- Case report
- Open Access
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report
BMC Medical Genetics volume 21, Article number: 10 (2020)
The role of deleterious copy number variations in schizophrenia is well established while data regarding pathogenic variations remain scarce. We report for the first time a case of schizophrenia in a child with a pathogenic mutation of the chromodomain helicase DNA binding protein 2 (CHD2) gene.
The proband was the second child of unrelated parents. Anxiety and sleep disorders appeared at the age of 10 months. He presented febrile seizures and, at the age of 8, two generalized tonic-clonic seizures. At the age of 10, emotional withdrawal emerged, along with a flat affect, disorganization and paranoid ideation, without seizures. He began to talk and giggle with self. Eventually, the patient presented daily auditory and visual hallucinations. The diagnosis of childhood onset schizophrenia (DSM V) was then evoked. Brain imaging was unremarkable. Wakefulness electroencephalography showed a normal background and some bilateral spike-wave discharges that did not explain the psychosis features. A comparative genomic hybridization array (180 K, Agilent, Santa Clara, CA, USA) revealed an 867-kb 16p13.3 duplication, interpreted as a variant of unknown significance confirmed by a quantitative PCR that also showed its maternal inheritance. Risperidone (1,5 mg per day), led to clinical improvement. At the age of 11, an explosive relapse of epilepsy occurred with daily seizures of various types. The sequencing of a panel for monogenic epileptic disorders and Sanger sequencing revealed a de novo pathogenic heterozygous transition in CHD2 (NM_001271.3: c.4003G > T).
This case underlines that schizophrenia may be, sometimes, underpinned by a Mendelian disease. It addresses the question of systematic genetic investigations in the presence of warning signs such as a childhood onset of the schizophrenia or a resistant epilepsy. It points that, in the absence of pathogenic copy number variation, the investigations should also include a search for pathogenic variations, which means that some of the patients with schizophrenia should benefit from Next Generation Sequencing tools. Last but not least, CHD2 encodes a member of the chromodomain helicase DNA-binding (CHD) family involved in chromatin remodeling. This observation adds schizophrenia to the phenotypic spectrum of chromodomain remodeling disorders, which may lead to innovative therapeutic approaches.
The growing access to comparative genomic hybridization arrays has allowed for better identification of schizophrenia cases associated with the presence of deleterious copy number variations [1,2,3,4,5]. However, data regarding schizophrenia linked to pathogenic variations remain scarce, despite an increasing availability of diagnostic techniques. There is a dire need to clarify the benefit and modality of high-throughput genetic investigations in schizophrenia. This step is crucial to provide accurate genetic counseling, to further understand the pathological mechanisms underlying the disease and to imagine new innovative therapies. We describe here for the first time a case of childhood onset schizophrenia eventually linked to the presence of a pathogenic variant of CHD2, which encodes a chromodomain protein involved in neurogenesis, chromatin remodeling and gene expression.
