Literature DB >> 30107084

The autism spectrum phenotype in ADNP syndrome.

Anne B Arnett1, Candace L Rhoads1, Kendra Hoekzema2, Tychele N Turner2, Jennifer Gerdts1, Arianne S Wallace1, Sandra Bedrosian-Sermone3, Evan E Eichler2,4, Raphael A Bernier1.   

Abstract

Pathogenic disruptions to the activity-dependent neuroprotector homeobox (ADNP) gene are among the most common heterozygous genetic mutations associated with autism spectrum disorders (ASDs). Individuals with ADNP disruptions share a constellation of medical and psychiatric features, including ASD, intellectual disability (ID), dysmorphic features, and hypotonia. However, the profile of ASD symptoms associated with ADNP may differ from that of individuals with another ASD-associated single gene disruption or with ASD without a known genetic cause. The current study examined the ASD phenotype in a sample of representative youth with ADNP disruptions. Participants (N = 116, ages 4-22 years) included a cohort with ADNP mutations (n = 11) and three comparison groups with either a mutation to CHD8 (n = 11), a mutation to another ASD-associated gene (other mutation; n = 53), or ASD with no known genetic etiology (idiopathic ASD; n = 41). As expected, individuals with ADNP disruptions had higher rates of ID but less severe social affect symptoms compared to the CHD8 and Idiopathic ASD groups. In addition, verbal intelligence explained more variance in social impairment in the ADNP group compared to CHD8, other mutation, and idiopathic ASD comparison groups. Restricted and repetitive behaviors in the ADNP group were characterized by high levels of stereotyped motor behaviors, whereas the idiopathic ASD group showed high levels of restricted interests. Taken together, these results underscore the role of ADNP in cognitive functioning and suggest that social impairments in ADNP syndrome are consistent with severity of verbal deficits. Autism Res 2018, 11: 1300-1310.
© 2018 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: Disruptions to the ADNP gene (i.e., ADNP syndrome) have been associated with autism spectrum disorder (ASD). This article describes intellectual disability, mild social difficulties, and severe repetitive motor movements in a group of 11 youth with ADNP Syndrome. We found lower rates of ASD than previously reported. Verbal skills explained individual variability in social impairment. This pattern suggests that the ADNP gene is primarily associated with learning and memory, and level of social difficulties is consistent with level of verbal impairment. © 2018 International Society for Autism Research, Wiley Periodicals, Inc.

Entities:  

Keywords:  ADNP; autism spectrum disorder; developmental disorder; genetic syndrome; intellectual disability

Mesh:

Substances:

Year:  2018        PMID: 30107084      PMCID: PMC6203613          DOI: 10.1002/aur.1980

Source DB:  PubMed          Journal:  Autism Res        ISSN: 1939-3806            Impact factor:   5.216


  29 in total

Review 1.  Intellectual disability and its relationship to autism spectrum disorders.

Authors:  Johnny L Matson; Mary Shoemaker
Journal:  Res Dev Disabil       Date:  2009-07-14

2.  Standardizing ADOS domain scores: separating severity of social affect and restricted and repetitive behaviors.

Authors:  Vanessa Hus; Katherine Gotham; Catherine Lord
Journal:  J Autism Dev Disord       Date:  2014-10

Review 3.  Treatments for the challenging behaviours of adults with intellectual disabilities.

Authors:  Johnny L Matson; Daniene Neal; Alison M Kozlowski
Journal:  Can J Psychiatry       Date:  2012-10       Impact factor: 4.356

4.  Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.

