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The experience of living with Niemann–Pick type C: a patient and caregiver perspective
BACKGROUND: Niemann–Pick disease type C (NPC) is a rare inherited lysosomal storage disease typified by accumulation of cholesterol and other lipids in late endosomes/lysosomes, thereby resulting in a spectrum of neurological, psychiatric, and systemic symptoms (notably liver disease). Though it is...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200045/ https://www.ncbi.nlm.nih.gov/pubmed/37210540 http://dx.doi.org/10.1186/s13023-023-02741-2 |
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author | Golden, Emma van Gool, Raquel Cay, Mariesa Goodlett, Benjamin Cao, Amanda Al-Hertani, Walla Upadhyay, Jaymin |
author_facet | Golden, Emma van Gool, Raquel Cay, Mariesa Goodlett, Benjamin Cao, Amanda Al-Hertani, Walla Upadhyay, Jaymin |
author_sort | Golden, Emma |
collection | PubMed |
description | BACKGROUND: Niemann–Pick disease type C (NPC) is a rare inherited lysosomal storage disease typified by accumulation of cholesterol and other lipids in late endosomes/lysosomes, thereby resulting in a spectrum of neurological, psychiatric, and systemic symptoms (notably liver disease). Though it is well-known that NPC exacts a physical and emotional toll on both patients and caregivers, the burden of NPC can vary between patients, while the challenges of living with NPC can evolve over time (i.e., from time of diagnosis to the present day). To further grasp patient and caregiver perceptions and experiences with NPC, we carried out focus group discussions with pediatric and adult individuals with NPC (N = 19), with partial or full representation of the patient by their caregiver. Furthermore, we utilized our NPC focus group discussion to provide guidance on study design parameters and feasibility of prospective investigations aiming to characterize the central manifestations of NPC using neuroimaging, specifically, magnetic resonance imaging (MRI) methodology. RESULTS: Focus group discussions revealed that neurological signs, including declining cognition, memory loss, and psychiatric symptoms, as well as increasingly impaired mobility and motor function, are among the most pressing past and current concerns for patients and caregivers. Moreover, several participants also expressed concern over a loss of independence, social exclusion, and uncertainty for what the future holds. Caregivers described the challenges that participation in research poses, which included logistical difficulties mainly due to traveling with medical equipment and the need for sedation in a minority of patients when undergoing MRI. CONCLUSIONS: The findings derived from focus group discussions highlight the outstanding challenges that NPC patients and their caregivers face daily, while also providing direction on the potential scope and feasibility of future studies focusing on the central phenotypes of NPC. |
format | Online Article Text |
id | pubmed-10200045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102000452023-05-22 The experience of living with Niemann–Pick type C: a patient and caregiver perspective Golden, Emma van Gool, Raquel Cay, Mariesa Goodlett, Benjamin Cao, Amanda Al-Hertani, Walla Upadhyay, Jaymin Orphanet J Rare Dis Research BACKGROUND: Niemann–Pick disease type C (NPC) is a rare inherited lysosomal storage disease typified by accumulation of cholesterol and other lipids in late endosomes/lysosomes, thereby resulting in a spectrum of neurological, psychiatric, and systemic symptoms (notably liver disease). Though it is well-known that NPC exacts a physical and emotional toll on both patients and caregivers, the burden of NPC can vary between patients, while the challenges of living with NPC can evolve over time (i.e., from time of diagnosis to the present day). To further grasp patient and caregiver perceptions and experiences with NPC, we carried out focus group discussions with pediatric and adult individuals with NPC (N = 19), with partial or full representation of the patient by their caregiver. Furthermore, we utilized our NPC focus group discussion to provide guidance on study design parameters and feasibility of prospective investigations aiming to characterize the central manifestations of NPC using neuroimaging, specifically, magnetic resonance imaging (MRI) methodology. RESULTS: Focus group discussions revealed that neurological signs, including declining cognition, memory loss, and psychiatric symptoms, as well as increasingly impaired mobility and motor function, are among the most pressing past and current concerns for patients and caregivers. Moreover, several participants also expressed concern over a loss of independence, social exclusion, and uncertainty for what the future holds. Caregivers described the challenges that participation in research poses, which included logistical difficulties mainly due to traveling with medical equipment and the need for sedation in a minority of patients when undergoing MRI. CONCLUSIONS: The findings derived from focus group discussions highlight the outstanding challenges that NPC patients and their caregivers face daily, while also providing direction on the potential scope and feasibility of future studies focusing on the central phenotypes of NPC. BioMed Central 2023-05-20 /pmc/articles/PMC10200045/ /pubmed/37210540 http://dx.doi.org/10.1186/s13023-023-02741-2 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Golden, Emma van Gool, Raquel Cay, Mariesa Goodlett, Benjamin Cao, Amanda Al-Hertani, Walla Upadhyay, Jaymin The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title | The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title_full | The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title_fullStr | The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title_full_unstemmed | The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title_short | The experience of living with Niemann–Pick type C: a patient and caregiver perspective |
title_sort | experience of living with niemann–pick type c: a patient and caregiver perspective |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200045/ https://www.ncbi.nlm.nih.gov/pubmed/37210540 http://dx.doi.org/10.1186/s13023-023-02741-2 |
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