Abstract

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.

Details

Title
The reliability and validity of DSM 5 diagnostic criteria for neurocognitive disorder and relationship with plasma neurofilament light in a down syndrome population
Author
Pape, Sarah E 1 ; al Janabi Tamara 2 ; Ashton, Nicholas J 3 ; Hye Abdul 4 ; Sheehan, Rory 5 ; Gallagher, Paul 6 ; Knight, Bernice 7 ; Prins Anne-Marije 8 ; Courtenay, Ken 9 ; Jordanova Vesna 10 ; Bini, Thomas 11 ; Nagarajan, Perumal 12 ; Forbes, Craig 13 ; Hassiotis, Angela 5 ; Strydom, Andre 14 

 King’s College London, Institute of Psychiatry, Psychology, and Neuroscience, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764); South London and Maudsley NHS Foundation Trust, London, UK (GRID:grid.37640.36) (ISNI:0000 0000 9439 0839); King’s College London, Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology, and Neuroscience, London, England (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764) 
 King’s College London, Centre for Developmental Neurobiology and MRC Centre for Neurodevelopmental Disorders, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764) 
 King’s College London, Institute of Psychiatry, Psychology, and Neuroscience, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764); NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia, London, UK (GRID:grid.454378.9); Sahlgrenska Academy at the University of Gothenburg, Department of Psychiatry and Neurochemistry, Mölndal, Sweden (GRID:grid.8761.8) (ISNI:0000 0000 9919 9582); University of Gothenburg, Wallenberg Centre for Molecular and Translational Medicine, Gothenburg, Sweden (GRID:grid.8761.8) (ISNI:0000 0000 9919 9582) 
 King’s College London, Institute of Psychiatry, Psychology, and Neuroscience, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764); NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia, London, UK (GRID:grid.454378.9) 
 University College London, Division of Psychiatry, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201) 
 East London NHS Foundation Trust, London, UK (GRID:grid.450709.f) (ISNI:0000 0004 0426 7183) 
 Camden and Islington Mental Health Foundation Trust, London, UK (GRID:grid.474126.2) (ISNI:0000 0004 0381 1108) 
 Parnassia Psychiatric Institute, The Hague, The Netherlands (GRID:grid.474126.2) 
 University College London, Division of Psychiatry, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201); Barnet Enfield and Haringey Mental Health NHS Trust, London, UK (GRID:grid.439448.6) (ISNI:0000 0004 0399 6472) 
10  South London and Maudsley NHS Foundation Trust, London, UK (GRID:grid.37640.36) (ISNI:0000 0000 9439 0839) 
11  North East London NHS Foundation Trust, London, UK (GRID:grid.451079.e) (ISNI:0000 0004 0428 0265) 
12  NHS Foundation Trust, Lancashire and South Cumbria, Lancashire, UK (GRID:grid.451052.7) (ISNI:0000 0004 0581 2008) 
13  Southern Health NHS Foundation Trust, London, UK (GRID:grid.467048.9) (ISNI:0000 0004 0465 4159) 
14  King’s College London, Institute of Psychiatry, Psychology, and Neuroscience, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764); South London and Maudsley NHS Foundation Trust, London, UK (GRID:grid.37640.36) (ISNI:0000 0000 9439 0839) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2546399136
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.