Association of SERPINE1 rs1799889 polymorphism with arterial ischemic stroke in children: a systematic review and meta-analysis

被引:1
|
作者
Bahrami, Reza [1 ]
Dastgheib, Seyed Alireza [2 ]
Mirjalili, Hamid [3 ]
Setayesh, Sepideh [4 ]
Shaker, Seyed Hossein [5 ]
Mirjalili, Seyed Reza [6 ]
Noorishadkam, Mahmood [6 ]
Neamatzadeh, Hossein [5 ,7 ]
机构
[1] Shiraz Univ Med Sci, Neonatal Res Ctr, Shiraz, Iran
[2] Shiraz Univ Med Sci, Sch Med, Dept Med Genet, Shiraz, Iran
[3] Shahid Sadoughi Univ Med Sci, Dept Emergency Med, Yazd, Iran
[4] Shiraz Univ Med Sci, Sch Med, Shiraz, Iran
[5] Iran Univ Med Sci, Dept Emergency Med, Tehran, Iran
[6] Shahid Sadoughi Univ Med Sci, Mother & Newborn Hlth Res Ctr, Yazd, Iran
[7] Shahid Sadoughi Univ Med Sci, Dept Med Genet, Yazd, Iran
关键词
Arterial ischemic stroke; SERPINE1; polymorphism; meta-analysis; 4G/5G PROMOTER POLYMORPHISM; ACTIVATOR INHIBITOR-1 PAI-1; RISK-FACTORS; SUSCEPTIBILITY; GENE; POPULATION; FIBRINOLYSIS; KEY;
D O I
10.1080/15257770.2021.1966798
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inherited thrombophilias are well-established predisposing factors for venous thromboembolism, but their role in arterial ischemic stroke (AIS) in children, remains unclear. The association between SERPINE1 rs1799889 polymorphism and AIS in children was evaluated by several studies, whereas the results were conflicting. Thus, we performed this meta-analysis to combine and analyze the available studies in order to provide a more accurate result on the association. PubMed, Scopus, EMBASE, SciELO, MedRxiv, China Biology Medicine Disk, DeepDyve, CNKI, and Web of Science were used to identify all relevant articles published up to 30 November 2020, without any restrictions on ethnicity. Summary odds ratios (ORs) with 95% confidence intervals (CIs) were used to determine the strength of the associations. A total of eight case-control studies with 600 cases and 2,156 controls were selected. No significant association between SERPINE1 rs1799889 polymorphism and AIS in children susceptibility was noted. In the stratified analyses by ethnicity, source of controls, genotyping methods, and age groups, there was still no significant association between SERPINE1 rs1799889 polymorphism and AIS risk in children. This study suggested that SERPINE1 rs1799889 polymorphism might be not related to etiology of AIS in children. Moreover, well-designed, large-scale and multicenter clinical studies are required to improve and validate these results. Supplemental data for this article is available online at https://doi.org/10.1080/15257770.2021.1966798 .
引用
收藏
页码:1018 / 1035
页数:18
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