- Case report
- Open Access
Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children
BMC Pediatrics volume 18, Article number: 338 (2018)
Autism spectrum disorder (ASD) is a heterogeneous group of neurodevelopmental disorders. Genetically based subtype identification may prove more beneficial not only in illuminating the course and prognosis, but also for individualized treatment targets of an ASD sub-group. Increasing evidence has shown that de novo loss-of-function mutations in the chromodomain helicase DNA-binding protein 8 (CHD8) gene are associated with an ASD sub-group.
Here we describe two ASD cases in children with mild intellectual disability, early motor deficits, and speech delay, without distinct structural or EEG brain anomalies. Exome sequencing revealed a novel heterozygous nonsense/missense mutations(c.2647C > A/p.E883X and c.1677C > A/p.M559I respectively) in CHD8 gene.
There were few cases in the literature reporting de novo mutation of CHD8 in ASD. As demonstrated in our patients, along with other previously reported studies support that disruption of the CHD8 gene represents a specific genetic sub-type of ASD.
Autism spectrum disorder (ASD) is a heterogeneous group of neurodevelopmental conditions with significant genotypic complexity usually diagnosed in early childhood that are characterized by impairments in communication, social interaction, and by repetitive patterns of behavior [1, 2]. There may be as many as 10 to 20 million people affected by ASD in China . However, the cause of ASD remains unknown in approximately 80% of patients . Although more than 100 genes and genomic regions have been associated with ASD , and > 800 genes have been suggested to play a role in ASD [6,7,8,9], these have not been tied to the ASD’s complicate sub-type phenotypes. Increasing evidences suggesting that genetically based subtype identification may prove more beneficial not only in illuminating the course and prognosis of a sub-group of individuals with ASD, but also for individualized treatment targets .
The chromodomain helicase DNA binding protein 8 (CHD8) on 14q11.2 has been reported to be associated with ASD. It has been reported with a variety of genotypes including chromosomal microdeletions , balanced chromosomal abnormalities , haploinsufficiency of the gene due to a 2.89 Mb deletion , and a recurrent ~ 100 Kb microdeletion . In addition to cytogenetic studies, next-generation sequencing (NGS) technologies performed in ASD cohorts have discovered loci associated with an increased risk of ASD [7,8,9]. Increasing evidence has indicated that de novo loss of function mutations contribute to ASD risk [14,15,16]. It has been reported that CHD8 mutations could result in a behavioral profile consistent with ASD, together with macrocephaly, distinct facial features, and gastrointestinal complaints . In this paper, we report two cases of children with ASD and global developmental delays diagnosed based on the clinical findings and confirmed by genetic tests with a de novo mutation of CHD8 that has not been previously reported.
The 24-month-old boy was the first child of healthy nonconsanguineous parents. Pregnancy and delivery were normal. He was born at term with normal measurements (birth weight: 3550 g, 50-85th percentile). The physical development seemed over growth of his infanthood, as his weight, length and head circumference was 5200 g (> 85th percentile), 59.5 cm (> 97th percentile) and 40 cm (> 97th percentile) separately at 1-month old, as well as 11.6 kg (85-97th percentile), 86 cm (> 97th percentile) and 47.5 cm (> 85th percentile) separately at 1-year old. He was irritable when kept in the crawling position at 3–4 months old presenting with crying constantly. He was neither to respond to his name nor to learn to talk since then. He presented with a general developmental delay and dysmorphic feature (Fig. 1a and b). He started sitting at 7-months old and walking at 15-months old but had never walked on all fours. He was always found tumbling head over heels without awareness of self protection. General learning difficulties were also observed. Subsequently, there were concerns about his delayed language development and abnormal behavior. He also showed symptoms of diarrhea and constipation alternately. Half month to 20 days with a dilute stool (3–4 stools/day), alternately turn to constipation (one stool/2–3 days) after medication, without anal fissure. He further had a halitosis in the morning due to the gastroesophageal reflux. He had an initial developmental evaluation at 17-months old with a subsequent follow-up. His hearing evaluation at 20-months of age was normal. He was not found with funicular hydrocele on the right until 12-months old and received repairing operation at 20-months old. There was no similar disease in the other member of the family. In the present study, the Bayley scales was chosen as an instrument to assess his neuropsychological profiles. The scales is an individually administered instrument, which assesses the cognitive, language, and motor functioning of infants and young children aged 1–42 months. The patient was assessed at 26 months old and the cognitive score was < 50 (18-19 months) and the motor score was 56 (19 months).
