告的抑郁症状(患者健康问卷-9)。结果:测试了组、时间和x组时间效应的线性混合模型,预测抑郁轨迹,调整基线抑郁/炎症、年龄、伴侣状态、教育程度、吸烟史和癌症治疗。总体而言,抑郁症状没有随时间变化(P=0.26),但正如预测的那样,只有队列4(抑郁+炎症)的相互作用显著[F(24,945)=-0.04, P=0.001],患者的抑郁轨迹升高。结论:新的数据有助于抑郁症病理生理学文献显示抑郁症和炎症共同发生预测抑郁症。临床上,数据提示了一种新的生物行为指标来识别LC患者的抑郁维持。Clinicaltrialsgov识别码:NCT03199651。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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