Effects of sertraline on depressive symptoms, serum brain-derived neurotrophic factor (BDNF), 5-HT, and inflammatory cytokine expression in pediatric depression patients.

IF 2.4 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Zhenbo Wu, Hongyu Chen, Li Li, Yanyan Huang, Qinghua Lan, Hanjun Zhu, Songmei Luo
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Abstract

This study investigated the therapeutic effects of sertraline in pediatric patients diagnosed with depression, focusing on its impact on serum levels of brain-derived neurotrophic factor (BDNF), serotonin (5-HT), and inflammatory cytokines. A total of 164 pediatric patients were randomly divided into two groups: the sertraline and control groups, with 82 participants in each. Depressive symptoms were evaluated at 2 and 4 weeks using the 17-item Hamilton Depression Rating Scale (HAMD-17) and the Children's Depression Rating Scale-Revised (CDRS-R). Serum concentrations of BDNF, 5-HT, and inflammatory cytokines (interleukin-1β, interleukin-6, and tumor necrosis factor-α) were quantified using ELISA. Results demonstrated no significant differences in baseline characteristics between the groups. After 4 weeks, both groups showed reductions in HAMD-17 and CDRS-R scores and interleukin-1β and tumor necrosis factor-α levels, as well as increases in BDNF and 5-HT levels. Notably, at the 2-week mark, the sertraline group had significantly lower scores in both depression scales and inflammatory cytokines compared to the control group (fluoxetine treatment), indicating an early onset of action. Despite these findings, by 4 weeks, differences in HAMD-17 and CDRS-R scores, BDNF, and 5-HT levels between the two groups were no longer significant, although the sertraline group maintained lower levels of inflammatory cytokines. Additionally, the sertraline group reported higher rates of early improvement and adverse events, though no significant differences in remission or response rates were found between the groups. Overall, sertraline demonstrates effectiveness in alleviating depressive symptoms in children during the initial treatment period, potentially via mechanisms involving BDNF, 5-HT, and inflammation modulation, although it presents a less favorable safety profile compared to fluoxetine. (PsycInfo Database Record (c) 2025 APA, all rights reserved).

舍曲林对儿童抑郁症患者抑郁症状、血清脑源性神经营养因子(BDNF)、5-HT及炎性细胞因子表达的影响
本研究探讨舍曲林对儿童抑郁症患者的治疗效果,重点关注其对血清脑源性神经营养因子(BDNF)、血清素(5-HT)和炎症因子水平的影响。164例患儿随机分为舍曲林组和对照组,每组82人。在第2周和第4周使用17项汉密尔顿抑郁评定量表(HAMD-17)和修订儿童抑郁评定量表(CDRS-R)评估抑郁症状。ELISA法测定血清BDNF、5-HT、炎症因子(白细胞介素-1β、白细胞介素-6、肿瘤坏死因子-α)浓度。结果显示两组间基线特征无显著差异。4周后,两组均显示HAMD-17和CDRS-R评分、白细胞介素-1β和肿瘤坏死因子-α水平降低,BDNF和5-HT水平升高。值得注意的是,在2周时,舍曲林组在抑郁量表和炎症细胞因子方面的得分都明显低于对照组(氟西汀治疗),这表明起效早。尽管有这些发现,到4周时,两组之间HAMD-17和CDRS-R评分、BDNF和5-HT水平的差异不再显著,尽管舍曲林组保持较低的炎症细胞因子水平。此外,舍曲林组报告了更高的早期改善率和不良事件发生率,尽管两组之间在缓解率或反应率方面没有发现显著差异。总体而言,舍曲林在最初治疗期间显示出缓解儿童抑郁症状的有效性,可能是通过涉及BDNF、5-HT和炎症调节的机制,尽管与氟西汀相比,舍曲林的安全性较差。(PsycInfo Database Record (c) 2025 APA,版权所有)。
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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来源期刊
CiteScore
4.20
自引率
8.70%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Experimental and Clinical Psychopharmacology publishes advances in translational and interdisciplinary research on psychopharmacology, broadly defined, and/or substance abuse.
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