We used Peabody developmental motor scales 2nd edition (PDMS-2) to assessed the patient’s motor development which including subtest scores: balance ability (19 months), locomotion (18 months), grasping (20 months), visual-motor (V-M) integration (19 months), and standardized motor quotients: gross (GMQ) (74), fine (FMQ) (82), total motor(TMQ) (75).
Autism Diagnostic Observation Schedule (ADOS)  was used to evaluate communication, social interaction abilities, creativity and the imaginative use of objects (Table 1). In the “communication” category, it was noted that he did not respond to his name, retrieve objects, initiate interactions, imitation, or point to pictures or objects. He did not differentially respond to his mother’s voice from others. He still had not developed speech appropriately. We also observed poor and limited eye contact in reciprocal social interactions during the ADOS examination. He had abnormal social interactions with repetitive patterns of behavior, poor eye contacts and restricted interests. In terms of behavior, he was hyperactive with difficulty in sustaining attention on using specific objects, and was unable to follow one-step directions. He did not respond or react to the examiner’s emotional state (ADOS Social interaction score: 13; Autism Cut-Off: 7/ASD Cut-Off: 4) . Concerning imagination, he did not initiate any spontaneous creative actions or pretend plays, even when he was invited to do so. His behavior did not reveal any unusual sensory interests, but the examiner noted the presentation with hyperactive behavior in sustaining attention on using specific objects and not to follow one-step directions. He also chewed on and ate non-edible objects. He showed little awareness of potential dangers. These findings confirmed our primary developmental diagnosis of ASD, which has finally been aligned to the American Psychiatric Association’s Diagnostic and Statistical Manual for Mental Disorders, 5th Edition (DSM5) criteria.
MRI showed the enlargement of skull anteroposterior diameter (17.6 cm at 17-months, Fig. 1c), increased signal in T2 in the white matter territories adjacent to the lateral ventricles and subcortical zone, and retardation of brain development (Fig. 1d). EEG showed non specific slow background activity, as well as no epileptiform discharges.
Genetic analyses were performed after obtaining the patient’s signed informed consent and approved by our hospital ethical committee. Exome sequencing revealed a novel heterozygous nonsense mutations, c.2647C > A (p.E883X) in CHD8 gene which was further validated by Sanger sequencing (Fig. 1. E1).
The proband is a 28-month-old boy who was born full term without major prenatal complications. The patient was the second child of healthy nonconsanguineous parents. His 5-year-old sister is healthy. Pregnancy and delivery were normal (birth weight: 3200 g, 50th percentile; length: 52 cm, 50-85th percentile). There were no major postnatal complications or congenital findings. The physical development also seemed over growth of his infanthood, as the weight, length and head circumference was 5200 g (50-85th percentile), 60 cm (97th percentile), and 40.4 cm (> 97th percentile) separately at 42-days old, as well as 17.5 kg (>97th percentile), 104 cm (>97th percentile), and 52 cm (> 97th percentile) separately at 2-years old. No facial or corporeal dysmorphic features have been detected (Fig. 2a and b). He was described by his parents as a very quiet infant who rarely crying even when receiving vaccinations. He seemed to develop normally, make eye contact, and interact spontaneously until approximately 5-months of age as he no longer made good eye contact afterward. He had gastrointestinal discomfort. The main clinical manifestation was constipation (one stool/3–4 days), with dry knot hard to discharge, and often accompanied by anal fissure. Also he showed a gastroesophageal reflux and a halitosis in the morning. His symptoms relieved after improvement of dietary habits before sleeping, stop the night milk, and improve sleep posture. He had an initial developmental evaluation at 6-months old with a subsequent follow-up. There were concerns about his delayed motor development. He exhibited developmental delays, sitting at 10-months and walking after 18-months of age. He was irritable and cried constantly. He had abnormal social interactions with poor eye contact and stereotypic behaviors. His hearing evaluation at 23-months was normal. By 18-months of age, he had not developed speech appropriately. There were no reports of clinical seizures in this patient. There was no similar disease in the other member of the family.
The patient was assessed by using Bayley scales at 30 months old and the cognitive score was < 50 (22–23 months) and the motor score was 55 (19 months).
The scores of PDMS-2: balance ability (20 months), locomotion (17 months), grasping (23 months), V-M integration (21 months), and standardized motor quotients: GMQ (53), FMQ (76), TMQ (59).
