Major depressive disorder and serum inflammatory biomarkers as predictors of reward processing dysfunction in an American Indian sample.

IF 4.8
Lizbeth Rojas, Eric Mann, Xi Ren, Danielle Bethel, Nicole Baughman, Kaiping Burrows, Rayus Kuplicki, Leandra K Figueroa-Hall, Robin L Aupperle, Jennifer L Stewart, Salvador M Guinjoan, Sahib S Khalsa, Jonathan Savitz, Martin P Paulus, Ricardo A Wilhelm, Neha A John-Henderson, Hung-Wen Yeh, Evan J White
{"title":"Major depressive disorder and serum inflammatory biomarkers as predictors of reward processing dysfunction in an American Indian sample.","authors":"Lizbeth Rojas, Eric Mann, Xi Ren, Danielle Bethel, Nicole Baughman, Kaiping Burrows, Rayus Kuplicki, Leandra K Figueroa-Hall, Robin L Aupperle, Jennifer L Stewart, Salvador M Guinjoan, Sahib S Khalsa, Jonathan Savitz, Martin P Paulus, Ricardo A Wilhelm, Neha A John-Henderson, Hung-Wen Yeh, Evan J White","doi":"10.1016/j.bpsc.2025.08.015","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>American Indians (AI) experience chronic stressors which may be associated with disproportionate prevalence rates of major depressive disorder (MDD). Stress affects mental health through increased inflammatory processes and has been associated with increased risk of MDD and disruptions to reward processing. This study investigated the role of inflammation in reward processing disruptions among AI individuals with lifetime MDD; a population at heightened risk due to chronic stressors.</p><p><strong>Method: </strong>Participants (n=73) completed a monetary incentive delay task during simultaneous electroencephalography (EEG) and functional magnetic resonance imaging (fMRI). Blood samples were analyzed for pro-inflammatory (tumor necrosis factor [TNF], interleukin-6 [IL-6], C-reactive protein [CRP]) and anti-inflammatory (interleukin-10 [IL-10]) biomarkers. Depression severity was assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) depression scale. Covariates were included and assessed from self-report measures.</p><p><strong>Results: </strong>Regression analyses revealed that elevated TNF concentrations and sex were associated with reduced activation across subregions of the basal ganglia during gain anticipation. Similarly, TNF and CRP concentrations, as well as medication, were associated with reduced activation within basal ganglia subregions across loss anticipation. IL-10, IL-6, and P300 showed limited predictive value for neural responses.</p><p><strong>Conclusions: </strong>These findings suggest that inflammation may contribute to reward processing disruptions by impairing striatal function amongst a sample with lifetime MDD. The observed associations underscore the importance of inflammation's potential role and association in the pathophysiology of MDD, particularly in contexts of chronic stress. This study highlights the need for addressing the disproportionate mental health burden among AI communities through a biopsychosocial approach.</p>","PeriodicalId":93900,"journal":{"name":"Biological psychiatry. Cognitive neuroscience and neuroimaging","volume":" ","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological psychiatry. Cognitive neuroscience and neuroimaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.bpsc.2025.08.015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: American Indians (AI) experience chronic stressors which may be associated with disproportionate prevalence rates of major depressive disorder (MDD). Stress affects mental health through increased inflammatory processes and has been associated with increased risk of MDD and disruptions to reward processing. This study investigated the role of inflammation in reward processing disruptions among AI individuals with lifetime MDD; a population at heightened risk due to chronic stressors.

Method: Participants (n=73) completed a monetary incentive delay task during simultaneous electroencephalography (EEG) and functional magnetic resonance imaging (fMRI). Blood samples were analyzed for pro-inflammatory (tumor necrosis factor [TNF], interleukin-6 [IL-6], C-reactive protein [CRP]) and anti-inflammatory (interleukin-10 [IL-10]) biomarkers. Depression severity was assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) depression scale. Covariates were included and assessed from self-report measures.

Results: Regression analyses revealed that elevated TNF concentrations and sex were associated with reduced activation across subregions of the basal ganglia during gain anticipation. Similarly, TNF and CRP concentrations, as well as medication, were associated with reduced activation within basal ganglia subregions across loss anticipation. IL-10, IL-6, and P300 showed limited predictive value for neural responses.

Conclusions: These findings suggest that inflammation may contribute to reward processing disruptions by impairing striatal function amongst a sample with lifetime MDD. The observed associations underscore the importance of inflammation's potential role and association in the pathophysiology of MDD, particularly in contexts of chronic stress. This study highlights the need for addressing the disproportionate mental health burden among AI communities through a biopsychosocial approach.

在美国印第安人样本中,重度抑郁症和血清炎症生物标志物作为奖励处理功能障碍的预测因子。
美国印第安人(AI)经历慢性压力源,这可能与严重抑郁症(MDD)的不成比例的患病率有关。压力通过增加炎症过程影响心理健康,并与重度抑郁症风险增加和奖励处理中断有关。本研究探讨了炎症在患有终身重度抑郁症的AI个体奖励加工中断中的作用;由于慢性压力而处于高风险的人群。方法:73名被试在同时进行脑电图(EEG)和功能磁共振成像(fMRI)时完成一项货币激励延迟任务。分析血样中促炎(肿瘤坏死因子[TNF]、白细胞介素-6 [IL-6]、c反应蛋白[CRP])和抗炎(白细胞介素-10 [IL-10])生物标志物。使用患者报告结果测量信息系统(PROMIS)抑郁量表评估抑郁严重程度。从自我报告测量中纳入并评估协变量。结果:回归分析显示,TNF浓度的升高和性别与增加预期期间基底神经节亚区激活的减少有关。同样,TNF和CRP浓度,以及药物,与基底神经节亚区在损失预期中的激活降低有关。IL-10、IL-6和P300对神经反应的预测价值有限。结论:这些发现表明,炎症可能通过损害终生重度抑郁症患者的纹状体功能而导致奖励处理中断。观察到的关联强调了炎症在重度抑郁症病理生理中的潜在作用和关联的重要性,特别是在慢性应激的背景下。这项研究强调需要通过生物心理社会方法解决人工智能社区中不成比例的心理健康负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信