Authors:  Maricela Alarcón; Rita M Cantor; Jianjun Liu; T Conrad Gilliam; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2001-12-06       Impact factor: 11.025

5.  Validating the Repetitive Behavior Scale-revised in young children with autism spectrum disorder.

Authors:  Pat Mirenda; Isabel M Smith; Tracy Vaillancourt; Stelios Georgiades; Eric Duku; Peter Szatmari; Susan Bryson; Eric Fombonne; Wendy Roberts; Joanne Volden; Charlotte Waddell; Lonnie Zwaigenbaum
Journal:  J Autism Dev Disord       Date:  2010-12

6.  De novo mutations revealed by whole-exome sequencing are strongly associated with autism.

Authors:  Stephan J Sanders; Michael T Murtha; Abha R Gupta; John D Murdoch; Melanie J Raubeson; A Jeremy Willsey; A Gulhan Ercan-Sencicek; Nicholas M DiLullo; Neelroop N Parikshak; Jason L Stein; Michael F Walker; Gordon T Ober; Nicole A Teran; Youeun Song; Paul El-Fishawy; Ryan C Murtha; Murim Choi; John D Overton; Robert D Bjornson; Nicholas J Carriero; Kyle A Meyer; Kaya Bilguvar; Shrikant M Mane; Nenad Sestan; Richard P Lifton; Murat Günel; Kathryn Roeder; Daniel H Geschwind; Bernie Devlin; Matthew W State
Journal:  Nature       Date:  2012-04-04       Impact factor: 49.962

7.  The Simons Simplex Collection: a resource for identification of autism genetic risk factors.

Authors:  Gerald D Fischbach; Catherine Lord
Journal:  Neuron       Date:  2010-10-21       Impact factor: 17.173

8.  The contribution of de novo coding mutations to autism spectrum disorder.

Authors:  Ivan Iossifov; Brian J O'Roak; Stephan J Sanders; Michael Ronemus; Niklas Krumm; Dan Levy; Holly A Stessman; Kali T Witherspoon; Laura Vives; Karynne E Patterson; Joshua D Smith; Bryan Paeper; Deborah A Nickerson; Jeanselle Dea; Shan Dong; Luis E Gonzalez; Jeffrey D Mandell; Shrikant M Mane; Michael T Murtha; Catherine A Sullivan; Michael F Walker; Zainulabedin Waqar; Liping Wei; A Jeremy Willsey; Boris Yamrom; Yoon-ha Lee; Ewa Grabowska; Ertugrul Dalkic; Zihua Wang; Steven Marks; Peter Andrews; Anthony Leotta; Jude Kendall; Inessa Hakker; Julie Rosenbaum; Beicong Ma; Linda Rodgers; Jennifer Troge; Giuseppe Narzisi; Seungtai Yoon; Michael C Schatz; Kenny Ye; W Richard McCombie; Jay Shendure; Evan E Eichler; Matthew W State; Michael Wigler
Journal:  Nature       Date:  2014-10-29       Impact factor: 69.504

9.  Synaptic, transcriptional and chromatin genes disrupted in autism.

Authors:  Silvia De Rubeis; Xin He; Arthur P Goldberg; Christopher S Poultney; Kaitlin Samocha; A Erucment Cicek; Yan Kou; Li Liu; Menachem Fromer; Susan Walker; Tarinder Singh; Lambertus Klei; Jack Kosmicki; Fu Shih-Chen; Branko Aleksic; Monica Biscaldi; Patrick F Bolton; Jessica M Brownfeld; Jinlu Cai; Nicholas G Campbell; Angel Carracedo; Maria H Chahrour; Andreas G Chiocchetti; Hilary Coon; Emily L Crawford; Sarah R Curran; Geraldine Dawson; Eftichia Duketis; Bridget A Fernandez; Louise Gallagher; Evan Geller; Stephen J Guter; R Sean Hill; Juliana Ionita-Laza; Patricia Jimenz Gonzalez; Helena Kilpinen; Sabine M Klauck; Alexander Kolevzon; Irene Lee; Irene Lei; Jing Lei; Terho Lehtimäki; Chiao-Feng Lin; Avi Ma'ayan; Christian R Marshall; Alison L McInnes; Benjamin Neale; Michael J Owen; Noriio Ozaki; Mara Parellada; Jeremy R Parr; Shaun Purcell; Kaija Puura; Deepthi Rajagopalan; Karola Rehnström; Abraham Reichenberg; Aniko Sabo; Michael Sachse; Stephan J Sanders; Chad Schafer; Martin Schulte-Rüther; David Skuse; Christine Stevens; Peter Szatmari; Kristiina Tammimies; Otto Valladares; Annette Voran; Wang Li-San; Lauren A Weiss; A Jeremy Willsey; Timothy W Yu; Ryan K C Yuen; Edwin H Cook; Christine M Freitag; Michael Gill; Christina M Hultman; Thomas Lehner; Aaarno Palotie; Gerard D Schellenberg; Pamela Sklar; Matthew W State; James S Sutcliffe; Christiopher A Walsh; Stephen W Scherer; Michael E Zwick; Jeffrey C Barett; David J Cutler; Kathryn Roeder; Bernie Devlin; Mark J Daly; Joseph D Buxbaum
Journal:  Nature       Date:  2014-10-29       Impact factor: 49.962

10.  Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children.

