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March 14, 2026Journal of Hypertension0 citations

Biological age acceleration in primary aldosteronism: associations with renin, aldosterone, aldosterone-to-renin ratio, and left ventricular mass index

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NLNing LiNLNingpeng LiangXZXiangtao Zhang

Key Result

In patients with primary aldosteronism, higher aldosterone-to-renin ratio was associated with increased biological age acceleration and greater left ventricular mass index (β = 0.640, P = 0.001).

Key Points

  • The study aims to understand how aldosterone and renin levels relate to biological age differences and cardiac mass in primary aldosteronism compared to essential hypertension.
  • Conducted a retrospective cross-sectional study of 1201 hypertensive adults
  • Compared biological age differences using the Gompertz law in primary aldosteronism and essential hypertension groups
  • Evaluated associations of plasma aldosterone concentration, plasma renin activity, and aldosterone-to-renin ratio with biological age difference via multivariable linear regression
  • Patients with primary aldosteronism had a significantly higher biological age difference than those with essential hypertension
  • Aldosterone-to-renin ratio was positively associated with biological age difference in primary aldosteronism
  • Higher biological age difference correlated with greater left ventricular mass index and excessive left ventricular mass index in primary aldosteronism

Structured PICO

P
Population
1201 hypertensive adults (785 with primary aldosteronism and 416 with essential hypertension)
C
Comparator
Patients with essential hypertension (EHT)
O
Outcome
Gompertz law–based biological age difference (GOLD BioAgeDiff)surrogate

In patients with primary aldosteronism, elevated aldosterone-to-renin ratio is associated with accelerated biological aging, which correlates with increased left ventricular mass, suggesting a potential mediating role in cardiac remodeling.

Limitations

  • Cross-sectional design limits causal inference

Abstract

Objectives: To investigate the associations of plasma aldosterone concentration (PAC), plasma renin activity (PRA), and aldosterone-to-renin ratio (ARR) with Gompertz law–based biological age difference (GOLD BioAgeDiff) in patients with primary aldosteronism versus essential hypertension (EHT), and to determine whether GOLD BioAgeDiff relates to cardiac mass. Methods: We conducted a retrospective cross-sectional study of 1201 hypertensive adults (785 with primary aldosteronism and 416 with EHT). GOLD BioAgeDiff was defined as the calculated biological age minus chronological age. Multivariable linear regression was used to evaluate the associations of PAC, PRA, and ARR with GOLD BioAgeDiff. Furthermore, we assessed the relationship between GOLD BioAgeDiff and echocardiographic indices, including left ventricular mass index (LVMI) and excessive LVMI (eLVMI). Results: Primary aldosteronism patients demonstrated significantly higher GOLD BioAgeDiff than EHT patients. In fully adjusted models, ARR was positively associated with GOLD BioAgeDiff in the primary aldosteronism group ( β = 0.292, P = 0.008) but not in the EHT group ( P for interaction = 0.032). PAC and postcaptopril PAC were also positively associated with GOLD BioAgeDiff in primary aldosteronism. Furthermore, higher GOLD BioAgeDiff was associated with greater eLVMI ( β = 0.591, P < 0.001) and LVMI ( β = 0.640, P = 0.001) in primary aldosteronism patients, suggesting a potential mediating role in the relationship between ARR and cardiac remodeling. Conclusion: Among patients with primary aldosteronism, elevated ARR and PAC were independently associated with GOLD BioAgeDiff, and GOLD BioAgeDiff was correlated with LVMI/eLVMI and may be involved in the association between ARR and eLVMI. Prospective studies are required to confirm causality and evaluate the clinical utility of this biological aging marker.

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Cite This Study

Li et al. (2026) studied this question. In patients with primary aldosteronism, higher aldosterone-to-renin ratio was associated with increased biological age acceleration and greater left ventricular mass index (β = 0.640, P = 0.001).

synapsesocial.com/papers/69b4fc0eb39f7826a300c9b7https://doi.org/10.1097/hjh.0000000000004295
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