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The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population

The validity of dementia diagnostic criteria depends on their ability to distinguish dementia symptoms from pre-existing cognitive impairments. The study aimed to assess inter-rater reliability and concurrent validity of DSM-5 criteria for neurocognitive disorder in Down syndrome. The utility of mil...

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Autores principales: Pape, Sarah E., al Janabi, Tamara, Ashton, Nicholas J., Hye, Abdul, Sheehan, Rory, Gallagher, Paul, Knight, Bernice, Prins, Anne-Marije, Courtenay, Ken, Jordanova, Vesna, Thomas, Bini, Perumal, Nagarajan, Forbes, Craig, Hassiotis, Angela, Strydom, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241825/
https://www.ncbi.nlm.nih.gov/pubmed/34188117
http://dx.doi.org/10.1038/s41598-021-92887-5
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author Pape, Sarah E.
al Janabi, Tamara
Ashton, Nicholas J.
Hye, Abdul
Sheehan, Rory
Gallagher, Paul
Knight, Bernice
Prins, Anne-Marije
Courtenay, Ken
Jordanova, Vesna
Thomas, Bini
Perumal, Nagarajan
Forbes, Craig
Hassiotis, Angela
Strydom, Andre
author_facet Pape, Sarah E.
al Janabi, Tamara
Ashton, Nicholas J.
Hye, Abdul
Sheehan, Rory
Gallagher, Paul
Knight, Bernice
Prins, Anne-Marije
Courtenay, Ken
Jordanova, Vesna
Thomas, Bini
Perumal, Nagarajan
Forbes, Craig
Hassiotis, Angela
Strydom, Andre
author_sort Pape, Sarah E.
collection PubMed
description The validity of dementia diagnostic criteria depends on their ability to distinguish dementia symptoms from pre-existing cognitive impairments. The study aimed to assess inter-rater reliability and concurrent validity of DSM-5 criteria for neurocognitive disorder in Down syndrome. The utility of mild neurocognitive disorder as a distinct diagnostic category, and the association between clinical symptoms and neurodegenerative changes represented by the plasma biomarker neurofilament light were also examined. 165 adults with Down syndrome were included. Two clinicians independently applied clinical judgement, DSM-IV, ICD-10 and DSM-5 criteria for dementia (or neurocognitive disorder) to each case. Inter-rater reliability and concurrent validity were analysed using the kappa statistic. Plasma neurofilament light concentrations were measured for 55 participants as a marker of neurodegeneration and between group comparisons calculated. All diagnostic criteria showed good inter-rater reliability apart from mild neurocognitive disorder which was moderate (k = 0.494). DSM- 5 criteria had substantial concurrence with clinical judgement (k = 0.855). When compared to the no neurocognitive disorder group, average neurofilament light concentrations were higher in both the mild and major neurocognitive disorder groups. DSM-5 neurocognitive disorder criteria can be used reliably in a Down syndrome population and has higher concurrence with clinical judgement than the older DSM-IV and ICD-10 criteria. Whilst the inter-rater reliability of the mild neurocognitive disorder criteria was modest, it does appear to identify people in an early stage of dementia with underlying neurodegenerative changes, represented by higher average NfL levels.
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spelling pubmed-82418252021-07-06 The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population Pape, Sarah E. al Janabi, Tamara Ashton, Nicholas J. Hye, Abdul Sheehan, Rory Gallagher, Paul Knight, Bernice Prins, Anne-Marije Courtenay, Ken Jordanova, Vesna Thomas, Bini Perumal, Nagarajan Forbes, Craig Hassiotis, Angela Strydom, Andre Sci Rep Article The validity of dementia diagnostic criteria depends on their ability to distinguish dementia symptoms from pre-existing cognitive impairments. The study aimed to assess inter-rater reliability and concurrent validity of DSM-5 criteria for neurocognitive disorder in Down syndrome. The utility of mild neurocognitive disorder as a distinct diagnostic category, and the association between clinical symptoms and neurodegenerative changes represented by the plasma biomarker neurofilament light were also examined. 165 adults with Down syndrome were included. Two clinicians independently applied clinical judgement, DSM-IV, ICD-10 and DSM-5 criteria for dementia (or neurocognitive disorder) to each case. Inter-rater reliability and concurrent validity were analysed using the kappa statistic. Plasma neurofilament light concentrations were measured for 55 participants as a marker of neurodegeneration and between group comparisons calculated. All diagnostic criteria showed good inter-rater reliability apart from mild neurocognitive disorder which was moderate (k = 0.494). DSM- 5 criteria had substantial concurrence with clinical judgement (k = 0.855). When compared to the no neurocognitive disorder group, average neurofilament light concentrations were higher in both the mild and major neurocognitive disorder groups. DSM-5 neurocognitive disorder criteria can be used reliably in a Down syndrome population and has higher concurrence with clinical judgement than the older DSM-IV and ICD-10 criteria. Whilst the inter-rater reliability of the mild neurocognitive disorder criteria was modest, it does appear to identify people in an early stage of dementia with underlying neurodegenerative changes, represented by higher average NfL levels. Nature Publishing Group UK 2021-06-29 /pmc/articles/PMC8241825/ /pubmed/34188117 http://dx.doi.org/10.1038/s41598-021-92887-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pape, Sarah E.
al Janabi, Tamara
Ashton, Nicholas J.
Hye, Abdul
Sheehan, Rory
Gallagher, Paul
Knight, Bernice
Prins, Anne-Marije
Courtenay, Ken
Jordanova, Vesna
Thomas, Bini
Perumal, Nagarajan
Forbes, Craig
Hassiotis, Angela
Strydom, Andre
The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title_full The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title_fullStr The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title_full_unstemmed The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title_short The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
title_sort reliability and validity of dsm 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241825/
https://www.ncbi.nlm.nih.gov/pubmed/34188117
http://dx.doi.org/10.1038/s41598-021-92887-5
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