Pro-inflammatory markers are associated with response to sequential pharmacotherapy in major depressive disorder: a CAN-BIND-1 report.

IF 3.4 3区 医学 Q2 CLINICAL NEUROLOGY CNS Spectrums Pub Date : 2023-12-01 Epub Date: 2023-05-23 DOI:10.1017/S109285292300233X
M Ishrat Husain, Jane A Foster, Brittany L Mason, Sheng Chen, Haoyu Zhao, Wei Wang, Susan Rotzinger, Sakina Rizvi, Keith Ho, Raymond Lam, Glenda MacQueen, Roumen Milev, Benicio N Frey, Daniel Müller, Gustavo Turecki, Manish Jha, Madhukar Trivedi, Sidney H Kennedy
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Abstract

Objective: There is limited literature on associations between inflammatory tone and response to sequential pharmacotherapies in major depressive disorder (MDD).

Methods: In a 16-week open-label clinical trial, 211 participants with MDD were treated with escitalopram 10-20 mg daily for 8 weeks. Responders continued escitalopram while non-responders received adjunctive aripiprazole 2-10 mg daily for 8 weeks. Plasma levels of pro-inflammatory markers-C-reactive protein, interleukin (IL)-1β, IL-6, IL-17, interferon-gamma (IFN)-Γ, tumor necrosis factor (TNF)-α, and Chemokine C-C motif ligand-2 (CCL-2)-measured at baseline, and after 2, 8 and 16 weeks were included in logistic regression analyzes to assess associations between inflammatory markers and treatment response.

Results: Pre-treatment IFN-Γ and CCL-2 levels were significantly associated with a lower of odds of response to escitalopram at 8 weeks. Increases in CCL-2 levels from weeks 8 to 16 in escitalopram non-responders were significantly associated with higher odds of non-response to adjunctive aripiprazole at week 16.

Conclusion: Higher pre-treatment levels of IFN-Γ and CCL-2 were associated with non-response to escitalopram. Increasing levels of these pro-inflammatory markers may be associated with non-response to adjunctive aripiprazole. These findings require validation in independent clinical populations.

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前炎症标志物与重度抑郁症患者对连续药物治疗的反应有关:CAN-BIND-1 报告。
摘要关于重度抑郁障碍(MDD)患者炎症张力与连续药物治疗反应之间关系的文献有限:在一项为期16周的开放标签临床试验中,211名重度抑郁症患者接受了为期8周、每天10-20毫克的艾司西酞普兰治疗。有反应者继续接受艾司西酞普兰治疗,无反应者则接受阿立哌唑辅助治疗,每天2-10毫克,共8周。在基线、2周、8周和16周后测量的血浆促炎症标志物--反应蛋白、白细胞介素(IL)-1β、IL-6、IL-17、γ干扰素(IFN)-Γ、肿瘤坏死因子(TNF)-α和趋化因子C-C马达配体-2(CCL-2)的水平被纳入逻辑回归分析,以评估炎症标志物与治疗反应之间的关联:结果:治疗前的IFN-Γ和CCL-2水平与8周后对艾司西酞普兰产生反应的几率较低有显著关系。在第8周至第16周期间,艾司西酞普兰无应答者体内CCL-2水平的升高与第16周时对辅助阿立哌唑无应答的几率升高显著相关:结论:治疗前较高的IFN-Γ和CCL-2水平与对艾司西酞普兰无应答有关。这些促炎标志物水平的升高可能与阿立哌唑辅助治疗无效有关。这些发现需要在独立的临床人群中进行验证。
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来源期刊
CNS Spectrums
CNS Spectrums 医学-精神病学
CiteScore
6.20
自引率
6.10%
发文量
239
审稿时长
>12 weeks
期刊介绍: CNS Spectrums covers all aspects of the clinical neurosciences, neurotherapeutics, and neuropsychopharmacology, particularly those pertinent to the clinician and clinical investigator. The journal features focused, in-depth reviews, perspectives, and original research articles. New therapeutics of all types in psychiatry, mental health, and neurology are emphasized, especially first in man studies, proof of concept studies, and translational basic neuroscience studies. Subject coverage spans the full spectrum of neuropsychiatry, focusing on those crossing traditional boundaries between neurology and psychiatry.
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