Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

  • Claire Amiet1, 2,

    Affiliated with

    • Isabelle Gourfinkel-An3, 4,

      Affiliated with

      • Claudine Laurent1, 5,

        Affiliated with

        • Nicolas Bodeau1,

          Affiliated with

          • Bérengère Génin2,

            Affiliated with

            • Eric Leguern3, 4,

              Affiliated with

              • Sylvie Tordjman6 and

                Affiliated with

                • David Cohen1, 7Email author

                  Affiliated with

                  Molecular Autism20134:47

                  DOI: 10.1186/2040-2392-4-47

                  Received: 3 April 2013

                  Accepted: 13 September 2013

                  Published: 1 December 2013

                  Abstract

                  Background

                  Autism spectrum disorders (ASD) and epilepsy frequently occur together. Prevalence rates are variable, and have been attributed to age, gender, comorbidity, subtype of pervasive developmental disorder (PDD) and risk factors. Recent studies have suggested disparate clinical and genetic settings depending on simplex or multiplex autism. The aim of this study was to assess: 1) the prevalence of epilepsy in multiplex autism and its association with genetic and non-genetic risk factors of major effect, intellectual disability and gender; and 2) whether autism and epilepsy cosegregate within multiplex autism families.

                  Methods

                  We extracted from the Autism Genetic Resource Exchange (AGRE) database (n = 3,818 children from 1,264 families) all families with relevant medical data (n = 664 children from 290 families). The sample included 478 children with ASD and 186 siblings without ASD. We analyzed the following variables: seizures, genetic and non-genetic risk factors, gender, and cognitive functioning as assessed by Raven’s Colored Progressive Matrices (RCPM) and Vineland Adaptive Behavior Scales (VABS).

                  Results

                  The prevalence of epilepsy was 12.8% in cases with ASD and 2.2% in siblings without ASD (P <10-5). With each RCPM or VABS measure, the risk of epilepsy in multiplex autism was significantly associated with intellectual disability, but not with gender. Identified risk factors (genetic or non-genetic) of autism tended to be significantly associated with epilepsy (P = 0.052). When children with prematurity, pre- or perinatal insult, or cerebral palsy were excluded, a genetic risk factor was reported for 6/59 (10.2%) of children with epilepsy and 12/395 (3.0%) of children without epilepsy (P = 0.002). Finally, using a permutation test, there was significant evidence that the epilepsy phenotype co-segregated within families (P <10-4).

                  Conclusions

                  Epilepsy in multiplex autism may define a different subgroup in terms of clinical characteristics and genetic risk.

                  Keywords

                  Autism Multiplex pedigree Epilepsy Intellectual disability

                  Background

                  Autism spectrum disorders (ASD) and epilepsy frequently occur together. Approximately 5% to 40% of individuals with autism have epilepsy [1], whereas the prevalence of epilepsy in the general population is about 0.5% to 1%. Conversely, 5% to 30% of individuals with epilepsy have ASD [25], whereas the prevalence of ASD in the general population is about 1/150; although recent studies reached even higher rates: 1/80 [6]. The variability of prevalence rates have been attributed to the heterogeneity of samples with respect to age, gender, comorbidity, subtype of ASD, intellectual disability and risk factors [7, 8]. It may also result from the criteria used to diagnose epilepsy. Finally, the genetic background of autism may have a considerable impact on epilepsy rates in autism.

                  Recently, a meta-analysis of 24 reports on autism and epilepsy confirmed intellectual disability and female gender as major risk factors of epilepsy in autism [9]. The pooled prevalence of epilepsy was 21.4% in individuals with autism and intellectual disability versus 8% in individuals with autism without intellectual disability, and the more severe the intellectual disability, the more prevalent the epilepsy. With a male:female ratio of 2, the risk of epilepsy was found significantly higher for females [9]. However, this might reflect the known circumstance that females with autism tend to be more severely mentally disabled [10].

                  Autism and epilepsy are both complex and heterogeneous disorders. Recent literature reviews underline the important role of genetic factors in the etiology of ASD [1113]. Rare chromosomal abnormalities (for example maternally inherited duplications of chromosome 15q11–q13) and single gene syndromes (for example fragile X, tuberous sclerosis) are important risk factors of ASD. More recently, individual genes of major effect have been identified by resequencing or array-based methods, but variants at these and other loci are present in no more than 1% to 2% of children with ASD [14]. Some of these genes with major effects have been associated with ASD, intellectual disability and/or seizures, suggesting that the three disorders may share common genetic risk factors (Table 1). Recent whole genome DNA microarray studies have identified submicroscopic duplications and deletions (copy number variations (CNVs) located in many loci and mostly including de novo events) in the same developmental disorders (ASD, intellectual disability, epilepsy), and in schizophrenia as well [1517] (Table 2).
                  Table 1

                  Genes implicated in autism, epilepsy and/or intellectual disability

                  Gene

                  Locus

                  Mutation

                  Transmission

                  Phenotype

                  Protein

                  Reference(s)

                  SCN1A

                  2q24

                  Point mutation

                  De novo

                  ASD, E, ID

                  Nav1.1 (Na+ channel)

                  [1820]

                  Deletion

                  Dominant inheritance

                  SCN2A

                  2q23–q24.3

                  Deletion

                  De novo

                  ASD, E, ID

                  Nav1.2 (Na+ channel)

                  [2022]

                  Point mutation

                  Inherited

                  SCN3A

                  2q24

                  Deletion

                  De novo

                  E, ID

                  Nav1.3 (Na+ channel)

                  [23, 24]

                  SCN1B

                  19q13.1

                  Point mutation

                  Dominant inheritance

                  E

                  β1 subunit (Na+ channel)

                  [25]

                  KCNA1

                  12p13

                  Point mutation

                  Dominant inheritance

                  E, ID

                  Kv1.1 (K+ channel)

                  [26, 27]

                  KCNQ2

                  20q13.3

                  Point mutation

                  Dominant inheritance

                  E, ID

                  KV7.2 (K+ channel)

                  [28, 29]

                  Deletion

                  De novo

                  KCNQ3

                  8q24

                  Point mutation

                  Not known

                  E

                  KV7.3 (K+ channel)

                  [30]

                  KCNMA1

                  10q22

                  Point mutation

                  Dominant inheritance

                  ASD, E, ID

                  KCa1.1 (K+ channel)

                  [31, 32]

                  De novo

                  CACNA1A

                  19p13

                  Point mutation

                  De novo

                  E, ID

                  CaV2.1 (Ca2+ channel)

                  [33]

