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Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale
BACKGROUND: Niemann-Pick disease type C (NPC) is an ultra-rare, progressive, genetic disease leading to impaired lysosomal function and neurodegeneration causing serious morbidity and shortened life expectancy. The Niemann-Pick type C Clinical Severity Scale (NPCCSS) is a 17 domain, disease-specific...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881637/ https://www.ncbi.nlm.nih.gov/pubmed/33579322 http://dx.doi.org/10.1186/s13023-021-01719-2 |
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author | Patterson, Marc C. Lloyd-Price, Lucy Guldberg, Christina Doll, Helen Burbridge, Claire Chladek, Michael íDali, Christine Mengel, Eugen Symonds, Tara |
author_facet | Patterson, Marc C. Lloyd-Price, Lucy Guldberg, Christina Doll, Helen Burbridge, Claire Chladek, Michael íDali, Christine Mengel, Eugen Symonds, Tara |
author_sort | Patterson, Marc C. |
collection | PubMed |
description | BACKGROUND: Niemann-Pick disease type C (NPC) is an ultra-rare, progressive, genetic disease leading to impaired lysosomal function and neurodegeneration causing serious morbidity and shortened life expectancy. The Niemann-Pick type C Clinical Severity Scale (NPCCSS) is a 17 domain, disease-specific, clinician-reported outcome measure of disease severity and progression. An abbreviated 5-domain NPCCSS scale has been developed (measuring Ambulation, Swallow, Cognition, Speech, and Fine Motor Skills) and the scale reliability has been established. Additional psychometric properties and meaningful change of the scale need, however, to be assessed. METHODS: Mixed method studies were conducted to ascertain which NPCCSS domains were most important, as well as to explore meaningful change: 1) surveys in caregivers/patients (n = 49) and 2) interviews with clinicians (n = 5) as well as caregivers/patients (n = 28). Clinical trial data (n = 43) assessed construct validity and meaningful change through an anchor-based approach. RESULTS: Domains identified as most important by clinicians, caregivers, and patients (independent of current age, age of onset, and disease severity) were Ambulation, Swallow, Cognition, Speech, and Fine Motor Skills, indicating content validity of the 5-domain NPCCSS. Criterion validity was shown with the 5-domain NPCCSS being highly correlated with the 17-item NPCCSS total score (excluding hearing domains), r(2) = 0.97. Convergent validity was demonstrated against the 9 Hole Peg Test, r(2) = 0.65 (n = 31 patients), and the Scale for Assessment and Rating of Ataxia (SARA), r(2) = 0.86 (n = 49 patients). Any change was seen as meaningful by patients/caregivers across domains. Meaningful change using trial data and interviews with NPC experts (n = 5) and patients/caregivers (n = 28) suggested that a 1-category change on a domain is equivalent to 1-point change or greater in the 5-domain NPCCSS total score. CONCLUSIONS: Qualitative and quantitative data support content and construct validity of the 5-domain NPCCSS score as a valid endpoint in NPC trials. A 1-category change on any domain is equivalent to 1-point change or greater in the 5 domain NPCCSS total score, representing a clinically meaningful transition and reflecting loss of complex function and increased disability. Trial registration NCT02612129. Registered 23 November 2015, https://clinicaltrials.gov/ct2/show/NCT02612129 |
format | Online Article Text |
id | pubmed-7881637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78816372021-02-17 Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale Patterson, Marc C. Lloyd-Price, Lucy Guldberg, Christina Doll, Helen Burbridge, Claire Chladek, Michael íDali, Christine Mengel, Eugen Symonds, Tara Orphanet J Rare Dis Research BACKGROUND: Niemann-Pick disease type C (NPC) is an ultra-rare, progressive, genetic disease leading to impaired lysosomal function and neurodegeneration causing serious morbidity and shortened life expectancy. The Niemann-Pick type C Clinical Severity Scale (NPCCSS) is a 17 domain, disease-specific, clinician-reported outcome measure of disease severity and progression. An abbreviated 5-domain NPCCSS scale has been developed (measuring Ambulation, Swallow, Cognition, Speech, and Fine Motor Skills) and the scale reliability has been established. Additional psychometric properties and meaningful change of the scale need, however, to be assessed. METHODS: Mixed method studies were conducted to ascertain which NPCCSS domains were most important, as well as to explore meaningful change: 1) surveys in caregivers/patients (n = 49) and 2) interviews with clinicians (n = 5) as well as caregivers/patients (n = 28). Clinical trial data (n = 43) assessed construct validity and meaningful change through an anchor-based approach. RESULTS: Domains identified as most important by clinicians, caregivers, and patients (independent of current age, age of onset, and disease severity) were Ambulation, Swallow, Cognition, Speech, and Fine Motor Skills, indicating content validity of the 5-domain NPCCSS. Criterion validity was shown with the 5-domain NPCCSS being highly correlated with the 17-item NPCCSS total score (excluding hearing domains), r(2) = 0.97. Convergent validity was demonstrated against the 9 Hole Peg Test, r(2) = 0.65 (n = 31 patients), and the Scale for Assessment and Rating of Ataxia (SARA), r(2) = 0.86 (n = 49 patients). Any change was seen as meaningful by patients/caregivers across domains. Meaningful change using trial data and interviews with NPC experts (n = 5) and patients/caregivers (n = 28) suggested that a 1-category change on a domain is equivalent to 1-point change or greater in the 5-domain NPCCSS total score. CONCLUSIONS: Qualitative and quantitative data support content and construct validity of the 5-domain NPCCSS score as a valid endpoint in NPC trials. A 1-category change on any domain is equivalent to 1-point change or greater in the 5 domain NPCCSS total score, representing a clinically meaningful transition and reflecting loss of complex function and increased disability. Trial registration NCT02612129. Registered 23 November 2015, https://clinicaltrials.gov/ct2/show/NCT02612129 BioMed Central 2021-02-12 /pmc/articles/PMC7881637/ /pubmed/33579322 http://dx.doi.org/10.1186/s13023-021-01719-2 Text en © The Author(s) 2021 Open AccessThis 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/. 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 in a credit line to the data. |
spellingShingle | Research Patterson, Marc C. Lloyd-Price, Lucy Guldberg, Christina Doll, Helen Burbridge, Claire Chladek, Michael íDali, Christine Mengel, Eugen Symonds, Tara Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title | Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title_full | Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title_fullStr | Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title_full_unstemmed | Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title_short | Validation of the 5-domain Niemann-Pick type C Clinical Severity Scale |
title_sort | validation of the 5-domain niemann-pick type c clinical severity scale |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881637/ https://www.ncbi.nlm.nih.gov/pubmed/33579322 http://dx.doi.org/10.1186/s13023-021-01719-2 |
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