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Published on: September 15, 2017
Screening for primary aldosteronism in an argentinian population: a multicenter prospective study
Mariela Leal Reyna1, Reynaldo M Gómez2, Susana N Lupi3
1Complejo Médico Churruca-Visca, Buenos Aires, Argentina.
This study establishes cut-off values for aldosterone (ALD)/plasma renin activity (ARR) and ALD/plasma renin concentration (ARC) ratios in Argentinian hypertensive patients. The findings aim to improve screening for primary aldosteronism (PA) and guide future diagnostic approaches.
Area of Science:
- Endocrinology
- Clinical Diagnostics
- Hypertension Research
Background:
- Primary aldosteronism (PA) is a condition of autonomous aldosterone overproduction.
- The aldosterone (ALD)/plasma renin activity (ARR) ratio is a key screening tool, with increasing prevalence.
- Establishing reliable diagnostic cut-off values is crucial for accurate PA screening.
Purpose of the Study:
- To determine cut-off values (COV) for ARR and ALD/plasma renin concentration (ARC) ratios in an Argentinian population.
- To assess the diagnostic concordance (DC%) between ARR and ARC in PA screening.
- To evaluate the utility of these ratios for identifying PA in hypertensive patients.
Main Methods:
- A multicenter prospective study involving 353 subjects (104 controls, 249 hypertensive patients).
- Serum aldosterone, PRA, and ARR were measured. Plasma renin concentration (PRC) was measured in a subset for ARC determination.
- COVs were derived from the 95th percentile of control subjects.
Main Results:
- Established COVs: ARR of 36 and ARC of 2.39 (with ALD ≥ 15 ng/dL).
- ARR ≥ 36 identified PA in a higher percentage of hypertensive patients compared to previous reports.
- Diagnostic concordance between ARR and ARC was 79.1%, with significant correlation observed at higher renin levels.
Conclusions:
- This study provides the first Argentinian multicenter-derived COVs for ARR (36) and ARC (2.39).
- Applying ARR ≥ 36 increased PA confirmation rates in hypertensive patients.
- Further research is needed to establish the clinical utility of ARC due to its limited concordance at lower renin levels.
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