A Phase 4 interventional study of Eplerenone and Chlorthalidone with potassium chloride in Metabolic Syndrome, Hypertension and Overweight and Obesity, sponsored by Brigham and Women's Hospital. Completed at 1 site in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-09-15.
Sponsored by Brigham and Women's Hospital · Phase 4, Interventional, and Treatment
This study will evaluate whether the mineralocorticoid receptor antagonist eplerenone, when compared to chlorthalidone plus potassium chloride, can improve cardiac MRI-derived myocardial perfusion reserve and fibrosis, independent of blood pressure, and proportionately to the severity of autonomous aldosterone production.
Obesity is a dominant risk factor for the development of cardiovascular disease (CVD). The public health relevance of this relationship is underscored by the fact that 40% (93 million) of adult Americans are obese.
Activation of the mineralocorticoid receptor (MR) is a major mechanism implicated in the pathogenesis of obesity-associated CVD. MR activation causes vascular stiffness, inflammation, and fibrosis, and MR antagonists improve clinical outcomes in heart failure with reduced ejection fraction, especially in obesity. However, even in the absence of heart failure, multiple mechanisms of CVD in obesity are mediated by excessive activation of the MR. These mechanisms include: autonomous aldosterone production, increased cortisol action, high sympathetic nervous system activity, increased leptin, inflammation, and oxidative stress.
Autonomous aldosterone production is a highly prevalent and poorly recognized disorder that causes CVD independent of blood pressure (BP). Autonomous aldosterone production manifests across a wide severity spectrum, ranging from mild/subclinical (rarely recognized) to overt (primary aldosteronism). The investigators' work has characterized autonomous aldosterone production as a phenotype of non-physiologic, non-suppressible, and renin-independent aldosterone production that is highly prevalent in the general population of the U.S.A..
Autonomous aldosterone production and MR activation are especially enriched in obesity, particularly among obese/overweight individuals with hypertension and/or metabolic syndrome. Current treatment guidelines do not recommend the early use of MR antagonists in obesity or hypertension, thereby delaying or omitting a targeted therapy that may specifically mitigate the mechanism of CVD in this high-risk population.
The investigators have validated cardiac MRI methods to measure coronary microvascular function and myocardial fibrosis, both strong surrogates for CVD that correlate with aldosterone production and that improve with MR antagonist therapy.
Prospective studies to investigate the early mechanistic contribution of aldosterone-MR activation in the pathogenesis of CVD in obesity, and whether MR antagonists can prevent this, are lacking. Mechanistic studies, using innovative and robust intermediate phenotypes of clinical CVD outcomes in a cost-effective manner, could have a major public health impact by implicating a targeted medical therapy (MR antagonists) to prevent CVD in high-risk obesity (overweight/obese individuals with hypertension and/or metabolic syndrome).
HYPOTHESIS: MR antagonists in high-risk obesity improve cardiac MRI-derived myocardial perfusion reserve and fibrosis, independent of BP, and proportionately to the severity of autonomous aldosterone production.
STUDY DESIGN: This mechanistic study will investigate whether MR antagonist therapy in high-risk overweight or obese participants can be a targeted strategy to prevent CVD.
80 participants with overweight/obesity, untreated hypertension, and/or at least one other feature of the metabolic syndrome, will be enrolled. Participants will undergo a deep-phenotyping protocol to characterize aldosterone and cortisol physiology before randomization to eplerenone (25-100 mg/d) or chlorthalidone (6.25-25 mg/d + KCl 20 mEq/d) for one year. BP will be maintained in a target range to ensure outcomes are independent of BP control. Cardiac MRI-derived outcomes will be measured at baseline and after one year.
AIM 1: To investigate whether eplerenone therapy in high-risk obese/overweight participants, when compared to chlorthalidone + KCl, can improve coronary microvascular function independent of BP, as measured via stress cardiac MRI-derived myocardial perfusion reserve (a strong predictor for incident cardiovascular events and death that has been shown to improve with MR antagonist therapy).
AIM 2: To investigate whether eplerenone therapy in high-risk obese/overweight participants, when compared to chlorthalidone + KCl, can decrease myocardial fibrosis independent of BP, as measured via extracellular volume fraction on T1 mapping cardiac MRI (an established surrogate for myocardial fibrosis and inflammation that is also strongly associated with autonomous aldosterone production and mortality).
Exploratory Aims: To investigate whether the severity of autonomous aldosterone production is associated with cardiac MRI-derived outcomes and predicts the response to eplerenone therapy; and, to investigate whether eplerenone therapy can improve measures of cardiac fat content, arterial stiffness (via pulse-wave velocity), and inflammation (via inflammatory markers and adipocytokines), when compared to chlorthalidone + KCl.
