Kitao Takashi, Konishi Eriko, Itoh Noriaki, Hirata Ayumu
Department of Cardiology, Minoh City Hospital Osaka Japan.
Department of Diabetes/Endocrinology and Metabolism, Minoh City Hospital Osaka Japan.
Circ Rep. 2024 Dec 14;7(1):37-46. doi: 10.1253/circrep.CR-24-0142. eCollection 2025 Jan 10.
The urinary albumin-to-creatinine ratio (UACR) or urinary protein-to-creatinine ratio (UPCR) has been reported as predictors of cardiovascular and renal events. We aimed to evaluate the impact of changes in proteinuria severity on the prognosis of hypertensive patients post-esaxerenone initiation.
Hypertensive patients who commenced esaxerenone (n=164) were classified into 3 groups according to baseline UACR or UPCR, based on the modified proteinuria severity classification: A1 (normal; n=35); A2 (microalbuminuria/mild proteinuria; n=49); and A3 (macroalbuminuria/severe proteinuria; n=80). At 6 months post-esaxerenone initiation, these patients were then reclassified into 3 groups: Á1 (n=48); Á2 (n=66); and Á3 (n=50). Á2 was further subdivided into 2 groups: Á2a (n=34); and Á2b (n=32), the latter representing patients who improved from A3. The primary endpoint was defined as the composite of cardiovascular and renal death, heart failure hospitalization, non-fatal myocardial infarction, initiation of dialysis, and estimated glomerular filtration rate decline exceeding 40%. Severity of proteinuria improved significantly after 6 months (P=0.003). The incidence of the primary endpoint was significantly higher in Á3 compared with Á1 (log-rank P<0.001); however, no significant difference was observed between Á1 and Á2b (log-rank P=0.12).
Esaxerenone may ameliorate proteinuria severity and improve the prognosis of patients with macroalbuminuria or severe proteinuria.
尿白蛋白与肌酐比值(UACR)或尿蛋白与肌酐比值(UPCR)已被报道为心血管和肾脏事件的预测指标。我们旨在评估蛋白尿严重程度的变化对起始依普利酮治疗的高血压患者预后的影响。
根据改良的蛋白尿严重程度分类,将开始使用依普利酮的高血压患者(n = 164)按基线UACR或UPCR分为3组:A1(正常;n = 35);A2(微量白蛋白尿/轻度蛋白尿;n = 49);A3(大量白蛋白尿/重度蛋白尿;n = 80)。在开始使用依普利酮6个月后,这些患者再被重新分为3组:Á1(n = 48);Á2(n = 66);Á3(n = 50)。Á2进一步细分为2组:Á2a(n = 34);Á2b(n = 32),后者代表从A3改善的患者。主要终点定义为心血管和肾脏死亡、心力衰竭住院、非致命性心肌梗死、开始透析以及估计肾小球滤过率下降超过40%的复合终点。6个月后蛋白尿严重程度显著改善(P = 0.003)。Á3组主要终点的发生率显著高于Á1组(对数秩检验P < 0.001);然而,Á1组和Á2b组之间未观察到显著差异(对数秩检验P = 0.12)。
依普利酮可能改善蛋白尿严重程度并改善大量白蛋白尿或重度蛋白尿患者的预后。