RICORS 2040, Instituto de Salud Carlos III, Servicio de Nefrología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
RICORS 2040, Instituto de Salud Carlos III, Servicio de Nefrología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Hipertens Riesgo Vasc. 2024 Apr-Jun;41(2):95-103. doi: 10.1016/j.hipert.2023.11.005. Epub 2024 Mar 19.
Evidence about nefroprotective effect with RAAS blockers in elderly patients with chronic kidney disease (CKD) without proteinuria is lacking. The primary outcome of our study is to evaluate the impact of RAAS blockers in CKD progression in elderly patients without proteinuria.
Multicenter open-label, randomized controlled clinical trial including patients over 65 year-old with hypertension and CKD stages 3-4 without proteinuria. Patients were randomized in a 1:1 ratio to either receive RAAS blockers or other antihypertensive drugs and were followed up for three years. Primary outcome is estimated glomerular filtration rate (eGFR) decline at 3 years. Secondary outcome measures include BP control, renal and cardiovascular events and mortality.
88 patients were included with a mean age of 77.9±6.1 years and a follow up period of 3 years: 40 were randomized to RAAS group and 48 to standard treatment. Ethiology of CKD was: 53 vascular, 16 interstitial and 19 of unknown ethiology. In the RAAS group eGFR slope during follow up was -4.3±1.1ml/min, whereas in the standard treatment group an increase on eGFR was observed after 3 years (+4.6±0.4ml/min), p=0.024. We found no differences in blood pressure control, number of antihypertensive drugs, albuminuria, potassium serum levels, incidence of cardiovascular events nor mortality during the follow up period.
In elderly patients without diabetes nor cardiopathy and with non proteinuric CKD the use of RAAS blockers does not show a reduction in CKD progression. The PROERCAN (PROgresión de Enfermedad Renal Crónica en ANcianos) trial (trial registration: NCT03195023).
缺乏关于肾素-血管紧张素-醛固酮系统(RAAS)阻滞剂在无蛋白尿的老年慢性肾脏病(CKD)患者中的肾保护作用的证据。我们研究的主要结局是评估 RAAS 阻滞剂在无蛋白尿的老年 CKD 患者中的 CKD 进展中的影响。
这是一项多中心、开放标签、随机对照临床试验,纳入了年龄在 65 岁以上、患有高血压和 CKD 3-4 期且无蛋白尿的患者。患者以 1:1 的比例随机分为 RAAS 阻滞剂组或其他降压药物组,并随访 3 年。主要结局是 3 年内估计肾小球滤过率(eGFR)的下降。次要结局包括血压控制、肾脏和心血管事件以及死亡率。
共纳入 88 例患者,平均年龄为 77.9±6.1 岁,随访时间为 3 年:40 例患者被随机分为 RAAS 组,48 例患者被随机分为标准治疗组。CKD 的病因分别为:53 例血管性、16 例间质性和 19 例病因不明。在 RAAS 组中,eGFR 斜率在随访期间为-4.3±1.1ml/min,而在标准治疗组中,eGFR 在 3 年后增加(+4.6±0.4ml/min),p=0.024。我们发现,在随访期间,血压控制、降压药物数量、蛋白尿、血钾水平、心血管事件发生率和死亡率无差异。
在无糖尿病和心脏病且无蛋白尿的老年 CKD 患者中,使用 RAAS 阻滞剂并不能降低 CKD 的进展。该 PROERCAN(PROgresión de Enfermedad Renal Crónica en ANcianos)试验(试验注册:NCT03195023)。