重度抑郁症患者治疗期间血浆代谢谱的变化

IF 3.5 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Yujing Du, Xixuan Li, Shufang Zhang, Jingxuan Tan, Ying Zhu, Xuejia Zhai, Yongning Lu
{"title":"重度抑郁症患者治疗期间血浆代谢谱的变化","authors":"Yujing Du, Xixuan Li, Shufang Zhang, Jingxuan Tan, Ying Zhu, Xuejia Zhai, Yongning Lu","doi":"10.1007/s11011-025-01682-y","DOIUrl":null,"url":null,"abstract":"<p><p>Major depression disorder (MDD) is a mental condition that significantly threatens both physical and psychological health. This study aimed to discern variances in plasma metabolic profiles between MDD sufferers and healthy counterparts. Additionally, we tracked the hospitalization journey of MDD patients to investigate the normalization of metabolic irregularities through conventional treatment in the form of self-control. Ultra-Performance Liquid Chromatography - Mass Spectrometry was employed to analyze the metabolic profiles of 47 plasma samples, including 12 controls and 12 MDD patients at three distinct clinical stages (untreated baseline, 1-month post-treatment, and 2-month post-treatment). Multivariate statistical analysis and K-means clustering were executed to pinpoint significantly different metabolites between the groups and specific metabolites showing an ideal trend of variation. Subsequently, these metabolites were mapped onto Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways to preliminarily explore the potential mechanism of metabolic shifts in MDD. We identified 14 significantly different metabolites between MDD patients and controls. Among these, the relative levels of 9-hydroperoxy octadecadienoic acid, imidazoleacetic acid, thromboxane B2, and arachidonic acid displayed a regular trend of variation post-treatment. Further integration analysis yielded a novel metabolite-pathway network comprising these 4 specific metabolites and 8 pathways. These findings suggest that transitions in metabolic pathways during the onset and treatment of MDD are primarily governed by lipid metabolism and its associated signaling pathway system, with the involvement of histidine metabolism. The identified metabolites hold promise for diagnosing and evaluating the therapeutic efficacy of MDD, and provide a foundation for future research into the potential mechanisms underlying MDD.</p>","PeriodicalId":18685,"journal":{"name":"Metabolic brain disease","volume":"40 7","pages":"265"},"PeriodicalIF":3.5000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transformations in plasma metabolic profiles of patients with major depression disorder during treatment.\",\"authors\":\"Yujing Du, Xixuan Li, Shufang Zhang, Jingxuan Tan, Ying Zhu, Xuejia Zhai, Yongning Lu\",\"doi\":\"10.1007/s11011-025-01682-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Major depression disorder (MDD) is a mental condition that significantly threatens both physical and psychological health. This study aimed to discern variances in plasma metabolic profiles between MDD sufferers and healthy counterparts. Additionally, we tracked the hospitalization journey of MDD patients to investigate the normalization of metabolic irregularities through conventional treatment in the form of self-control. Ultra-Performance Liquid Chromatography - Mass Spectrometry was employed to analyze the metabolic profiles of 47 plasma samples, including 12 controls and 12 MDD patients at three distinct clinical stages (untreated baseline, 1-month post-treatment, and 2-month post-treatment). Multivariate statistical analysis and K-means clustering were executed to pinpoint significantly different metabolites between the groups and specific metabolites showing an ideal trend of variation. Subsequently, these metabolites were mapped onto Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways to preliminarily explore the potential mechanism of metabolic shifts in MDD. We identified 14 significantly different metabolites between MDD patients and controls. Among these, the relative levels of 9-hydroperoxy octadecadienoic acid, imidazoleacetic acid, thromboxane B2, and arachidonic acid displayed a regular trend of variation post-treatment. Further integration analysis yielded a novel metabolite-pathway network comprising these 4 specific metabolites and 8 pathways. These findings suggest that transitions in metabolic pathways during the onset and treatment of MDD are primarily governed by lipid metabolism and its associated signaling pathway system, with the involvement of histidine metabolism. The identified metabolites hold promise for diagnosing and evaluating the therapeutic efficacy of MDD, and provide a foundation for future research into the potential mechanisms underlying MDD.</p>\",\"PeriodicalId\":18685,\"journal\":{\"name\":\"Metabolic brain disease\",\"volume\":\"40 7\",\"pages\":\"265\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Metabolic brain disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11011-025-01682-y\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Metabolic brain disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11011-025-01682-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

