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Visualizing Vascular Mechanisms of Salt Sensitivity

Not Applicable
Completed
Conditions
Salt; Excess
Cardiovascular Risk Factor
Obesity
Interventions
Dietary Supplement: Low-salt diet
Dietary Supplement: High-salt diet
Registration Number
NCT03696433
Lead Sponsor
Vanderbilt University Medical Center
Brief Summary

This study aims to assess the salt sensitive blood pressure response to dietary salt load compared with radiological markers of salt handling.

Detailed Description

Hypertension is a major cause of heart disease, heart failure, and stroke. Hypertension, or high blood pressure, affects people differently and is related to the body's ability to maintain healthy circulation of salt. Some individuals may be affected by salt sensitive blood pressure (SSBP), when their blood pressure changes in response to dietary salt load. SSBP is a prevalent, independent risk factor for developing cardiovascular disease that preferentially affects black individuals. Current methods to assess SSBP require dietary salt loading over the course of days to weeks, and measurement of blood pressure following high salt diet and low salt diet. Such lengthy protocols are not feasible in a clinical setting to evaluate this risk factor for cardiovascular disease, and more importantly, these procedures provide incomplete information about mechanisms of salt sensitivity.

Our knowledge regarding salt handling in the body is limited. While renal dysfunction is partly responsible for SSBP, recent research points to the role of lymphatic vascular clearance in regulating tissue salt storage and blood pressure control. To better understand these mechanisms in vivo, we have recently developed a noninvasive magnetic resonance (MR) lymphangiography method sensitive to lymphatic vasculature, and applied standardized MR protocols for measuring tissue sodium and fat storage in adults with impaired lymphatic clearance. We found evidence of lymph stasis and tissue salt deposition that correlated with local subcutaneous fat volume. Here, we will test whether similar lymphatic pathways are impaired in persons with SSBP, leading to tissue salt and fat storage, in comparison to the involvement of renal dysfunction in SSBP tissue profiles.

The aims of this study are to improve our understanding of vascular mechanisms of human salt storage, and to provide standardized radiologic biomarkers sensitive to the SSBP phenotype. This study will test the primary hypothesis that the SSBP response is correlated with baseline tissue sodium storage, and elevated in persons with salt sensitivity. Secondary hypotheses will address whether the SSBP response is related to fat storage, lymphatic vascular function, renal vascular function, and impaired target organ responses to salt loading, including decreased urinary sodium excretion, and less suppression of plasma renin and serum aldosterone.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
19
Inclusion Criteria
  • Identification as black race
  • Age between 18 and 55 years
  • Body mass index between 25 and <35 kg/m2
  • Normotensive or pre-hypertensive
  • Willing to adhere to study diets
  • Able to provide informed consent and communicate with study personnel
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Exclusion Criteria
  • Prevalent cardiovascular disease or use of medications for cardiovascular disease
  • Current or prior history of hypertension or use of blood pressure lowering medications
  • Current or prior history of diabetes mellitus or use of anti-diabetic medications
  • Prevalent renal disease (eGFR < 60 ml/min/1.73m2), abnormal serum sodium or potassium
  • Current or prior smoker
  • Current pregnancy, or use of hormone replacement therapy or oral contraceptive
  • Current steroid use
  • Contraindications to MRI
  • Active infection or open wounds on the top of the feet or hands
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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Low- then high-salt dietLow-salt diet10 subjects will be enrolled and each will undergo study procedures at 4 separate visits. Subjects will be randomly assigned to this study arm, differing in the order of low and high salt diets. After a baseline visit to include a noninvasive MRI scan, the subject will begin this study diet: low-salt diet, then washout consisting of the subject's typical diet, then high-salt diet. Each dietary or washout period lasts for 7 days, and study visits will occur after each period.
Low- then high-salt dietHigh-salt diet10 subjects will be enrolled and each will undergo study procedures at 4 separate visits. Subjects will be randomly assigned to this study arm, differing in the order of low and high salt diets. After a baseline visit to include a noninvasive MRI scan, the subject will begin this study diet: low-salt diet, then washout consisting of the subject's typical diet, then high-salt diet. Each dietary or washout period lasts for 7 days, and study visits will occur after each period.
High- then low-salt dietLow-salt diet10 subjects will be enrolled and each will undergo study procedures at 4 separate visits. Subjects will be randomly assigned to this study arm, differing in the order of low and high salt diets. After a baseline visit to include a noninvasive MRI scan, the subject will begin this study diet: high-salt diet, then washout consisting of the subject's typical diet, then low-salt diet. Each dietary or washout period lasts for 7 days, and study visits will occur after each period.
High- then low-salt dietHigh-salt diet10 subjects will be enrolled and each will undergo study procedures at 4 separate visits. Subjects will be randomly assigned to this study arm, differing in the order of low and high salt diets. After a baseline visit to include a noninvasive MRI scan, the subject will begin this study diet: high-salt diet, then washout consisting of the subject's typical diet, then low-salt diet. Each dietary or washout period lasts for 7 days, and study visits will occur after each period.
Primary Outcome Measures
NameTimeMethod
Change in Salt-sensitive blood pressure after low salt dietFollowing completion of all dietary supplements and washout, in no less than 21 days.

Measured as the difference in mean arterial pressure following high-salt diet compared to low-salt diet

Secondary Outcome Measures
NameTimeMethod
Tissue sodium content of the legsAt baseline

Measured by sodium MRI

Fat fraction of the legsAt baseline

Measured by conventional MRI, in units of fat/water volume ratio

Kidney blood perfusion rateAt baseline

Measured by conventional noninvasive MRI

Lymphatic stasis of the legsAt baseline

Measured by noninvasive MR lymphangiography

Urinary sodium excretionAt baseline and each of 3 study visits occurring about every 7 days, to be completed in no less than 21 days.

Measured from 24-hour urine collection

Plasma reninAt baseline and each of 3 study visits occurring about every 7 days, to be completed in no less than 21 days.

Physiological parameter

Serum aldosteroneAt baseline and each of 3 study visits occurring about every 7 days, to be completed in no less than 21 days.

Physiological parameter

Trial Locations

Locations (1)

Vanderbilt University Medical Center

🇺🇸

Nashville, Tennessee, United States

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