                  Dominant inheritance

                  GABRA1

                  5q34–q35

                  Point mutation

                  Dominant inheritance

                  E

                  Α1 subunit (GABAA receptor)

                  [34]

                  GABRG2

                  5q34

                  Point mutation

                  Dominant inheritance

                  E, ID

                  γ subunit (GABAA receptor)

                  [35, 36]

                  CHRNA2

                  8p21

                  Point mutation

                  Dominant inheritance

                  E

                  α2 subunit (nACh receptor)

                  [37]

                  CHRNA4

                  20q13.2–q13.3

                  Point mutation

                  Dominant inheritance

                  E, ID

                  α4 subunit (nACh receptor)

                  [38, 39]

                  De novo

                  CHRNB2

                  1q21

                  Point mutation

                  Dominant inheritance

                  E

                  β2 subunit (nACh receptor)

                  [40]

                  De novo

                  NLGN3

                  Xq13.1

                  Point mutation

                  Inherited

                  ASD

                  Inhibitory synapse formation

                  [41]

                  NLGN4

                  Xp22.31

                  Point mutation

                  Inherited

                  ASD, ID

                  Synapse formation

                  [41, 42]

                  Deletion

                  CDH8

                  16q21

                  Deletion

                  Inherited

                  ASD

                  Synapse formation

                  [43]

                  PCDH10

                  4q28.3

                  Deletion

                  Inherited

                  ASD

                  Synapse formation

                  [44]

                  PCDH19

                  Xq22

                  Deletion

                  De novo

                  E, ID

                  Synapse formation

                  [45]

                  Point mutation

                  Inherited

                  NRXN1

                  2p16.3

                  Deletion

                  Recessive inheritance

                  ASD, E, ID, SCZ

                  Synapse formation

                  [4648]

                  Point mutation

                  De novo

                  CNTNAP2

                  7q35

                  Deletion

                  Recessive inheritance

                  ASD, E, ID, SCZ

                  Synapse formation

                  [4951]

                  Point mutation

                  De novo

                  SHANK2

                  11q13.4

                  Deletion

                  De novo

                  ASD, ID

                  Synapse scaffolding

                  [52]

                  Point mutation

                  Inherited

                  SHANK3

                  22q13.3

                  Deletion

                  De novo

                  ASD, ID, SCZ

                  Synapse scaffolding

                  [53, 54]

                  Point mutation

                  Inherited

                  SYNGAP1

                  6p21.3

                  Point mutation

                  De novo

                  ASD, E, ID

                  Synapse RasGAP

                  [55, 56]

                  Deletion

                  Inherited, de novo

                  CDKL5

                  Xp22

                  Point mutation

                  De novo

                  E, ID

                  Cyclin-dependent kinase-like 5

                  [57, 58]

                  Deletion

                  Inherited

                  ARX

                  Xp22.13

                  Duplication

                  Inherited

                  ASD, E, ID

                  Aristaless-related homeobox protein

                  [59, 60]

                  De novo

                  ATP1A2

                  1q21–23

                  Point mutation

                  Dominant inheritance

                  E, ID

                  Sodium-potassium ATPase

                  [61, 62]

                  SLC2A1

                  1p35–p31.1

                  Deletion

                  Dominant inheritance

                  E, ID

                  GLUT1

                  [63]

                  Point mutation

                  De novo

                     

                  Recessive inheritance

                  STXBP1

                  9q34.1

                  Point mutation

                  Inherited

                  E, ID

                  Syntaxin-binding protein

                  [64]

                     

                  De novo

                     

                  Adapted from Betancur [15] and Amiet [65]. ASD, autism spectrum disorders; E, epilepsy; GABA, γ-aminobutyric acid; GLUT1, glucose transporter type 1; ID, intellectual disability; nACh, nicotinic acetylcholine; RasGAP, Ras GTPase activating protein; SCZ, schizophrenia.

                  Table 2

                  Copy number variations (CNVs) associated with autism spectrum disorders (ASD), epilepsy, intellectual disability and schizophrenia

                  Cytoband

                  Maximum coordinates

                  Phenotype

                  Deletion/duplication

                  References

                  1q21.1

                  144.9–146.2

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [16, 6675]

                  3q29

                  197.1–198.9

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [16, 7481]

                  7q11.23

                  71.9–74.2

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [69, 75, 8289]

                  15q11.2–13.1

                  21.1–26.2

                  ASD, E, ID, SCZ

                  Duplication

                  [68, 69, 72, 83, 90, 91]

                  15q13.3

                  28.2–30.7

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [16, 6872, 75, 83, 92100]

                  16p11.2

                  29.4–30.1

                  ASD, E, ID, SCZ

                  Duplication

                  [16, 68, 74, 75, 83, 101107]

                  16p11.2

                  29.4–30.1

                  ASD, E, ID

                  Deletion

                  [68, 83, 92, 101, 102, 104110]

                  16p13.11

                  14.6–18.7

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [68, 69, 72, 73, 81, 90, 92, 111114]

                  17q12

                  31.5–33.1

                  ASD, E, ID, SCZ

                  Deletion/duplication

                  [73, 81, 115117]

                  22q11.2

                  16.9–20.6

                  ASD, E, ID, SCZ

                  Deletion

                  [16, 68, 69, 71, 72, 80, 92, 101],[118, 119]

                  Adapted from Betancur [15], Johnson and Shorvon [17], and Levinson et al.[120]. ASD, autism spectrum disorders; CNV, copy number variation; E, epilepsy; ID, intellectual disability; SCZ, schizophrenia.

                  However, all together, an identified genetic etiology is estimated to account for 10% to 20% of ASD cases [15]. Therefore, in the majority of epilepsy cases, most autism appears to be a multifactorial hereditary disorder, depending on polygenic heredity and environmental factors Environmental factors associated with autism are mainly pre-, peri- and postnatal, such as in utero exposure to teratogenic medications (for example thalidomide, valproate) [121], prematurity, neonatal encephalopathy and hyperbilirubinemia [122].

                  Most of the samples studied in autism are composed of autistic individuals without information about whether autism affects only one individual in the family (simplex autism) or multiple siblings in the family (multiplex autism). This is a major issue since higher genetic risk may be hypothesized in multiplex autism. Some recent studies have suggested disparate clinical and genetic settings depending on simplex or multiplex autism. More de novo rare mutations in genes of major effect have been associated with simplex autism [108], while an interactive effect of multiple common susceptibility alleles have long been hypothesized as risk factors of familial autistic syndromes [123, 124]. Whether some clinical variables may help to delineate more homogeneous subgroups in multiplex autism remains an open question. Regarding epilepsy and ASD, only one study specified that part of the sample included individuals with multiplex autism [125]. However, there was no separate analysis of these two groups except to observe that a similar incidence of electroencephalogram (EEG) abnormalities was found. Banach et al. examined gender differences and intellectual quotients (IQs), and found no difference in non-verbal IQ between females and males in multiplex families, while females had lower non-verbal IQ scores than males in simplex families [126]. However, the prevalence of major effect genetic risk factors as a function of epilepsy, intellectual disability and gender in multiplex families remains unknown.