The proband was the second child of unrelated parents with no remarkable medical history. The paternal grandfather had a history of simple, uncomplicated febrile seizures in infancy. The pregnancy and delivery were unremarkable, and the patients’ neurodevelopmental milestones were in the normal range. However, the mother described the appearance of sleep disorders at the age of 10 months that increased the sleep onset latency and nocturnal awakenings and ceased with co-sleeping. Not until the age of 6 could he sleep alone. The patient began school at the age of 3, but separation anxiety was severe and interfered with his learning. He was also described as a solitary child without other signs suggestive of an autism spectrum disorder. Between 19 months and 6 years of age, he experienced 7 typical febrile seizures. At 7 years of age, a global cognitive assessment revealed a heterogeneous profile with verbal intellectual quotient (IQ) of 78, perceptive IQ of 71 and speed processing index of 59. These results should, however, be interpreted with caution given the level of anxiety. At the age of 8, sodium valproate (400 mg per day, blood concentration: 52.4 mg/l) was introduced because of the occurrence of two spontaneous generalized tonic-clonic seizures with generalized spike-wave discharges upon interictal electroencephalography recording. Sodium valproate led to full seizure control. At the age of 9, anxiety escalation was noted, with death worries, iterative questioning, restlessness and panic attacks. At the age of 10, emotional withdrawal emerged, along with a flat affect, suicidal thoughts, irrelevant talk, delusions and paranoid ideation, with no recurrence of seizures. Confusion and disorganization were also noted. He began to talk and giggle with self. Eventually, the occurrence of daily auditory and visual hallucinations led to the patient’s hospitalization. The diagnosis of childhood onset schizophrenia (DSM V) was then evoked. This uncommon and severe phenotype associated with visual hallucinations led to further investigations. Brain magnetic resonance imaging was unremarkable. Wakefulness electroencephalography showed a normal background and some bilateral spike-wave discharges that did not explain the psychosis features and lacked contemporary clinical manifestation. Ammonemia, urinary organic acids, plasmatic amino acids, exchangeable copper, lysosphingolipids and oxysterols were in the normal ranges. A comparative genomic hybridization array (180 K, Agilent, Santa Clara, CA, USA) and quantitative polymerase chain reaction revealed an 867-kb 16p13.3 duplication inherited from the patient’s mother, which was interpreted as a variant of unknown significance (arr [hg19] 16p13.13p13.12(12,008,151-12,875,277) × 3 mat). (Fig. 1) The patient was given risperidone (1,5 mg per day), which led to a clinical improvement allowing hospital discharge. At the age of 11, an explosive relapse of epilepsy occurred with daily seizures of various types: absences, myoclonic fits, tonic and tonicoclonic seizures. No contemporary increase in behavioral disorders was noted. An electroencephalogram disclosed slow background activity, with bilateral diffuse spikes and waves predominating in the frontal area. Several tonic seizures were recorded. A photoparoxysmal response was recorded on electroencephalogram with photic stimulation. Progressive but significant improvement of epilepsy was obtained with lamotrigine (250 mg per day) in addition to valproic acid (1200 mg per day, blood concentration: 63.6 mg/l). The epilepsy phenotype, close to Lennox-Gastaut syndrome, led to the sequencing of a 93-gene panel for monogenic epileptic disorders. Capture was performed with the SeqCap EZ kit (Roche, Madison, WI, USA) and sequencing on a NextSeq500 (Illumina, San Diego, CA, USA). Gene panel sequencing disclosed the presence of a heterozygous transition in CHD2 (NM_001271.3: c.4003G > T) that was predicted to produce a premature stop codon, p.(Glu1335*). (Fig. 2) This transition had not been reported previously in patients or in database of control individuals (gnomAD). Sanger sequencing from the patient and his parents confirmed the presence of the variant and indicated its de novo occurrence. (Fig. 3) The present truncating variation likely brought on non-mediated decay (NMD) so that no protein could be produced.
