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Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability

BACKGROUND: Individuals with Down syndrome (DS) are at significant risk for early onset Alzheimer's disease (AD), likely due to the triplication of genes on chromosome 21 that facilitate AD neuropathology. To aid the effective early diagnosis of dementia in DS, we demonstrate the strategy of us...

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Autores principales: Oliver, Chris, Adams, Dawn, Holland, Anthony J., Brown, Stephanie S. G., Ball, Sarah, Dodd, Karen, Carr, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306607/
https://www.ncbi.nlm.nih.gov/pubmed/34994494
http://dx.doi.org/10.1002/gps.5674
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author Oliver, Chris
Adams, Dawn
Holland, Anthony J.
Brown, Stephanie S. G.
Ball, Sarah
Dodd, Karen
Carr, Janet
author_facet Oliver, Chris
Adams, Dawn
Holland, Anthony J.
Brown, Stephanie S. G.
Ball, Sarah
Dodd, Karen
Carr, Janet
author_sort Oliver, Chris
collection PubMed
description BACKGROUND: Individuals with Down syndrome (DS) are at significant risk for early onset Alzheimer's disease (AD), likely due to the triplication of genes on chromosome 21 that facilitate AD neuropathology. To aid the effective early diagnosis of dementia in DS, we demonstrate the strategy of using single point assessment of cognitive performance with scoring normed for degree of intellectual disability to generate age related prevalence data for acquired mild cognitive impairment (AMCI). METHODS: Four hundred and twelve adults with DS were assessed using the Neuropsychological Assessment of dementia in adults with Intellectual Disability. Normative data, banded by degree of intellectual disability, allowed identification of AMCI by atypical deviation from expected performance. RESULTS: AMCI was evident in approximately 20% of adults with DS aged 40 and under, 40% aged 41–50 and 45% aged 51 and over. Relative risk increased significantly in those aged 46 and over. Analysis of prevalence by 5‐year age bands revealed two peaks for higher prevalence of AMCI. CONCLUSIONS: Psychometric data indicate single point assessment of AMCI is possible for the majority of adults with DS. Two peaks for age‐related prevalence of AMCI suggest the risk for onset of AD conferred by trisomy of chromosome 21 is moderated by another factor, possibly ApoE status.
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spelling pubmed-93066072022-07-28 Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability Oliver, Chris Adams, Dawn Holland, Anthony J. Brown, Stephanie S. G. Ball, Sarah Dodd, Karen Carr, Janet Int J Geriatr Psychiatry Research Article BACKGROUND: Individuals with Down syndrome (DS) are at significant risk for early onset Alzheimer's disease (AD), likely due to the triplication of genes on chromosome 21 that facilitate AD neuropathology. To aid the effective early diagnosis of dementia in DS, we demonstrate the strategy of using single point assessment of cognitive performance with scoring normed for degree of intellectual disability to generate age related prevalence data for acquired mild cognitive impairment (AMCI). METHODS: Four hundred and twelve adults with DS were assessed using the Neuropsychological Assessment of dementia in adults with Intellectual Disability. Normative data, banded by degree of intellectual disability, allowed identification of AMCI by atypical deviation from expected performance. RESULTS: AMCI was evident in approximately 20% of adults with DS aged 40 and under, 40% aged 41–50 and 45% aged 51 and over. Relative risk increased significantly in those aged 46 and over. Analysis of prevalence by 5‐year age bands revealed two peaks for higher prevalence of AMCI. CONCLUSIONS: Psychometric data indicate single point assessment of AMCI is possible for the majority of adults with DS. Two peaks for age‐related prevalence of AMCI suggest the risk for onset of AD conferred by trisomy of chromosome 21 is moderated by another factor, possibly ApoE status. John Wiley and Sons Inc. 2022-01-07 2022-02 /pmc/articles/PMC9306607/ /pubmed/34994494 http://dx.doi.org/10.1002/gps.5674 Text en © 2021 The Authors. International Journal of Geriatric Psychiatry published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oliver, Chris
Adams, Dawn
Holland, Anthony J.
Brown, Stephanie S. G.
Ball, Sarah
Dodd, Karen
Carr, Janet
Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title_full Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title_fullStr Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title_full_unstemmed Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title_short Acquired mild cognitive impairment in adults with Down syndrome: Age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
title_sort acquired mild cognitive impairment in adults with down syndrome: age‐related prevalence derived from single point assessment data normed by degree of intellectual disability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306607/
https://www.ncbi.nlm.nih.gov/pubmed/34994494
http://dx.doi.org/10.1002/gps.5674
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