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CompletedNCT04519164Updated Sep 15, 2026Results posted

Aldosterone, the Mineralocorticoid Receptor, and Cardiovascular Disease in Obesity

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

Phase
Phase 4
Study type
Interventional
Enrollment
79
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Metabolic Syndrome
  • Hypertension
  • Overweight and Obesity

Keywords

  • aldosterone
  • mineralocorticoid receptor antagonist
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In context

Metabolic Syndrome

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. BMI ≥ 30 with at least one of the following, or BMI ≥ 25 with at least two of the following:

    1. Untreated Hypertension: Stage I (BP 120-139/80-89 mmHg) or stage II (BP 140-159/90-99 mmHg).
    2. Treated Hypertension: On one anti-hypertensive medication with BP\<140/90 mmHg and willing to undergo a 2-week washout of the medication before initiating eplerenone or chlorthalidone + KCl
    3. Dysglycemia: Impaired fasting plasma glucose (100-125 mg/dL) or glycated A1c 5.7-6.4%
    4. Dyslipidemia: Fasting triglyceride level > 150 mg/dL and HDL\< 40 mg/dL in men or \<50 mg/dL in women.
  2. Age between 18 and 70 years old

Exclusion criteria

Exclusion Criteria:

  • Estimated glomerular filtration rate \< 60 mL/min/1.73m2)
  • Serum potassium > 5.2 mEq/L
  • Known diagnosis or treatment for type 1 or type 2 diabetes
  • Known history of CVD (myocardial infarction, heart failure, atrial fibrillation, or stroke)
  • EKG with ischemic ST-segment or T-wave changes or Q waves in more than one territorial lead or a left bundle branch block
  • Pregnancy (verified with a pregnancy test) or breast-feeding
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
79 participants (actual)

Study arms

  • Experimental
    Eplerenone

    Participants will receive eplerenone, ranging from 25-100mg daily for one year.

    Drug: Eplerenone

  • Active comparator
    Chlorthalidone with potassium chloride

    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

Interventions

  • DrugEplerenone

    mineralocorticoid receptor antagonist and potassium-sparing diuretic

    Also known as: Inspra

  • DrugChlorthalidone with potassium chloride

    potassium-wasting diuretic with potassium chloride

    Also known as: hygroton

06

What researchers measure

Primary outcomes

  1. Change in Stress Myocardial Perfusion Reserve on Cardiac MRI

    Change in myocardial perfusion reserve

    Time frame: one year

Secondary outcomes

  1. Change in Extracellular Volume Fraction

    Change in extracellular volume fraction on cardiac MRI

    Time frame: one year

07

Results

Posted Sep 15, 2026
Limitations and caveats
Limitations: * this was a one year study: longer durations of treatment may have shown different results * the population was selected because they were known to be free of cardiac and coronary disease: the absence of these high risk features may have made potential treatment effects to small to detect * cardiac MRI was used as a surrogate of clinical events

Participant flow

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.

Participant flow — Overall Study
MilestoneEplerenone With PlaceboChlorthalidone With Potassium
Started4039
Completed3031
Not completed108
Withdrew: Withdrawal by subject43
Withdrew: Adverse event55
Withdrew: Physician decision10

Outcome measures

PrimaryChange in Stress Myocardial Perfusion Reserve on Cardiac MRI

Change in myocardial perfusion reserve

Time frame:
one year
Reported as:
Least squares mean · ratio of mL/min/g per mL/min/g
Change in Stress Myocardial Perfusion Reserve on Cardiac MRI
ratio of mL/min/g per mL/min/gEplerenone With PlaceboChlorthalidone With Potassium Chloride
Change in Stress Myocardial Perfusion Reserve on Cardiac MRI0.154 (-0.122 to 0.430)0.147 (-0.134 to 0.428)
Statistical analysis
  • Eplerenone With Placebo vs Chlorthalidone With Potassium Chloride · ANCOVA · p = 0.97
SecondaryChange in Extracellular Volume Fraction

Change in extracellular volume fraction on cardiac MRI

Time frame:
one year
Reported as:
Least squares mean · percentage
Change in Extracellular Volume Fraction
percentageEplerenone With PlaceboChlorthalidone With Potassium Chloride
Change in Extracellular Volume Fraction-0.474 (-1.091 to 0.142)-0.297 (-0.913 to 0.320)
Statistical analysis
  • Eplerenone With Placebo vs Chlorthalidone With Potassium Chloride · ANCOVA · p = 0.68

Adverse events

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.

Adverse event summary by group
GroupDeathsSeriousOther
Eplerenone With Placebo0/40 (0%)0/40 (0%)31/40 (77.5%)
Chlorthalidone With Potassium0/39 (0%)2/39 (5.1%)28/39 (71.8%)
Most frequent serious events
Most frequent serious events
EventEplerenone With PlaceboChlorthalidone With Potassium
Potassium DisordersEndocrine disorders0/401/39
DizzinessNervous system disorders—1/39
Most frequent other events
Most frequent other events
EventEplerenone With PlaceboChlorthalidone With Potassium
Other abnormal laboratory resultsInvestigations17/4015/39
viral infectionInfections and infestations10/4016/39
Trauma/InjuryMusculoskeletal and connective tissue disorders6/4010/39
Potassium DisordersEndocrine disorders2/409/39
OtherSocial circumstances6/405/39
LightheadednessCardiac disorders5/402/39
Gastrointestinal complaintsGastrointestinal disorders2/403/39
Incidental MRI abnormalityCardiac disorders3/401/39

Baseline characteristics

Age, Continuous
Age, Continuous(years)Eplerenone With PlaceboChlorthalidone With PotassiumTotal
Mean54.8 ± 9.555.6 ± 10.655.2 ± 10.0
Sex: Female, Male
Sex: Female, Male(Participants)Eplerenone With PlaceboChlorthalidone With PotassiumTotal
Female292655
Male111324
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Eplerenone With PlaceboChlorthalidone With PotassiumTotal
White343367
Black369
Asian000
More than one race202
Other101
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Study locations

1 site
  • Brigham and Women's Hospital
    Boston, Massachusetts 02115, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · Apr 11, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04519164
Lead sponsor
Brigham and Women's Hospital
Responsible party
Anand Vaidya (Associate Professor of Medicine, Brigham and Women's Hospital) — Principal investigator
First posted
Aug 19, 2020
Start date
Dec 1, 2020
Primary completion
Sep 17, 2025
Completion
Sep 17, 2025
Results posted
Sep 15, 2026
Last update
Sep 15, 2026

Study contacts

Anand Vaidya, MD
principal investigator · Brigham and Women's Hospital, Harvard Medical School

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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