Discussion and conclusion
De novo heterozygous truncating or missense variations of CHD2 have been described in children with childhood-onset epileptic encephalopathy (OMIM # 615369) [6,7,8,9]. The growing access to genomic testing begets the continuous discovery of new, moderate phenotypes related to rare monogenic variants that were only associated at first with severe clinical pictures and variable expressivity of pathogenic rare variants is particularly well known in neuropsychiatric disorders  In that vein, pathogenic single-nucleotide variations or deletions of CHD2 have also been linked to intellectual deficiency and behavioral disorders, including autism spectrum disorders, attention-deficit hyperactivity disorder, and challenging behaviors [6, 11,12,13,14,15,16,17,18,19,20]. Bernardo et al., described the occurrence of severe behavioral disorders and aberrant emotional and affective complex aspects disrupting social functioning in a 27 years old woman with a CHD2 mutation . Veroeven et al. reported on short-lasting psychotic episodes eventually linked to an untreated absence epilepsy as it disappeared concomitantly with the introduction of valproic acid . Thomas et al. (2015) described the occurrence of schizophrenia in a 29-year-old patient with CHD2 mutation and myoclonic seizures during infancy . (Table 1) However, given the prevalence of schizophrenia during adulthood, no definitive link between CHD2 and schizophrenia could be established at that time. In the present case, schizophrenia had a childhood onset, inaugurated the clinical degradation and was not improved by valproic acid. Seizures were well controlled during psychosis onset, and in particular, no myoclonic fit was observed during this period. Furthermore, when seizures reoccurred, psychosis was still well controlled. Overall, these findings suggest that schizophrenic disorders likely belong to the clinical spectrum of CHD2 haploinsufficiency, as a distinct phenotype in association with epilepsy. This observation is in line with previous genome-wide association studies and rare variants studies that applied common pathways between schizophrenia, epilepsy, and intellectual deficiency [21,22,23]. To our knowledge, the 16p13.3 duplication affects genes that have not been related to neurodevelopment. However, we cannot exclude a modulating role of this copy number variation on the phenotype, as has previously been described for double-hit carrier patients [24, 25].
CHD2 encodes the chromatin organization modifier (chromodomain) helicase DNA-binding protein2 and a SNF2-related helicase/ATPase domain, involved in neurogenesis and chromatin organization [6, 26,27,28,29]. Chromodomains are highly evolutionary conserved among eukaryotes and interact with DNA conformation [30, 31]. Converging evidence has suggested a link between schizophrenia and epigenetic processes [32, 33]. However, most of our knowledge on this subject comes from in vivo animal studies, which are unable to reproduce the complexity of human mental disorders. In a murine model, CHD2 prevents suppressive chromatin formation in neurodevelopmentally regulated genes and allows the maintenance of embryonic stem cells in an undifferentiated state. It also remodels chromatin into a permissive state  via the replacement of histone H3 with histone H3.3 . In human embryonic stem cells, CHD2 haploinsufficiency seems to impair cortical interneurons specification, which may in turn lead to the electrophysiological dysfunction of these interneurons . The impairment of the local inhibition usually provided by these interneurons may be involved in the occurrence of epilepsy and schizophrenia in children with CHD2 haploinsufficiency. Interestingly Lamar suggests that, in a near future previously developed cancer drug such as Histone Deacetylase (HDAC) Inhibitors may be useful in neurological disease linked to CHD2 dysfunction . Given the data from this case report, schizophrenia might also benefit from such breakthrough in drugs development. Last but not least, to allow for better identification of schizophrenia cases associated with rare genetic disorders, the presence of warning signs (‘red flags’) would be greatly helpful [32, 33]. Previous data suggested that intolerance and resistance to psychotropic medication could be used as such red flags [35,36,37]. Based on the present case, we propose that schizophrenia onset before 13 years of age, visual hallucinations and resistant epilepsy should lead to genetic investigations. The role of pathogenic copy number variations in schizophrenia is now well established. We suggest that an exhaustive etiological investigation of patients with childhood onset schizophrenia, especially in the presence of other ‘red flags’ and in the absence of pathogenic copy number variation, should seek for intragenic pathogenic variants.
In conclusion, this case brings new elements in favor of a link between CHD2 and schizophrenia. It highlights that schizophrenia may be, in some cases, a Mendelian disorder. We propose that a childhood onset of schizophrenia should be considered as a red flag and should lead to systematic genetic investigations. This case also underlines that, in the absence of pathogenic copy number variations, the investigations should also include a search for pathogenic variations, which means that some patients with schizophrenia should benefit from Next Generation Sequencing tools. Last but not least, CHD2 encodes a member of the chromodomain helicase DNA-binding (CHD) family involved in chromatin remodeling. Thus, this observation adds schizophrenia to the phenotypic spectrum of chromodomain remodeling disorders, which may lead to innovative therapeutic approaches.
