Zhanxin Zhu, Jin Zhao, Yunlong Qin, Jinguo Yuan, Yumeng Zhang, Anjing Wang, Mei Han, Qiao Zheng, Xiaoxuan Ning, Shiren Sun
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Additionally, a reverse MR analysis was conducted to evaluate any potential reverse causal effects.</p><p><strong>Results: </strong>The IVW analysis provided strong evidence supporting a causal link between CRC and MN (odds ratio (OR), 1.485; 95% confidence interval (CI), 1.131 - 1.951, p = 0.004). Similar findings were obtained from the weighted median analysis (OR, 1.515; 95% CI, 1.120 - 2.051, p = 0.007) and the weighted mode (OR, 1.572; 95% CI, 0.996 - 2.480, p = 0.084). The MR-Egger regression results indicated that the presence of horizontal pleiotropy was unlikely to bias the findings (intercept, -0.047; p = 0.611). MR-Egger regression did not show any causal association between CRC and MN (OR, 2.075; 95% CI, 0.584 - 7.373, p = 0.292). Reverse MR analysis suggested that MN is not a causative factor for CRC. Cochran's Q test, the funnel plot, and leave-one-out sensitivity analysis demonstrated the robustness of the MR study.</p><p><strong>Conclusion: </strong>Based on the genetic evidence obtained from this MR study, it can be concluded that CRC may serve as a risk factor for the development of MN. 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引用次数: 0
摘要
背景:研究表明结直肠癌(CRC)和膜性肾病(MN)可能相互关联。然而,现有的常规研究方法未能建立两者之间的结论性关系。材料和方法:CRC和MN的全基因组关联数据来自先前发表的全基因组关联研究(GWAS)。采用逆方差加权(IVW)、加权中位数、加权模式和孟德尔随机化(MR)-Egger回归对数据进行分析。采用异质性检验、多效性检验和留一检验进行敏感性分析。此外,还进行了反向磁共振分析,以评估任何潜在的反向因果效应。结果:IVW分析提供了强有力的证据支持CRC和MN之间的因果关系(优势比(OR), 1.485;95%置信区间(CI), 1.131 ~ 1.951, p = 0.004)。加权中位数分析(OR, 1.515; 95% CI, 1.120 - 2.051, p = 0.007)和加权模型(OR, 1.572; 95% CI, 0.996 - 2.480, p = 0.084)也得到了类似的结果。MR-Egger回归结果表明,水平多效性的存在不太可能影响结果(截距,-0.047;p = 0.611)。MR-Egger回归未显示CRC和MN之间存在任何因果关系(OR, 2.075; 95% CI, 0.584 - 7.373, p = 0.292)。反向MR分析提示MN不是结直肠癌的致病因素。Cochran’s Q检验、漏斗图和留一敏感性分析证明了MR研究的稳健性。结论:基于本MR研究获得的遗传学证据,可以得出结论,CRC可能是MN发展的危险因素。这些发现将有助于未来对MN机制的理解。
The causal association of colorectal cancer on the risk of membranous nephropathy: A Mendelian randomization study.
Background: Studies have suggested that colorectal cancer (CRC) and membranous nephropathy (MN) could be associated with each other. However, the existing conventional research methods fail to establish a conclusive relationship between the two conditions.
Materials and methods: The genome-wide association data for CRC and MN were obtained from previously published genome-wide association studies (GWAS). Inverse variance weighted (IVW), weighted median, weighted mode, and Mendelian randomization (MR)-Egger regression, were employed to analyze the data. Sensitivity analyses were conducted using the heterogeneity test, pleiotropic test, and leave-one-out test. Additionally, a reverse MR analysis was conducted to evaluate any potential reverse causal effects.
Results: The IVW analysis provided strong evidence supporting a causal link between CRC and MN (odds ratio (OR), 1.485; 95% confidence interval (CI), 1.131 - 1.951, p = 0.004). Similar findings were obtained from the weighted median analysis (OR, 1.515; 95% CI, 1.120 - 2.051, p = 0.007) and the weighted mode (OR, 1.572; 95% CI, 0.996 - 2.480, p = 0.084). The MR-Egger regression results indicated that the presence of horizontal pleiotropy was unlikely to bias the findings (intercept, -0.047; p = 0.611). MR-Egger regression did not show any causal association between CRC and MN (OR, 2.075; 95% CI, 0.584 - 7.373, p = 0.292). Reverse MR analysis suggested that MN is not a causative factor for CRC. Cochran's Q test, the funnel plot, and leave-one-out sensitivity analysis demonstrated the robustness of the MR study.
Conclusion: Based on the genetic evidence obtained from this MR study, it can be concluded that CRC may serve as a risk factor for the development of MN. These findings will facilitate a future understanding of the mechanisms underlying MN.
期刊介绍:
Clinical Nephrology appears monthly and publishes manuscripts containing original material with emphasis on the following topics: prophylaxis, pathophysiology, immunology, diagnosis, therapy, experimental approaches and dialysis and transplantation.