Cardiorenal Protective Effects of Finerenone in Patients with Type 2 Diabetes Mellitus.

Archives of internal medicine research Pub Date : 2026-06-01 Epub Date: 2026-05-02 DOI:10.26502/aimr.0241
Talia Radparvar, Ilana Radparvar, Devendra K Agrawal
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Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder characterized by insulin resistance and progressive β-cell dysfunction, resulting in persistent hyperglycemia and long-term vascular complications. The global prevalence of T2DM continues to rise and is strongly associated with cardiovascular disease, chronic kidney disease, and the broader cardiovascular-kidney-metabolic (CKM) syndrome. This review summarizes the pathophysiology of T2DM, with emphasis on insulin resistance, endothelial dysfunction, oxidative stress, and activation of the renin-angiotensin-aldosterone system, all of which contribute to progressive end-organ damage. Chronic hyperglycemia further promotes inflammatory and fibrotic pathways that accelerate diabetic kidney disease and atherosclerotic cardiovascular disease. Finerenone, a non-steroidal mineralocorticoid receptor antagonist, has emerged as a therapeutic option for patients with T2DM and chronic kidney disease. Clinical trial data demonstrate that finerenone reduces albuminuria and provides cardiovascular and renal protection by reducing inflammation and fibrosis. Its use is associated with a generally acceptable safety profile, although hyperkalemia remains an important adverse effect requiring routine monitoring. Overall, T2DM is a multifactorial disease that requires comprehensive management targeting metabolic dysregulation as well as inflammatory and hormonal pathways. Finerenone represents an important advancement in cardiorenal protection. Understanding the interconnected mechanisms underlying CKM syndrome is essential for improving long-term outcomes in individuals with T2DM.

芬尼酮对2型糖尿病患者心脏肾脏的保护作用。
2型糖尿病(T2DM)是一种以胰岛素抵抗和进行性β细胞功能障碍为特征的慢性代谢紊乱,可导致持续性高血糖和长期血管并发症。2型糖尿病的全球患病率持续上升,并与心血管疾病、慢性肾脏疾病和更广泛的心血管-肾脏代谢(CKM)综合征密切相关。本文综述了T2DM的病理生理学,重点是胰岛素抵抗、内皮功能障碍、氧化应激和肾素-血管紧张素-醛固酮系统的激活,所有这些都有助于进行性终末器官损伤。慢性高血糖进一步促进炎症和纤维化途径,加速糖尿病肾病和动脉粥样硬化性心血管疾病。非甾体类矿物皮质激素受体拮抗剂非芬那酮已成为T2DM和慢性肾脏疾病患者的治疗选择。临床试验数据表明,细芬烯酮可减少蛋白尿,并通过减少炎症和纤维化提供心血管和肾脏保护。尽管高钾血症仍然是一个需要常规监测的重要不良反应,但它的使用具有普遍可接受的安全性。总的来说,T2DM是一种多因素疾病,需要针对代谢失调以及炎症和激素途径进行综合管理。芬尼酮在心肾保护方面取得了重要进展。了解CKM综合征的相互关联机制对于改善T2DM患者的长期预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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