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Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

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 cell...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933737/
https://www.ncbi.nlm.nih.gov/pubmed/31878865
http://dx.doi.org/10.1186/s11689-019-9288-7
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author 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.
author_facet 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.
author_sort Baker, Emma K.
collection PubMed
description 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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spelling pubmed-69337372019-12-30 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. J Neurodev Disord Research 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. BioMed Central 2019-12-26 /pmc/articles/PMC6933737/ /pubmed/31878865 http://dx.doi.org/10.1186/s11689-019-9288-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
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.
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title_full Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title_fullStr Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title_full_unstemmed Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title_short Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
title_sort intellectual functioning and behavioural features associated with mosaicism in fragile x syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933737/
https://www.ncbi.nlm.nih.gov/pubmed/31878865
http://dx.doi.org/10.1186/s11689-019-9288-7
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