Han Siliang, Xue Ling, Chen Chunhong, Xie Junmin, Kong Fanchang, Zhang Fang
Department of Cardiology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Department of Cardiology, Affiliated Hospital of Hebei University, Baoding, Hebei, China.
Front Cardiovasc Med. 2024 Oct 18;11:1416412. doi: 10.3389/fcvm.2024.1416412. eCollection 2024.
Observational studies have found that vascular endothelial growth factor (VEGF) levels are associated with the risk of cardiovascular disease. However, it remains unclear whether VEGF levels have a causal effect on the risk of atrial fibrillation.
A two-sample Mendelian randomization (MR) study was conducted to explore the causal relationship between VEGF levels and the risk of atrial fibrillation. Genetic variants associated with VEGF [VEGF-A, VEGF-C, VEGF-D, VEGF receptor-2 (VEGFR-2), VEGFR-3] and atrial fibrillation (atrial fibrillation, atrial fibrillation and flutter) were used as instrumental variables. Data on genetic variants were obtained from published genome-wide association studies (GWAS) or the IEU Open GWAS project. Inverse-variance weighted (IVW) analysis was used as the primary basis for the results, and sensitivity analyses were used to reduce bias. Causal relationships were expressed as odds ratio (OR) with 95% confidence interval (CI), and a -value of <0.1 corrected for False Discovery Rate (FDR) ( < 0.1) was considered to have a significant causal relationship.
Genetically predicted high levels of VEGF-A [OR = 1.025 (95%CI: 1.004-1.047), = 0.060] and VEGF-D [OR = 1.080 (95%CI: 1.039-1.123), = 0.001]] were associated with an increased risk of atrial fibrillation, while no causal relationship was observed between VEGF-C ( = 0.419), VEGFR-2 ( = 0.784), and VEGFR-3 ( = 0.899) and atrial fibrillation risk. Moreover, only genetically predicted high levels of VEGF-D [OR = 1.071 (95%CI: 1.014-1.132), = 0.087] increased the risk of atrial fibrillation and flutter. Sensitivity analysis demonstrated that the relationship between VEGF-D levels and the risk of atrial fibrillation was robust.
This study supports a causal association between high VEGF-D levels and increased risk of atrial fibrillation.
观察性研究发现血管内皮生长因子(VEGF)水平与心血管疾病风险相关。然而,VEGF水平对心房颤动风险是否具有因果效应仍不清楚。
进行了一项两样本孟德尔随机化(MR)研究,以探讨VEGF水平与心房颤动风险之间的因果关系。与VEGF [VEGF-A、VEGF-C、VEGF-D、血管内皮生长因子受体-2(VEGFR-2)、VEGFR-3]和心房颤动(心房颤动、心房颤动合并扑动)相关的基因变异用作工具变量。基因变异数据来自已发表的全基因组关联研究(GWAS)或IEU Open GWAS项目。采用逆方差加权(IVW)分析作为结果的主要依据,并进行敏感性分析以减少偏倚。因果关系以比值比(OR)及其95%置信区间(CI)表示,校正错误发现率(FDR)后的P值<0.1(P<0.1)被认为具有显著因果关系。
遗传预测的高水平VEGF-A [OR = 1.025(95%CI:1.004 - 1.047),P = 0.060]和VEGF-D [OR = 1.080(95%CI:1.039 - 1.123),P = 0.001]与心房颤动风险增加相关,而未观察到VEGF-C(P = 0.419)、VEGFR-2(P = 0.784)和VEGFR-3(P = 0.899)与心房颤动风险之间存在因果关系。此外,仅遗传预测的高水平VEGF-D [OR = 1.071(95%CI:1.014 - 1.132),P = 0.087]增加了心房颤动合并扑动的风险。敏感性分析表明VEGF-D水平与心房颤动风险之间的关系是稳健的。
本研究支持高水平VEGF-D与心房颤动风险增加之间存在因果关联。