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Modifying chronic kidney disease progression with the mineralocorticoid receptor antagonist finerenone in patients with type 2 diabetes
被引:15
|作者:
DeFronzo, Ralph A.
[1
]
Bakris, George L.
[2
]
机构:
[1] UT Hlth & Texas Diabet Inst, Dept Med, Diabet Div, San Antonio, TX USA
[2] Univ Chicago, Dept Med, Sch Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
来源:
关键词:
chronic kidney disease;
mineralocorticoid receptor antagonist;
type;
2;
diabetes;
ANGIOTENSIN-ALDOSTERONE SYSTEM;
BASE-LINE CHARACTERISTICS;
CHRONIC HEART-FAILURE;
RENAL INJURY;
US ADULTS;
OXIDATIVE STRESS;
BLOCKADE;
OUTCOMES;
NEPHROPATHY;
MORTALITY;
D O I:
10.1111/dom.14696
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
In patients with type 2 diabetes, chronic kidney disease (CKD) is the most common cause of kidney failure. With its increasing prevalence and limited treatment options, CKD is a major contributor to the global burden of disease. Although recent guidelines for the control of hypertension and hyperglycaemia, as well as the use of renin-angiotensin system inhibitors and, more recently, sodium-glucose co-transporter-2 inhibitors, have improved outcomes for patients with CKD and diabetes, there is still a high residual risk of CKD progression and adverse cardiovascular events. In this review, we discuss the recently published FIDELIO-DKD and FIGARO-DKD studies and FIDELITY prespecified individual patient analysis. Together, these studies have established finerenone, a novel non-steroidal mineralocorticoid receptor antagonist, as an effective treatment for kidney and cardiovascular protection and welcome addition to the pillars of treatment to slow CKD progression in patients with type 2 diabetes.
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页码:1197 / 1205
页数:9
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