Authors:  I Gozes; A Van Dijck; G Hacohen-Kleiman; I Grigg; G Karmon; E Giladi; M Eger; Y Gabet; M Pasmanik-Chor; E Cappuyns; O Elpeleg; R F Kooy; S Bedrosian-Sermone
Journal:  Transl Psychiatry       Date:  2017-02-21       Impact factor: 6.222

View more
  18 in total

1.  The Need for a Developmentally Based Measure of Social Communication Skills.

Authors:  Somer Bishop; Cristan Farmer; Aaron Kaat; Stelios Georgiades; Stephen Kanne; Audrey Thurm
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2019-06       Impact factor: 8.829

2.  Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation.

Authors:  Joseph Levine; David Cohen; Carole Herman; Alain Verloes; Vincent Guinchat; Lautaro Diaz; Cora Cravero; Anne Mandel; Illana Gozes
Journal:  J Mol Neurosci       Date:  2019-07       Impact factor: 3.444

3.  Neuroprotective Peptide NAPVSIPQ Antagonizes Ethanol Inhibition of L1 Adhesion by Promoting the Dissociation of L1 and Ankyrin-G.

Authors:  Xiaowei Dou; Jerry Y Lee; Michael E Charness
Journal:  Biol Psychiatry       Date:  2019-09-05       Impact factor: 13.382

4.  ADNP differentially interact with genes/proteins in correlation with aging: a novel marker for muscle aging.

Authors:  Oxana Kapitansky; Illana Gozes
Journal:  Geroscience       Date:  2019-07-01       Impact factor: 7.713

5.  Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders.

Authors:  Danijela Krgovic; Mario Gorenjak; Nika Rihar; Iva Opalic; Spela Stangler Herodez; Hojka Gregoric Kumperscak; Peter Dovc; Nadja Kokalj Vokac
Journal:  Front Mol Neurosci       Date:  2022-06-23       Impact factor: 6.261

6.  Transcriptional subtyping explains phenotypic variability in genetic subtypes of autism spectrum disorder.

Authors:  Sandy Trinh; Anne Arnett; Evangeline Kurtz-Nelson; Jennifer Beighley; Marta Picoto; Raphael Bernier
Journal:  Dev Psychopathol       Date:  2020-10

7.  Developmental Predictors of Cognitive and Adaptive Outcomes in Genetic Subtypes of Autism Spectrum Disorder.

Authors:  Anne B Arnett; Jennifer S Beighley; Evangeline C Kurtz-Nelson; Kendra Hoekzema; Tianyun Wang; Raphe A Bernier; Evan E Eichler
Journal:  Autism Res       Date:  2020-09-12       Impact factor: 5.216

8.  Sex-and Region-Dependent Expression of the Autism-Linked ADNP Correlates with Social- and Speech-Related Genes in the Canary Brain.

Authors:  Gal Hacohen-Kleiman; Stan Moaraf; Oxana Kapitansky; Illana Gozes
Journal:  J Mol Neurosci       Date:  2020-09-14       Impact factor: 3.444

9.  Exposure to sevoflurane results in changes of transcription factor occupancy in sperm and inheritance of autism†.

Authors:  Hsiao-Lin V Wang; Samantha Forestier; Victor G Corces
Journal:  Biol Reprod       Date:  2021-09-14       Impact factor: 4.285

10.  ADNP Regulates Cognition: A Multitasking Protein.

Authors:  Illana Gozes
Journal:  Front Neurosci       Date:  2018-11-26       Impact factor: 4.677

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.