Venous thromboembolism and ovarian cancer risk: a Mendelian randomized study

被引:0
作者
Liu, Xiaolin [1 ]
Wang, Shan [1 ]
Lv, Hongwei [1 ]
Chen, Enli [1 ]
Yu, Jing [1 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Canc Ctr, 95 Yong Rd, Beijing 100050, Peoples R China
基金
北京市自然科学基金;
关键词
Venous thromboembolism; Ovarian cancer; Mendelian randomization; TISSUE FACTOR; COAGULATION-FACTORS; SIGNALING PATHWAY; THROMBOSIS; PROGRESSION; MECHANISMS; MORTALITY; BIOLOGY; TARGET;
D O I
10.1007/s12672-024-01446-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction A potential link between venous thromboembolism and the risk of ovarian cancer has been identified in clinical practice. However, it is unclear whether there is a causal relationship between the two. In this study, we applied a univariate two-sample Mendelian randomization method to explain the possible link between venous thromboembolism and ovarian cancer pathogenesis at the genetic level, and pointed out that lipid metabolism and ovarian cancer pathogenesis have innovative basic experimental directions. Objective This study explored the causal effect between a history of venous thromboembolism and the risk of ovarian cancer. Methods Genome-Wide Association Study (GWAS) data of venous thromboembolism patients (n = 9176) of the same ethnicity were selected as study exposures, and GWAS data of ovarian cancer patients (n = 1218) of the same ethnicity were selected as study exposures. In this study, univariate two-sample Mendelian randomization analysis (UVMR) was performed separately using inverse variance weighted (IVW), MR-Egger regression, and weighted median (WM) to assess causal effects. In this study, Cochran's Q test, MR-Egger regression intercept term, MR-PRESSO, and leave-one-out method were used for sensitivity analysis to assess the stability and reliability of the results. Results The GWAS data screened in this study were all European ethnicity data. In this study, we found that genetically predicted history of venous thromboembolism was associated with an upward trend in ovarian cancer incidence, and the results of Weighted median, Simple mode, Weighted mode, and MR Egger showed a similar trend (OR = 1.0006, 95% CI: 1.00007-1.0013, p < 0.05). There was no heterogeneity of results (p = 0.18) and no horizontal pleiotropy (p = 0.77). The instrumental variables selected for venous thromboembolism in this study were all strong instrumental variables (F = 669.7). The results of the sensitivity analysis remained consistent. Conclusion The results of this study indicate that patients with a history of venous thromboembolism are at increased risk of developing ovarian cancer and point to possible associations between lipid metabolism genes, such as CYP4V2, and the development of ovarian cancer, which provide interesting directions for further basic research.
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页数:11
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