• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

患者重度抑郁症的血浆代谢组分析。

Plasma metabolome analysis of patients with major depressive disorder.

机构信息

Kawamura Clinic for General Practice, Gyouki-Kai Medical Corporation, Tokyo, Japan.

Human Metabolome Technologies Inc., Tsuruoka, Japan.

出版信息

Psychiatry Clin Neurosci. 2018 May;72(5):349-361. doi: 10.1111/pcn.12638. Epub 2018 Mar 3.

DOI:10.1111/pcn.12638
PMID:29356314
Abstract

AIM

This study sought to characterize the plasma metabolite profiling of patients with major depressive disorder (MDD).

METHODS

Psychiatric assessments were made with the Structured Clinical Interview for DSM-IV Axis I Disorders. In the exploratory cohort, plasma metabolite profiles of 34 MDD patients and 31 mentally healthy controls were compared using capillary electrophoresis-mass spectrometry. Among the candidate metabolites, we focused on a metabolite showing the largest difference. The absolute concentrations were measured in two cohorts from a psychiatric primary care clinic to characterize the accuracy of the metabolite biomarker.

RESULTS

Among 23 metabolites significantly lower in the MDD group than in healthy controls, we focused on phosphoethanolamine (PEA) as a candidate. The reduction of PEA levels in MDD was checked in independent clinical sample sets. An ion-chromatography-fluorescence detection method was developed to measure plasma PEA levels. In the preliminary cohort, we examined 34 MDD and 43 non-MDD subjects. The area under the receiver-operator curve (AUC) was 0.92, with sensitivity/specificity greater than 88%, at a cut-off of 1.46 μM. In the checking cohort, with 10 MDD and 13 non-MDD subjects, AUC was 0.89, with sensitivity/specificity of 86% and 100%, respectively, at a cut-off of 1.48 μM. Plasma PEA inversely correlated with MDD severity, depressed mood, loss of interest, and psychomotor retardation.

CONCLUSION

These results suggest that plasma PEA level could be a candidate biomarker of MDD in the clinical setting. Further studies comparing MDD and mentally healthy controls are needed to confirm the utility of PEA as a biomarker for depression.

摘要

目的

本研究旨在描述重性抑郁障碍(MDD)患者的血浆代谢组特征。

方法

采用DSM-IV轴 I 障碍定式临床访谈对精神状态进行评估。在探索性队列中,采用毛细管电泳-质谱联用技术比较了 34 例 MDD 患者和 31 例心理健康对照者的血浆代谢组谱。在候选代谢物中,我们关注显示最大差异的代谢物。在精神科初级保健诊所的两个队列中测量绝对浓度,以表征代谢物生物标志物的准确性。

结果

在 MDD 组显著低于健康对照组的 23 种代谢物中,我们选择磷酸乙醇胺(PEA)作为候选物。在独立的临床样本集中检查了 MDD 患者中 PEA 水平的降低。开发了离子色谱-荧光检测法来测量血浆 PEA 水平。在初步队列中,我们检查了 34 例 MDD 和 43 例非 MDD 患者。在 1.46 μM 的截止值时,曲线下面积(AUC)为 0.92,灵敏度/特异性大于 88%。在检查队列中,有 10 例 MDD 和 13 例非 MDD 患者,AUC 为 0.89,灵敏度/特异性分别为 86%和 100%,截止值为 1.48 μM。血浆 PEA 与 MDD 严重程度、抑郁情绪、兴趣丧失和精神运动迟缓呈负相关。

结论

这些结果表明,血浆 PEA 水平可能是临床环境中 MDD 的候选生物标志物。需要进一步比较 MDD 和心理健康对照者的研究来确认 PEA 作为抑郁生物标志物的效用。

