Liu Bin, Gao Xin, Teng Haolin, Zhou Honglan, Gao Baoshan, Li Faping
Department of Urology II, The First Hospital of Jilin University, Changchun, 130021, Jilin, China.
Sci Rep. 2024 Sep 16;14(1):20346. doi: 10.1038/s41598-024-68448-x.
Chronic Kidney Disease (CKD) stands as a substantial challenge within the global health landscape. The elevated metabolic demands essential for sustaining normal kidney function have propelled an increasing interest in unraveling the intricate relationship between mitochondrial dysfunction and CKD. However, the authentic causal relationship between these two factors remains to be conclusively elucidated. This study endeavors to address this knowledge gap through the Mendelian Randomization (MR) method. We utilized large-scale QTL datasets (including 31,684 eQTLs samples, 1980 mQTLs samples, and 35,559 pQTLs samples) to precisely identify key genes related to mitochondrial function as exposure factors. Subsequently, we employed GWAS datasets (comprising 480,698 CKD samples and 1,004,040 eGFRcrea samples) as outcome factors. Through a comprehensive multi-level analysis (encompassing expression, methylation, and protein quantification loci), we evaluated the causal impact of these genes on CKD and estimated glomerular filtration rate (eGFR). The integration and validation of diverse genetic data, complemented by the application of co-localization analysis, bi-directional MR analysis, and various MR methods, notably including inverse variance weighted, have collectively strengthened our confidence in the robustness of these findings. Lastly, we validate the outcomes through examination in human RNA sequencing datasets encompassing various subtypes of CKD. This study unveils significant associations between the glycine amidinotransferase (GATM) and CKD, as well as eGFR. Notably, an augmentation in GATM gene and protein expression corresponds to a diminished risk of CKD, whereas distinct methylation patterns imply an increased risk. Furthermore, a discernible reduction in GATM expression is observed across diverse pathological subtypes of CKD, exhibiting a noteworthy positive correlation with GFR. These findings establish a causal relationship between GATM and CKD, thereby highlighting its potential as a therapeutic target. This insight lays the foundation for the development of potential therapeutic interventions for CKD, presenting substantial clinical promise.
慢性肾脏病(CKD)是全球健康领域面临的一项重大挑战。维持正常肾功能所需的代谢需求增加,促使人们越来越关注线粒体功能障碍与CKD之间的复杂关系。然而,这两个因素之间真正的因果关系仍有待最终阐明。本研究试图通过孟德尔随机化(MR)方法来填补这一知识空白。我们利用大规模QTL数据集(包括31684个eQTL样本、1980个mQTL样本和35559个pQTL样本)精确识别与线粒体功能相关的关键基因作为暴露因素。随后,我们将全基因组关联研究(GWAS)数据集(包括480698个CKD样本和1004040个估算肾小球滤过率(eGFRcrea)样本)用作结果因素。通过全面的多层次分析(包括表达、甲基化和蛋白质定量位点),我们评估了这些基因对CKD和估算肾小球滤过率(eGFR)的因果影响。不同遗传数据的整合与验证,辅之以共定位分析、双向MR分析以及各种MR方法(特别是逆方差加权法)的应用,共同增强了我们对这些发现稳健性的信心。最后,我们通过在包含CKD各种亚型的人类RNA测序数据集中进行检验来验证结果。本研究揭示了甘氨酸脒基转移酶(GATM)与CKD以及eGFR之间的显著关联。值得注意的是,GATM基因和蛋白质表达的增加对应着CKD风险的降低,而不同的甲基化模式则意味着风险增加。此外,在CKD的各种病理亚型中均观察到GATM表达明显降低,与肾小球滤过率(GFR)呈显著正相关。这些发现确立了GATM与CKD之间的因果关系,从而突出了其作为治疗靶点的潜力。这一见解为开发针对CKD的潜在治疗干预措施奠定了基础,展现出巨大的临床前景。