Blood pressure and Cardiorenal Outcomes With Finerenone in Chronic Kidney Disease in Type 2 Diabetes

被引:30
|
作者
Ruilope, Luis M. [1 ,2 ,3 ,4 ]
Agarwal, Rajiv [5 ,6 ]
Anker, Stefan D. [7 ,8 ]
Filippatos, Gerasimos [9 ]
Pitt, Bertram [10 ]
Rossing, Peter [11 ,12 ]
Sarafidis, Pantelis [13 ]
Schmieder, Roland E. [14 ]
Joseph, Amer [15 ]
Rethemeier, Nicole [16 ]
Nowack, Christina [17 ]
Bakris, George L. [18 ]
机构
[1] Inst Res Imas12, Cardiorenal Translat Lab, Madrid, Spain
[2] Inst Res Imas12, Hypertens Unit, Madrid, Spain
[3] Hosp Univ 12 Octubre, CIBER CV, Madrid, Spain
[4] European Univ Madrid, Fac Sport Sci, Madrid, Spain
[5] Richard L Roudebush VA Med Ctr, Indianapolis, IN USA
[6] Indiana Univ, Indianapolis, IN 46204 USA
[7] Charite, Dept Cardiol CVK, Berlin, Germany
[8] Charite, Berlin Inst Hlth Ctr Regenerat Therapies, German Ctr Cardiovasc Res, Partner Site Berlin, Berlin, Germany
[9] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Sch Med, Dept Cardiol, Athens, Greece
[10] Univ Michigan, Sch Med, Dept Med, Ann Arbor, MI 48104 USA
[11] Steno Diabet Ctr Copenhagen, Herlev, Denmark
[12] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[13] Aristotle Univ Thessaloniki, Hippokration Hosp, Dept Nephrol, Thessaloniki, Greece
[14] Univ Hosp Erlangen, Dept Nephrol & Hypertens, Erlangen, Germany
[15] Bayer AG, Cardiol & Nephrol Clin Dev, Berlin, Germany
[16] Bayer AG, Stat & Data Insights, Wuppertal, Germany
[17] Bayer AG, Clin Dev Operat, Res & Dev, Wuppertal, Germany
[18] Univ Chicago Med, Dept Med, Chicago, IL USA
关键词
blood pressure; chronic kidney diseases; finerenone; mineralocorticoid receptor antagonist; systolic blood pressure; type; 2; diabetes; DOUBLE-BLIND; HYPERTENSION; SPIRONOLACTONE; ASSOCIATION; FAILURE;
D O I
10.1161/HYPERTENSIONAHA.122.19744
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
BACKGROUND: Chronic kidney disease is frequently associated with hypertension and poorly controlled blood pressure can lead to chronic kidney disease progression. Finerenone, a nonsteroidal mineralocorticoid receptor antagonist, significantly improves cardiorenal outcomes in patients with chronic kidney disease and type 2 diabetes. This analysis explored the relationship between office systolic blood pressure (SBP) and cardiorenal outcomes with finerenone in FIDELIO-DKD trial (Finerenone in Reducing Kidney Failure and Disease Progression in Diabetic Kidney Disease). METHODS: Patients with type 2 diabetes, urine albumin-to-creatinine ratio 30 to 5000 mg/g, and estimated glomerular filtration rate of 25 to <75 mL/min per 1.73 m(2) receiving optimized renin-angiotensin system blockade, were randomized to finerenone or placebo. For this analysis, patients (N=5669) were grouped by baseline office SBP quartiles. RESULTS: Finerenone reduced office SBP across the baseline office SBP quartiles, including patients with baseline office SBP of >148 mm Hg. Overall, patients with lower baseline office SBP quartile and greater declines from baseline in SBP were associated with better cardiorenal outcomes. The risk of primary kidney and key secondary cardiovascular composite outcomes was consistently reduced with finerenone versus placebo irrespective of baseline office SBP quartiles (Pfor interaction 0.87 and 0.78, respectively). A time-varying analysis revealed that 13.8% and 12.6% of the treatment effect with finerenone was attributed to the change in office SBP for the primary kidney composite outcome and the key secondary cardiovascular outcome, respectively. CONCLUSIONS: In FIDELIO-DKD, cardiorenal outcomes improved with finerenone irrespective of baseline office SBP. Reductions in office SBP accounted for a small proportion of the treatment effect on cardiorenal outcomes.
引用
收藏
页码:2685 / 2695
页数:11
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