De Cosmo Salvatore, Pontremoli Roberto, Giandalia Annalisa, Manicardi Valeria, Rocca Alberto, Nicolucci Antonio, Rossi Maria Chiara, Lucisano Giuseppe, Graziano Giusi, Di Bartolo Paolo, Di Cianni Graziano, Candido Riccardo, Russo Giuseppina T
Department of Medical Sciences, Scientific Institute "Casa Sollievo Della Sofferenza", San Giovanni Rotondo, FG, Italy.
Department of Internal Medicine, University of Genoa and I.R.C.C.S., Viale Benedetto XV, 16125, Genoa, Italy.
J Nephrol. 2025 Mar;38(2):589-596. doi: 10.1007/s40620-024-02171-8. Epub 2024 Dec 15.
We evaluated the proportion of Type 2 diabetes (T2D) patients with chronic kidney disease (CKD) participating in the AMD (Association of Medical Diabetologists) Annals initiative who met the eligibility criteria for phase III-studies on finerenone, showing its renal and cardiovascular benefits.
This analysis involved all T2D patients seen in 2019 in 282 diabetes centers in Italy, for whom data on kidney function (estimated glomerular filtration rate and albuminuria) were available. Data are presented separately for different scenarios, covering the population with main eligibility criteria for inclusion in the FIDELIO-DKD and FIGARO-DKD trials.
Among 343,037 T2D patients involved in the analysis, 5.4% met the eligibility criteria of the FIDELIO-DKD study (13.3% if we consider the population with fundus data) and 22.3% met those of the FIGARO-DKD trial. Overall, 110,000 (33%) patients were eligible for treatment with finerenone, with a male prevalence, an average age of 71 years, and good control of the main risk factors (HbA1c 7.3%; BP 138/76 mmHg; LDL-c 87 mg/dl), albeit with large percentages of not well controlled patients (50% with SBP > 140 mmHg; > 30% with LDL-c > 100 mg/dl). Over 12% were on sodium/glucose cotransporter 2 inhibitors or glucagon-like peptide 1 receptor agonists. Based on the event rate from the FIDELITY pooled analysis, the number of potentially avoidable events was 21.7 per 1000 eligible patients for the cardiovascular composite outcome and 16.7 for the renal outcome.
This analysis showed that approximately 33% of patients with T2D present the main eligibility criteria for treatment with finerenone and could therefore benefit from it in the near future.
我们评估了参与AMD(糖尿病医生协会)年鉴计划的2型糖尿病(T2D)合并慢性肾脏病(CKD)患者中,符合非奈利酮III期研究资格标准的患者比例,该研究显示了非奈利酮对肾脏和心血管的益处。
该分析纳入了2019年在意大利282个糖尿病中心就诊的所有T2D患者,这些患者有肾功能数据(估计肾小球滤过率和蛋白尿)。数据按不同情况分别呈现,涵盖了符合FIDELIO-DKD和FIGARO-DKD试验主要纳入标准的人群。
在参与分析的343,037例T2D患者中,5.4%符合FIDELIO-DKD研究的资格标准(若考虑有眼底数据的人群,则为13.3%),22.3%符合FIGARO-DKD试验的资格标准。总体而言,110,000例(33%)患者有资格接受非奈利酮治疗,男性患病率较高,平均年龄为71岁,主要危险因素控制良好(糖化血红蛋白7.3%;血压138/76 mmHg;低密度脂蛋白胆固醇87 mg/dl),尽管仍有很大比例的患者控制不佳(50%收缩压>140 mmHg;>30%低密度脂蛋白胆固醇>100 mg/dl)。超过12%的患者正在使用钠-葡萄糖协同转运蛋白2抑制剂或胰高血糖素样肽1受体激动剂。根据FIDELITY汇总分析的事件发生率,每1000例符合条件的患者中,心血管复合结局的潜在可避免事件数为21.7,肾脏结局为16.7。
该分析表明,约33%的T2D患者具备接受非奈利酮治疗的主要资格标准,因此在不久的将来可能从中获益。