Assani Mohamed-Zakaria, Novac Marius Bogdan, Dijmărescu Anda Lorena, Stroe-Ionescu Alexandra-Ștefania, Boldeanu Mihail Virgil, Siloși Isabela, Boldeanu Lidia
Doctoral School, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Department of Immunology, Faculty of Medicine, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Life (Basel). 2025 Aug 13;15(8):1287. doi: 10.3390/life15081287.
Chronic kidney disease (CKD) is a multifactorial disorder increasingly recognized as a systemic condition marked by persistent inflammation, oxidative stress, dyslipidemia, and endothelial dysfunction. Diabetic nephropathy, a leading cause of CKD, amplifies cardiovascular risk through intertwined mechanisms beyond traditional risk factors. This review synthesizes current evidence on the interplay between inflammation, oxidative stress, and atherosclerosis in CKD, with a special focus on emerging molecular biomarkers-PCSK9, EPHX2, AOPPs, and TBARSs-and their integration with clinical indices. These markers illuminate pathophysiological networks underlying CKD progression and cardiovascular complications, offering novel insights into risk stratification, disease monitoring, and targeted therapy. By exploring molecular and clinical intersections, this review underscores the potential of a personalized, biomarker-driven approach to CKD management.
慢性肾脏病(CKD)是一种多因素疾病,越来越被认为是一种全身性疾病,其特征为持续炎症、氧化应激、血脂异常和内皮功能障碍。糖尿病肾病是CKD的主要病因,它通过超越传统危险因素的相互交织机制增加心血管风险。本综述综合了目前关于CKD中炎症、氧化应激和动脉粥样硬化之间相互作用的证据,特别关注新兴分子生物标志物——前蛋白转化酶枯草溶菌素9(PCSK9)、环氧水解酶2(EPHX2)、晚期氧化蛋白产物(AOPPs)和硫代巴比妥酸反应物(TBARSs)——以及它们与临床指标的整合。这些标志物揭示了CKD进展和心血管并发症背后的病理生理网络,为风险分层、疾病监测和靶向治疗提供了新的见解。通过探索分子与临床的交叉点,本综述强调了个性化、生物标志物驱动的CKD管理方法的潜力。