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Adaptive behaviour deficits in individuals with 3q29 deletion syndrome.
Pollak, R M; Burrell, T L; Cubells, J F; Klaiman, C; Murphy, M M; Saulnier, C A; Walker, E F; White, S P; Mulle, J G.
Afiliação
  • Pollak RM; Center for Advanced Biotechnology and Medicine, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
  • Burrell TL; Department of Pediatrics, School of Medicine, Emory University, Atlanta, GA, USA.
  • Cubells JF; Department of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA.
  • Klaiman C; Department of Psychiatry and Behavioral Sciences, School of Medicine, Emory University, Atlanta, GA, USA.
  • Murphy MM; Department of Pediatrics, School of Medicine, Emory University, Atlanta, GA, USA.
  • Saulnier CA; Marcus Autism Center, Children's Healthcare of Atlanta and Emory University, Atlanta, GA, USA.
  • Walker EF; Department of Pediatrics, School of Medicine, Emory University, Atlanta, GA, USA.
  • White SP; Department of Pediatrics, School of Medicine, Emory University, Atlanta, GA, USA.
  • Mulle JG; Neurodevelopmental Assessment & Consulting Services, Atlanta, GA, USA.
J Intellect Disabil Res ; 68(2): 113-127, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37740553
ABSTRACT

BACKGROUND:

3q29 deletion syndrome (3q29del) is associated with a significantly increased risk for neurodevelopmental and neuropsychiatric phenotypes. Mild to moderate intellectual disability (ID) is common in this population, and previous work by our team identified substantial deficits in adaptive behaviour. However, the full profile of adaptive function in 3q29del has not been described nor has it been compared with other genomic syndromes associated with elevated risk for neurodevelopmental and neuropsychiatric phenotypes.

METHODS:

Individuals with 3q29del (n = 32, 62.5% male) were evaluated using the Vineland Adaptive Behaviour Scales, Third Edition, Comprehensive Parent/Caregiver Form (Vineland-3). We explored the relationship between adaptive behaviour and cognitive function, executive function, and neurodevelopmental and neuropsychiatric comorbidities in our 3q29del study sample, and we compared subjects with 3q29del with published data on fragile X syndrome, 22q11.2 deletion syndrome and 16p11.2 deletion and duplication syndromes.

RESULTS:

Individuals with 3q29del had global deficits in adaptive behaviour that were not driven by specific weaknesses in any given domain. Individual neurodevelopmental and neuropsychiatric diagnoses had a small effect on adaptive behaviour, and the cumulative number of comorbid diagnoses was significantly negatively associated with Vineland-3 performance. Both cognitive ability and executive function were significantly associated with adaptive behaviour, and executive function was a better predictor of Vineland-3 performance than cognitive ability. Finally, the severity of adaptive behaviour deficits in 3q29del was distinct from previously published data on comparable genomic disorders.

CONCLUSIONS:

Individuals with 3q29del have significant deficits in adaptive behaviour, affecting all domains assessed by the Vineland-3. Executive function is a better predictor of adaptive behaviour than cognitive ability in this population and suggests that interventions targeting executive function may be an effective therapeutic strategy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Intellect Disabil Res Assunto da revista: TRANSTORNOS MENTAIS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Intellect Disabil Res Assunto da revista: TRANSTORNOS MENTAIS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos