Department of Pharmaceutical Technology, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Sosnowiec, Poland.
Department of Paediatric Neurology, School of Medicine in Katowice, Medical University of Silesia in Katowice, Katowice, Poland.
Clin Appl Thromb Hemost. 2019 Jan-Dec;25:1076029619869500. doi: 10.1177/1076029619869500.
The role of genetic risk factors for ischemic stroke seems to be in particular significance in pediatric patients. Numerous polymorphic variants of genes encoding proteins, that is, plasminogen activator inhibitor as well as coagulation factors, involved in the coagulation cascade may be related to arterial ischemic stroke (AIS) both in adults and children. We performed systematic review and 2 meta-analyses to assess possible correlations between common plasminogen activator inhibitor () and polymorphisms and ischemic stroke in children. We searched PubMed to identify available data published before October 2018 using appropriate keywords and inclusion criteria. Finally, 12 case-control studies were included: 8 analyzing polymorphism (600 children with stroke and 2152 controls) and 4- polymorphism (358 children with stroke and 451 controls). R and Comprehensive Meta-Analysis software were used to analyze the impact of the particular polymorphism in the following models: dominant, recessive, additive, and allelic. No publication bias was observed in both meta-analyses. In case of polymorphism, we observed no relation between 4G4G genotype of 4G allele and ischemic stroke in children. We also demonstrated lack of association between polymorphism and childhood ischemic stroke. In children with AIS, the and polymorphisms are not risk factors for the disease.
遗传风险因素在缺血性卒中中的作用在儿科患者中似乎尤为重要。许多编码蛋白质的基因(即纤溶酶原激活物抑制剂和凝血因子)的多态性变异与成年人和儿童的动脉缺血性卒中(AIS)有关。我们进行了系统评价和 2 项荟萃分析,以评估常见的纤溶酶原激活物抑制剂()和多态性与儿童缺血性卒中之间的可能相关性。我们使用适当的关键词和纳入标准在 PubMed 上搜索了 2018 年 10 月之前发表的可用数据。最终纳入了 12 项病例对照研究:8 项分析 多态性(600 名卒中患儿和 2152 名对照)和 4-多态性(358 名卒中患儿和 451 名对照)。使用 R 和 Comprehensive Meta-Analysis 软件在以下模型中分析特定多态性的影响:显性、隐性、相加和等位基因。这两项荟萃分析均未观察到发表偏倚。在 多态性方面,我们没有观察到 4G 等位基因的 4G4G 基因型与儿童缺血性卒中之间存在关系。我们还表明,多态性与儿童缺血性卒中之间没有关联。在 AIS 患儿中,和多态性不是疾病的危险因素。