                  The aims of the current study are: 1) to assess the prevalence of seizures in multiplex autism and compare it to the prevalence of siblings without ASD. Since autism and epilepsy share common genetic risk factors, we hypothesize a higher risk of epilepsy in individuals with autism than siblings without ASD; 2) to compare the prevalence of major effect genetic risk factors in multiplex autism with and without epilepsy. We hypothesize the group with epilepsy to have an increased risk; 3) to assess whether autism and epilepsy co-segregate within multiplex autism families; and 4) to assess whether higher prevalence of epilepsy in multiplex autism is mediated by intellectual disability and gender as it has been shown in the literature [9].

                  Methods

                  Participants

                  Data were ascertained from all families participating in the Autism Genetic Resource Exchange (AGRE) in September 2011. Families with two or more members diagnosed with autism, pervasive developmental disorder-not otherwise specified (PDD-NOS) or Asperger syndrome may enroll in the AGRE program. Families register to the program then AGRE recruitment staff follow-up with families to confirm eligibility and complete the intake process. Families were excluded from the AGRE program if they had participated in another genetic study, a confirmed neurogenetic disorder, a pre- or perinatal injury, prematurity defined as delivery before 35 weeks of gestational age for single births or before 33 weeks of gestational age for twin births, a known chromosomal abnormality, or an abnormal neurological examination.

                  The diagnosis of autism was made using the standard Autism Diagnostic Interview-Revised (ADI-R) [127] with three affected status categories based on ADI-R results: autism, not quite autism (NQA) and broad spectrum. In the current report, we fused the last two categories as PDD-NOS. To meet the criteria for autism, the individual must exceed the ADI-R cutoff for autism in all domains. Children meeting the following criteria were classified as PDD-NOS: 1a) must meet cutoff scores for autism on the three core domains (social, communication, behavior) but not on the age of onset domain, or 1b) must be no more than one point below the cutoff score on any of the three core domains, while also meeting the cutoff for the age of onset domain; and 2) must meet one or more of the following: a) show a severe deficit in at least one domain, b) show more moderate deficits in at least two domains, and/or c) show only minimal deficits in all three domains.

                  The AGRE database consisted of 3,819 children from 1,264 families. We excluded the 3,150 children (1,837 children with autistic disorder, 226 children with PDD-NOS and 1,087 children without autism) whose clinical data gave no information about the presence or absence of epileptic seizure. We excluded five more individuals who were reported by their family with a diagnosis of Asperger syndrome without any ADI-R available. We included the 664 children from 290 families (417 children with autistic disorder, 61 children with PDD-NOS and 186 children without autism) whose characteristics are discussed below. We found no significant differences between excluded and included individuals for age at ADI-R clinical assessment (mean (± SD)) (8.5 years (± 4.9) versus 8.1 years (± 4.7), respectively; P = 0.098), gender (68.1% versus 69.7% of boys, respectively; P = 0.43) and Raven’s nonverbal IQ (100.2 (± 19.3) versus 99.8 (± 18), respectively; P = 0.76). We found a significant difference in the percentage of autistic disorder, PDD-NOS and unaffected children (P = 0.002), but the difference accounted for a higher percentage of unaffected children in the excluded sample (34.6% versus 28.0%). In contrast with Raven’s nonverbal IQ, we found a significant difference for Vineland composite standard score (62.6 (± 21.6) versus 54.4 (± 20.4), respectively; P <10-10).

                  Measures

                  Data relevant to epilepsy

                  Most of the AGRE families had an extensive evaluation by pediatricians, psychiatrists and/or neurodevelopmental specialists in order to obtain medical and family history information. Data relevant to epilepsy were extracted from probands, and unaffected children’s medical history files were provided by the AGRE database. These data were collected through a standardized method by AGRE and consist of the occurrence or not of afebrile seizures or remote febrile seizures, the age of onset, and the number of seizures and their type. After extraction from the AGRE database, data were reviewed by a neurologist and three groups were formed: epilepsy, remote febrile seizures (meaning febrile seizures with an identified antecedent classified as a risk factor for epilepsy) and only one seizure. Epilepsy was defined as two or more afebrile seizures.

                  Genetic and non-genetic risk factors of autism

                  For each of the 478 included individuals with ASD, we determined whether there were known genetic and non-genetic risk factors of autism. Despite the exclusionary criteria described above, the database flags: 1) possible syndromic autism based on clinical (significant dysmorphology, abnormal neurologic exams) and morphologic criteria (abnormal imaging or medical tests); and 2) pre- or perinatal injuries and prematurity (defined as delivery before 35 weeks of gestational age for single births and before 33 weeks of gestational age for twin births). Also noted were: comorbid medical or psychiatric disorders and genetic abnormalities identified by clinical genetic investigation [128]. Most of the families of the AGRE dataset were screened for fragile X syndrome using PCR technique. About half of the AGRE families had been karyotyped, and 228 (47.7%) were analyzed for small nuclear ribonucleoprotein polypeptide N (SNRPN) duplication at 15q12 and 393 for telomere analyses for small-scale deletions and duplications. A sample of 943 families was genotyped using the HumanHap550 BeadChip (Illumina, San Diego, CA, USA) [129] and a sample of 777 families was genotyped using the 5.0 Chip (Affymetrix, Santa Clara, CA, USA) [130]. The details of these screenings are available on the AGRE website (http://​www.​agre.​org).

                  Of the 664 children included in this analysis, 35 (5.3%) children from 33 families (31 children with autistic disorder, two children with PDD-NOS and two children without autism) were flagged as having strong risk factors for both autism and seizures: pre- or perinatal insult, prematurity before 35 weeks of gestational age (19 children), chromosomal abnormality (eight children with a known trisomy, translocation or inversion, and one child with significant dysmorphology), or an abnormal neurological or cerebral imaging examination (seven children). We found no significant differences between these children and their siblings and the children with no flag for age on ADI-R clinical assessment (P = 024), gender (P = 0.42), mean Raven’s non-verbal IQ (P = 0.17), mean Vineland composite standard score (P = 0.80), or the percentage of autistic disorder, PDD-NOS and unaffected children (P = 0.17).

