肠道微生物群和代谢组学途径在调节SSRIs治疗重度抑郁症疗效中的作用。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Ying Jiang, Yucai Qu, Lingyi Shi, Mengmeng Ou, Zhiqiang Du, Zhenhe Zhou, Hongliang Zhou, Haohao Zhu
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引用次数: 0

摘要

本研究旨在探讨肠道菌群通过代谢途径影响血清素再摄取抑制剂(SSRIs)抗抑郁作用的机制。共有126名患者进行了肠道微生物群和代谢组学分析。患者接受SSRI治疗,并根据治疗前后汉密尔顿抑郁评定量表(HAMD-17)评分的变化分为有反应组和无反应组。通过16S rRNA基因测序和代谢组学分析,研究肠道菌群组成与SSRIs疗效之间的关系,并建立预测模型。因此,研究发现,反应组和耐药组之间的肠道微生物群组成存在显著差异。特定的分类群,如瘤胃球菌、双歧杆菌和粪杆菌,在反应组中更为丰富。功能分析显示,反应组醋酸酯降解和神经递质合成途径上调。机器学习模型表明,肠道微生物群和代谢物是预测SSRIs疗效的潜在生物标志物。综上所述,肠道菌群通过代谢途径影响SSRIs的抗抑郁作用。肠道菌群的多样性和功能可以作为预测治疗反应的生物标志物,为个性化治疗提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of gut microbiota and metabolomic pathways in modulating the efficacy of SSRIs for major depressive disorder.

This study aims to explore the mechanism by which gut microbiota influences the antidepressant effects of serotonin reuptake inhibitors (SSRIs) through metabolic pathways. A total of 126 patients were analyzed for their gut microbiota and metabolomics. Patients received SSRI treatment and were categorized into responder and non-responder groups based on changes in their Hamilton Depression Rating Scale (HAMD-17) scores before and after treatment. The association between gut microbiota composition and the efficacy of SSRIs was investigated through 16S rRNA gene sequencing and metabolomic analysis, and a predictive model was developed. As a result, the study found significant differences in gut microbiota composition between the responder and resistant groups. Specific taxa, such as Ruminococcus, Bifidobacterium, and Faecalibacterium, were more abundant in the responder group. Functional analysis revealed upregulation of acetate degradation and neurotransmitter synthesis pathways in the responder group. The machine learning model indicated that gut microbiota and metabolites are potential biomarkers for predicting SSRIs efficacy. In conclusion, gut microbiota influences the antidepressant effects of SSRIs through metabolic pathways. The diversity and function of gut microbiota can serve as biomarkers for predicting the treatment response, providing new insights for personalized treatment.

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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.
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