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Low iron storage in children and adolescents with neurally mediated syncope
Imad T Jarjour1, Laila K Jarjour
1Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA. jarjour@bcm.tmc.edu
Insights
Low iron storage, indicated by low serum ferritin (SF), is linked to neurally mediated syncope (NMS) in children. This suggests iron deficiency may play a role in the condition.
Area of Science:
- Pediatric Neurology
- Hematology
Background:
- Neurally mediated syncope (NMS) is a common cause of syncope in children.
- The underlying pathophysiology of NMS is not fully understood.
Purpose of the Study:
- To determine if low iron storage, measured by serum ferritin (SF), is associated with NMS in pediatric patients.
- To investigate the potential role of iron deficiency in NMS.
Main Methods:
- A retrospective study of 206 children evaluated for syncope.
- Serum ferritin (SF), iron, transferrin saturation, and hemoglobin levels were measured.
- Iron deficiency (ID) was defined as SF <12 microg/L; low iron storage as SF ≤25 microg/L.
Main Results:
- Children with NMS (71/106) showed a significantly higher prevalence of low iron storage (57% vs 17%) compared to other syncope causes.
- Patients with NMS had lower mean SF, transferrin saturation, and hemoglobin levels.
- Iron deficiency and anemia were exclusively observed in the NMS group.
Conclusions:
- Low iron storage and low serum ferritin are significantly associated with NMS in children.
- These findings suggest that iron deficiency may be a contributing pathophysiologic factor in NMS.
Objective:
To investigate whether neurally mediated syncope (NMS) is associated with low iron storage or serum ferritin (SF).
Study Design:
206 children evaluated between 2000 and 2004 for probable syncope at a tertiary care Pediatric Neurology Clinic were included in a retrospective study. Serum ferritin (SF), iron, total iron binding capacity, and hemoglobin were measured prospectively after initial history taking and physical examination, along with other diagnostic testing. We defined iron deficiency (ID) as SF <12 microg/L, and low iron storage as SF =25 microg/L.
Results:
Among 106 included patients with syncope, 71 had NMS and 35 had other causes of syncope. Patients with NMS, when compared with those with other causes of syncope, had a higher prevalence of low iron storage (57% vs 17%, P < .001) and lower mean values of SF (27 vs 46 microg/L, P < .001), transferrin saturation (23 vs 31 %, P < .01), and hemoglobin (13.3 vs 14 g/dL, P < .05). Only patients with NMS had ID (15%), anemia (11%), or ID with anemia (7%).
Conclusions:
Low iron storage or serum ferritin is associated with NMS and is a potentially pathophysiologic factor in NMS.
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