Urinary peptidomics identifies potential biomarkers for major depressive disorder

被引:37
作者
Wang, Ying [1 ,2 ,3 ]
Chen, Jianjun [2 ,3 ]
Chen, Liang [1 ,2 ,3 ]
Zheng, Peng [1 ,2 ,3 ]
Xu, Hong-Bo [1 ,2 ,3 ]
Lu, Jia [1 ,2 ,3 ]
Zhong, Jiaju [1 ,2 ,3 ]
Lei, Yang [1 ,2 ,3 ]
Zhou, Chanjuan [1 ,2 ,3 ]
Ma, Qingwei [4 ]
Li, Yan [4 ]
Xie, Peng [1 ,2 ,3 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Neurol, Chongqing 400016, Peoples R China
[2] Chongqing Key Lab Neurobiol, Chongqing, Peoples R China
[3] Chongqing Med Univ, Inst Neurosci, Chongqing 400016, Peoples R China
[4] Bioyong Beijing Technol Co Ltd, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Depression; MDD; Diagnosis; Diagnostic; Peptide pattern; Urine; PERFORMANCE-CHARACTERISTICS; PROTEOMIC ANALYSIS; PROTEIN; PLASMA; SERUM; DIAGNOSIS; DISCOVERY; FRAGMENT; BURDEN; BRAIN;
D O I
10.1016/j.psychres.2014.02.029
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Major depressive disorder (MDD) is a debilitating psychiatric illness with no available objective laboratory-based diagnostic test. In this study, matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS)-based peptidomics was applied to identify potential urinary diagnostic biomarkers for MDD. A training set of 42 first-episode drug-naive MDD patients and 28 age- and gender-matched healthy controls (HC) was used to develop a peptide diagnostic pattern. Then, the diagnostic efficacy of this pattern was assessed in an independent blinded test set consisting of 24 MDD patients and 13 age- and gender-matched HC. A combination of five potential biomarkers was identified, yielding a sensitivity of 91.7% and specificity of 84.6% in the test set. Moreover, the protein precursors of four of the five peptides were identified by tandem mass spectrometric analysis: serum albumin, apolipoprotein A-I, protein AMBP, and basement membrane-specific heparan sulfate proteoglycan core protein. Taken together, the peptide pattern may be valuable for establishing an objective laboratory-based diagnostic test for MDD. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:25 / 33
页数:9
相关论文
共 52 条
[1]   Heme-scavenging role of α1-microglobulin in chronic ulcers [J].
Allhorn, M ;
Lundqvist, K ;
Schmidtchen, A ;
Åkerström, B .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (03) :640-646
[2]   Performance Characteristics of a New Hybrid Quadrupole Time-of-Flight Tandem Mass Spectrometer (TripleTOF 5600) [J].
Andrews, Genna L. ;
Simons, Brigitte L. ;
Young, J. Bryce ;
Hawkridge, Adam M. ;
Muddiman, David C. .
ANALYTICAL CHEMISTRY, 2011, 83 (13) :5442-5446
[3]   Evaluation of endogenous plasma peptide extraction methods for mass spectrometric biomarker discovery [J].
Aristoteli, Lina P. ;
Molloy, Mark P. ;
Baker, Mark S. .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (02) :571-581
[4]   DETERMINATION OF NON-ENZYMATICALLY GLYCATED APOLIPOPROTEIN-A1 [J].
CAINES, PS ;
THIBERT, RJ ;
DRAISEY, TF ;
FOREBACK, CC ;
CHU, JW .
CLINICAL BIOCHEMISTRY, 1989, 22 (04) :285-287
[5]   STRATEGIES FOR PROTEOMIC ANALYSIS OF NON-ENZYMATICALLY GLYCATED PROTEINS [J].
Capote, Feliciano Priego ;
Sanchez, Jean-Charles .
MASS SPECTROMETRY REVIEWS, 2009, 28 (01) :135-146
[6]   Use of glycan targeting antibodies to identify cancer-associated glycoproteins in plasma of breast cancer patients [J].
Cho, Wonryeon ;
Jung, Kwanyoung ;
Regnier, Fred E. .
ANALYTICAL CHEMISTRY, 2008, 80 (14) :5286-5292
[7]  
Connor TJ, 2003, HANDB EXP PHARMACOL, P117
[8]   Genetics of affective (mood) disorders [J].
Craddock, Nick ;
Forty, Liz .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (06) :660-668
[9]   PLASMA APOLIPOPROTEINS-AI, APOLIPOPROTEIN-AII, APOLIPOPROTEIN-B, APOLIPOPROTEIN-CI, AND APOLIPOPROTEIN-E ARE GLUCOSYLATED IN HYPERGLYCEMIC DIABETIC SUBJECTS [J].
CURTISS, LK ;
WITZTUM, JL .
DIABETES, 1985, 34 (05) :452-461
[10]   Urine in Clinical Proteomics [J].
Decramer, Stephane ;
de Peredo, Anne Gonzalez ;
Breuil, Benjamin ;
Mischak, Harald ;
Monsarrat, Bernard ;
Bascands, Jean-Loup ;
Schanstra, Joost P. .
MOLECULAR & CELLULAR PROTEOMICS, 2008, 7 (10) :1850-1862