Quality of Life Changes in Early-Onset Multiple Sclerosis: A 4-Year Follow-Up Study

Laura Rosa1, Maria Petracca2,3, Antonio Carotenuto2

  • 1Department of Public Health, University of Naples Federico II, 80131 Naples, Italy.

Insights

Early-onset multiple sclerosis (MS) patients showed improved social functioning but decreased emotional functioning over four years. Relapses impacted social functioning changes, highlighting the need to support emotional acceptance and social connections.

Area of Science:

  • Neurology
  • Quality of Life Research
  • Pediatric Health

Background:

  • Early-onset multiple sclerosis (MS) significantly impacts young individuals' lives.
  • Longitudinal data on health-related quality of life (HRQoL) in this demographic is crucial for understanding disease progression and support needs.

Purpose of the Study:

  • To investigate longitudinal changes in HRQoL among early-onset MS patients.
  • To determine the influence of disease activity, specifically relapses, on these HRQoL changes over time.

Main Methods:

  • A cohort of individuals with MS onset between 12-25 years was followed for four years.
  • Health-related quality of life was assessed using the Paediatric Quality of Life inventory (PedsQL) at baseline and year 4.
  • Paired samples t-tests and linear mixed-effects models were used to analyze HRQoL changes and the effect of relapses.

Main Results:

  • No significant longitudinal changes were found in overall PedsQL scores or physical, school, and psychological functioning.
  • A significant increase in social functioning (p < 0.001) and a decrease in emotional functioning (p = 0.006) were observed.
  • Relapses significantly affected changes in social functioning (p = 0.044) but not emotional functioning.

Conclusions:

  • Juvenile-onset MS leads to distinct longitudinal HRQoL changes, with social functioning improving and emotional functioning declining.
  • Disease activity, indicated by relapses, plays a role in altering social functioning over time.
  • Interventions should focus on fostering emotional acceptance of limitations and maintaining social connections to preserve quality of life in young MS patients.

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