Unmasking Hormonal Mechanisms of Hypertension in Obesity
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Background
Understanding hormonal mechanisms of obesity-related hypertension may inform the optimal approach to targeted therapy.
Objectives
To interrogate hormonal phenotypes of obesity-related hypertension.
Methods
77 participants with obesity and hypertension underwent deep-phenotyping of adrenocortical hormones at baseline and following multiple dynamic maneuvers to suppress and stimulate hormone production, including: the seated saline suppression (SST), oral sodium loading (OSLT) test, dexamethasone suppression test (DST), and ACTH-stimulation (ACTHstim). Participants were classified into 3 aldosteronism phenotypes: (1) primary aldosteronism (PA) phenotype (low renin with non-suppressible aldosterone), low-renin phenotype (low renin and low aldosterone), and renin-dependent aldosteronism (high renin with renin-mediated aldosteronism). The DST was used to evaluate for ACTH-independent hypercortisolism and ACTHstim was used to evaluate ACTH-modulated adrenocortical hormone production.
Results
Participants were 55.4 ± 9.4 years, 66.2% women, and had a BMI of 34.8 ± 5.2 kg/m 2 . At baseline, 37.7% of participants had a PA phenotype. Following sodium loading with SST, a persistent PA phenotype was seen in 28.5% and unmasked in an additional 23.4% of participants (total 51.9%). Participants with an unmasked PA phenotype had renin-dependent aldosteronism prior to SST, and thus were not identified during baseline testing. Persistent renin-dependent aldosteronism following SST was identified in 23.4% of the cohort and was characterized by greater kaliuresis and higher aldosterone levels (at baseline and following dynamic maneuvers to modulate ACTH and angiotensin II). These patterns were all reproduced following sodium loading with the OSLT. The DST identified ACTH-independent hypercortisolism in 9.2% of participants.
Conclusions
Over 80% of participants with obesity-related hypertension reproducibly exhibited pathologic phenotypes of aldosteronism and/or hypercortisolism. These overlapping hormonal mechanisms reveal the multi-factorial nature of obesity-related hypertension and provide evidence to support aldosterone- and cortisol-directed therapies to treat hypertension in people with obesity.
CONDENSED ABSTRACT
Understanding hormonal mechanisms of obesity-related hypertension may inform targeted therapy. Participants with obesity and hypertension underwent deep-phenotyping procedures to detect the: primary aldosteronism (PA) phenotype, low-renin phenotype, renin-dependent aldosteronism phenotype, and ACTH-independent hypercortisolism. In total, 51.9% of participants had a PA phenotype, of which approximately half also had superimposed renin-dependent aldosteronism. Another 23.4% participants had just renin-dependent aldosteronism that was characterized by higher aldosterone levels and kaliuresis, and 9.2% of participants had hypercortisolism. Over 80% of individuals with obesity-related hypertension exhibited overlapping pathologic phenotypes of aldosteronism and/or hypercortisolism, providing mechanistic evidence to support the efficacy of aldosterone- and cortisol-directed therapy ( Central Illustration ).
