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The quality of life in children with spinal muscular atrophy: a case–control study

OBJECTIVES: This study aimed to analyze the health-related quality of life (HRQoL) of patients with spinal muscular atrophy (SMA) based on the type of SMA, demographic and clinical features and compare HRQoL of these patients with a matched healthy control group.  METHODS: This was a case–control st...

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Autores principales: Zamani, Gholamreza, Ashrafi, Mahmoud Reza, Ghabeli, Homa, Akbari, Masood Ghahvechi, Mohammadi, Mahmoud, Badv, Reza Shervin, Hosseinpour, Sareh, Haghighi, Roya, Pourbakhtyaran, Elham, Khosroshahi, Nahid, Heidari, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743571/
https://www.ncbi.nlm.nih.gov/pubmed/36503502
http://dx.doi.org/10.1186/s12887-022-03751-y
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author Zamani, Gholamreza
Ashrafi, Mahmoud Reza
Ghabeli, Homa
Akbari, Masood Ghahvechi
Mohammadi, Mahmoud
Badv, Reza Shervin
Hosseinpour, Sareh
Haghighi, Roya
Pourbakhtyaran, Elham
Khosroshahi, Nahid
Heidari, Morteza
author_facet Zamani, Gholamreza
Ashrafi, Mahmoud Reza
Ghabeli, Homa
Akbari, Masood Ghahvechi
Mohammadi, Mahmoud
Badv, Reza Shervin
Hosseinpour, Sareh
Haghighi, Roya
Pourbakhtyaran, Elham
Khosroshahi, Nahid
Heidari, Morteza
author_sort Zamani, Gholamreza
collection PubMed
description OBJECTIVES: This study aimed to analyze the health-related quality of life (HRQoL) of patients with spinal muscular atrophy (SMA) based on the type of SMA, demographic and clinical features and compare HRQoL of these patients with a matched healthy control group.  METHODS: This was a case–control study of Patients with SMA in Iran. Sixty-six patients with SMA type II and III aged 8–18 years and also 264 healthy age, sex, and socio-economic matched individuals were enrolled. To assess the quality of life, we used the Persian version of the KIDSCREEN-27. RESULTS: The health-related quality of life between children with type II and type III SMA was not significant in all 5 subscales. However, HRQoL in healthy children was significantly higher than in SMA children in all 5 subscales. CONCLUSION: The quality of life in children with SMA was lower than the healthy control group in all subscales, and physical well-being and psychosocial aspects are the main domains of life impaired by SMA disease. However, no significant difference between the quality of life in children with SMA type II and type III was observed. 
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spelling pubmed-97435712022-12-13 The quality of life in children with spinal muscular atrophy: a case–control study Zamani, Gholamreza Ashrafi, Mahmoud Reza Ghabeli, Homa Akbari, Masood Ghahvechi Mohammadi, Mahmoud Badv, Reza Shervin Hosseinpour, Sareh Haghighi, Roya Pourbakhtyaran, Elham Khosroshahi, Nahid Heidari, Morteza BMC Pediatr Research OBJECTIVES: This study aimed to analyze the health-related quality of life (HRQoL) of patients with spinal muscular atrophy (SMA) based on the type of SMA, demographic and clinical features and compare HRQoL of these patients with a matched healthy control group.  METHODS: This was a case–control study of Patients with SMA in Iran. Sixty-six patients with SMA type II and III aged 8–18 years and also 264 healthy age, sex, and socio-economic matched individuals were enrolled. To assess the quality of life, we used the Persian version of the KIDSCREEN-27. RESULTS: The health-related quality of life between children with type II and type III SMA was not significant in all 5 subscales. However, HRQoL in healthy children was significantly higher than in SMA children in all 5 subscales. CONCLUSION: The quality of life in children with SMA was lower than the healthy control group in all subscales, and physical well-being and psychosocial aspects are the main domains of life impaired by SMA disease. However, no significant difference between the quality of life in children with SMA type II and type III was observed.  BioMed Central 2022-12-12 /pmc/articles/PMC9743571/ /pubmed/36503502 http://dx.doi.org/10.1186/s12887-022-03751-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (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
Zamani, Gholamreza
Ashrafi, Mahmoud Reza
Ghabeli, Homa
Akbari, Masood Ghahvechi
Mohammadi, Mahmoud
Badv, Reza Shervin
Hosseinpour, Sareh
Haghighi, Roya
Pourbakhtyaran, Elham
Khosroshahi, Nahid
Heidari, Morteza
The quality of life in children with spinal muscular atrophy: a case–control study
title The quality of life in children with spinal muscular atrophy: a case–control study
title_full The quality of life in children with spinal muscular atrophy: a case–control study
title_fullStr The quality of life in children with spinal muscular atrophy: a case–control study
title_full_unstemmed The quality of life in children with spinal muscular atrophy: a case–control study
title_short The quality of life in children with spinal muscular atrophy: a case–control study
title_sort quality of life in children with spinal muscular atrophy: a case–control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743571/
https://www.ncbi.nlm.nih.gov/pubmed/36503502
http://dx.doi.org/10.1186/s12887-022-03751-y
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