Effects of Sodium Chloride or Its Substitute Salt Potassium Chloride on Vascular Function

Healthy Clinical Trial

— ESCAPE-SALT  

Official title:

Effects of Sodium Chloride or Its Substitute Salt Potassium Chloride on Vascular Function and Immune Response - a Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05970601
• Other study ID #: 2022-1844
• Status: Not yet recruiting
• Phase: N/A
• Start date: August 1, 2023
• Est. completion date: October 2026

Study information

• Verified date: July 2023
• Source: Heinrich-Heine University, Duesseldorf
• Contact: Johannes Stegbauer, Prof.Dr.med.
• Phone: +492118117502
• Email: johannes.stegbauer[@]med.uni-duesseldorf.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, monocentric, randomized trial to investigate how sodium chloride or its substitute potassium chloride acutely affects vascular function by ingestion via a salted soup. Furthermore we want to get insights on the pathophysiology by analyzing metabolism and cell function in relation to vascular reaction.

Description:

Some of the leading death causes in western countries are attributed to artheriosclerosis with its consequences especially cardiovascular events. Beside lifestyle risk factors such as physical inactivity, adipositas and stress, high dietary sodium intake is one of the easiest modifiable factors to reduce development and progession of artheriosclerosis. Unfortunately high sodium diet is one of the hallmarks of western diet. Epidemiologic and experimental data have provided compelling evidence that high salt and its induced elevation in bloodpressure is an important factor in the development and progression of cardiovascular disease, artheriosclerosis with its endorgan failure. To analyze the reasons for the hazardous effects of high oral sodium chloride exposure on vascular damage and a possible protective mechanism by the salt substitute potassium chloride, we intend to conduct a single-center randomized trial (ESCAPE-SALT). We aim to measure vascular function by flow mediated dilation (FMD) and dynamic vessel analysis (DVA) of retinal mircocirculation. Participants will be divided into 3 groups. Each group will be served a soup with different salt content. The salt composition is as follows: soup A (9 g sodium chloride), soup B (6 g sodium chloride plus 3 g potassium chloride), and soup C (6 g sodium chloride). The effects on blood pressure, body composition markers, electrolytes, inflammatory and metabolic response, and vascular function are measured before, 4 and 24 h after ingestion of the soup. Furthermore we will investigate the underlying mechanism by performing metabolomic, transcriptomic and proteomic anyalysis.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 60
• Est. completion date: October 2026
• Est. primary completion date: June 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• full-aged
• signed informed consent
• no dietary restrictions
• access to retina for microvascular measurement

Exclusion Criteria:

• age <18 y
• no retinal access for microvascular measurement
• known glaucoma
• antibiotic therapy within the last 4 weeks
• immunosuppressive Therapie within the last 4 weeks (e.g. glucocorticoids)
• s.p. malignancy
• unknown fever within the last 4 weeks
• salt wasting syndroms (e.g. renal tubular acidosis, Diabetes insipidus)
• chronic kidney disease stage 4-5
• known electrolyte disorder (e.g. hyperkalaemia, hypokalaemia, hypernatriaemia, hyponatriaema)
• no or rejected informed consent

Related Conditions & MeSH terms

• Diabetes
• Healthy
• Vascular Function

Intervention

Dietary Supplement:
• Soup
Intake of a single soup with different sodium chloride and potassium chloride content

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Prof. Dr. med. Johannes Stegbauer

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on fluid body composition.	Analysis of fluid body composition and intra- and extracellular water amount by bioimpendance monitoring at baseline, 4 and 24 hours after salt intake. The changes in body composition between the three timepoints will be measured.	Baseline, 4 hours, 24 hours
Other	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on blood pressure.	Analysis of blood pressure by automated office blood pressure device at baseline, 4 hours and 24 hours after salt intake. The changes in blood pressure between the three timepoints will be measured.	Baseline, 4 hours, 24 hours
Other	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on renin-angiotensine-aldosterone system.	Analysis of renin, angiotensine and aldosterone levels at baseline, 4 hours and 24 hours after salt intake, measurement will be done in the clinical routine laboratory and the difference between timepoints will be analyzed.	Baseline, 4 hours, 24 hours
Other	Effect of a single oral high-sodium chloride load or a partial substitution by potassium on fecal microbiome.	Analysis of the change of fecal microbiome composition in microbiology of probes before and after salt intake.	up to 48 hours before and after salt intake
Other	Effect of a single oral high-sodium chloride load or a partial substitution by potassium on metabolomics in stool.	Analysis of the change of metabolomics in stool and serum after salt intake using liquid chromotagraphy and high resolution tandem mass spectrometry.	up to 48 hours before and after salt intake
Primary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on retinal vessel diameter and the flicker-light-induced retinal vessel dilatation.	Flicker-induced dilatation and diameter of fundus vessels will be measured via funduscopy in a static an dynamic analysis before, 4 hours and 24 hours after ingestion of a salty soup and the change between the timepoints will be analyzed. First the diameter of venoles and arterioles in µm and their ratio are measured in a standardized fundus picture. In a second step we will film the fundus during three flicker-light periods of 20 seconds and measure the dilatation in percent during the flicker period.	Baseline, 4 hours, 24 hours
Primary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on hypoxia-induced dilatation of brachial artery.	Flow mediated dilatation (FMD) as a marker for macrovascular function will be measured at baseline, 4 hours and 24 hours after ingestion of a salty soup. We will measure FMD by ultrasound based measurement of brachial artery diameter in mm before and after induced hypoxia for 5 minutes. The change of dilatation in percentage between the different timepoints will be analyzed.	Baseline, 4 hours, 24 hours
Secondary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on mitochondrial respiration capacity in PBMC.	Analysis of mitochondrial respiration capacity via seahorse technology in isolated PBMC from baseline, 4 and 24 hours after salt intake. The oxygen consumption rate (OCR) will be measured and the changes between the timepoints will be analyzed.	Baseline, 4 hours, 24 hours
Secondary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium chloride on NO metabolism in serum and red blood cells.	We will measure the amount of nitrite and nitrate in red blood cells and serum by gas chemiluminescence at baseline, 4 and 24 hours after salt intake. The change between the three timepoints will be measured.	Baseline, 4 hours, 24 hours
Secondary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium on metabolic profile in PBMC and plasma.	We will investigate the effect of a single oral high-sodium chloride load or a partial substitution by potassium on the metabolic profile in PBMCs and theplasma. The metabolites will be measured by liquid chromotagraphy and high resolution tandem mass spectrometry at baseline, 4 hours and 24 hours after salt intake. The difference between the timepoints will be analyzed.	Baseline, 4 hours, 24 hours
Secondary	Effect of a single oral high-sodium chloride load or a partial substitution by potassium on systemic inflammation markers.	Inflammatory markers such as cytokines will be meassured at baseline, 4 and 24 hours after salt intake by ELISA and OLINK. Changes of these markers between the three timepoints will be analyzed.	Baseline, 4 hours, 24 hours