Early treatment-related changes in dorsolateral prefrontal cortex activity and functional connectivity as potential biomarkers for antidepressant response in major depressive disorder.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Han Zhang, Cun Li, Ke Shi, Ye Xia, Yanhui Song, Jie Feng, Ziwei Wang, Kai Wang, Yuan Yang
{"title":"Early treatment-related changes in dorsolateral prefrontal cortex activity and functional connectivity as potential biomarkers for antidepressant response in major depressive disorder.","authors":"Han Zhang, Cun Li, Ke Shi, Ye Xia, Yanhui Song, Jie Feng, Ziwei Wang, Kai Wang, Yuan Yang","doi":"10.1038/s41398-025-03576-0","DOIUrl":null,"url":null,"abstract":"<p><p>Cognitive deficits are prevalent in major depressive disorder (MDD). Given that the dorsolateral prefrontal cortex (DLPFC) is a crucial region within the executive control network, its activity and functional connectivity (FC) may serve as potential indicators of antidepressant response. This prospective cohort study recruited 115 MDD patients and 43 healthy controls. Psychological assessments, electroencephalogram and event-related potential recordings were performed at baseline and 1 week after venlafaxine treatment, with a 12-week follow-up. Independent sample t-tests and Mann-Whitney U tests analyzed group differences, while linear mixed-effects models and logistic regression evaluated associations between DLPFC activity/FC changes and clinical outcomes. The MDD group showed significantly reduced right DLPFC current density during the N2 time window evoked by oddball stimuli (p = 0.028). Higher right DLPFC current density during the N2 time window was correlated with lower HAMD-21 scores one week after treatment (p = 0.041, n = 46). Furthermore, an early increase predicted remission at week 12 (p = 0.005). Decreased beta-band FC between the left DLPFC and both side of posterior cingulate cortex (PCC) (left: p = 0.003; right: p = 0.004) were correlated with lower HAMD-21 scores (n = 71). Moreover, an early reduction in these connectivity measures (left: odds ratio (OR) = 0.534, 95% confidence interval (CI): 0.297-0.972, p = 0.036; right: OR = 0.533, 95% CI: 0.299-0.950, p = 0.033) predicted remission at week 12. Early changes in DLPFC activity and FC may serve as biomarkers for monitoring treatment efficacy and predicting clinical outcomes, informing personalized treatment approaches.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"350"},"PeriodicalIF":6.2000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501012/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03576-0","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0

Abstract

Cognitive deficits are prevalent in major depressive disorder (MDD). Given that the dorsolateral prefrontal cortex (DLPFC) is a crucial region within the executive control network, its activity and functional connectivity (FC) may serve as potential indicators of antidepressant response. This prospective cohort study recruited 115 MDD patients and 43 healthy controls. Psychological assessments, electroencephalogram and event-related potential recordings were performed at baseline and 1 week after venlafaxine treatment, with a 12-week follow-up. Independent sample t-tests and Mann-Whitney U tests analyzed group differences, while linear mixed-effects models and logistic regression evaluated associations between DLPFC activity/FC changes and clinical outcomes. The MDD group showed significantly reduced right DLPFC current density during the N2 time window evoked by oddball stimuli (p = 0.028). Higher right DLPFC current density during the N2 time window was correlated with lower HAMD-21 scores one week after treatment (p = 0.041, n = 46). Furthermore, an early increase predicted remission at week 12 (p = 0.005). Decreased beta-band FC between the left DLPFC and both side of posterior cingulate cortex (PCC) (left: p = 0.003; right: p = 0.004) were correlated with lower HAMD-21 scores (n = 71). Moreover, an early reduction in these connectivity measures (left: odds ratio (OR) = 0.534, 95% confidence interval (CI): 0.297-0.972, p = 0.036; right: OR = 0.533, 95% CI: 0.299-0.950, p = 0.033) predicted remission at week 12. Early changes in DLPFC activity and FC may serve as biomarkers for monitoring treatment efficacy and predicting clinical outcomes, informing personalized treatment approaches.

Abstract Image

Abstract Image

Abstract Image

早期治疗相关的背外侧前额叶皮层活动和功能连通性变化作为重度抑郁症抗抑郁反应的潜在生物标志物
认知缺陷在重度抑郁症(MDD)中很普遍。鉴于背外侧前额叶皮层(DLPFC)是执行控制网络中的一个关键区域,其活性和功能连接(FC)可能作为抗抑郁反应的潜在指标。这项前瞻性队列研究招募了115名重度抑郁症患者和43名健康对照者。在基线和文拉法辛治疗后1周进行心理评估、脑电图和事件相关电位记录,随访12周。独立样本t检验和Mann-Whitney U检验分析组间差异,而线性混合效应模型和逻辑回归评估DLPFC活性/FC变化与临床结果之间的关联。MDD组在古怪刺激引起的N2时间窗内,右侧DLPFC电流密度显著降低(p = 0.028)。N2时间窗内右侧DLPFC电流密度越高,治疗后1周HAMD-21评分越低(p = 0.041, n = 46)。此外,早期升高预测在第12周缓解(p = 0.005)。左侧DLPFC和两侧后扣带皮层(PCC)之间β带FC减少(左:p = 0.003;右:p = 0.004)与HAMD-21评分降低相关(n = 71)。此外,这些连通性指标的早期降低(左:优势比(OR) = 0.534, 95%可信区间(CI): 0.297-0.972, p = 0.036;右:OR = 0.533, 95% CI: 0.299-0.950, p = 0.033)预测第12周缓解。DLPFC活性和FC的早期变化可以作为监测治疗效果和预测临床结果的生物标志物,为个性化治疗方法提供信息。
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
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
×
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