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Differences in iron deficiency anemia and mean platelet volume between children with simple and complex febrile
Eda Ozaydin1, Ebru Arhan, Bilge Cetinkaya
1The Ministry of Health, Ankara Children's Health and Diseases Hematology-Oncology, Education and Research Hospital, Infancy Service, Turkey. eozaydin2001@yahoo.com
Insights
Iron deficiency anemia is more common in complex febrile seizures (CFS) than simple febrile seizures (SFS). Lower mean platelet volume (MPV) in CFS suggests brain inflammation, potentially linking iron metabolism, inflammation, and epilepsy development.
Area of Science:
- Pediatric Neurology
- Hematology
- Epilepsy Research
Background:
- Febrile seizures (FSs) are common in children.
- Iron deficiency anemia (IDA) has been previously linked to FSs.
- Mean platelet volume (MPV) is an emerging inflammatory marker.
Purpose of the Study:
- To compare iron deficiency anemia, demographic characteristics, and MPV between simple febrile seizures (SFS) and complex febrile seizures (CFS).
- To investigate the role of MPV as an inflammatory marker in differentiating SFS and CFS.
Main Methods:
- Retrospective analysis of 493 children aged 6 months to 6 years diagnosed with SFS or CFS.
- Comparison of demographic data, gestational age, birth weight, family history, and hematological parameters including Hb, Htc, MCV, Plt, RDW, and MPV.
- Statistical analysis to determine significant differences between the SFS and CFS groups.
Main Results:
- No significant differences in mean age, gender ratio, or family history of FS between SFS and CFS groups.
- Significant differences observed in gestational age, consanguinity, family history of epilepsy, and birth weight.
- Children with CFS showed significantly lower Hb, Htc, MCV, and MPV levels, and higher Plt and RDW levels compared to SFS.
- Iron deficiency anemia was more prevalent in the CFS group (16.2%) than the SFS group (12.1%).
Conclusions:
- Iron deficiency anemia is more frequently observed in children with complex febrile seizures.
- Lower MPV levels in CFS suggest an underlying inflammatory process in the brain.
- Findings support the hypothesis that inflammation plays a role in the development of epilepsy following complex febrile seizures.
- Further research is needed to elucidate the interplay between iron metabolism, inflammation, and seizure activity.
Objective:
The relationship between iron deficiency anemia and febrile seizures (FSs) were examined in several studies before. The aim of our study is to find out the differences regarding iron deficiency anemia, demographic characteristics and mean platelet volume (MPV) which is an inflammatory marker between simple and complex febrile seizure groups.
Methods:
In this study, the authors investigated the recordings of 493 children with a diagnosis of simple and complex febrile seizure, aged between 6 months and 6 years, followed between 2002 and 2010 retrospectively.
Results:
Mean age and male/female ratio were similar in two groups. There was no significant difference regarding with age, gender and family history of FS between two groups. We found significant difference statistically with respect to gestational age, consanguinity, family history of epilepsy and birth weight between two groups. The mean levels of Hb, Htc, MCV were lower and Plt and RDW levels were higher in children with CFS than SFS group, the differences were statistically significant (p: 0.001). A higher proportion of children with CFS (16.2%) had iron deficiency anemia compared to SFS group (12.1%). Mean platelet volume (MPV) of CFS (7.99±0.96fL) were significantly lower than that of SFS group (8.77±0.75) (p<0.001).
Conclusions:
The results of this study suggests that iron deficiency anemia is more frequently seen among the patients with CFS than the patients with SFS. The lower levels of MPV as an inflammatory marker, supports the idea that CFS is a brain inflammatory disease and the consequence of this inflammatory mechanism is the development of the epilepsy. Further studies are necessary to highlight the relationship between iron metabolism, inflammation and seizures.
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