相似文献

1
Plasma metabolome analysis of patients with major depressive disorder.患者重度抑郁症的血浆代谢组分析。
Psychiatry Clin Neurosci. 2018 May;72(5):349-361. doi: 10.1111/pcn.12638. Epub 2018 Mar 3.
2
Diagnosis of major depressive disorder based on changes in multiple plasma neurotransmitters: a targeted metabolomics study.基于多种血浆神经递质变化的重度抑郁症诊断:一项靶向代谢组学研究。
Transl Psychiatry. 2018 Jul 10;8(1):130. doi: 10.1038/s41398-018-0183-x.
3
Discovery and validation of plasma biomarkers for major depressive disorder classification based on liquid chromatography-mass spectrometry.基于液相色谱-质谱联用技术的重度抑郁症分类血浆生物标志物的发现与验证
J Proteome Res. 2015 May 1;14(5):2322-30. doi: 10.1021/acs.jproteome.5b00144. Epub 2015 Mar 26.
4
Divergent Urinary Metabolic Phenotypes between Major Depressive Disorder and Bipolar Disorder Identified by a Combined GC-MS and NMR Spectroscopic Metabonomic Approach.采用气相色谱-质谱联用和核磁共振光谱代谢组学方法鉴定重度抑郁症和双相情感障碍之间不同的尿液代谢表型。
J Proteome Res. 2015 Aug 7;14(8):3382-9. doi: 10.1021/acs.jproteome.5b00434. Epub 2015 Jul 20.
5
Tryptophan-kynurenine and lipid related metabolites as blood biomarkers for first-episode drug-naïve patients with major depressive disorder: An exploratory pilot case-control study.色氨酸-犬尿氨酸和脂质相关代谢物作为首发未用药的重性抑郁障碍患者的血液生物标志物:一项探索性的病例对照研究。
J Affect Disord. 2018 Apr 15;231:74-82. doi: 10.1016/j.jad.2018.01.014. Epub 2018 Jan 31.
6
Metabolite signature for diagnosing major depressive disorder in peripheral blood mononuclear cells.外周血单个核细胞中用于诊断重度抑郁症的代谢物特征
J Affect Disord. 2016 May;195:75-81. doi: 10.1016/j.jad.2016.02.008. Epub 2016 Feb 5.
7
A novel urinary metabolite signature for diagnosing major depressive disorder.一种用于诊断重度抑郁症的新型尿代谢物特征。
J Proteome Res. 2013 Dec 6;12(12):5904-11. doi: 10.1021/pr400939q. Epub 2013 Nov 26.
8
Plasma amino acid profile in major depressive disorder: Analyses in two independent case-control sample sets.重性抑郁障碍患者的血浆氨基酸谱:两个独立病例对照样本集的分析。
J Psychiatr Res. 2018 Jan;96:23-32. doi: 10.1016/j.jpsychires.2017.09.014. Epub 2017 Sep 19.
9
Discovery of serum protein biomarkers in drug-free patients with major depressive disorder.在未服用药物的重度抑郁症患者中发现血清蛋白生物标志物。
Prog Neuropsychopharmacol Biol Psychiatry. 2016 Aug 1;69:60-8. doi: 10.1016/j.pnpbp.2016.04.009. Epub 2016 Apr 19.
10
Plasma Nervonic Acid Is a Potential Biomarker for Major Depressive Disorder: A Pilot Study.血浆壬酸是重度抑郁症的一个潜在生物标志物:一项初步研究。
Int J Neuropsychopharmacol. 2018 Mar 1;21(3):207-215. doi: 10.1093/ijnp/pyx089.

引用本文的文献

1
Rapamycin immunomodulation utilizes time-dependent alterations of lymph node architecture, leukocyte trafficking, and gut microbiome.雷帕霉素免疫调节利用淋巴结结构、白细胞运输和肠道微生物群的时间依赖性改变。
JCI Insight. 2025 Apr 22;10(8). doi: 10.1172/jci.insight.186505.
2
Using an Interpretable Amino Acid-Based Machine Learning Method to Enhance the Diagnosis of Major Depressive Disorder.使用一种基于可解释氨基酸的机器学习方法来加强对重度抑郁症的诊断。
J Clin Med. 2024 Feb 21;13(5):1222. doi: 10.3390/jcm13051222.
3
Metabolite Biomarkers of Prolonged and Intensified Pain and Distress in Head and Neck Cancer Patients Undergoing Radio- or Chemoradiotherapy by Means of NMR-Based Metabolomics-A Preliminary Study.
基于核磁共振代谢组学对头颈部癌患者在接受放疗或放化疗期间疼痛和痛苦持续加剧的代谢物生物标志物——一项初步研究
Metabolites. 2024 Jan 17;14(1):60. doi: 10.3390/metabo14010060.
4
Wide-scope targeted analysis of bioactive lipids in human plasma by LC/MS/MS.通过液相色谱/串联质谱法对人血浆中的生物活性脂质进行广泛靶向分析。
J Lipid Res. 2024 Jan;65(1):100492. doi: 10.1016/j.jlr.2023.100492. Epub 2023 Dec 20.
5
The changes in metabolomics profile induced by intermittent theta burst stimulation in major depressive disorder: an exploratory study.间歇 theta 爆破刺激诱导的重性抑郁障碍代谢组学特征的变化:一项探索性研究。
BMC Psychiatry. 2023 Jul 29;23(1):550. doi: 10.1186/s12888-023-05044-9.
6
Circulating metabolites and depression: a bidirectional Mendelian randomization.循环代谢物与抑郁症:双向孟德尔随机化研究
Front Neurosci. 2023 Apr 21;17:1146613. doi: 10.3389/fnins.2023.1146613. eCollection 2023.
7
Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids.代谢组学研究重度抑郁症发现多不饱和脂肪酸的潜在因果关联。
Biol Psychiatry. 2023 Oct 15;94(8):630-639. doi: 10.1016/j.biopsych.2023.01.027. Epub 2023 Feb 9.
8
Relationship between Urinary Metabolomic Profiles and Depressive Episode in Antarctica.南极环境下尿液代谢组学特征与抑郁发作的关系。
Int J Mol Sci. 2023 Jan 4;24(2):943. doi: 10.3390/ijms24020943.
9
Discovery and validation of acetyl-L-carnitine in serum for diagnosis of major depressive disorder and remission status through metabolomic approach.通过代谢组学方法发现并验证血清中乙酰左旋肉碱用于诊断重度抑郁症及缓解状态
Front Psychiatry. 2022 Nov 15;13:1002828. doi: 10.3389/fpsyt.2022.1002828. eCollection 2022.
10
Salivary microRNA and Metabolic Profiles in a Mouse Model of Subchronic and Mild Social Defeat Stress.社交挫败应激致慢性轻度应激小鼠唾液 microRNA 和代谢组学特征
Int J Mol Sci. 2022 Nov 21;23(22):14479. doi: 10.3390/ijms232214479.