ADOS  was used to assess communication, social interaction abilities, creativity and the imaginative use of objects (Table 1). In the “communication” category, it was noted that he did not respond to his name as the patient 1. His verbal and non-verbal communication capabilities were so weak that, at that age, it was clearly observed that the quality of his eye contact, as well as social interactions, were in the autistic spectrum range. He did also have repetitive behaviors. His socialization skills were variable: did not interact with children in his same age and was unable to appreciate social cues. His ADOS scores (Table 1) suggested that the child was in the range of the autistic spectrum. This finding confirmed our primary developmental diagnosis of ASD.
MRI showed the increased signal in T2 in the white matter territories adjacent to the lateral ventricles and subcortical zone, and retardation of brain development (Fig. 2c). EEG showed non specific slow background activity, as well as no epileptiform discharges.
Genetic analyses were performed after obtaining the patient’s signed informed consent and approved by our hospital ethical committee. Exome sequencing revealed a novel heterozygous missense mutations, c.1677C > A (p.M559I) in CHD8 gene which was further validated by Sanger sequencing (Fig. 2. E1). The variant (p.M559I) was determined to be pathogenic which was classified basing on American College of Medical Genetics and Genomics guideline.
Discussion and conclusions
In the present study, we report de novo heterozygous missense/nonsense mutations of the CHD8 gene in two children with autism and global developmental delay that has not been previously reported. This provides additional evidence that disruption of the CHD8 gene could result in the development of ASD. Increasing evidences from exome sequencing to targeted analysis have showed that de novo loss-of-function mutations in the CHD8 gene are associated with ASD [7,8,9,10, 17, 19]. A decrease in functional CHD8 in human neural progenitor cells may be another cause of the development of ASD as it induced transcriptional alterations . There are lots of de novo loss of function mutations have been found contribute to ASD risk [14,15,16]. Many of these genes appear to be involved in regulation of transcription and modification of chromatin . CHD8 binds to β-catenin in its function in chromatin remodeling  and as a potential regulator of Wnt signaling which plays an important role in development . CHD8 also interacts with other ASD risk genes in neurodevelopment . All these suggest that CHD8 regulates co-expressing genes during human brain development and most of these genes are associated with ASD. Therefore, CHD8 mutations could result in intellectual disability and developmental delay as a behavioral profile consistent with ASD, together with macrocephaly with rapid postnatal growth, increased incidences of gastrointestinal problems and sleep disturbance . We performed review of all other 16 cases of CHD8 nonsense/missense mutations reported in the Human Gene Mutation Database (HGMD) [8, 17, 19, 25,26,27,28,29] (Table 2). Notably, our two CHD8 nonsense/missence mutation case (c.2647C > A and c.1677C > A) has not been previously reported. CHD8 mutations are associated with mild intellectual disability, early motor deficits, and speech delay, without distinct structural or EEG brain anomalies. Our patients have these common phenotypic features. In conclusion, we describe two cases of a novel heterozygous missense/nonsense mutations of CHD8 gene in two Chinese children with autism and global developmental delay, along with other previously reported studies support that disruption of the CHD8 gene represents a specific genetic sub-type of ASD.
Autism diagnostic observation schedule
Autism spectrum disorders
- CHD8 :
Chromodomain helicase DNA-binding protein 8
Diagnostic and Statistical Manual for Mental Disorders 5th Edition
Fine motor quotient
Gross motor quotient
Human gene mutation database
Peabody developmental motor scales 2nd edition
Total motor quotient
Schaefer GB, Mendelsohn NJ. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders. Genet Med. 2008;10(4):301–5.
Schaefer GB, Mendelsohn NJ. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. Genet Med. 2013;15(5):399–407.
Jiang L, Li G, Hao L, Guo R, Yang C, Du Y. Epidemiological investigation on autism spectrum disorders among preschool children in Shanghai. Zhonghua Liu Xing Bing Xue Za Zhi. 2015;36(12):1365–8.
Carter MT, Scherer SW. Autism spectrum disorder in the genetics clinic: a review. Clin Genet. 2013;83(5):399–407.
Betancur C. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res. 2011;1380:42–77.
Iossifov I, Ronemus M, Levy D, Wang Z, Hakker I, Rosenbaum J, Yamrom B, Lee YH, Narzisi G, Leotta A, et al. De novo gene disruptions in children on the autistic spectrum. Neuron. 2012;74(2):285–99.
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, et al. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 2012;485(7397):242–5.
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature. 2012;485(7397):246–50.
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 2012;485(7397):237–41.
