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非奈利酮的心脏肾脏获益:保护肾脏和心脏。

Cardiorenal benefits of finerenone: protecting kidney and heart.

机构信息

Cardiology Department, Hospital Clínico Universitario Santiago de Compostela, Centro de investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), Santiago de Compostela, Spain.

Nephrology Department, Hospital Clínico Universitario de Valencia, Universidad de Valencia, Valencia, Spain.

出版信息

Ann Med. 2023 Dec;55(1):502-513. doi: 10.1080/07853890.2023.2171110.

Abstract

Persons with diabetes and chronic kidney disease (CKD) have a high residual risk of developing cardiovascular (CV) complications despite treatment with renin-angiotensin system blockers and sodium-glucose cotransporter type 2 inhibitors. Overactivation of mineralocorticoid receptors plays a key role in the progression of renal and CV disease, mainly by promoting inflammation and fibrosis. Finerenone is a nonsteroidal selective mineralocorticoid antagonist. Recent clinical trials, such as FIDELIO-DKD and FIGARO-DKD and the combined analysis FIDELITY have demonstrated that finerenone decreases albuminuria, risk of CKD progression, and CV risk in subjects with type 2 diabetes (T2D) and CKD. As a result, finerenone should thus be considered as part of a holistic approach to kidney and CV risk in persons with T2D and CKD. In this narrative review, the impact of finerenone treatment on the CV system in persons with type 2 diabetes and CKD is analyzed from a practical point of view.Key messages:Despite inhibition of renin-angiotensin system and sodium-glucose cotransporter type 2, persons with type 2 diabetes (T2D) and chronic kidney disease (CKD) remain on high cardiovascular (CV) residual risk.Overactivation of mineralocorticoid receptors plays a key role in the progression of renal and CV disease, mainly by promoting inflammation and fibrosis that is not targeted by traditional treatments.Finerenone is a nonsteroidal selective mineralocorticoid antagonist that decreases not only albuminuria, but also the risk of CKD progression, and CV risk in subjects with T2D and CKD.

摘要

尽管抑制了肾素-血管紧张素系统和钠-葡萄糖协同转运蛋白 2,患有 2 型糖尿病(T2D)和慢性肾脏病(CKD)的患者仍面临较高的心血管(CV)残余风险。

矿皮质激素受体的过度激活在肾脏和心血管疾病的进展中起着关键作用,主要通过促进炎症和纤维化来实现,而传统治疗方法并不能针对这一过程。

非奈利酮是一种非甾体类选择性盐皮质激素拮抗剂,可降低 T2D 和 CKD 患者的蛋白尿、CKD 进展风险和 CV 风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a114/9891162/8a7a47aa0dc9/IANN_A_2171110_F0001_C.jpg

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