Impact of endocrine dysregulation on disability and non-motor symptoms in pediatric onset multiple sclerosis

Justin Abe1, Saba Jafarpour2, My H Vu3

  • 1John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, United States.

Frontiers in Neurology
|December 22, 2023
PubMed

Insights

Pediatric onset multiple sclerosis (POMS) is associated with altered sex and stress hormones, including lower testosterone and cortisol. However, these endocrine changes did not correlate with disease severity or non-motor symptoms in children with POMS.

Area of Science:

  • Pediatric Endocrinology
  • Neuroimmunology
  • Pediatric Neurology

Background:

  • Pediatric onset multiple sclerosis (POMS) often coincides with significant endocrine shifts.
  • The relationship between endocrine status and POMS disease severity remains under-explored.

Purpose of the Study:

  • To investigate the impact of sex and stress hormones on motor and non-motor disease severity in pediatric patients with multiple sclerosis.
  • To compare endocrine profiles of children with POMS to healthy controls.

Main Methods:

  • A single-center case-control study involving 40 children with POMS and 40 controls.
  • Three morning blood draws per participant to assess hormone levels (testosterone, cortisol, ACTH, progesterone).
  • Standardized questionnaires evaluated fatigue (Epworth Sleepiness Scale), depression (PHQ-9), and quality of life (PedsQL).

Main Results:

  • Children with POMS exhibited lower free testosterone, cortisol, and ACTH, alongside higher progesterone levels compared to controls.
  • No significant association was found between endocrine variables and relapse rates or Expanded Disability Status Scale (EDSS) scores.
  • The POMS group reported significantly higher fatigue and depression scores and lower quality of life.

Conclusions:

  • Children with POMS display distinct alterations in key sex and stress hormones.
  • Despite hormonal differences, endocrine status did not appear to influence motor disease markers or non-motor symptoms in this cohort.
Abstract

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