The Fifth Clinical Medical College of Shanxi Medical University, Taiyuan, Shanxi 030001, China.
School of Public Health, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
J Immunol Res. 2022 Apr 28;2022:9284204. doi: 10.1155/2022/9284204. eCollection 2022.
To investigate the potential diagnostic and predictive significance of immune-related genes in IgA nephropathy (IgAN) and discover the abnormal glomerular inflammation in IgAN.
GSE116626 was used as a training set to identify different immune-related genes (DIRGs) and establish machine learning models for the diagnosis of IgAN; then, a nomogram model was generated based on GSE116626, and GSE115857 was used as a test set to evaluate its clinical value. Short Time-Series Expression Miner (STEM) analysis was also performed to explore the changing trend of DIRGs with the progression of IgAN lesions. GSE141344 was used with DIRGs to establish the ceRNA network associated with IgAN progression. Finally, ssGSEA analysis was performed on the GSE141295 dataset to discover the abnormal inflammation in IgAN.
Machine learning (ML) performed excellently in diagnosing IgAN using six DIRGs. A nomogram model was constructed to predict IgAN based on the six DIRGs. Three trends related to IgAN lesions were identified using STEM analysis. A ceRNA network associated with IgAN progression which contained 8 miRNAs, 14 lncRNAs, and 3 mRNAs was established. A higher macrophage ratio and lower CD4+ T cell ratio in IgAN compared to controls were observed, and the correlation between macrophages and monocytes in the glomeruli of IgAN patients was inverse compared to controls.
This study reveals the diagnostic and predictive significance of DIRGs in IgAN and finds that the imbalance between macrophages and CD4+ immune cells may be an important pathomechanism of IgAN. These results provide potential directions for the treatment and prevention of IgAN.
探讨免疫相关基因(DIRGs)在 IgA 肾病(IgAN)中的潜在诊断和预测意义,并发现 IgAN 中异常的肾小球炎症。
使用 GSE116626 作为训练集,以识别不同的免疫相关基因(DIRGs)并建立用于诊断 IgAN 的机器学习模型;然后,基于 GSE116626 生成列线图模型,并使用 GSE115857 作为测试集评估其临床价值。还进行了短时间序列表达挖掘(STEM)分析,以探讨 DIRGs 随 IgAN 病变进展的变化趋势。使用 GSE141344 与 DIRGs 建立与 IgAN 进展相关的 ceRNA 网络。最后,对 GSE141295 数据集进行 ssGSEA 分析,以发现 IgAN 中的异常炎症。
使用六个 DIRGs,机器学习(ML)在诊断 IgAN 方面表现出色。构建了一个列线图模型,基于这六个 DIRGs 预测 IgAN。通过 STEM 分析确定了与 IgAN 病变相关的三个趋势。建立了一个与 IgAN 进展相关的 ceRNA 网络,其中包含 8 个 miRNA、14 个 lncRNA 和 3 个 mRNA。与对照组相比,IgAN 患者的巨噬细胞比例较高,CD4+T 细胞比例较低,并且 IgAN 患者肾小球中巨噬细胞与单核细胞之间的相关性与对照组相反。
本研究揭示了 DIRGs 在 IgAN 中的诊断和预测意义,并发现巨噬细胞和 CD4+免疫细胞之间的失衡可能是 IgAN 的重要发病机制。这些结果为 IgAN 的治疗和预防提供了潜在的方向。