IMPACT: Obesity/overweight status is enriched with autonomous aldosterone production and MR activation, mechanisms known to cause CVD. This study will investigate targeted mechanisms for the prevention of MR-mediated CVD in high-risk obesity using innovative physiologic phenotyping and surrogate imaging outcomes. This study will establish a mechanistic foundation for future outcome studies in obesity with incident CVD events.
1,964 studies on the registry are indexed under Metabolic Syndrome; 330 are open to participants now.
This study's enrollment of 79 is above the median of 60 across 1,460 interventional studies indexed under Metabolic Syndrome.
Browse Metabolic Syndrome studies →Brigham and Women's Hospital is the lead sponsor of 1,236 studies on the registry; 224 are open to participants now.
Of its 116 completed or terminated interventional studies of FDA-regulated products, 64 (55%) have results posted.
Counted across the registry records on this site, refreshed daily.
BMI ≥ 30 with at least one of the following, or BMI ≥ 25 with at least two of the following:
Exclusion Criteria:
Participants will receive eplerenone, ranging from 25-100mg daily for one year.
Drug: Eplerenone
Participants will receive chlorthalidone (6.25-25mg daily for one year) along with potassium chloride (up to 20 mEq daily for one year)
Drug: Chlorthalidone with potassium chloride
mineralocorticoid receptor antagonist and potassium-sparing diuretic
Also known as: Inspra
potassium-wasting diuretic with potassium chloride
Also known as: hygroton
Change in Stress Myocardial Perfusion Reserve on Cardiac MRI
Change in myocardial perfusion reserve
Time frame: one year
Change in Extracellular Volume Fraction
Change in extracellular volume fraction on cardiac MRI
Time frame: one year
223 participants from the greater Boston metropolitan area assessed for eligibility, of which 88 were enrolled to undergo phenotyping visits, of which 79 were randomized to study medication intervention. Broad inclusion criteria overweight/obese status with high blood pressure.
| Milestone | Eplerenone With Placebo | Chlorthalidone With Potassium |
|---|---|---|
| Started | 40 | 39 |
| Completed | 30 | 31 |
| Not completed | 10 | 8 |
| Withdrew: Withdrawal by subject | 4 | 3 |
| Withdrew: Adverse event | 5 | 5 |
| Withdrew: Physician decision | 1 | 0 |
Change in myocardial perfusion reserve
| ratio of mL/min/g per mL/min/g | Eplerenone With Placebo | Chlorthalidone With Potassium Chloride |
|---|---|---|
| Change in Stress Myocardial Perfusion Reserve on Cardiac MRI | 0.154 (-0.122 to 0.430) | 0.147 (-0.134 to 0.428) |
Change in extracellular volume fraction on cardiac MRI
| percentage | Eplerenone With Placebo | Chlorthalidone With Potassium Chloride |
|---|---|---|
| Change in Extracellular Volume Fraction | -0.474 (-1.091 to 0.142) | -0.297 (-0.913 to 0.320) |
Collected over From randomization to the end of study follow-up (up to one year). Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Eplerenone With Placebo | 0/40 (0%) | 0/40 (0%) | 31/40 (77.5%) |
| Chlorthalidone With Potassium | 0/39 (0%) | 2/39 (5.1%) | 28/39 (71.8%) |
| Event | Eplerenone With Placebo | Chlorthalidone With Potassium |
|---|---|---|
| Potassium DisordersEndocrine disorders | 0/40 | 1/39 |
| DizzinessNervous system disorders | — | 1/39 |
| Event | Eplerenone With Placebo | Chlorthalidone With Potassium |
|---|---|---|
| Other abnormal laboratory resultsInvestigations | 17/40 | 15/39 |
| viral infectionInfections and infestations | 10/40 | 16/39 |
| Trauma/InjuryMusculoskeletal and connective tissue disorders | 6/40 | 10/39 |
| Potassium DisordersEndocrine disorders | 2/40 | 9/39 |
| OtherSocial circumstances | 6/40 | 5/39 |
| LightheadednessCardiac disorders | 5/40 | 2/39 |
| Gastrointestinal complaintsGastrointestinal disorders | 2/40 | 3/39 |
| Incidental MRI abnormalityCardiac disorders | 3/40 | 1/39 |
| Age, Continuous(years) | Eplerenone With Placebo | Chlorthalidone With Potassium | Total |
|---|---|---|---|
| Mean | 54.8 ± 9.5 | 55.6 ± 10.6 | 55.2 ± 10.0 |
| Sex: Female, Male(Participants) | Eplerenone With Placebo | Chlorthalidone With Potassium | Total |
|---|---|---|---|
| Female | 29 | 26 | 55 |
| Male | 11 | 13 | 24 |
| Race/Ethnicity, Customized(Participants) | Eplerenone With Placebo | Chlorthalidone With Potassium | Total |
|---|---|---|---|
| White | 34 | 33 | 67 |
| Black | 3 | 6 | 9 |
| Asian | 0 | 0 | 0 |
| More than one race | 2 | 0 | 2 |
| Other | 1 | 0 | 1 |
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