Yenkoyan K, Grigoryan A, Fereshetyan K, Yepremyan D. Advances in understanding the pathophysiology of autism spectrum disorders. Behav Brain Res. 2017;331:92–101.
Terrone G, Cappuccio G, Genesio R, Esposito A, Fiorentino V, Riccitelli M, Nitsch L, Brunetti-Pierri N, Del Giudice E. A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of wolf-Hirschhorn syndrome. Am J Med Genet A. 2014;164A(1):190–3.
Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A, Ernst C, Hanscom C, Rossin E, Lindgren AM, et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 2012;149(3):525–37.
Prontera P, Ottaviani V, Toccaceli D, Rogaia D, Ardisia C, Romani R, Stangoni G, Pierini A, Donti E. Recurrent approximately 100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. Am J Med Genet A. 2014;164A(12):3137–41.
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, et al. Strong association of de novo copy number mutations with autism. Science. 2007;316(5823):445–9.
Gilman SR, Iossifov I, Levy D, Ronemus M, Wigler M, Vitkup D. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron. 2011;70(5):898–907.
Levy D, Ronemus M, Yamrom B, Lee YH, Leotta A, Kendall J, Marks S, Lakshmi B, Pai D, Ye K, et al. Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron. 2011;70(5):886–97.
Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, et al. Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 2014;158(2):263–76.
Lord C, Risi S, Lambrecht L, Cook EH Jr, Leventhal BL, DiLavore PC, Pickles A, Rutter M. The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord. 2000;30(3):205–23.
O'Roak BJ, Vives L, Fu W, Egertson JD, Stanaway IB, Phelps IG, Carvill G, Kumar A, Lee C, Ankenman K, et al. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science. 2012;338(6114):1619–22.
Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes. Transl Psychiatry. 2015;5:e568.
Krumm N, O'Roak BJ, Shendure J, Eichler EE. A de novo convergence of autism genetics and molecular neuroscience. Trends Neurosci. 2014;37(2):95–105.
Thompson BA, Tremblay V, Lin G, Bochar DA. CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes. Mol Cell Biol. 2008;28(12):3894–904.
Nishiyama M, Skoultchi AI, Nakayama KI. Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-beta-catenin signaling pathway. Mol Cell Biol. 2012;32(2):501–12.
Cotney J, Muhle RA, Sanders SJ, Liu L, Willsey AJ, Niu W, Liu W, Klei L, Lei J, Yin J, et al. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nat Commun. 2015;6:6404.
McCarthy SE, Gillis J, Kramer M, Lihm J, Yoon S, Berstein Y, Mistry M, Pavlidis P, Solomon R, Ghiban E, et al. De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Mol Psychiatry. 2014;19(6):652–8.
O'Roak BJ, Stessman HA, Boyle EA, Witherspoon KT, Martin B, Lee C, Vives L, Baker C, Hiatt JB, Nickerson DA, et al. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nat Commun. 2014;5:5595.
D'Gama AM, Pochareddy S, Li M, Jamuar SS, Reiff RE, Lam AN, Sestan N, Walsh CA. Targeted DNA sequencing from autism Spectrum disorder brains implicates multiple genetic mechanisms. Neuron. 2015;88(5):910–7.
Cappi C, Brentani H, Lima L, Sanders SJ, Zai G, Diniz BJ, Reis VN, Hounie AG, Conceicao do Rosario M, Mariani D, et al. Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways. Transl Psychiatry. 2016;6:e764.
Merner N, Forgeot d'Arc B, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF, Michaud JL, Mottron L, et al. A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): a case report and literature review. Am J Med Genet A. 2016;170A(5):1225–35.
The authors would like to thank the family who agreed to publication of their clinical details for the benefit of other families.
This publication was supported by the National Natural Science Foundation of China (81571263, 81300975 and 81871012), the Zhejiang Provincial Technology Plan (2015C37105), and by the Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, and the Key Laboratory for Diagnosis and Therapy of Neonatal Diseases of Zhejiang Province.
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Ethics approval is deemed unnecessary according to national regulations because all family members were seen in a medical consultation for a diagnostic purpose and they gave their written consent to participate and benefit from molecular analysis, the parents gave their written consent on behalf of both patients.
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Each family member gave written consent for clinical data and images to be published (the parents gave their written consent on behalf of both patients).
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Wang, J., Liu, J., Gao, Y. et al. Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children. BMC Pediatr 18, 338 (2018). https://doi.org/10.1186/s12887-018-1307-4
- Autism spectrum disorders
- Chromodomain helicase DNA-binding protein 8
- Next-generation sequencing