Abstract | Rationale & Objective:
Heart failure treatment relies on loop diuretics to induce natriuresis and decongestion, but the therapy is often limited by diuretic resistance. We explored the association of renin-angiotensin-aldosterone system (RAAS) activation with diuretic response. Study Design: Observational cohort. Setting & Population: Euvolemic ambulatory adults with chronic heart failure were administered torsemide in a monitored environment. Predictors: Outcomes: Analytical Approach: Robust linear regression models estimated the associations of each RAAS intermediate with outcomes. Results: The analysis included 56 participants, and the median age was 65 years; 50% were women, and 41% were Black. The median home diuretic dose was 80-mg furosemide equivalents. In unadjusted and multivariable-adjusted models, higher levels of RAAS measures were generally associated with lower diuretic efficiency. Higher plasma total renin remained significantly associated with lower sodium output per doubling of diuretic dose (β = -0.41 [-0.76, -0.059] per SD change) with adjustment; higher plasma total and active renin were significantly associated with lower fractional excretion of sodium per doubling of diuretic dose (β = -0.48 [-0.83, -0.14] and β = -0.51 [-0.95, -0.08], respectively) in adjusted models. Stratification by RAAS inhibitor use did not substantially alter these associations. Limitations: Small sample size; highly selected participants; associations may not be causal. Conclusions: Among multiple measures of RAAS activation, higher plasma total and active renin levels were consistently associated with lower diuretic response. These findings highlight the potential drivers of diuretic resistance and underscore the need for high-quality trials of decongestive therapy enhanced by RAAS blockade.
|
Authors | Jonathan G Amatruda, Rebecca Scherzer, Veena S Rao, Juan B Ivey-Miranda, Michael G Shlipak, Michelle M Estrella, Jeffrey M Testani |
Journal | Kidney medicine
(Kidney Med)
Vol. 4
Issue 6
Pg. 100465
(Jun 2022)
ISSN: 2590-0595 [Electronic] United States |
PMID | 35620081
(Publication Type: Journal Article)
|