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Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
Baker, Emma K; Arpone, Marta; Vera, Solange Aliaga; Bretherton, Lesley; Ure, Alexandra; Kraan, Claudine M; Bui, Minh; Ling, Ling; Francis, David; Hunter, Matthew F; Elliott, Justine; Rogers, Carolyn; Field, Michael J; Cohen, Jonathan; Maria, Lorena Santa; Faundes, Victor; Curotto, Bianca; Morales, Paulina; Trigo, Cesar; Salas, Isabel; Alliende, Angelica M; Amor, David J; Godler, David E.
Afiliação
  • Baker EK; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia. emma.baker@mcri.edu.au.
  • Arpone M; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia. emma.baker@mcri.edu.au.
  • Vera SA; School of Psychology and Public Health, La Trobe University, Bundoora, VIC, Australia. emma.baker@mcri.edu.au.
  • Bretherton L; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Ure A; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
  • Kraan CM; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Bui M; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Ling L; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Francis D; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
  • Hunter MF; Neurodisability and Rehabilitation, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Elliott J; Royal Children's Hospital, Melbourne, VIC, Australia.
  • Rogers C; Department of Pediatrics, Monash University, Clayton, VIC, Australia.
  • Field MJ; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Cohen J; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
  • Maria LS; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Carlton, VIC, Australia.
  • Faundes V; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Curotto B; Victorian Clinical Genetics Services and Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Morales P; Department of Pediatrics, Monash University, Clayton, VIC, Australia.
  • Trigo C; Monash Genetics, Monash Health, Melbourne, VIC, Australia.
  • Salas I; Victorian Clinical Genetics Services and Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Alliende AM; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW, Australia.
  • Amor DJ; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW, Australia.
  • Godler DE; Fragile X Alliance Inc, Centre for Developmental Disability Health Victoria, Monash University, North Caulfield, Clayton, VIC, Australia.
J Neurodev Disord ; 11(1): 41, 2019 12 26.
Article em En | MEDLINE | ID: mdl-31878865
ABSTRACT

BACKGROUND:

Fragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM CGG ≥ 200), increased DNA methylation of the FMR1 promoter and silencing of the gene. Mosaicism for presence of cells with either methylated FM or smaller unmethylated pre-mutation (PM CGG 55-199) alleles in the same individual have been associated with better cognitive functioning. This study compares age- and sex-matched FM-only and PM/FM mosaic individuals on intellectual functioning, ASD features and maladaptive behaviours.

METHODS:

This study comprised a large international cohort of 126 male and female participants with FXS (aged 1.15 to 43.17 years) separated into FM-only and PM/FM mosaic groups (90 males, 77.8% FM-only; 36 females, 77.8% FM-only). Intellectual functioning was assessed with age appropriate developmental or intelligence tests. The Autism Diagnostic Observation Schedule-2nd Edition was used to examine ASD features while the Aberrant Behavior Checklist-Community assessed maladaptive behaviours.

RESULTS:

Comparing males and females (FM-only + PM/FM mosaic), males had poorer intellectual functioning on all domains (p < 0.0001). Although females had less ASD features and less parent-reported maladaptive behaviours, these differences were no longer significant after controlling for intellectual functioning. Participants with PM/FM mosaicism, regardless of sex, presented with better intellectual functioning and less maladaptive behaviours compared with their age- and sex-matched FM-only counterparts (p < 0.05). ASD features were similar between FM-only and PM/FM mosaics within each sex, after controlling for overall intellectual functioning.

CONCLUSIONS:

Males with FXS had significantly lower intellectual functioning than females with FXS. However, there were no significant differences in ASD features and maladaptive behaviours, after controlling for intellectual functioning, independent of the presence or absence of mosaicism. This suggests that interventions that primarily target cognitive abilities may in turn reduce the severity of maladaptive behaviours including ASD features in FXS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sintomas Comportamentais / Transtorno do Espectro Autista / Síndrome do Cromossomo X Frágil / Deficiência Intelectual / Mosaicismo Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Neurodev Disord Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sintomas Comportamentais / Transtorno do Espectro Autista / Síndrome do Cromossomo X Frágil / Deficiência Intelectual / Mosaicismo Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Neurodev Disord Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália