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Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs.
Cunningham, Adam C; Hall, Jeremy; Einfeld, Stewart; Owen, Michael J; van den Bree, Marianne B M.
Afiliação
  • Cunningham AC; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
  • Hall J; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
  • Einfeld S; Faculty of Health Sciences, University of Sydney, Sydney, Australia.
  • Owen MJ; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
  • van den Bree MBM; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
Psychol Med ; 52(3): 574-586, 2022 02.
Article em En | MEDLINE | ID: mdl-32643597
ABSTRACT

BACKGROUND:

A number of genomic conditions caused by copy number variants (CNVs) are associated with a high risk of neurodevelopmental and psychiatric disorders (ND-CNVs). Although these patients also tend to have cognitive impairments, few studies have investigated the range of emotion and behaviour problems in young people with ND-CNVs using measures that are suitable for those with learning difficulties.

METHODS:

A total of 322 young people with 13 ND-CNVs across eight loci (mean age 9.79 years, range 6.02-17.91, 66.5% male) took part in the study. Primary carers completed the Developmental Behaviour Checklist (DBC).

RESULTS:

Of the total, 69% of individuals with an ND-CNV screened positive for clinically significant difficulties. Young people from families with higher incomes (OR = 0.71, CI = 0.55-0.91, p = .008) were less likely to screen positive. The rate of difficulties differed depending on ND-CNV genotype (χ2 = 39.99, p < 0.001), with the lowest rate in young people with 22q11.2 deletion (45.7%) and the highest in those with 1q21.1 deletion (93.8%). Specific patterns of strengths and weaknesses were found for different ND-CNV genotypes. However, ND-CNV genotype explained no more than 9-16% of the variance, depending on DBC subdomain.

CONCLUSIONS:

Emotion and behaviour problems are common in young people with ND-CNVs. The ND-CNV specific patterns we find can provide a basis for more tailored support. More research is needed to better understand the variation in emotion and behaviour problems not accounted for by genotype.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variações do Número de Cópias de DNA / Lista de Checagem Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Psychol Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variações do Número de Cópias de DNA / Lista de Checagem Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Psychol Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido