The 2025 European Society of Endocrinology criteria increased primary aldosteronism detection to 16.1% compared to 8.8% with 2016 criteria (p=0.009), identifying milder phenotypes.
Observational (n=137)
No
Do the 2025 European Society of Endocrinology criteria increase the detection of primary aldosteronism compared to 2016 criteria in hypertensive patients?
The 2025 European Society of Endocrinology criteria nearly double the detection of primary aldosteronism by identifying milder phenotypes, supporting the shift towards a biochemical phenotype-driven approach.
Effect estimate: 92% relative increase
Absolute Event Rate: 16.1% vs 8.8%
p-value: p=0.009
Objective: Primary aldosteronism is the most common cause of secondary hypertension, affecting up to 10% of hypertensive patients with disproportionate cardiovascular morbidity. The 2025 European Society of Endocrinology guidelines fundamentally revised diagnostic criteria by abandoning mandatory confirmatory testing in favor of a biochemical phenotype-driven approach. We compared primary aldosteronism prevalence and diagnostic performance using 2016 versus 2025 algorithms in hypertensive patients referred to a specialized center. Design and method: We retrospectively analyzed 137 consecutive patients referred for secondary hypertension work-up between June 2024 and June 2025. Plasma renin, aldosterone, and aldosterone-to-renin ratio were assessed before and after saline loading. Primary aldosteronism was defined according to 2016 criteria and 2025 criteria using locally validated thresholds. Results: rimary aldosteronism prevalence increased from 8.8% with 2016 criteria to 16.1% with 2025 criteria (p=0.009), representing a 92% relative increase. Diagnostic concordance reached 91.7% (k=0.61). Net reclassification improvement ranged from +148% to +175%. Newly diagnosed patients exhibited milder phenotypes with less severe/resistant hypertension (27% vs 73%, p=0.03), lower baseline aldosterone levels (95 vs 185 ng/L, p<0.001), and 82% negative saline infusion tests versus 18% in classical cases (p=0.002). Among 2025-diagnosed patients, 91% of newly identified cases showed intermediate lateralization probability, suggesting predominantly bilateral disease requiring medical management. The saline infusion test demonstrated a 50% false-negative rate. Despite this limitation, positive saline test remained the sole independent predictor of primary aldosteronism diagnosis (OR=3.25, 95%CI 1.22-8.67, p=0.019). Conclusions: The 2025 criteria nearly double primary aldosteronism detection by identifying milder phenotypes characterized by lower aldosterone levels and negative confirmatory tests. The high saline infusion test false-negative rate supports abandoning mandatory confirmatory testing. Implementation requires laboratory-specific threshold validation and prospective studies to confirm cardiovascular benefits of earlier identification.
Cordeanu et al. (Fri,) conducted a observational in Secondary hypertension (n=137). 2025 European Society of Endocrinology criteria vs. 2016 criteria was evaluated on Primary aldosteronism prevalence (92% relative increase, p=0.009). The 2025 European Society of Endocrinology criteria increased primary aldosteronism detection to 16.1% compared to 8.8% with 2016 criteria (p=0.009), identifying milder phenotypes.