Pervasive developmental disorder behavior in adolescents with intellectual disability and co-occurring somatic chronic diseases

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Abstract

Evidence on the association between somatic chronic diseases in ID-adolescents and the full range of pervasive developmental disorder behavior (PDD behavior) is scarce. The aim of the present study is to assess the association between somatic chronic diseases in ID-adolescents and mild PDD behavior. We obtained data on 1044 ID-adolescents, aged 12–18, attending secondary schools in the Netherlands. Parents of the adolescents completed the Dutch version of the Children's Social Behavior Questionnaire (CSBQ) parent version, covering a wide range of PDD behavior, and questions about chronic diseases and background characteristics of their child. ID-adolescents with somatic chronic diseases showed more PDD behavior, in particular milder forms, than their peers without chronic diseases. In addition, ID-adolescents with somatic chronic diseases in combination with pervasive development disorders (PDD) and attention deficit hyperactivity disorder (ADHD) also showed more PDD behavior than their peers with only PDD/ADHD. Clinicians should be extra alert on PDD behavior, in particular the milder forms, in ID-adolescents when somatic chronic diseases are present. However, to strengthen our results about the relationship between somatic chronic diseases in ID-adolescents and PDD behavior studies are needed using both the CSBQ and standardized diagnostic instruments.

Introduction

Studies on the association between somatic chronic diseases in adolescents with intellectual disability (ID-adolescents) and the full range of pervasive developmental disorder behavior (PDD behavior), in particular milder forms of PDD behavior (mild PDD behavior), are hardly available. Mild PDD behavior is a term reserved for those who do not meet the criteria for severe PDD behavior like in autism or Asperger syndrome. Mild PDD behavior is widespread among ID-adolescents and has a profound effect on their daily functioning (de Bildt et al., 2005a, de Bildt et al., 2005b, Hartman et al., 2006, Kraijer, 2000).

Literature shows a positive association between severity of ID and mild PDD behavior in adolescents (de Bildt et al., 2005a). This positive association is caused by the fact that ID-adolescents, especially those with lower levels of ID, have a greater chance on both pervasive development disorders (PDD) (de Bildt et al., 2005a, Harris et al., 2008, Matson and Shoemaker, 2009, Walker et al., 2004) and attention deficit hyperactivity disorder (ADHD) (Emerson and Hatton, 2007, Matson and Shoemaker, 2009). Although ADHD and PDD have different nosological diagnoses, both diagnostic categories partly include similar symptoms like deficits in social interaction, impulsivity, attention and hyperactivity deficit (Gallagher, Bellgrove, Hawi, Segurado, & Fitzgerald, 2007). These deficits are also associated with mild PDD behavior (de Bildt et al., 2005a, Hartman et al., 2006, Nijmeijer et al., 2009).

Literature also suggests that adolescents with somatic chronic diseases show more PDD behavior than adolescents in the general population (Ekström et al., 2008, Fombonne, 2009, Freeman et al., 2005, Hendriksen and Vles, 2008, Kilincaslan and Mukaddes, 2009, Nordin and Gillberg, 1996, Steffenburg et al., 1996, Thome-Souza et al., 2004), but only two studies have focused explicitly on ID-adolescents with somatic chronic diseases (Nordin and Gillberg, 1996, Steffenburg et al., 1996). None of the aforementioned studies used instruments that were suitable for screening or diagnosing mild PDD behavior (Hartman et al., 2006).

Studies on the association between somatic chronic diseases in ID-adolescents and PDD behavior, in particular milder forms of PDD behavior, are highly needed. Professionals do not always recognize mild PDD behavior in (ID-)adolescents (de Bildt et al., 2005b, Kilincaslan and Mukaddes, 2009). Evidence on an association between somatic chronic diseases in ID-adolescents and mild PDD behavior may thus increase the attentiveness of professionals for mild PDD behavior, enabling earlier diagnosis and treatment. PDD behavior is very disabling in social and interpersonal situations and hinder successful participation in society (de Bildt et al., 2005a, Haccou and Hamond, 2006, Matson et al., 2008).

The aim of this study is to assess the association between somatic chronic diseases in ID-adolescents and PDD behavior, in particular the milder forms of PDD behavior.

Section snippets

Participants and procedure

We collected data on adolescents with a borderline, mild, moderate or severe ID aged 12–18 years in two provinces in the north of the Netherlands: Groningen and Drenthe (total population about 1.1 million people).

Nearly all adolescents of the target population attended secondary schools (schools for practical training) or special secondary schools (regional expertise centers). ID-adolescents attending schools for practical training can be classified as mainly educable and have IQs between 60

Results

Table 1 shows the background characteristics of the adolescents. The gender ratio, 58.2% boys and 41.8% girls, was similar to the ratio boys and girls with ID in the Netherlands (van Schrojenstein Lantman-de Valk et al., 2002).

Table 2, Table 3 shows the mean scores and standard deviations of the four subgroups of ID-adolescents on all CSBQ scales.

Table 2 shows that, adjusted for level of ID, ID-adolescents with somatic chronic diseases had statistically significant higher mean scores on all

Discussion

ID-adolescents with somatic chronic diseases have more PDD behavior than those without chronic diseases, in particular milder forms of PDD behavior. This association is independent of having PDD/ADHD or not. Our findings suggest a relationship between somatic chronic diseases in ID-adolescents and mild PDD behavior.

Differences are rather large, whereas effect sizes are mostly relative low. This can be explained by the fact that the differences in mean scores on the CSBQ scales between the

Acknowledgement

The authors want to thank Dr. C.A. Hartman from the Department of Psychiatry, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands for her useful comments on earlier drafts of the article.

References (32)

  • J.L. Matson et al.

    Intellectual disability and its relationship to autism spectrum disorders

    Research in Developmental Disabilities

    (2009)
  • S. Thome-Souza et al.

    Which factors may play a pivotal role on determining the type of psychiatric disorder in children and adolescents with epilepsy?

    Epilepsy and Behavior

    (2004)
  • D.R. Walker et al.

    Specifying PDD-NOS: A comparison of PDD-NOS, Asperger syndrome, and autism

    Journal of The American Academy of Child and Adolescent Psychiatry

    (2004)
  • J. Cohen

    Statistical power analysis for the behavioural sciences

    (1988)
  • A. de Bildt et al.

    Validity of the Children's Social Behavior Questionnaire (CSBQ) in children with intellectual disability: Comparing the CSBQ with ADI-R, ADOS, and Clinical DSM-IV-TR Classification

    Journal of Autism and Developmental Disorders

    (2009)
  • A. de Bildt et al.

    Social skills in children with intellectual disabilities with and without autism

    Journal of Intellectual Disability Research

    (2005)
  • A. de Bildt et al.

    Prevalence of pervasive developmental disorders in children and adolescents with mental retardation

    Journal of Child Psychology and Psychiatry

    (2005)
  • M.C. Dekker et al.

    Emotional and behavioral problems in children and adolescents with and without intellectual disability

    Journal of Child Psychology and Psychiatry

    (2002)
  • Dutch Eurydice Unit

    The Education System in the Netherlands 2007

    (2007)
  • A.B. Ekström et al.

    Autism spectrum conditions in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    (2008)
  • E. Emerson et al.

    Mental health of children and adolescents with intellectual disabilities in Britain

    British Journal of Psychiatry

    (2007)
  • E. Fombonne

    Epidemiology of pervasive developmental disorders

    Pediatric Research

    (2009)
  • S.J. Freeman et al.

    Type 1 diabetes and autism: Is there a link?

    Diabetes Care

    (2005)
  • M. Gallagher et al.

    ADHD, autism spectrum disorders and Tourette's syndrome: Investigating the evidence for clinical and genetic overlap

  • R. Haccou et al.

    Gaining and proving yourself in social competence

    (2006)
  • J.M. Harris et al.

    Autistic traits and cognitive performance in young people with mild intellectual impairment

    Journal of Autism and Developmental Disorders

    (2008)
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