A proteomic analysis of urine biomarkers in autism spectrum disorder

被引:16
作者
Wang, Yan [1 ,2 ]
Zhang, Jishui [2 ]
Song, Wenqi [2 ]
Tian, Xiaoyi [2 ]
Liu, Ying [2 ]
Wang, Yanfei [2 ]
Ma, Jie [2 ]
Wang, Chengbin [1 ,3 ]
Yan, Guangtao [1 ,3 ]
机构
[1] Med Sch Chinese PLA, 28 Fuxing Rd, Beijing 100853, Peoples R China
[2] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Beijing, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Lab Med, Beijing, Peoples R China
关键词
Autism spectrum disorder; Proteomics; Parallel reaction monitoring; Biomarkers; ATP-SYNTHASE; EXPRESSION; CHILDREN; PROTEIN; METABOLOMICS; PREVALENCE; DIAGNOSIS; MARKERS; GENES;
D O I
10.1016/j.jprot.2021.104259
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by early-onset socialcommunication challenges, restricted and repetitive behaviors, or unusual sensory-motor behaviors. A lack of specific biomarkers hinders the early diagnosis and treatment of this disease in many children. This study analyzes and validates potential urinary biomarkers using mass spectrometry proteomics. Global proteomics profiles of urine from 19 ASD patients and 19 healthy control subjects were compared to identify significantly changed proteins. These proteins were validated with targeted proteomics using parallel reaction monitoring (PRM) in an independent validation set consisting of samples from 40 ASD patients and 38 healthy controls. A total of 34 significantly changed proteins were found in the discovery set, among which seven proteins were identified as potential biomarkers for ASD through PRM assays in the validation set. Of these seven proteins, immunoglobulin kappa variable 4-1, immunoglobulin kappa variable 3-20, and immunoglobulin lambda variable 1-51 were up-regulated, while ATP synthase F1 subunit alpha, 10 kDa heat shock protein, apolipoprotein CIII, and arylsulfatase F were down-regulated. Six of these seven proteins support previous findings that ASD is accompanied by altered immune response and lipid metabolism, as well as mitochondrial dysfunction. This study lays the groundwork for additional research using biomarkers to clinically diagnose ASD. The proteomics and PRM raw data of this study have been deposited under the accession number IPX0002592000 at iProX. Significance: This study identified 34 proteins in urine of ASD patients that were significantly changed from the urinary proteins of healthy subjects using LC-MS/MS-based proteomics in a discovery set. Seven of these proteins were validated by PRM analysis in an independent validation set. This report represents the first description of combined label-free quantitative proteomics and PRM analysis of targeted proteins for discovery of ASD urinary biomarkers. The results will be helpful for early diagnosis and can provide additional insight into the molecular mechanisms of ASD.
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页数:8
相关论文
共 43 条
[1]   Downregulation of the Expression of Mitochondrial Electron Transport Complex Genes in Autism Brains [J].
Anitha, Ayyappan ;
Nakamura, Kazuhiko ;
Thanseem, Ismail ;
Matsuzaki, Hideo ;
Miyachi, Taishi ;
Tsujii, Masatsugu ;
Iwata, Yasuhide ;
Suzuki, Katsuaki ;
Sugiyama, Toshiro ;
Mori, Norio .
BRAIN PATHOLOGY, 2013, 23 (03) :294-302
[2]  
[Anonymous], 2018, BIOMOLECULES
[3]   Advanced glycation endproducts, dityrosine and arginine transporter dysfunction in autism - a source of biomarkers for clinical diagnosis [J].
Anwar, Attia ;
Abruzzo, Provvidenza Maria ;
Pasha, Sabah ;
Rajpoot, Kashif ;
Bolotta, Alessandra ;
Ghezzo, Alessandro ;
Marini, Marina ;
Posar, Annio ;
Visconti, Paola ;
Thornalley, Paul J. ;
Rabbani, Naila .
MOLECULAR AUTISM, 2018, 9
[4]   Mutation Update of ARSA and PSAP Genes Causing Metachromatic Leukodystrophy [J].
Cesani, Martina ;
Lorioli, Laura ;
Grossi, Serena ;
Amico, Giulia ;
Fumagalli, Francesca ;
Spiga, Ivana ;
Filocamo, Mirella ;
Biffi, Alessandra .
HUMAN MUTATION, 2016, 37 (01) :16-27
[5]   Outcomes and moderators of Early Start Denver Model intervention in young children with autism spectrum disorder delivered in a mixed individual and group setting [J].
Contaldo, Annarita ;
Colombi, Costanza ;
Pierotti, Caterina ;
Masoni, Patrizia ;
Muratori, Filippo .
AUTISM, 2020, 24 (03) :718-729
[6]   A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins [J].
Corbett, B. A. ;
Kantor, A. B. ;
Schulman, H. ;
Walker, W. L. ;
Lit, L. ;
Ashwood, P. ;
Rocke, D. M. ;
Sharp, F. R. .
MOLECULAR PSYCHIATRY, 2007, 12 (03) :292-306
[7]   Expression and oxidative modifications of plasma proteins in autism spectrum disorders: Interplay between inflammatory response and lipid peroxidation [J].
Cortelazzo, Alessio ;
De Felice, Claudio ;
Guerranti, Roberto ;
Signorini, Cinzia ;
Leoncini, Silvia ;
Zollo, Gloria ;
Leoncini, Roberto ;
Timperio, Anna Maria ;
Zolla, Lello ;
Ciccoli, Lucia ;
Hayek, Joussef .
PROTEOMICS CLINICAL APPLICATIONS, 2016, 10 (11) :1103-1112
[8]   Early Behavioral Intervention Is Associated With Normalized Brain Activity in Young Children With Autism [J].
Dawson, Geraldine ;
Jones, Emily J. H. ;
Merkle, Kristen ;
Venema, Kaitlin ;
Lowy, Rachel ;
Faja, Susan ;
Kamara, Dana ;
Murias, Michael ;
Greenson, Jessica ;
Winter, Jamie ;
Smith, Milani ;
Rogers, Sally J. ;
Webb, Sara J. .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2012, 51 (11) :1150-1159
[9]   Reconstitution of composite actin and keratin networks in vesicles [J].
Deek, J. ;
Maan, R. ;
Loiseau, E. ;
Bausch, A. R. .
SOFT MATTER, 2018, 14 (10) :1897-1902
[10]   Metabolomics Study of Urine in Autism Spectrum Disorders Using a Multiplatform Analytical Methodology [J].
Dieme, Binta ;
Mavel, Sylvie ;
Blasco, Helene ;
Tripi, Gabriele ;
Bonnet-Brilhault, Frederique ;
Malvy, Joelle ;
Bocca, Cinzia ;
Andres, Christian R. ;
Nada-Desbarats, Lydie ;
Emond, Patrick .
JOURNAL OF PROTEOME RESEARCH, 2015, 14 (12) :5273-5282