BMC Pediatrics (Dec 2022)

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

  • Gholamreza Zamani,
  • Mahmoud Reza Ashrafi,
  • Homa Ghabeli,
  • Masood Ghahvechi Akbari,
  • Mahmoud Mohammadi,
  • Reza Shervin Badv,
  • Sareh Hosseinpour,
  • Roya Haghighi,
  • Elham Pourbakhtyaran,
  • Nahid Khosroshahi,
  • Morteza Heidari

DOI
https://doi.org/10.1186/s12887-022-03751-y
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 5

Abstract

Read online

Abstract 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.

Keywords