Association between the plasminogen activator inhibitor-1 4G/5G polymorphism and risk of venous thromboembolism: A meta-analysis

• Published in: Thrombosis research Vol. 134; no. 6; pp. 1241 - 1248
• Main Authors: Wang, Jiarong, Wang, Chengdi, Chen, Nan, Shu, Chi, Guo, ‍Xiaojiang, He, Yazhou, Zhou, Yanhong
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.12.2014
• Subjects: 4G/5G polymorphism; Genetic Markers - genetics; Genetic Predisposition to Disease - epidemiology; Genetic Predisposition to Disease - genetics; Genetic susceptibility; Hematology, Oncology and Palliative Medicine; Humans; Incidence; Meta-analysis; Mutation - genetics; PAI-1; Plasminogen Activator Inhibitor 1 - genetics; Polymorphism, Single Nucleotide - genetics; Risk Factors; Venous thromboembolism; Venous Thromboembolism - epidemiology; Venous Thromboembolism - genetics; OR; DVT; Genetic susceptibility; CI; VTE; odds ratio; HT; Meta-analysis; factor V Leiden; Hardy–Weinberg equilibrium; PE; venous thromboembolism; HWE; PAI-1; confidence interval; hormone therapy; antiphospholipid antibody syndrome; deep venous thrombosis; pulmonary embolism; FVL; APL; 4G/5G polymorphism; Venous thromboembolism
• ISSN: 0049-3848; 1879-2472
• DOI: 10.1016/j.thromres.2014.09.035

Abstract Introduction The plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism was considered to be associated with risk of venous thromboembolism (VTE), while evidence remains inadequate. To provide a more accurate estimation of this relationship, we performed an updated meta-analysis of all eligible studies. Materials and Methods A systematical search was performed in PubMed, EMBASE, Wanfang, China National Knowledge Infrastructure (CNKI) and Cqvip databases to identify relevant studies published before March 6th 2014. The odds ratios (ORs) with 95% confidence intervals (CIs) were pooled using the fixed/random-effects model using Review Manager 5.1 and STATA 12.0. Results A total of 34 studies with 3561 cases and 5693 controls were analyzed. Overall, significant association between the PAI-1 4G/5G variant and VTE risk in total population (dominant model: OR = 1.32, 95%CI: 1.13-1.54) was observed. And this variant was also related to the deep vein thrombosis risk (dominant model: OR = 1.60, 95%CI: 1.24-2.06, P = 0.0003). In the subgroup analyses on ethnicity, significant results were obtained in both Asians (dominant model: OR = 2.08, 95%CI: 1.29-3.35, P = 0.003) and Caucasians (dominant model: OR = 1.31, 95%CI: 1.10-1.56, P = 0.003). However, no significant association was found in patients with provoked VTE. In terms of subgroup analyses on co-existence of other thrombotic risk factors, the PAI-1 4G/5G polymorphism was significantly associated with VTE risk in patients with factor V Leiden mutation (dominant model: OR = 1.72, 95%CI: 1.17-2.53), but not in patients with cancer or surgery. Conclusion Our findings demonstrate the role of PAI-1 4G/5G polymorphism being a risk candidate locus for VTE susceptibility, especially in patients with other genetic thrombophilic disorders.