Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment

被引:97
作者
Hicks, Steven D. [1 ]
Ignacio, Cherry [2 ]
Gentile, Karen [3 ]
Middleton, Frank A. [3 ,4 ,5 ]
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Dept Pediat, Hershey, PA 17033 USA
[2] Partek Inc, St Louis, MO USA
[3] SUNY Upstate Med Univ, Dept Neurosci & Physiol, 750 East Adams St, Syracuse, NY 13210 USA
[4] SUNY Upstate Med Univ, Dept Psychiat & Behav Sci, Syracuse, NY 13210 USA
[5] SUNY Upstate Med Univ, Dept Biochem & Mol Biol, Syracuse, NY 13210 USA
来源
BMC PEDIATRICS | 2016年 / 16卷
关键词
miRNA; Next generation sequencing; RNA-Seq; Biomarker; Saliva; MENTAL-RETARDATION PROTEIN; MICRORNA;
D O I
10.1186/s12887-016-0586-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Autism spectrum disorder (ASD) is a common neurodevelopmental disorder that lacks adequate screening tools, often delaying diagnosis and therapeutic interventions. Despite a substantial genetic component, no single gene variant accounts for > 1 % of ASD incidence. Epigenetic mechanisms that include microRNAs (miRNAs) may contribute to the ASD phenotype by altering networks of neurodevelopmental genes. The extracellular availability of miRNAs allows for painless, noninvasive collection from biofluids. In this study, we investigated the potential for saliva-based miRNAs to serve as diagnostic screening tools and evaluated their potential functional importance. Methods: Salivary miRNA was purified from 24 ASD subjects and 21 age-and gender-matched control subjects. The ASD group included individuals with mild ASD (DSM-5 criteria and Autism Diagnostic Observation Schedule) and no history of neurologic disorder, pre-term birth, or known chromosomal abnormality. All subjects completed a thorough neurodevelopmental assessment with the Vineland Adaptive Behavior Scales at the time of saliva collection. A total of 246 miRNAs were detected and quantified in at least half the samples by RNA-Seq and used to perform between-group comparisons with non-parametric testing, multivariate logistic regression and classification analyses, as well as Monte Carlo Cross-Validation (MCCV). The top miRNAs were examined for correlations with measures of adaptive behavior. Functional enrichment analysis of the highest confidence mRNA targets of the top differentially expressed miRNAs was performed using the Database for Annotation, Visualization, and Integrated Discovery (DAVID), as well as the Simons Foundation Autism Database (AutDB) of ASD candidate genes. Results: Fourteen miRNAs were differentially expressed in ASD subjects compared to controls (p < 0.05; FDR < 0.15) and showed more than 95 % accuracy at distinguishing subject groups in the best-fit logistic regression model. MCCV revealed an average ROC-AUC value of 0.92 across 100 simulations, further supporting the robustness of the findings. Most of the 14 miRNAs showed significant correlations with Vineland neurodevelopmental scores. Functional enrichment analysis detected significant over-representation of target gene clusters related to transcriptional activation, neuronal development, and AutDB genes. Conclusion: Measurement of salivary miRNA in this pilot study of subjects with mild ASD demonstrated differential expression of 14 miRNAs that are expressed in the developing brain, impact mRNAs related to brain development, and correlate with neurodevelopmental measures of adaptive behavior. These miRNAs have high specificity and cross-validated utility as a potential screening tool for ASD.