                  Raven’s Colored Progressive Matrices (RCPM)

                  Non-verbal intellectual capacity was measured by Raven’s Colored Progressive Matrices (RCPM) [131]. The RCPM is a standardized test designed to measure non-verbal intellectual capacity in children from the age of 5 years. Scores on the RCPM correlate highly with scores on tests of general intellectual capacity [132]. The RCPM consist of 36 items, presented in three sets of 12, which become progressively more difficult. Each item contains a pattern problem with one part removed and six pictured potential inserts, one of which contains the correct pattern. The number of correct answers is transformed to a non-verbal IQ score based on age-dependent normative data.

                  Vineland Adaptive Behavior Scales (VABS)

                  The adaptive functioning level was assessed by the Vineland Adaptive Behaviors Scales (VABS). The VABS is a semi-structured parental interview that evaluates adaptive functioning in four domains: communication, daily living skills, socialization and motor skills. Age equivalent scores and standard scores are provided for each domain. Scores across domains can be combined to create an overall adaptive behavior composite standard score. Depending on the time of inclusion in AGRE, one of the two forms of the VABS was used: the survey form [133] and the second edition of the VABS (Vineland II) [134]. For the purposes of the current study, the overall adaptive behavior composite standard score was used.

                  Statistical analysis

                  R software, version 2.12.2, was used for the statistical analysis. First, we compared affected individuals with individuals without epilepsy. Fisher’s exact test was used for analysis of the association between the qualitative variables. A Student’s t-test was used for the analysis of the association between the quantitative variables and the group variables. Second, we tested whether epilepsy co-segregated within families. To do so, from the 290 families, we first extracted the 179 families in which pairs of two affected siblings had a complete dataset for epilepsy, since permutation tests cannot be applied on missing data. Each sib-pair was designated either concordant or discordant for epilepsy status. In each of the 20,000 permutations, the individuals with epilepsy were randomly assigned among the 179 families, and the resulting number of concordant sib-pairs was recorded. The P value is the fraction of permutation in which the number of concordant sib-pairs exceeded the number in the observed data. Third, admixture analysis was used to determine the best-fit model for the age at onset of seizure in ASD. Given the literature, we hypothesized a model with two subgroups, including one with seizure onset before the age of 5 years and another with seizure onset close to adolescence. Finally, a multivariate analysis (logistic regression) was performed to assess which variables contribute to the risk of seizures.

                  To assess whether the inclusion of the 35 children from 33 families who were flagged with strong risk factors for autism and seizures biased our results, we performed secondary analyses excluding all families with such children. These analyses were performed on 586 children from 257 families who had medical data about presence or absence of epilepsy: 362 (61.8%) children with autistic disorder, 53 (9%) children with PDD-NOS and 171 (29.2%) children without autism.

                  Results

                  Primary analyses were performed on 664 children from 290 families who had informative data about presence or absence of epilepsy: 417 (62.8%) children with autistic disorder, 61 (9.2%) children with PDD-NOS and 186 (28%) children without autism (Table 3). Secondary analyses were performed on 586 children from 257 families after exclusion of children with strong risk factors for autism and seizures.
                  Table 3

                  Sample characteristics and prevalence of epilepsy according to clinical status

                  Characteristics

                  Autistic disorder

                  PDD-NOS

                  Total (ASD)

                  Siblings without autism

                  Total (n)

                  417

                  61

                  478

                  186

                  Gender (male/female)

                  334/83

                  48/13

                  382/96

                  81/105

                  Mean age (years)

                  9.33 (± 5.02)

                  8.67 (± 5.01)

                  9.24 (± 5.02)

                  10.56 (± 6.59)

                  Epilepsy

                  56 (13.4%)

                  5 (8.2%)

                  61 (12.8%)

                  4 (2.2%)

                  Remote febrile seizures

                  16 (3.8%)

                  6 (9.8%)

                  22 (4.6%)

                  5 (2.7%)

                  One afebrile seizure

                  14 (3.4%)

                  0 (0%)

                  14 (2.9%)

                  1 (0.5%)

                  Risk factors for ASD

                  39 (9.6%)

                  3 (5.4%)

                  42 (8.8%)

                  0

                  Risk factors for ASD and comorbid seizures

                  10 (2.5%)

                  0

                  10 (2.2%)

                  0

                  Performed on 664 children and 290 families. ASD, autism spectrum disorders; PDD-NOS, pervasive developmental disorder-not otherwise specified.

                  Prevalence and type of epilepsy

                  The prevalence of epilepsy was 13.4% (56/417) among cases with an autistic disorder, 8.2% (5/61) among cases with PDD-NOS and 2.2% (4/186) among siblings without autism (P <10-4). The risk of epilepsy was sevenfold higher for children with ASD (autistic disorder or PDD-NOS) when compared with their siblings without ASD (odds ratio (OR) = 0.15; 95% confidence interval (CI): 0 to 0.4; P <10-5). The prevalence of remote febrile seizures was 4.6% (22/478) in cases with an ASD and 2.7% (5/186) in siblings without ASD (OR = 1.75; 95% CI: 0.63 to 5.99; P = 0.38). The prevalence of one afebrile seizure was 14/478 (2.9%) in cases with an ASD and 0.5% (1/186) in siblings without ASD (OR = 5.57; 95% CI: 0.84 to 237.1; P = 0.08). Secondary analyses excluding children with strong risk factors for autism and seizures yielded similar results: the prevalence of epilepsy was 12.2% (44/362) in cases with an autistic disorder, 5.7% (3/53) in cases with PDD-NOS and 2.3% (4/171) in siblings without autism (P = 0.0002).

                  The mean age of children with ASD was 9.2 years (± 5.0) at the time of their clinical assessment. Children with ASD and epilepsy were significantly older (mean age: 12.8 years ± 8.6) than children with ASD without epilepsy (mean age: 8.7 years ± 4.0) (P <10-8). Mean age of the first seizure was 4.7 years (± 3.8). Figure 1 summarizes the distribution of seizure onset according to age. Given the 4-year older age of children with epilepsy, the distribution of age of individuals with ASD without epilepsy, and of individuals with ASD and epilepsy, is also given. As several reports showed that there may be distinct ages at onset of subgroups among individuals with epilepsy, we conducted an admixture analysis to test whether the observed distribution for age at onset in individuals with ASD and seizure (n = 55) was a mixture of Gaussian distributions. A parametric bootstrap with B = 500 replications of the likelihood ratio statistic was performed for testing the null hypothesis of a one-component fit versus the alternative hypothesis of a two-component fit. The result was significant (P <0.001) and therefore the model with two components was adequate. The mean ages estimated in this model were 2.3 years (± 1.3) and 8.3 years (± 3.5) (Figure 2). All types of seizures were reported in children with autism and epilepsy (n = 61): 12 (19.7%) children had generalized seizures, 17 (27.9%) children had absences, 14 (23.0%) children had complex partial seizures, 11 (18.0%) children had multiple seizure types, and the type of seizure was unknown for seven (11.5%) children.
                  http://static-content.springer.com/image/art%3A10.1186%2F2040-2392-4-47/MediaObjects/13229_2013_Article_97_Fig1_HTML.jpg
                  Figure 1