摘要

重度抑郁症(MDD)是一种严重威胁身体和心理健康的精神疾病。这项研究的目的是辨别重度抑郁症患者和健康人血浆代谢谱的差异。此外,我们跟踪了MDD患者的住院过程,以研究通过自我控制形式的常规治疗对代谢异常的正常化。采用超高效液相色谱-质谱法分析47份血浆样本的代谢谱,包括12名对照组和12名处于三个不同临床阶段(未治疗基线、治疗后1个月和治疗后2个月)的MDD患者。通过多变量统计分析和K-means聚类,找出组间存在显著差异的代谢物和表现出理想变化趋势的特定代谢物。随后,这些代谢物被定位到京都基因与基因组百科全书(KEGG)通路上,初步探索MDD代谢变化的潜在机制。我们在重度抑郁症患者和对照组之间发现了14种显著不同的代谢物。其中,9-羟基十八烯酸、咪唑乙酸、血栓素B2和花生四烯酸的相对含量在处理后呈规律性变化趋势。进一步的整合分析得到了一个由这4种特定代谢物和8条通路组成的新的代谢物通路网络。这些发现表明,MDD发病和治疗过程中代谢途径的转变主要受脂质代谢及其相关信号通路系统的控制,其中包括组氨酸代谢。鉴定出的代谢物有望诊断和评估重度抑郁症的治疗效果,并为进一步研究重度抑郁症的潜在机制奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transformations in plasma metabolic profiles of patients with major depression disorder during treatment.

Major depression disorder (MDD) is a mental condition that significantly threatens both physical and psychological health. This study aimed to discern variances in plasma metabolic profiles between MDD sufferers and healthy counterparts. Additionally, we tracked the hospitalization journey of MDD patients to investigate the normalization of metabolic irregularities through conventional treatment in the form of self-control. Ultra-Performance Liquid Chromatography - Mass Spectrometry was employed to analyze the metabolic profiles of 47 plasma samples, including 12 controls and 12 MDD patients at three distinct clinical stages (untreated baseline, 1-month post-treatment, and 2-month post-treatment). Multivariate statistical analysis and K-means clustering were executed to pinpoint significantly different metabolites between the groups and specific metabolites showing an ideal trend of variation. Subsequently, these metabolites were mapped onto Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways to preliminarily explore the potential mechanism of metabolic shifts in MDD. We identified 14 significantly different metabolites between MDD patients and controls. Among these, the relative levels of 9-hydroperoxy octadecadienoic acid, imidazoleacetic acid, thromboxane B2, and arachidonic acid displayed a regular trend of variation post-treatment. Further integration analysis yielded a novel metabolite-pathway network comprising these 4 specific metabolites and 8 pathways. These findings suggest that transitions in metabolic pathways during the onset and treatment of MDD are primarily governed by lipid metabolism and its associated signaling pathway system, with the involvement of histidine metabolism. The identified metabolites hold promise for diagnosing and evaluating the therapeutic efficacy of MDD, and provide a foundation for future research into the potential mechanisms underlying MDD.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Metabolic brain disease
Metabolic brain disease 医学-内分泌学与代谢
CiteScore
5.90
自引率
5.60%
发文量
248
审稿时长
6-12 weeks
期刊介绍: Metabolic Brain Disease serves as a forum for the publication of outstanding basic and clinical papers on all metabolic brain disease, including both human and animal studies. The journal publishes papers on the fundamental pathogenesis of these disorders and on related experimental and clinical techniques and methodologies. Metabolic Brain Disease is directed to physicians, neuroscientists, internists, psychiatrists, neurologists, pathologists, and others involved in the research and treatment of a broad range of metabolic brain disorders.
×
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