Association between endothelial dysfunction and otoneurological symptoms in children with sickle cell disease

Mara Renata Rissatto-Lago1,2, Cristina Salles1, Fernando Gesteira Campos de Pinho1

  • 1a Bahiana School of Medicine and Public Health , Salvador , Brazil.

Insights

Children with sickle cell disease (SCD) experience more otoneurological symptoms like vertigo. Endothelial dysfunction is linked to these symptoms and vaso-occlusive events in pediatric SCD patients.

Area of Science:

  • Pediatric Hematology
  • Vascular Biology
  • Otolaryngology

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder.
  • Endothelial dysfunction and otoneurological symptoms are potential complications in SCD.
  • Vaso-occlusive phenomena are characteristic of SCD.

Purpose of the Study:

  • To investigate the association between endothelial dysfunction and otoneurological symptoms in children with SCD.
  • To explore the link between endothelial dysfunction, otoneurological symptoms, and vaso-occlusive phenomena in pediatric SCD.

Main Methods:

  • A cross-sectional study involving 54 children (6-19 years) with SCD (genotype SS) and healthy controls (genotype AA).
  • Oto-neurological symptoms were assessed via questionnaires.
  • Endothelial function was evaluated using flow-mediated dilation (FMD) of the brachial artery via Doppler ultrasound.

Main Results:

  • Otoneurological symptoms, including tinnitus and vertigo, were significantly more prevalent in the SCD group (46.4%) compared to controls (15.4%).
  • A negative correlation was found between FMD percentage and the duration of vertigo in SCD patients (r = -0.432, p = 0.022).
  • Linear regression indicated that reduced FMD was associated with increased vertigo duration, and painful crises correlated with vertigo duration (r = 0.3, p = 0.04).

Conclusions:

  • Vascular endothelial damage in the labyrinthine artery may contribute to otoneurological symptoms, such as vertigo, in SCD patients.
  • The study confirms an association between endothelial dysfunction, otoneurological symptoms, and vaso-occlusive phenomena in children with sickle cell disease.
Abstract

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