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A Thrombotic Stroke Model Based On Transient Cerebral Hypoxia-ischemia
Published on: August 18, 2015
Inherited prothrombotic risk factors in children with first ischemic stroke
Renata Zadro1, Désirée Coen Herak
1Clinical Hospital Center Zagreb University School of Medicine, Department of Laboratory Diagnostics, Zagreb, Croatia. rzadro@mef.hr
Insights
Inherited prothrombotic factors are more common in children with stroke, but a single factor is a mild risk. Further research is needed to understand childhood stroke mechanisms and improve prevention.
Area of Science:
- Pediatric Neurology
- Genetics
- Hematology
Background:
- Childhood stroke is a complex condition with numerous identified risk factors.
- Genetic predisposition plays a role, with inherited prothrombotic conditions being a key area of investigation.
Purpose of the Study:
- To review inherited prothrombotic risk factors in pediatric ischemic stroke.
- To analyze the consistency of findings across studies investigating these factors in children.
Main Methods:
- Review of meta-analyses and studies investigating inherited prothrombotic risk factors in pediatric first ischemic stroke.
- Analysis of discrepancies in results attributed to methodological variations.
Main Results:
- Several inherited prothrombotic factors are investigated in pediatric stroke, including Factor V Leiden and protein deficiencies.
- Meta-analyses show inconsistent results for many factors due to methodological differences.
- Inherited prothrombotic factors are more frequent in pediatric stroke but are mild risk factors individually.
Conclusions:
- While inherited prothrombotic factors are elevated in pediatric stroke, they do not fully explain stroke occurrence.
- Multi-center studies are crucial for robust data collection and understanding childhood stroke.
- Further research is essential for improved primary and secondary prevention strategies for childhood stroke.
Abstract:
Stroke in children is a heterogeneous disorder. Over 100 risk factors for stroke have been reported and genetic predisposition to stroke has been established. The most frequently reported risk factors are congenital heart malformations, hemolytic anemias, collagen vascular diseases, some rare inborn metabolic disorders, trauma, infection and thrombophilia. The aim of this article is to provide an overview of investigated inherited prothrombotic risk factors in children with first ischemic stroke. Various prothrombotic risk factors have been investigated in pediatric stroke including elevated homocysteine and lipoprotein (a), antithrombin, protein C and protein S deficiency, Factor V Leiden, Factor II G20210A and plasminogen activator inhibitor-1 4G/5G polymorphism. Despite similar criteria for inclusion of different studies in meta-analyses investigating first ischemic stroke in children, the obtained results were not consistent for all prothrombotic risk factors. The discrepancies found could be explained by methodological issues like different sample sizes, patient populations included and lack of controls. In order to provide the necessary power for randomized control trials, multi-center, multi-national approaches like International Pediatric Stroke Study have been initiated with the aim to describe risk factors for childhood stroke and explore their relationship with presentation, age, geography, and infarct characteristics. Although it is evident from numerous studies that the frequency of inherited prothrombotic factors is increased in pediatric stroke, single thrombophilia does not fully explain stroke in a child as it represents only a mild risk factor. Further studies are needed, as improved understanding of underlying mechanisms will improve primary and secondary prevention of childhood stroke.
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