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Cited 7 time in webofscience Cited 7 time in scopus
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Integrative analyses of genes about venous thromboembolism: An umbrella review of systematic reviews and meta-analysesopen access

Authors
Lee, SangyeobLee, Chang HanSeo, Min SeokYoo, Jun-Il
Issue Date
Oct-2022
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
femoral head osteonecrosis; genetic variant; polymorphism; steroid; umbrella review
Citation
Medicine, v.101, no.43, pp E31162
Indexed
SCIE
SCOPUS
Journal Title
Medicine
Volume
101
Number
43
Start Page
E31162
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/29812
DOI
10.1097/MD.0000000000031162
ISSN
0025-7974
1536-5964
Abstract
Background: In recent years, many studies have found possible links between gene polymorphisms and venous thromboembolism (VTE). By identifying genetic risk factors before facing environmental risk factors such as surgical interventions and COVID-19 vaccination, we could rapidly respond to the risk of VTE. The aim of this study was to perform an umbrella review of genetic variants related to VTE. Integrative gene analysis of VTE was performed to identify critical genetic variations. Methods: This study conducted an umbrella review of systematic reviews and meta-analyses. All included studies were selected from the PubMed/MEDLINE database. To select eligible studies, the following variables were extracted: first author name; effect size of each study genetic variant; year of publication; the number of studies included in each article; ethnicity, sample size, P values, and heterogeneity estimates. To assess cumulative evidence in genetic epidemiology about effects of gene polymorphisms on VTE, Human Genome Epidemiology Network's Venice criteria were used. Methodological quality assessment was conducted with JBI Critical Appraisal Checklist for Systematic Reviews and Research Syntheses. Results: Genes provided in the present study with genetic variants associated with VTE were FVL (G1691A), Prothrombin (G20210A), MTHFR (C677T, A1298C), PAI-1 (4G/5G), factor VII activating protease (1601G > A), and endothelial protein C receptor (g.6936A_G, c.4600A_G). Among them, variants in FVL, Prothrombin, MTHFR, and PAI-1 showed high significance. Particularly, variants in Prothrombin (G20210A), MTHFR (C677T), and PAI-1 (4G/5G) had more than 2 types of model significance. Conclusion: The present study performed a systematic review of genetic variants associated with VTE. Our results could lead to a more comprehensive understanding of VTE etiology. These results could give a strategy of prediagnosis about evaluating individual risks of VTE who might be exposed to environmental risk factors.
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