Nephrology and, †Epidemiology Departments, Nice University Hospital, Nice, France;, ‡ASH Comprehensive Hypertension Center, University of Chicago, Chicago, Illinois, §Institut National de la Santé et de la Recherche Médicale U1081, Nice Sophia-Antipolis University, Nice, France.
Clin J Am Soc Nephrol. 2013 Oct;8(10):1694-701. doi: 10.2215/CJN.06960712. Epub 2013 Aug 8.
Inhibition of the renin-angiotensin-aldosterone system decreases proteinuria and slows estimated GFR decline in patients with type 2 diabetes mellitus with overt nephropathy. Serum aldosterone levels may increase during renin-angiotensin-aldosterone system blockade. The determinants and consequences of this aldosterone breakthrough remain unknown.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: This study examined the incidence, determinants, and changes associated with aldosterone breakthrough in a posthoc analysis of a randomized study that compared the effect of two angiotensin II receptor blockers in patients with type 2 diabetes mellitus with overt nephropathy.
Of 567 of 860 participants included in this posthoc analysis, 28% of participants developed aldosterone breakthrough, which was defined by an increase greater than 10% over baseline values of serum aldosterone levels after 1 year of angiotensin II receptor blocker treatment. Factors independently associated with aldosterone breakthrough at 1 year were lower serum aldosterone and potassium levels at baseline, higher decreases in sodium intake, systolic BP, and estimated GFR from baseline to 1 year, and use of losartan versus telmisartan. Aldosterone breakthrough at 6 months was not sustained at 1 year in 69% of cases, and it did not predict estimated GFR decrease and proteinuria increase between 6 months and 1 year.
Aldosterone breakthrough is a frequent event 1 year after initiating renin-angiotensin-aldosterone system blockade, particularly in participants exposed to intensive lowering of BP with sodium depletion and short-acting angiotensin II receptor blockers. Short-term serum aldosterone level increases at 6 months are not associated with negative kidney outcomes between 6 months and 1 year.
抑制肾素-血管紧张素-醛固酮系统可减少蛋白尿并减缓 2 型糖尿病显性肾病患者的估算肾小球滤过率下降。在肾素-血管紧张素-醛固酮系统阻断期间,血清醛固酮水平可能会升高。这种醛固酮突破的决定因素和后果仍不清楚。
设计、设置、参与者和测量:本研究在一项比较两种血管紧张素 II 受体阻滞剂对 2 型糖尿病显性肾病患者影响的随机研究的事后分析中,研究了醛固酮突破的发生率、决定因素和变化。
在这项事后分析中,纳入了 860 名参与者中的 567 名,其中 28%的参与者出现了醛固酮突破,定义为在血管紧张素 II 受体阻滞剂治疗 1 年后,血清醛固酮水平比基线值升高超过 10%。1 年内与醛固酮突破相关的独立因素包括基线时血清醛固酮和钾水平较低、钠摄入量、收缩压和估算肾小球滤过率从基线到 1 年的降幅较高,以及使用氯沙坦与替米沙坦。在 69%的情况下,6 个月时的醛固酮突破在 1 年内并未持续,并且它不能预测 6 个月至 1 年内估算肾小球滤过率下降和蛋白尿增加。
在开始肾素-血管紧张素-醛固酮系统阻断后 1 年内,醛固酮突破是一种常见事件,尤其是在接受强化降压和短期作用血管紧张素 II 受体阻滞剂治疗的患者中。6 个月时短期血清醛固酮水平升高与 6 个月至 1 年内的肾脏不良结局无关。