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Renin-to-Aldosterone Ratio Is Associated with Ambulatory Blood Pressure Levels and Control in Treated Hypertensive
Matteo Landolfo1,2, Francesco Spannella3,4, Alessandro Gezzi3
1Clinical and Molecular Sciences Department, "Politecnica delle Marche" University, Ancona, Italy, m.landolfo@univpm.it.
Insights
The renin-to-aldosterone ratio (RAR) is linked to better blood pressure control in treated hypertension, irrespective of obesity. Higher RAR, driven by renin levels, indicates improved outcomes in patients on renin-angiotensin system inhibitors.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Pharmacology
Background:
- Hypertension management involves combination therapy modulating the Renin-Angiotensin-Aldosterone System (RAAS).
- Excess adiposity can disrupt RAAS, leading to blood pressure variability and treatment resistance.
- The study investigates the renin-to-aldosterone ratio (RAR) in overweight/obese hypertensive patients.
Purpose of the Study:
- To evaluate the association between RAR and ambulatory blood pressure monitoring (ABPM) in treated hypertensive patients with overweight (OW) or obesity (OB).
- To determine if central obesity affects the relationship between RAR and blood pressure control.
Main Methods:
- Cross-sectional study of 97 OW/OB hypertensive adults and 97 normal-weight controls on stable therapy (RASi + TZD and/or CCB).
- 24-hour ABPM, direct renin concentration (DRC), and plasma aldosterone concentration (PAC) measurements were performed.
- RAR calculated as DRC/PAC, with values normalized using natural logarithm (Ln).
Main Results:
- Higher LnRAR and LnDRC correlated with greater odds of achieving 24-hour, daytime, and night-time blood pressure control in both OW/OB and normal-weight groups.
- LnRAR and LnDRC were inversely associated with ABP levels in controls, but not in OW/OB patients.
- Patients with controlled ABP exhibited higher median LnRAR and LnDRC values than those with uncontrolled ABP, irrespective of weight status.
Conclusions:
- RAR, influenced by higher DRC levels, demonstrates a mechanism-based association with blood pressure control in treated hypertension.
- This association persists regardless of the presence of visceral obesity.
- The findings suggest a pharmacologic response to RAS inhibition contributes to RAR's role in blood pressure management.
Introduction:
Combination therapy, including a renin-angiotensin system inhibitor (RASi) and a thiazide diuretic (TZD) or a calcium channel blocker (CCB), is the first-line approach in hypertension management and modulates circulating markers of the renin-angiotensin-aldosterone system. Excess adiposity may induce renin-aldosterone axis dysregulation and contribute to blood pressure variability and treatment resistance. This study aimed to evaluate the association between the renin-to-aldosterone ratio (RAR) and ambulatory blood pressure monitoring (ABPM) in treated hypertensive patients with central overweight (OW) or obesity (OB).
Methods:
In a cross-sectional design, 97 adults with essential hypertension and OW/OB on stable RASi + TZD and/or CCB therapy were matched with 97 normal-weight hypertensive controls. All participants underwent 24-h ABPM and orthostatic direct renin concentration (DRC) and plasma aldosterone concentration (PAC) measurements. RAR was calculated as the ratio between DRC and PAC. For the analyses, values were normalized using natural logarithm (Ln).
Results:
LnRAR and LnDRC were inversely associated with 24-h, daytime, and night-time ABP levels in controls, but not in OW/OB patients. However, higher LnRAR and LnDRC values were linked to greater odds of achieving ABP control in both OW/OB and normal-weight for 24h [LnRAR OR 1.74 (1.25-2.42), p = 0.001 in OW/OB], daytime, and night-time periods, whereas LnPAC showed no significant associations. Two-way ANOVA confirmed that patients with controlled ABP had higher median LnRAR and LnDRC values than those with uncontrolled ABP, regardless of weight status (p for interaction >0.05).
Conclusion:
RAR, primarily driven by higher DRC levels and likely linked to a pharmacologic response to RAS inhibition, shows a mechanism-based association with ABP control in treated hypertension, regardless of the presence of visceral OB.
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