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Health comorbidities and cognitive abilities across the lifespan in Down syndrome

BACKGROUND: Down syndrome (DS) is associated with variable intellectual disability and multiple health and psychiatric comorbidities. The impact of such comorbidities on cognitive outcomes is unknown. We aimed to describe patterns of physical health and psychiatric comorbidity prevalence, and recept...

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Autores principales: Startin, Carla M., D’Souza, Hana, Ball, George, Hamburg, Sarah, Hithersay, Rosalyn, Hughes, Kate M. O., Massand, Esha, Karmiloff-Smith, Annette, Thomas, Michael S. C., Strydom, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979347/
https://www.ncbi.nlm.nih.gov/pubmed/31973697
http://dx.doi.org/10.1186/s11689-019-9306-9
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author Startin, Carla M.
D’Souza, Hana
Ball, George
Hamburg, Sarah
Hithersay, Rosalyn
Hughes, Kate M. O.
Massand, Esha
Karmiloff-Smith, Annette
Thomas, Michael S. C.
Strydom, Andre
author_facet Startin, Carla M.
D’Souza, Hana
Ball, George
Hamburg, Sarah
Hithersay, Rosalyn
Hughes, Kate M. O.
Massand, Esha
Karmiloff-Smith, Annette
Thomas, Michael S. C.
Strydom, Andre
author_sort Startin, Carla M.
collection PubMed
description BACKGROUND: Down syndrome (DS) is associated with variable intellectual disability and multiple health and psychiatric comorbidities. The impact of such comorbidities on cognitive outcomes is unknown. We aimed to describe patterns of physical health and psychiatric comorbidity prevalence, and receptive language ability, in DS across the lifespan, and determine relationships with cognitive outcomes. METHODS: Detailed medical histories were collected and cognitive abilities measured using standardised tests for 602 individuals with DS from England and Wales (age range 3 months to 73 years). Differences in prevalence rates between age groups and between males and females were determined using chi-squared or Fisher’s exact tests. In adults, rates for psychiatric comorbidities were compared to expected population rates using standardised morbidity ratios (SMRs). Adapted ANCOVA functions were constructed to explore age and sex associations with receptive language ability across the lifespan, and regression analyses were performed to determine whether the presence of health comorbidities or physical phenotypes predicted cognitive abilities. RESULTS: Multiple comorbidities showed prevalence differences across the lifespan, though there were few sex differences. In adults, SMRs were increased in males and decreased in females with DS for schizophrenia, bipolar disorder, and anxiety. Further, SMRs were increased in both males and females with DS for dementia, autism, ADHD, and depression, with differences more pronounced in females for dementia and autism, and in males for depression. Across the lifespan, receptive language abilities increasingly deviated from age-typical levels, and males scored poorer than females. Only autism and epilepsy were associated with poorer cognitive ability in those aged 16–35 years, with no relationships for physical health comorbidities, including congenital heart defects. CONCLUSIONS: Our results indicate the prevalence of multiple comorbidities varies across the lifespan in DS, and in adults, rates for psychiatric comorbidities show different patterns for males and females relative to expected population rates. Further, most health comorbidities are not associated with poorer cognitive outcomes in DS, apart from autism and epilepsy. It is essential for clinicians to consider such differences to provide appropriate care and treatment for those with DS and to provide prognostic information relating to cognitive outcomes in those with comorbidities.
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spelling pubmed-69793472020-01-29 Health comorbidities and cognitive abilities across the lifespan in Down syndrome Startin, Carla M. D’Souza, Hana Ball, George Hamburg, Sarah Hithersay, Rosalyn Hughes, Kate M. O. Massand, Esha Karmiloff-Smith, Annette Thomas, Michael S. C. Strydom, Andre J Neurodev Disord Research BACKGROUND: Down syndrome (DS) is associated with variable intellectual disability and multiple health and psychiatric comorbidities. The impact of such comorbidities on cognitive outcomes is unknown. We aimed to describe patterns of physical health and psychiatric comorbidity prevalence, and receptive language ability, in DS across the lifespan, and determine relationships with cognitive outcomes. METHODS: Detailed medical histories were collected and cognitive abilities measured using standardised tests for 602 individuals with DS from England and Wales (age range 3 months to 73 years). Differences in prevalence rates between age groups and between males and females were determined using chi-squared or Fisher’s exact tests. In adults, rates for psychiatric comorbidities were compared to expected population rates using standardised morbidity ratios (SMRs). Adapted ANCOVA functions were constructed to explore age and sex associations with receptive language ability across the lifespan, and regression analyses were performed to determine whether the presence of health comorbidities or physical phenotypes predicted cognitive abilities. RESULTS: Multiple comorbidities showed prevalence differences across the lifespan, though there were few sex differences. In adults, SMRs were increased in males and decreased in females with DS for schizophrenia, bipolar disorder, and anxiety. Further, SMRs were increased in both males and females with DS for dementia, autism, ADHD, and depression, with differences more pronounced in females for dementia and autism, and in males for depression. Across the lifespan, receptive language abilities increasingly deviated from age-typical levels, and males scored poorer than females. Only autism and epilepsy were associated with poorer cognitive ability in those aged 16–35 years, with no relationships for physical health comorbidities, including congenital heart defects. CONCLUSIONS: Our results indicate the prevalence of multiple comorbidities varies across the lifespan in DS, and in adults, rates for psychiatric comorbidities show different patterns for males and females relative to expected population rates. Further, most health comorbidities are not associated with poorer cognitive outcomes in DS, apart from autism and epilepsy. It is essential for clinicians to consider such differences to provide appropriate care and treatment for those with DS and to provide prognostic information relating to cognitive outcomes in those with comorbidities. BioMed Central 2020-01-23 /pmc/articles/PMC6979347/ /pubmed/31973697 http://dx.doi.org/10.1186/s11689-019-9306-9 Text en © The Author(s). 2020 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
Startin, Carla M.
D’Souza, Hana
Ball, George
Hamburg, Sarah
Hithersay, Rosalyn
Hughes, Kate M. O.
Massand, Esha
Karmiloff-Smith, Annette
Thomas, Michael S. C.
Strydom, Andre
Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title_full Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title_fullStr Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title_full_unstemmed Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title_short Health comorbidities and cognitive abilities across the lifespan in Down syndrome
title_sort health comorbidities and cognitive abilities across the lifespan in down syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979347/
https://www.ncbi.nlm.nih.gov/pubmed/31973697
http://dx.doi.org/10.1186/s11689-019-9306-9
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