                  Distribution of age of first seizure, age of individuals with ASD and epilepsy, and age of individuals with ASD without epilepsy. Age of first seizure (n = 55, black), age of individuals with ASD and epilepsy (n = 61, green or grey), and age of individuals with ASD without epilepsy (n = 417, white and blue). ASD, autism spectrum disorders.

                  http://static-content.springer.com/image/art%3A10.1186%2F2040-2392-4-47/MediaObjects/13229_2013_Article_97_Fig2_HTML.jpg
                  Figure 2

                  Theoretical distribution of ages of onset of seizures for 55 individuals with comorbid multiplex autism with epilepsy. Distribution shows two subgroups with early onset of seizures (mean = 2.3 years (± 1.3)) and late onset of seizures (mean = 8.3 years (± 3.5)). A parametric bootstrap with B = 500 replications of the likelihood ratio statistic was performed for testing the null hypothesis of a one-component fit versus the alternative hypothesis of a two-component fit. The result was significant (P = 0) and therefore the model with two components was adequate.

                  Secondary analyses excluding children with strong risk factors for autism and seizures yielded similar results: mean age of ASD children = 9.1 years (± 4.7); mean age of ASD and epilepsy children = 12.4 years (± 7.0) versus mean age of ASD children without epilepsy = 8.7 years (± 4.1) (P <10-6); mean age at the first seizures = 5.2 years (± 4.1); similar proportions of generalized seizures (21.3%), absences (27.7%), complex partial seizures (23.4%), multiple seizures types (19.1%), and unknown (8.5%).

                  Co-segregation analyses and prevalence of genetic and non-genetic risk factors as a function of epilepsy

                  Of the 478 children with ASD, 464 (97.1%) children underwent genetic testing (karyotyping and/or array comparative genomic hybridization (aCGH), and/or genome-wide association (GWA)). A total of 42 (8.8%) children had a known possible genetic or non-genetic risk factor for autism (39 children with autistic disorder, three children with PDD-NOS; Table 4). In decreasing frequency, we found prematurity and/or pre- or perinatal insult (n = 19), chromosomal abnormality (n = 14), abnormal cerebral imaging or significant developmental abnormality (n = 3), comorbid medical disease associated with ASD (n = 4), and cerebral palsy (n = 2). An epilepsy was reported for ten children (all had autistic disorder). Genetic or non-genetic risk factors of autism tended to be significantly associated with epilepsy (OR = 2.25; 95% CI: 0.93 to 5.04; P = 0.052). When children with prematurity, pre- or perinatal insult, or cerebral palsy were excluded, a known or possible genetic risk factor was reported for 10.2% (6/59) of children with epilepsy and 3.0% (12/395) of children without epilepsy (OR = 3.6; 95% CI: 1.06 to 10.9; P = 0.02).
                  Table 4

                  Risk factors of autism in the AGRE sample according to epilepsy

                  Risk factors

                   

                  Total (n)

                  Epilepsy (n)

                  No epilepsy (n)

                  Total of individuals

                  478

                  63

                  415

                  Chromosomal abnormality or genetic condition

                  14 (2.92%)

                  4 (6.35%)

                  10 (2.4%)

                   

                  16p11.2 deletion/duplication

                  4

                  2

                  2

                   

                  15q11–13 duplication

                  3

                  1

                  2

                   

                  22q11.21 duplication

                  1

                  0

                  1

                   

                  22q13.33 duplication

                  1

                  0

                  1

                   

                  t(2;9)(p13;q34.3)

                  1

                  1

                  0

                   

                  Mosaic t(3;16)

                  1

                  0

                  1

                   

                  Mosaic t(3;14)

                  1

                  0

                  1

                   

                  Trisomy 21

                  1

                  0

                  1

                   

                  Mosaic trisomy 12

                  1

                  0

                  1

                  Prematuritya/pre- or perinatal insult

                  19 (3.98%)

                  3 (4.76%)

                  16 (3.9%)

                  Cerebral palsy

                   

                  2 (0.42%)

                  0

                  2 (0.48%)

                  Abnormal cerebral imaging

                  3 (0.63%)

                  2 (3.17%)

                  1 (0.24%)

                   

                  Agenesis of corpus callosum

                  1

                  1

                  0

                   

                  Left frontal damage

                  1

                  1

                  0

                   

                  Not given

                  1

                  0

                  1

                  Other significant abnormality

                  4 (0.84%)

                  1 (1.59%)

                  3 (0.72%)

                   

                  Significant dysmorphology

                  2

                  0

                  2

                   

                  Mitochondrial disorder, mild tonsillectomy (premature puberty)

                  1

                  1

                  0

                   

                  Cranial nerve paralysis (congenital versus traumatic)

                  1

                  0

                  1

                  Total of individuals with abnormalitiesb

                  42 (8.8%)

                  10 (15.9%)

                  32 (7.71%)

                  aDefined as delivery before 35 weeks of gestational age for single births or before 33 weeks of gestational age for twin births; bP = 0.052. AGRE, Autism Genetic Resource Exchange.

                  Finally, there was significant evidence that epilepsy co-segregated within autism sib-pairs. Indeed, among the 179 families with sib-pairs affected by ASD, we found 154 sib-pairs concordant (meaning both siblings with ASD had epilepsy or did not have epilepsy) for associated epilepsy, while 25 sib-pairs were discordant (permutation: P <10-4). Secondary analyses excluding children with strong risk factors for autism and seizures yielded similar results: among the 155 families with sib-pairs affected by ASD, we found 132 sib-pairs concordant for associated epilepsy, while 23 sib-pairs were discordant (permutation test: P = 0.0049). Table 5 details the 11 AGRE families with two children with ASD and comorbid epilepsy, showing clinical status, type of seizure and known risk factors in all siblings.
                  Table 5

                  AGRE families with two children with ASD and comorbid epilepsy (n = 11): clinical status, type of seizures and risk factors in all siblings a

                  Family

                  Gender

                  Autism diagnosis

                  Type of seizureb

                  Risk factor of ASD and/or epilepsy

                  AU0025

                  M

                  Autism

                  Partial

                  Mitochondrial disorder, mild tonsillectomy (premature puberty)

                   

                  M

                  Autism

                  Multiple

                  No risk reported

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                  AU0051

                  M

                  Autism

                  Absence

                  No risk reported

                   

                  M

                  Autism

                  Absence

                  Agenesis of corpus callosum

                  AU0123

                  F

                  Autism

                  Partial

                  Prematurityc/pre- or perinatal insult

                   

                  M

                  Autism

                  Multiple

                  Unknown

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                  AU0176

                  F

                  Autism

                  Partial

                  No risk reported

                   

                  M

                  Autism

                  Partial

                  No risk reported

                   

                  M

                  Unaffected

                  No seizure

                  Unknown

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                  AU0275

                  M

                  Autism

                  Multiple

                  No risk reported

                   

                  M

                  Autism

                  Not indicated

                  Unknown

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                  AU0461

                  M

                  Autism

                  Generalized

                  No risk reported

                   

                  M

                  Autism

                  Generalized

                  Unknown

                  AU0548

                  F

                  Autism

                  Absence

                  No risk reported

                   

                  M

                  Autism

                  Not indicated

                  No risk reported

                   

                  F

                  Unaffected

                  No seizure

                  Unknown

                  AU0731

                  M

                  Autism

                  Generalized

                  Prematurityc/pre- or perinatal insult

                   

                  M

                  PDD-NOS

                  Not indicated

                  Unknown

                  AU0765

                  M

                  Autism

                  Absence

                  Unknown

                   

                  F

                  PDD-NOS

                  Not indicated

                  t(2;9)(p13;q34.3)

                   

                  M

                  Unaffected

                  No seizure

                  Unknown

                  AU0922

                  M

                  Autism

                  Partial

                  No risk reported

                   

                  F

                  Autism

                  Partial

                  Unknown

                  AU1208

                  M

                  Autism

                  Multiple

                  15q11–13 duplication

                   

                  M

                  Autism

                  Absence

                  Unknown

                  aFrom the 154 families included in the co-segregation analysis, the families with ASD children and without epilepsy are not detailed in this table; bnot indicated means that the type of seizures was not given in the AGRE database, although the patient exhibits epilepsy; cdefined as delivery before 35 weeks of gestational age for single births or before 33 weeks of gestational age for twin births. AGRE, Autism Genetic Resource Exchange; ASD, autism spectrum disorders; PDD-NOS, pervasive developmental disorder-not otherwise specified.

                  Epilepsy and non-verbal IQ/adaptive level

                  Given the heterogeneity of general cognitive function in ASD, we used two measures to assess whether epilepsy was associated with intellectual disability in multiplex autism. An assessment with the RCPM was applied to 438 children with ASD (381 children with an autistic disorder and 57 children with PDD-NOS). One hundred forty-three children were not testable and ten children scored above the highest possible age-specific non-verbal IQ, without numeric scores available. The mean non-verbal IQ of children with ASD (n = 285) was 99.6 (± 18.0). Stratification of cases into two categories: IQ <70 (n = 17) and IQ ≥70 (n = 278) showed a fivefold increased risk of epilepsy for children with an IQ <70 (7/17; 41.2%) comparing children with an IQ ≥70 (31/278; 11.2%) (OR = 5.5; 95% CI: 1.7 to 17.5; P = 0.005).

                  An assessment with VABS was performed in 386 children with ASD (336 children with an autistic disorder and 50 children with PDD-NOS). The mean overall adaptive behavior composite standard score of children with ASD was 54.0 (± 20.2). Stratification of cases into two categories: composite standard score <70 (n = 294) and composite standard score ≥70 (n = 92) showed a threefold increased risk of epilepsy for children with a composite standard score <70 (45/294 (15.3%)) comparing children with a composite standard score ≥70 (5/92 (5.4%) (OR = 3.1; 95% CI: 1.2 to 10.5; P = 0.015). Figure 1 depicts the frequency of comorbid epilepsy in individuals with ASD as a function of composite standard score. The more severe the impairment of adaptive level, the more prevalent the epilepsy (P = 0.002).

                  Epilepsy and gender

                  Among the 96 females with a diagnosis of ASD (autistic disorder or PDD-NOS), 16.7% (n = 16/96) had epilepsy. For the 382 males with ASD, 11.8% (45/382) had epilepsy. The male:female ratio was 4.2 for the children with ASD without epilepsy, and 2.9 for the children with ASD and with epilepsy. However, the difference was not statistically significant (OR = 0.7; 95% CI: 0.3 to 1.3; P = 0.268). Considering all the children with ASD regardless of their epileptic status, the male:female ratio was not significantly different when the sample was stratified into two groups (normal intelligence versus intellectual disability) based on the non-verbal IQ (RCPM: ≥70, n = 278; <70, n = 17) (male:female ratio = 3.3 versus 4.5, respectively) (OR = 0.7; 95% CI: 0.2 to 3.2; P = 0.788) or the adaptive level (VABS: ≥70, n = 92; <70, n = 294) (male:female ratio = 3.4 versus 3.9, respectively) (OR = 1.2; 95% CI: 0.6 to 2.1; P = 0.664). Furthermore, there was no difference when the sample was stratified into four groups based on the adaptive level (<40, 40 to 54, 55 to 69, ≥70; P = 0.591).

                  Multivariate analysis

                  To confirm univariate variables associated with the risk of seizures, we used a logistic regression. ASD (estimate = 2.49, P = 1.1 10-5; OR = 12; 95% CI: 4.46 to 43.1), age (estimate = 0.11, P = 1.1 10-6; OR = 1.15; 95% CI: 1.07 to 1.17) and gender (male: estimate = -0.61, P = 0.049; OR = 0.54; 95% CI: 0.3 to 1.013) were associated with the risk of seizure. In ASD individuals only, gender was not significantly associated, whereas age and intellectual disability were significantly associated, whether intellectual disability was measured with VABS (estimate = 1.15, P = 0.02; OR = 3.2; 95% CI: 1.3 to 9.6) or with RCPM (estimate = 1.57, P = 0.005; OR = 4.85; 95% CI: 1.53 to 14.56).

                  Discussion

                  Epilepsy in autism has been a subject of increasing interest, and reported prevalence rates of seizures in this condition vary from 5% to 40% [1]. The variability of rates have been attributed to the heterogeneity of samples with respect to age, gender, comorbidity, subtype of pervasive developmental disorder (PDD), intellectual disability and risk factors [9]. But most of the studies have been conducted in samples with simplex autism; for example the prevalence found in the Simons Simplex Collection (a large multisite phenotypic and DNA collection that includes families (n = 2,644) in which there is only one child (aged 4 to 17 years) with ASD) is 2.4% [135]. In multiplex families, we found that 13.4% of children with autism and 8.2% of children with PDD-NOS had epilepsy. These results are in the range of prevalence rates described in the literature. In these multiplex families, we found that 2.2% of the siblings without autism had epilepsy. This prevalence rate is high compared to the general population where 0.7% to 0.8% of children up to the age of 15 years have repeated seizures [136]. Moreover, the permutation tests performed in this study show significant evidence that epilepsy phenotypes co-segregated within families.

                  Studies suggest that there are two peaks of onset of seizures in autism, one in early childhood (before the age of 5 years old), and one near adolescence [137]. In the sample studied here, the admixture analysis confirms this two-peak model: 62% of the children had their first seizures before the age of 5 years. Mean age of onset for the second peak is in pre/early adolescence as only 9% of the children had their first seizure after the age of 12 years. However, with a mean age of 9.2 years, the children studied are relatively young and many of them had not yet reached adolescence. Therefore, it is likely that our estimate of the age of onset for the later peak may be spuriously low as we cannot rule out that epilepsy could begin later for some individuals. Unfortunately, conducting a subanalysis with individuals aged 16 years and older was not possible given the sample size.

                  The risk of epilepsy in individuals with simplex autism was significantly associated with intellectual disability and gender. In a meta-analysis of 17 studies, the pooled prevalence of epilepsy was 21.5% in individuals with autism and intellectual disability, against 8% in individuals with autism and normal intelligence [9]. Of note, the increased risk with gender in simplex autism may reflect the known circumstance that females with autism tend to have more severe intellectual disability: the more severe the intellectual disability, the lower the male:female ratio [10]. In the present study, the respective prevalence rates of epilepsy was 41.2% in individuals with autism and intellectual disability, against 11.1% in individuals with autism and normal intelligence (P = 0.005), and the more the adaptive behavior level was impaired, the higher the prevalence of epilepsy (Figure 3). However, there was no increase of epilepsy linked to gender in individuals with ASD. Furthermore, no significant difference in IQ among males and females was found in the AGRE sample. A similar result was suggested in previous reports of multiplex families [126, 138].
                  http://static-content.springer.com/image/art%3A10.1186%2F2040-2392-4-47/MediaObjects/13229_2013_Article_97_Fig3_HTML.jpg
                  Figure 3

                  Frequencies of comorbid epilepsy in children (n = 386) with autism from multiplex families as function of the Vineland Adaptive Behavior Scales (VABS) composite standard score.

                  Identification or strong suspicion of a risk factor for autism (genetic or not) tended to increase the prevalence of epilepsy. The non-genetic risk factors identified were mainly perinatal fetal distress, the implication of which for autism, epilepsy and intellectual disability is well known. The prevalence of epilepsy remained significantly higher even when only identified or suspected genetic risk factors were considered. Genetic risk factors may be more often implicated when autism and epilepsy are associated [139]. This is also the case in multiplex families.

                  Interpretation of the informative families presented in Table 5 requires consideration of the AGRE database limitations, which include: excluding individuals with major perinatal risk factors or with known genetic abnormalities (for example fragile X syndrome) (but some siblings with such risk factors may have been included); and in many individuals, data are unknown or missing (for example not all individuals underwent CNV search; see Methods). Also, large family histories including epilepsy and ASD statuses of all members were not available. Careful scrutiny of Table 5 shows that several combinations of risk can lead to a multiplex pedigree: 1) the existence of a common risk factor for epilepsy and autism leading to the suggestion of screening for known genetic risk factors of epilepsy in AGRE families AU25, AU51, AU176, AU275, AU461, AU548 and AU922; and 2) the co-occurrence of two different risk factors (genetic and non-genetic ones) leading to a false ‘multiplex pedigree’, such as in families AU731, AU123, AU765 and AU1208; and 3) combinations of major and minor risk factors as it cannot be excluded that a) in some families interpretation of genotype/phenotype relationship may be particularly complex (for example AU25, AU51) and b) the same ASD genetic risk factor may be responsible for increased risk of prematurity (for example AU731).

                  In terms of pathophysiological mechanisms, several hypotheses have been proposed to explain the comorbidity between autism and epilepsy: 1) accidental co-occurrence given the high frequency of both conditions; 2) altered internal organization of minicolumns in the cortex of autistic individuals may be associated with a defect in inhibitory local circuit projection, and the defect in γ-aminobutyric acid (GABA)ergic fibers may correlate with the increased prevalence of seizures in autism [140, 141]; 3) common genetic or neurodevelopmental risk factors; and 4) epilepsy by itself may induce the development of autistic symptoms [142]. Indeed, early-life seizures may affect synaptic plasticity through alteration of neurotransmitter receptor systems and molecules essential for intrinsic neuronal function, and changes that may contribute to an enhanced risk of autism [143, 144]. Supporting this hypothesis, infantile spasms and/or early-onset seizures have been significantly associated with autism [145147]. In the present study, few children had seizures in their first year of life (11/63, 17%) and none had infantile spasms. Thus, this mechanism may not account for much of the high prevalence found. As stated previously, in individuals with autism from multiplex families, common pathophysiological mechanisms appear to be more prevalent and may be genetic. If both autism and epilepsy can be considered as disorders of synaptic plasticity [143, 144], autism and epilepsy may be the consequences of the same pathophysiological mechanisms, resulting in abnormal plasticity of genetic origin. Numerous genetic conditions that associate autism and epilepsy in their phenotypic features are caused by mutations in genes implicated in synaptic development, functioning and/or plasticity, such as Angelman syndrome [148], fragile X syndrome [149], Rett syndrome [150] and tuberous sclerosis [120, 151]. Furthermore, missense and nonsense mutations of several genes involved in neurodevelopment have been identified in individuals with epilepsy, autism or both (Table 1). Most of those genes are involved in cerebral development pathways and functioning: synaptic formation (NLGN4, NRXN1, CDH8, PCDH19, SHANK3), ionic channel subunits (SCN1A, SCN2A, SCN1B, KCNMA1, KCNQ2, CACNA1A) and neurotransmitter receptors (GABRG2, CHRNA4). Similarly, CNVs such as 1q21.1, 3q29, 7q11.23, 15q11–13, 15q13.3, 16p11.2, 16p13.11, 17q12 and 22q11.2 have been implicated in different developmental disorders, such as ASD, intellectual disability and epilepsy [15, 17, 152], as well as schizophrenia [16, 152, 153] (Table 2). Autism, epilepsy and intellectual disability may share alteration of common pathways involved in neurodevelopmental maturation and neural functioning. We propose that these genes need to be more systematically investigated as major and minor risk factors.

