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非奈利酮用于患有慢性肾脏病和2型糖尿病的西班牙裔患者:一项事后FIDELITY分析

Finerenone in Hispanic Patients With CKD and Type 2 Diabetes: A Post Hoc FIDELITY Analysis.

作者信息

Rosas Sylvia E, Ruilope Luis M, Anker Stefan D, Pitt Bertram, Rossing Peter, Bonfanti Andres Angelo Cadena, Correa-Rotter Ricardo, González Fernando, Munoz Carlos Francisco Jaramillo, Pergola Pablo, Umpierrez Guillermo E, Scalise Andrea, Scott Charlie, Lawatscheck Robert, Joseph Amer, Bakris George L

机构信息

Kidney and Hypertension Unit, Joslin Diabetes Center and Harvard Medical School, Boston, MA.

Cardiorenal Translational Laboratory and Hypertension Unit, Institute of Research imas12, CIBER-CV, Hospital Universitario 12 de Octubre, and Faculty of Sport Sciences, European University of Madrid, Madrid, Spain.

出版信息

Kidney Med. 2023 Aug 1;5(10):100704. doi: 10.1016/j.xkme.2023.100704. eCollection 2023 Oct.

Abstract

RATIONALE & OBJECTIVE: In FIDELITY, finerenone improved cardiorenal outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes. This analysis explores the efficacy and safety of finerenone in Hispanic patients.

STUDY DESIGN

Post hoc analysis of the FIDELITY prespecified pooled analysis of the FIDELIO-DKD and FIGARO-DKD randomized control trials.

SETTING & PARTICIPANTS: Patients with type 2 diabetes and CKD (urinary albumin-to-creatinine ratio [UACR] of ≥30 to <300 mg/g and estimated glomerular filtration rate [eGFR] of ≥25-≤90 mL/min/1.73 m, or UACR of ≥300 to ≤5,000 and eGFR of ≥25 mL/min/1.73 m) on optimized renin-angiotensin system blockade.

INTERVENTION

Finerenone or placebo.

OUTCOMES

Cardiovascular composite (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure); kidney composite (kidney failure, sustained ≥57% eGFR decline, or renal death); change in UACR.

RESULTS

Of 13,026 patients, 2,099 (16.1%) self-identified as Hispanic. Median follow-up was 3.0 years. The cardiovascular composite outcome occurred in 10.0% of Hispanic patients receiving Finerenone and in 12.3% of Hispanic patients receiving placebo (HR, 0.80; 95% CI, 0.62-1.04). This was consistent with non-Hispanic patients (HR, 0.87; 95% CI, 0.79-0.97; = 0.59). The kidney composite outcome occurred in 6.5% and 6.6% of Hispanic patients with finerenone and placebo, respectively (HR, 0.94; 95% CI, 0.67-1.33). The risk reduction was consistent with that observed in non-Hispanic patients (HR, 0.75; 95% CI, 0.64-0.87; = 0.22). Finerenone reduced UACR by 32% at month 4 in both Hispanic and non-Hispanic patients versus placebo ( < 0.001 for both patient groups). The safety profile of finerenone and incidence of hyperkalemia was similar between Hispanic and non-Hispanic patient groups.

LIMITATIONS

Small sample size, short follow-up time, and lower treatment adherence in the Hispanic population.

CONCLUSIONS

Overall, the efficacy and safety of finerenone were similar in Hispanic and non-Hispanic patients with CKD and type 2 diabetes.

FUNDING

Bayer AG.

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT02540993, NCT02545049.

PLAIN-LANGUAGE SUMMARY: Chronic kidney disease (CKD) in patients with type 2 diabetes occurs more frequently in Hispanic patients than in non-Hispanic patients, with a more rapid progression to kidney failure. Treatment with finerenone reduces the risk of having a kidney or heart event (such as starting dialysis or having a heart attack) in patients with CKD and type 2 diabetes. Because clinical trials that investigate treatments for CKD and type 2 diabetes have not included enough Hispanic patients, the benefits of treatments particularly for Hispanic patients are frequently unknown. This study explores the benefits of finerenone in Hispanic patients. Overall, the study shows that finerenone can provide kidney and heart benefits in Hispanic patients with CKD and type 2 diabetes, as it does in non-Hispanic patients.

摘要

原理与目的

在FIDELITY研究中,非奈利酮改善了慢性肾脏病(CKD)合并2型糖尿病患者的心肾结局。本分析探讨非奈利酮在西班牙裔患者中的疗效和安全性。

研究设计

对FIDELIO-DKD和FIGARO-DKD随机对照试验的FIDELITY预先指定的汇总分析进行事后分析。

设置与参与者

接受优化肾素-血管紧张素系统阻断治疗的2型糖尿病合并CKD患者(尿白蛋白与肌酐比值[UACR]≥30至<300mg/g,估计肾小球滤过率[eGFR]≥25-≤90mL/min/1.73m²,或UACR≥300至≤5000mg/g且eGFR≥25mL/min/1.73m²)。

干预措施

非奈利酮或安慰剂。

结局指标

心血管复合结局(心血管死亡、非致死性心肌梗死、非致死性卒中或因心力衰竭住院);肾脏复合结局(肾衰竭、eGFR持续下降≥57%或肾脏死亡);UACR变化。

结果

在13026例患者中,2099例(16.1%)自我认定为西班牙裔。中位随访时间为3.0年。接受非奈利酮的西班牙裔患者中心血管复合结局发生率为10.0%,接受安慰剂的西班牙裔患者中为12.3%(风险比[HR],0.80;95%置信区间[CI],0.62-1.04)。这与非西班牙裔患者一致(HR,0.87;95%CI,0.79-0.97;P=0.59)。接受非奈利酮和安慰剂的西班牙裔患者中肾脏复合结局发生率分别为6.5%和6.6%(HR,0.94;95%CI,0.67-1.33)。风险降低与非西班牙裔患者中观察到的情况一致(HR,0.75;CC,0.64-0.87;P=0.22)。与安慰剂相比,非奈利酮在第4个月时使西班牙裔和非西班牙裔患者的UACR均降低了32%(两组患者P均<0.001)。非奈利酮的安全性概况和高钾血症发生率在西班牙裔和非西班牙裔患者组中相似。

局限性

样本量小、随访时间短以及西班牙裔人群中治疗依从性较低。

结论

总体而言,非奈利酮在西班牙裔和非西班牙裔CKD合并2型糖尿病患者中的疗效和安全性相似。

资助

拜耳公司。

试验注册

ClinicalTrials.gov标识符:NCT02540993、NCT02545049。

通俗易懂的总结

2型糖尿病患者中的慢性肾脏病(CKD)在西班牙裔患者中比在非西班牙裔患者中更常见,且向肾衰竭进展更快。非奈利酮治疗可降低CKD合并2型糖尿病患者发生肾脏或心脏事件(如开始透析或心脏病发作)的风险。由于研究CKD和2型糖尿病治疗方法的临床试验未纳入足够多的西班牙裔患者,因此治疗对西班牙裔患者的益处往往未知。本研究探讨了非奈利酮对西班牙裔患者的益处。总体而言,该研究表明非奈利酮可为CKD合并2型糖尿病的西班牙裔患者带来肾脏和心脏方面的益处,就如同对非西班牙裔患者一样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b54c/10514441/9be8c320c85d/gr1.jpg

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