Chromodomain helicase DNA-binding
- CHD2 :
Chromodomain helicase DNA-binding 2
Ahn K, Gotay N, Andersen TM, Anvari AA, Gochman P, Lee Y, et al. High rate of disease-related copy number variations in childhood onset schizophrenia. Mol Psychiatry. 2014;19:568–72.
Ahn K, An SS, Shugart YY, Rapoport JL. Common polygenic variation and risk for childhood-onset schizophrenia. Mol Psychiatry. 2016;21:94–6.
Marshall CR, Howrigan DP, Merico D, Thiruvahindrapuram B, Wu W, Greer DS, et al. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nat Genet. 2017;49:27–35.
Stefansson H, Meyer-Lindenberg A, Steinberg S, Magnusdottir B, Morgen K, Arnarsdottir S, et al. CNVs conferring risk of autism or schizophrenia affect cognition in controls. Nat. 2014;505:361–6.
Kushima I, Aleksic B, Nakatochi M, Shimamura T, Okada T, Uno Y, et al. Comparative analyses of copy-number variation in autism Spectrum disorder and schizophrenia reveal etiological overlap and biological insights. Cell Rep. 2018;24:2838–56.
Carvill GL, Heavin SB, Yendle SC, McMahon JM, O'Roak BJ, Cook J, et al. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nat Genet. 2013;45:825–30.
Suls A, Jaehn JA, Kecskes A, Weber Y, Weckhuysen S, Craiu DC, et al. De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. Am J Hum Genet. 2013;93:967–75.
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet. 2012;380:1674–82.
Krupp DR, Barnard RA, Duffourd Y, Evans SA, Mulqueen RM, Bernier R, et al. Exonic mosaic mutations contribute risk for autism Spectrum disorder. Am J Hum Genet. 2017;101:369–90.
Moreno-De-Luca A, Myers SM, Challman TD, Moreno-De-Luca D, Evans DW, Ledbetter DH. Variable expressivity of pathogenic rare variants is well known in neuropsychiatric disorders. Lancet Neurol. 2013;12:406–14.
Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, Rajan D, et al. DECIPHER: database of chromosomal imbalance and phenotype in humans using Ensembl resources. Am J Hum Genet. 2009;84:524–33.
Verhoeven WM, Egger JI, Knegt AC, Zuydam J, Kleefstra T. Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2. Neuropsychiatr Dis Treat. 2016;12:1135–9.
O'Roak BJ, Stessman HA, Boyle EA, Witherspoon KT, Martin B, Lee C, et al. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nat Commun. 2014;5:5595.
McRae J, Clayton S, Fitzgerald T, Kaplanis J, Prigmore E, Rajan D, et al. Prevalence and architecture of de novo mutations in developmental disorders. Nat. 2017;542:433–8.
Chénier S, Yoon G, Argiropoulos B, Lauzon J, Laframboise R, Ahn JW, et al. CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. J Neurodev Disord. 2014;6:9.
Thomas RH, Zhang LM, Carvill GL, Archer JS, Heavin SB, Mandelstam SA, et al. CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures. Neurol. 2015;84:951–8.
Lebrun N, Parent P, Gendras J, Billuart P, Poirier K, Bienvenu T. Autism spectrum disorder recurrence, resulting of germline mosaicism for a CHD2 gene missense variant. Clin Genet. 2017;92:669–70.
Lund C, Brodtkorb E, Øye AM, Røsby O, Selmer KK. CHD2 mutations in Lennox-Gastaut syndrome. Epilepsy Behav. 2014;33:18–21.
Pinto AM, Bianciardi L, Mencarelli MA, Imperatore V, Di Marco C, Furini SE, et al. Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation. Brain and Development. 2016;38:590–6.
Bernardo P, Galletta D, Iasevoli F, D'Ambrosio L, Troisi S, Gennaro E, et al. CHD2 mutations: only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation. Seizure. 2017;51:186–9.
