Comorbidity of Neurally Mediated Syncope and Allergic Disease in Children

Yaru Wang1,2, Junbao Du1, Hongfang Jin1,2

  • 1Department of Pediatrics, Peking University First Hospital, Beijing, China.

Frontiers in Immunology
|September 28, 2020
PubMed

Insights

Pediatric neurally mediated syncope (NMS) frequently co-occurs with allergic diseases, affecting up to 40% of patients. Understanding this link is crucial for diagnosing and treating children with syncope and allergies.

Area of Science:

  • Pediatric Cardiology
  • Allergy and Immunology
  • Autonomic Nervous System Research

Background:

  • Neurally mediated syncope (NMS), encompassing vasovagal syncope (VVS), postural tachycardia syndrome (POTS), and situational syncope, is common in children.
  • Allergic diseases are highly prevalent in pediatric populations across various systems.
  • Growing evidence suggests a significant comorbidity between NMS and allergic diseases in children.

Purpose of the Study:

  • To review the clinical manifestations and pathogenesis of NMS and allergic disease comorbidity in children.
  • To highlight the prevalence and unique clinical features of this combined condition.
  • To explore potential underlying mechanisms linking NMS and allergies.

Main Methods:

  • Literature review of clinical studies on pediatric syncope and allergic diseases.
  • Analysis of reported comorbidity rates and clinical characteristics.
  • Examination of proposed etiological factors and regulatory pathways.

Main Results:

  • Approximately 30-40% of children with VVS and/or POTS have coexisting allergic diseases.
  • Children with this comorbidity exhibit distinct clinical presentations.
  • Potential contributing factors include autonomic nervous system (ANS) dysfunction, vasoactive element imbalance, and autoimmunity.
  • A strong association exists between asthma and cough syncope, a type of situational syncope.

Conclusions:

  • The comorbidity of NMS and allergic diseases is a significant concern in pediatric patients.
  • Autonomic dysfunction, allergic responses, and autoimmunity are implicated in the pathogenesis.
  • Further research is essential for improved diagnosis and therapeutic strategies for affected children.

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