Genetic analysis of very obese children with autism spectrum disorder

被引:7
作者
Cortes, Herman D. [1 ]
Wevrick, Rachel [1 ]
机构
[1] Univ Alberta, Dept Med Genet, Edmonton, AB, Canada
关键词
SSC; Autism spectrum disorder; Obesity; Wnt; Gene Ontology; DE-NOVO MUTATIONS; INTELLECTUAL DISABILITY; NUMBER; ONTOLOGY; PHOSPHORYLATION; IDENTIFICATION; PREVALENCE; DISRUPTION; OVERWEIGHT; DISCOVERY;
D O I
10.1007/s00438-018-1418-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autism spectrum disorder (ASD) is defined by the triad of deficits in social interactions, deficits in communication, and repetitive behaviors. Common co-morbidities in syndromic forms of ASD include intellectual disability, seizures, and obesity. We asked whether very obese children with ASD had different behavioral, physical and genetic characteristics compared to children with ASD who were not obese. We found that very obese children with ASD had significantly poorer scores on standardized behavioral tests. Very obese boys with ASD had lower full scale IQ and increased impairments with respect to stereotypies, communication and social skills. Very obese girls with ASD had increased impairments with respect to irritability and oppositional defiant behavior. We identified genetic lesions in a subset of the children with ASD and obesity and attempted to identify enriched biological pathways. Our study demonstrates the value of identifying co-morbidities in children with ASD as we move forward towards understanding the biological processes that contribute to this complex disorder and prepare to design customized treatments that target the diverse genetic lesions present in individuals with ASD.
引用
收藏
页码:725 / 736
页数:12
相关论文
共 68 条
  • [1] [Anonymous], NEURAL PLAST
  • [2] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [3] ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks
    Bindea, Gabriela
    Mlecnik, Bernhard
    Hackl, Hubert
    Charoentong, Pornpimol
    Tosolini, Marie
    Kirilovsky, Amos
    Fridman, Wolf-Herman
    Pages, Franck
    Trajanoski, Zlatko
    Galon, Jerome
    [J]. BIOINFORMATICS, 2009, 25 (08) : 1091 - 1093
  • [4] MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus
    Blanchet, Patricia
    Bebin, Martina
    Bruet, Shaam
    Cooper, Gregory M.
    Thompson, Michelle L.
    Duban-Bedu, Benedicte
    Gerard, Benedicte
    Piton, Amelie
    Suckno, Sylvie
    Deshpande, Charu
    Clowes, Virginia
    Vogt, Julie
    Turnpenny, Peter
    Williamson, Michael P.
    Alembik, Yves
    Glasgow, Eric
    McNeill, Alisdair
    [J]. PLOS GENETICS, 2017, 13 (08):
  • [5] Prevalence of Overweight and Obesity in a Large Clinical Sample of Children With Autism
    Broder-Fingert, Sarabeth
    Brazauskas, Karissa
    Lindgren, Kristen
    Iannuzzi, Dorothea
    Van Cleave, Jeanne
    [J]. ACADEMIC PEDIATRICS, 2014, 14 (04) : 408 - 414
  • [6] Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome
    Bunn, Kieran J.
    Daniel, Phil
    Roesken, Heleen S.
    O'Neill, Adam C.
    Cameron-Christie, Sophia R.
    Morgan, Tim
    Brunner, Han G.
    Lai, Angeline
    Kunst, Henricus P. M.
    Markie, David M.
    Robertson, Stephen P.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 96 (04) : 623 - 630
  • [7] Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression
    Casanova, Emily L.
    Sharp, Julia L.
    Chakraborty, Hrishikesh
    Sumi, Nahid Sultana
    Casanova, Manuel F.
    [J]. MOLECULAR AUTISM, 2016, 7
  • [8] Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism
    Chahrour, Maria H.
    Yu, Timothy W.
    Lim, Elaine T.
    Ataman, Bulent
    Coulter, Michael E.
    Hill, R. Sean
    Stevens, Christine R.
    Schubert, Christian R.
    Greenberg, Michael E.
    Gabriel, Stacey B.
    Walsh, Christopher A.
    [J]. PLOS GENETICS, 2012, 8 (04): : 236 - 244
  • [9] Patterns of autism spectrum symptomatology in individuals with Down syndrome without comorbid autism spectrum disorder
    Channell, Marie Moore
    Phillips, B. Allyson
    Loveall, Susan J.
    Conners, Frances A.
    Bussanich, Paige M.
    Klinger, Laura Grofer
    [J]. JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2015, 7
  • [10] Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese
    Chen, Guanjie
    Zhang, Zhenjian
    Adebamowo, Sally N.
    Liu, Guozheng
    Adeyemo, Adebowale
    Zhou, Yanxun
    Doumatey, Ayo P.
    Wang, Chuntao
    Zhou, Jie
    Yan, Wenqiang
    Shriner, Daniel
    Tekola-Ayele, Fasil
    Bentley, Amy R.
    Jiang, Congqing
    Rotimi, Charles N.
    [J]. PLOS ONE, 2017, 12 (03):