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页数:11
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共 28 条
  • [11] Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
    Jin, P
    Zarnescu, DC
    Ceman, S
    Nakamoto, M
    Mowrey, J
    Jongens, TA
    Nelson, DL
    Moses, K
    Warren, ST
    [J]. NATURE NEUROSCIENCE, 2004, 7 (02) : 113 - 117
  • [12] Comprehensive analysis of the functional microRNA-mRNA regulatory network identifies miRNA signatures associated with glioma malignant progression
    Li, Yongsheng
    Xu, Juan
    Chen, Hong
    Bai, Jing
    Li, Shengli
    Zhao, Zheng
    Shao, Tingting
    Jiang, Tao
    Ren, Huan
    Kang, Chunsheng
    Li, Xia
    [J]. NUCLEIC ACIDS RESEARCH, 2013, 41 (22) : e203
  • [13] Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
    MacDermot, KD
    Bonora, E
    Sykes, N
    Coupe, AM
    Lai, CSL
    Vernes, SC
    Vargha-Khadem, F
    McKenzie, F
    Smith, RL
    Monaco, AP
    Fisher, SE
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (06) : 1074 - 1080
  • [14] Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
    Pinto, Dalila
    Delaby, Elsa
    Merico, Daniele
    Barbosa, Mafalda
    Merikangas, Alison
    Klei, Lambertus
    Thiruvahindrapuram, Bhooma
    Xu, Xiao
    Ziman, Robert
    Wang, Zhuozhi
    Vorstman, Jacob A. S.
    Thompson, Ann
    Regan, Regina
    Pilorge, Marion
    Pellecchia, Giovanna
    Pagnamenta, Alistair T.
    Oliveira, Barbara
    Marshall, Christian R.
    Magalhaes, Tiago R.
    Lowe, Jennifer K.
    Howe, Jennifer L.
    Griswold, Anthony J.
    Gilbert, John
    Duketis, Eftichia
    Dombroski, Beth A.
    De Jonge, Maretha V.
    Cuccaro, Michael
    Crawford, Emily L.
    Correia, Catarina T.
    Conroy, Judith
    Conceicao, Ines C.
    Chiocchetti, Andreas G.
    Casey, Jillian P.
    Cai, Guiqing
    Cabrol, Christelle
    Bolshakova, Nadia
    Bacchelli, Elena
    Anney, Richard
    Gallinger, Steven
    Cotterchio, Michelle
    Casey, Graham
    Zwaigenbaum, Lonnie
    Wittemeyer, Kerstin
    Wing, Kirsty
    Wallace, Simon
    van Engeland, Herman
    Tryfon, Ana
    Thomson, Susanne
    Soorya, Latha
    Roge, Bernadette
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 94 (05) : 677 - 694
  • [15] Screening for autism spectrum disorders in primary care settings
    Robins, Diana L.
    [J]. AUTISM, 2008, 12 (05) : 537 - 556
  • [16] Characteristics and Concordance of Autism Spectrum Disorders Among 277 Twin Pairs
    Rosenberg, Rebecca E.
    Law, J. Kiely
    Yenokyan, Gayane
    McGready, John
    Kaufmann, Walter E.
    Law, Paul A.
    [J]. ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2009, 163 (10): : 907 - 914
  • [17] Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines
    Sarachana, Tewarit
    Zhou, Rulun
    Chen, Guang
    Manji, Husseini K.
    Hu, Valerie W.
    [J]. GENOME MEDICINE, 2010, 2
  • [18] Gene and miRNA expression profiles in autism spectrum disorders
    Seno, Mohammad M. Ghahramani
    Hu, Pingzhao
    Gwadry, Fuad G.
    Pinto, Dalila
    Marshall, Christian R.
    Casallo, Guillermo
    Scherer, Stephen W.
    [J]. BRAIN RESEARCH, 2011, 1380 : 85 - 97
  • [19] Comprehensive survey of human brain microRNA by deep sequencing
    Shao, Ning-Yi
    Hu, Hai Yang
    Yan, Zheng
    Xu, Ying
    Hu, Hao
    Menzel, Corinna
    Li, Na
    Chen, Wei
    Khaitovich, Philipp
    [J]. BMC GENOMICS, 2010, 11
  • [20] miR-23a regulation of X-linked inhibitor of apoptosis (XIAP) contributes to sex differences in the response to cerebral ischemia
    Siegel, Chad
    Li, Jun
    Liu, Fudong
    Benashski, Sharon E.
    McCullough, Louise D.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (28) : 11662 - 11667