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Impact of endocrine dysregulation on disability and non-motor symptoms in pediatric onset multiple sclerosis.
Abe, Justin; Jafarpour, Saba; Vu, My H; O'Brien, Devon; Boyd, Natalie K; Vogel, Benjamin N; Nguyen, Lina; Paulsen, Kelli C; Saucier, Laura E; Ahsan, Nusrat; Mitchell, Wendy G; Santoro, Jonathan D.
Afiliação
  • Abe J; John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, United States.
  • Jafarpour S; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Vu MH; Biostatistics and Data Management Core, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • O'Brien D; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Boyd NK; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Vogel BN; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Nguyen L; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Paulsen KC; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Saucier LE; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Ahsan N; Department of Neurology, Keck School of Medicine of USC, Los Angeles, CA, United States.
  • Mitchell WG; Division of Neurology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Santoro JD; Department of Neurology, Keck School of Medicine of USC, Los Angeles, CA, United States.
Front Neurol ; 14: 1304610, 2023.
Article em En | MEDLINE | ID: mdl-38130835
ABSTRACT

Background:

Pediatric onset multiple sclerosis (POMS) commonly occurs at the time of various endocrine changes. Evaluation of the impact of endocrine status on disease severity in POMS has not been previously explored.

Objective:

This study sought to evaluate if sex and stress hormones in children with POMS impact motor and non-motor diseases severity.

Methods:

A single-center case control study was performed. Individuals with POMS were compared to individuals without neurologic disease. Each individual had three blood draws assessing stress and sex hormones between 0700 and 0900. Measures of fatigue (Epworth sleepiness scale), depression (PHQ-9), and quality of life (PedsQL) assessed at each visit.

Results:

Forty individuals with POMS and 40 controls were enrolled. Individuals with POMS had lower free testosterone (p = 0.003), cortisol (p < 0.001), and ACTH (p < 0.001) and had higher progesterone (p = 0.025) levels than controls. Relapses and EDSS were not impacted by endocrine variables. The POMS cohort had a significantly higher Epworth score (p < 0.001), PHQ-9 score (p < 0.001), and lower PQL score (p < 0.001) than controls. Non-motor measures were not associated with endocrine status.

Conclusion:

Free testosterone, cortisol, ACTH, and progesterone were abnormal in children with POMS although there was no association between endocrine status and markers of disease severity or non-motor symptoms of MS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article