教育程度与静脉血栓栓塞发生的因果关系。

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY
Sitong Guo, Sitao Tan, Shiran Qin, Dandan Xu, Henghai Su, Xiaoyu Chen
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引用次数: 0

摘要

背景:教育程度(EA)与动脉血栓性疾病之间的关系已被报道,但教育程度(EA)与静脉血栓栓塞(VTE)之间的因果关系尚不清楚。我们的目的是使用双样本孟德尔随机化(MR)方法评估EA对静脉血栓栓塞的因果影响。方法:利用暴露因子EA和结局因子VTE对全基因组关联研究(GWAS)进行数据挖掘。采用双样本孟德尔随机化(TSMR)分析,结果采用随机效应逆方差加权法(IVW)。多效性分析采用MR-Egger法,敏感性分析留一种方法,以验证数据的可靠性。结果:在FinnGen联盟和UK Biobank中,基因预测的EA降低与VTE风险降低相关(FinnGen-VTE: OR = 0.848;95% ci 0.776-0.927;p = 2.84 × 10-4;Ukb-vte or = 0.996;95% ci 0.994-0.999;P = 0.008)在乘法随机效应IVW模型下。所有敏感性分析结果一致,未检测到水平多效性。结论:磁共振技术提示EA与静脉血栓栓塞的发生之间存在潜在的负相关关系。因此,低EA患者应更加警惕VTE的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Causal relationship between educational attainment and the occurrence of venous thromboembolism.

Background: The association between educational attainment (EA) and arterial thrombotic disease has been reported, but the causal relationship between EA and venous thromboembolism (VTE) is not clear. We aimed to assess the causal effect of EA on VTE using the two-sample mendelian randomization (MR) method.

Methods: Data mining was conducted on the genome wide association studies (GWAS), with exposure factor EA and outcome factor VTE. Two-sample Mendelian Randomization (TSMR) analysis was conducted, with the results obtained from the random effects inverse variance weighted method (IVW). Use the MR-Egger method for pleiotropy analysis and leave one method for sensitivity analysis to verify the reliability of the data.

Results: Genetically predicted decreased EA was associated with a decreased risk of VTE in both the FinnGen consortium and UK Biobank (FinnGen-VTE: OR = 0.848; 95% CI 0.776-0.927; P = 2.84 × 10-4; UKB-VTE OR = 0.996; 95% CI 0.994-0.999; P = 0.008) under a multiplicative random-effects IVW model. Results were consistent in all sensitivity analyses and no horizontal pleiotropy was detected.

Conclusions: The MR technique instructed a potential inverse causative relationship between EA and occurrence of VTE. Therefore, patients with low EA should be more vigilant about the occurrence of VTE.

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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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