Key result
Aldosterone breakthrough occurred in 28% of patients with type 2 diabetes and overt nephropathy 1 year after initiating angiotensin II receptor blocker treatment, but did not predict kidney outcomes.
Why the study?
What are the determinants and consequences of aldosterone breakthrough after angiotensin II receptor blockade in patients with type 2 diabetes with overt nephropathy?
RCT (n=567)
What are the determinants and consequences of aldosterone breakthrough after angiotensin II receptor blockade in patients with type 2 diabetes with overt nephropathy?
Aldosterone breakthrough is common after 1 year of ARB therapy in diabetic nephropathy, particularly with short-acting agents and intensive BP lowering, but short-term increases do not predict worsening kidney function.
Answers are grounded in this paper and cite their sources.
Aldosterone breakthrough after ARB does not predict kidney outcomes in diabetic nephropathy; leaves open whether monitoring or add-on therapy is warranted.
BACKGROUND AND OBJECTIVES: 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. RESULTS: 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. CONCLUSIONS: 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.
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Moranne et al. (2013) conducted an RCT in Type 2 diabetes mellitus with overt nephropathy (n=567). Angiotensin II receptor blockers (losartan or telmisartan) was evaluated on Aldosterone breakthrough (increase >10% over baseline serum aldosterone levels). Aldosterone breakthrough occurred in 28% of patients with type 2 diabetes and overt nephropathy 1 year after initiating angiotensin II receptor blocker treatment, but did not predict kidney outcomes.
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