Literature DB >> 23111923

Identification and validation of urinary metabolite biomarkers for major depressive disorder.

Peng Zheng1, Ying Wang, Liang Chen, Deyu Yang, Huaqing Meng, Dezhi Zhou, Jiaju Zhong, Yang Lei, N D Melgiri, Peng Xie.   

Abstract

Major depressive disorder (MDD) is a widespread and debilitating mental disorder. However, there are no biomarkers available to aid in the diagnosis of this disorder. In this study, a nuclear magnetic resonance spectroscopy-based metabonomic approach was employed to profile urine samples from 82 first-episode drug-naïve depressed subjects and 82 healthy controls (the training set) in order to identify urinary metabolite biomarkers for MDD. Then, 44 unselected depressed subjects and 52 healthy controls (the test set) were used to independently validate the diagnostic generalizability of these biomarkers. A panel of five urinary metabolite biomarkers-malonate, formate, N-methylnicotinamide, m-hydroxyphenylacetate, and alanine-was identified. This panel was capable of distinguishing depressed subjects from healthy controls with an area under the receiver operating characteristic curve (AUC) of 0.81 in the training set. Moreover, this panel could classify blinded samples from the test set with an AUC of 0.89. These findings demonstrate that this urinary metabolite biomarker panel can aid in the future development of a urine-based diagnostic test for MDD.

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Year:  2012        PMID: 23111923      PMCID: PMC3536901          DOI: 10.1074/mcp.M112.021816

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  37 in total

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Review 9.  Brain oxygenation and energy metabolism: part I-biological function and pathophysiology.

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Authors:  Roman Fischer; David C Trudgian; Cynthia Wright; Gethin Thomas; Linda A Bradbury; Matthew A Brown; Paul Bowness; Benedikt M Kessler
Journal:  Mol Cell Proteomics       Date:  2011-10-13       Impact factor: 5.911

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  73 in total

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3.  Combined Metabolomics and Proteomics Analysis of Major Depression in an Animal Model: Perturbed Energy Metabolism in the Chronic Mild Stressed Rat Cerebellum.

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Journal:  OMICS       Date:  2015-07

4.  A Load to Find Clinically Useful Biomarkers for Depression.

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5.  Comprehensive urinary metabolomic characterization of a genetically induced mouse model of prostatic inflammation.

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6.  Gut microbiome remodeling induces depressive-like behaviors through a pathway mediated by the host's metabolism.

Authors:  P Zheng; B Zeng; C Zhou; M Liu; Z Fang; X Xu; L Zeng; J Chen; S Fan; X Du; X Zhang; D Yang; Y Yang; H Meng; W Li; N D Melgiri; J Licinio; H Wei; P Xie
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7.  D-serine plasma concentration is a potential biomarker of (R,S)-ketamine antidepressant response in subjects with treatment-resistant depression.

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9.  Assessment of trimethylamine N-oxide (TMAO) as a potential biomarker of severe stress in patients vulnerable to posttraumatic stress disorder (PTSD) after acute myocardial infarction.

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10.  Metabolic Profiling Indicates Diversity in the Metabolic Physiologies Associated With Maternal Postpartum Depressive Symptoms.

Authors:  Emma Bränn; Christina Malavaki; Emma Fransson; Maria-Konstantina Ioannidi; Hanna E Henriksson; Fotios C Papadopoulos; George P Chrousos; Maria I Klapa; Alkistis Skalkidou
Journal:  Front Psychiatry       Date:  2021-06-25       Impact factor: 4.157

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