                  Although the current study was conducted in the largest available sample of multiplex families, limitations should be listed. First, we cannot exclude biases in recruitment due to exclusion criteria as evidenced by the very low rate of infantile spasm in the sample. Furthermore, of the 664 children included in this analysis, 35 children (31 children with autistic disorder, two children with PDD-NOS and two children without autism) had strong risk factors for autism and seizures, such as pre- or perinatal insult/prematurity before 35 weeks (n = 19), chromosomal abnormality (n = 8), or abnormal neurological or brain imaging examination (n = 7). However, when analyses were performed excluding these children and their siblings, the results remained unchanged (see also Additional file 1). Second, individuals’ ages were significantly different in children with autism with epilepsy, and children with autism without epilepsy, and the small number of adolescents may have reduced the prevalence of late onset seizures. Third, given the heterogeneity of intellectual functioning in autism and the heterogeneity of intellectual disability measures, we used two standardized tools for the cognitive and adaptive assessment: RCPM and VABS. Assessing a broad sample of 38 autistic children, Dawson et al. found scores on the RCPM to be, on average, 30 percentile points higher than their scores on the Wechsler scale of intelligence [154]. The VABS assess the adaptive functioning with a parent interview. Strong positive relationships have been found between Vineland composite and Vineland subscales (communication, socialization, daily living skills) and IQ, particularly when considering low functioning individuals [155]. Therefore, the two scales can be considered as complementary for the cognitive assessment of children with autism. The fact that we found similar results in the AGRE sample strengthens this view. Fourth, we cannot exclude that the absence of association with gender was related to our final sample size and a lack of statistical power. To assess this issue, we decided to perform a meta-analysis in a larger sample including other studies reporting IQ in multiplex pedigrees [126, 138]. The standardized mean difference between mean non-verbal IQ in males versus females from multiplex pedigrees was 0.01 (95% CI: –0.17; 0.19), meaning that there is no difference between mean non-verbal IQ according to gender (Additional file 2: Figure S1). The meta-analysis confirmed our results.

                  Conclusion

                  We conclude that epilepsy in multiplex autism may define a different subgroup in terms of clinical characteristics and genetic risk: association with intellectual disability, no association with gender and possible common risk factors. Future studies should be encouraged to increase knowledge of common genetic risk factors between ASD and epilepsy.

                  Abbreviations

                  aCGH: 

                  Array comparative genomic hybridization

                  ADI-R: 

                  Autism diagnostic interview-revised

                  AGRE: 

                  Autism genetic resource exchange

                  ASD: 

                  Autism spectrum disorders

                  CI: 

                  Confidence interval

                  CNV: 

                  Copy number variation

                  EEG: 

                  Electroencephalogram

                  GABA: 

                  γ-aminobutyric acid

                  GLUT1: 

                  Glucose transporter type 1

                  GWA: 

                  Genome-wide association

                  ID: 

                  Intellectual disability

                  IQ: 

                  Intellectual quotient

                  nACh: 

                  Nicotinic acetylcholine

                  NQA: 

                  Not quite autism

                  OR: 

                  Odds ratio

                  PCR: 

                  Polymerase chain reaction

                  PDD: 

                  Pervasive developmental disorder

                  PDD-NOS: 

                  Pervasive developmental disorder-not otherwise specified

                  RasGAP: 

                  Ras GTPase activating protein

                  RCPM: 

                  Raven’s colored progressive matrices

                  SCZ: 

                  Schizophrenia

                  SD: 

                  Standard deviation

                  SNRPN: 

                  Small nuclear ribonucleoprotein protein N

                  VABS: 

                  Vineland adaptive behavior scales.

                  Declarations

                  Acknowledgements

                  We gratefully acknowledge the resources provided by the AGRE Consortium and the participating AGRE families. The AGRE is a program of Autism Speaks and is supported, in part, by grant 1U24MH081810 from the National Institute of Mental Health to Clara M Lajonchere (principal investigator). This work was supported by the Orange Foundation.

                  The AGRE Consortium comprises: Dan Geschwind MD PhD UCLA, Los Angeles, CA, USA; Maja Bucan PhD, University of Pennsylvania, Philadelphia, PA, USA; W Ted Brown MD PhD FACMG, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA; Rita M Cantor PhD, UCLA School of Medicine, Los Angeles, CA, USA; John N Constantino MD, Washington University School of Medicine, St Louis, MO, USA; T Conrad Gilliam PhD, University of Chicago, Chicago, IL, USA; Martha Herbert MD PhD, University of Texas, Houston, TX, USA; Clara Lajonchere PhD, Cure Autism Now, Los Angeles, CA, USA; David H Ledbetter PhD, Emory University, Atlanta, GA, USA; Christa Lese-Martin PhD, Emory University, Atlanta, GA, USA; Janet Miller, JD, PhD, Cure Autism Now, Los Angeles, CA, USA; Stanley F Nelson MD, UCLA School of Medicine, Los Angeles, CA, USA; Gerard D Schellenberg PhD, University of Washington, Seattle, WA, USA; Carol A Samango-Sprouse EdD, George Washington University, Washington, DC, USA; Sarah Spence MD PhD, Harvard University, Boston, MA, USA; Matthew State MD PhD, Yale University, New Haven, CT, USA; Rudolph E Tanzi PhD, Massachusetts General Hospital, Boston, MA, USA.

                  Authors’ Affiliations

                  (1)
                  Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalier Pitié-Salpêtrière, Université Pierre et Marie Curie
                  (2)
                  IntegraGen
                  (3)
                  Center of Epileptology, Reference Center for Rare Epilepsies, AP-HP, Groupe Hospitalier Pitié-Salpêtrière
                  (4)
                  Department of Genetics, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Université Pierre et Marie Curie
                  (5)
                  Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CR-ICM), Université Pierre et Marie Curie/Institut national de la santé et de la recherche médicale (INSERM) Unité Mixte de Recherche (UMR) S975/Centre National de la Recherche Scientifique (CNRS) UMR 7225, Département Biotechnologies et Biothérapies, Groupe Hospitalier Pitié-Salpêtrière
                  (6)
                  Department of Child and Adolescent Psychiatry, Groupe Hospitalier Guillaume Régnier, Université de Rennes
                  (7)
                  Institut des Systèmes Intelligents et Robotiques (ISIR), CNRS UMR 7222, Université Pierre et Marie Curie

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                  This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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