Li Z, Chen J, Yu H, He L, Xu Y, Zhang D, et al. Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. Nat Genet. 2017;49:1576–83.
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nat. 2014;506:185–90.
Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nat. 2014;511:421–7.
Vorstman JAS, Olde Loohuis LM, GROUP Investigators, Kahn RS, Ophoff RA. Double hits in schizophrenia. Hum Mol Genet. 2018;27:2755–61.
Jensen M, Kooy RF, Simon TJ, Reyniers E, Girirajan S, Tassone F. A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome. Eur J Med Genet. 2018;61:209–12.
Meganathan K, Lewis EMA, Gontarz P, Liu S, Stanley EG, Elefanty AG, et al. Regulatory networks specifying cortical interneurons from human embryonic stem cells reveal roles for CHD2 in interneuron development. Proc Natl Acad Sci U S A. 2017;114:E11180–9.
Liu JC, Ferreira CG, Yusufzai T. Human CHD2 is a chromatin assembly ATPase regulated by its chromo- and DNA-binding domains. J Biol Chem. 2015;290:25–34.
Nieto-Estevez V, Hsieh J. CHD2: One Gene. Many Roles Neuron. 2018;100:1014–6.
Lamar KJ, Carvill GL. Chromatin remodeling proteins in epilepsy: lessons from CHD2-associated epilepsy. Front Mol Neurosci. 2018;11:208.
de Dieuleveult M, Yen K, Hmitou I, Depaux A, Boussouar F, Bou Dargham D, et al. Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells. Nat. 2016;530:113–6.
Brehm A, Tufteland KR, Aasland R, Becker PB. The many colours of chromodomains. BioEssays. 2004;26:133–40.
Piton A, Gauthier J, Hamdan FF, Lafrenière RG, Yang Y, Henrion E, et al. Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia. Mol Psychiatry. 2001;16:867–80.
Gilman SR, Chang J, Xu B, Bawa TS, Gogos JA, Karayiorgou M, et al. Diverse types of genetic variation converge on functional gene networks involved in schizophrenia. Nat Neurosci. 2012;15:1723–8.
Semba Y, Harada A, Maehara K, Oki S, Meno C, Ueda J, et al. Chd2 regulates chromatin for proper gene expression toward differentiation in mouse embryonic stem cells. Nucleic Acids Res. 2017;45:8758–72.
Poisson A, Schluth Bolard C, Martin B, Babinet MN, Sanlaville D, Demily C. 16q12.2q21: a new susceptibility locus for schizophrenia? Schizophr Res. 2016;178:109–11.
Poisson A, Favre E, Peyroux E, Nicolas A, Schlutz Bolard C, Demily C. An ambiguous psychiatric diagnosis resolved by genetic investigations. Schizophr Res. 2018;195:577–8.
Kushima I, Aleksic B, Nakatochi M, Shimamura T, Shiino T, Yoshimi A, et al. High-resolution copy number variation analysis of schizophrenia in Japan. Mol Psychiatry. 2017;22:430–40.
We thank the patient and family for their agreement for this publication. We also thank the Vinatier Hospital and Ms. Chantal Silarakis from Lyon University Hospital’s library.
Availability of data and material
The variant have been submitted to ClinVar (accession number: RCV000856837.1).
Ethics approval and consent to participate
The French Ethic committee CPP (Comité pour la Protection des Personnes) Sud Est IV gave its approval for the study (ID-RCB: 2015-A01992–47, CPP: 16/005). The patient and his parents gave their written consent to participate.
Consent for publication
The patient and his parents gave their written consent for publication.
The authors declare that they have no competing interests.
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Cite this article
Poisson, A., Chatron, N., Labalme, A. et al. Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report. BMC Med Genet 21, 10 (2020). https://doi.org/10.1186/s12881-019-0946-0
- Childhood onset schizophrenia
- Genetic counselling
- Chromodomain helicase DNA-binding