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Deciphering the Role of Dietary Fatty Acids on Extracellular Vesicles-mediated Intercellular Communication (DIETEVOME)

Primary Purpose

Obesity, Metabolic Syndrome, Metabolic Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Oral lipid emulsions
Sponsored by
University of Seville
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Obesity

Eligibility Criteria

35 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: • Clinical diagnosis of metabolic syndrome Exclusion Criteria: Allergy to dairy products Allergy to fish oil Vegetarian Tobacco smoker Current or recent (<4 wk) use of fish oil supplements or more than four times fish/week Received innoculations within 2 mo of starting the study or planned to during the study Donated or intended to donate blood from 2 mo before the study till 2 mo after the study Unstable body weight (no weight gain/loss >3 kg)

Sites / Locations

  • University of Seville

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Metabolic Syndrome patients

Healthy patients

Arm Description

Outcomes

Primary Outcome Measures

Evolution of cytokines in postprandial state
Pro-inflammatory and anti-inflammatory cytokines, including NFα, IL-1β, IL-6, IL-8, IL-10, ICAM-1, MCP-1, leptin, and adiponectin, in plasma will be measured using appropriate methods (EIA, ELISA, and/or Bioplex multiplex system) (mg/dl).
Evolution of inflammatory markers in postprandial state. [Time Frame: Up to 6 hours]
The acute phase protein (hsCRP), PAI-1, fibrinogen, transferrin, albumin, and myeloperoxidase (MPO) will be measured using appropriate methods (EIA, ELISA, and/or Bioplex multiplex system) (mg/dl).
Effect of EVs on gene expression in PBMCs
PBMCs will be isolated from the subjects' peripheral blood and treated with autologous circulating EVs for different times.
EV proteome
The quantification of exosome-derived proteins will be performed by nLC-MS/MS
EV lipidome
The analysis of intact lipids derived from exosomes will be performed by LC-MS
Ev microtranscriptome
Enriched RNA and miRNA derived from exosomes will be determined by Next Generation Sequencing (NGS)

Secondary Outcome Measures

Full Information

First Posted
September 5, 2023
Last Updated
September 19, 2023
Sponsor
University of Seville
Collaborators
Spanish National Research Council
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1. Study Identification

Unique Protocol Identification Number
NCT06051461
Brief Title
Deciphering the Role of Dietary Fatty Acids on Extracellular Vesicles-mediated Intercellular Communication
Acronym
DIETEVOME
Official Title
Deciphering the Role of Dietary Fatty Acids on Extracellular Vesicles-mediated Intercellular Communication and Their Implication in Atherosclerosis and Metabolic Syndrome: a Multi-omics Approach to Precision Nutrition
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 1, 2023 (Anticipated)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Seville
Collaborators
Spanish National Research Council

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Dietary interventions have been consistently proposed as a part of a comprehensive strategy to lower the incidence and severity of atherosclerosis and coronary vascular disease. Excessive comsumption of fats enriched in saturated fatty acids (SFAs) is associated with an increased risk of atherosclerosis and other cardiovascular diseases (CVD). In contrasts, replacement of SFAs with monounsaturated fatty acids (MUFAs) and omega-3 long chain polyunsaturated fatty acids (ω3-LCPUFAs) has been reported to be inversely associated with risk of atherosclerosis. This is partly due to the ability of MUFAs (and ω3-LCPUFAs) to modulate lipoprotein composition, oxidation state, and consequently their functionality, among others. While most of the nutritional studies have focused on elucidating the mechanisms by which dietary fats affect lipoprotein particles, little or nothing is known about the regulatory effect of dietary fatty acids on extracellular vesicles (EVs). EVs are small phospholipid particles that convey molecular bioactive cargoes and play essential roles in intercellular communication and, hence, a multifaceted role in health and disease. For the first time, the purpose of this project is to establish whether the type of major fatty acids present on a diet (SFAs, MUFAs, or ω3-LCPUFAs) may alter the structure, cargo, and functionality of postprandial- and long-term-EVs. In the precision nutrition era, the investigators expect to offer a new insight on EVs and their relationship with dietary fatty acids through the following objectives: 1) To map changes in the lipidome, proteome, microtranscriptome, and functional properties of circulating EVs in healthy subjects and patients with metabolic syndrome (MetS) both at fasting and at postprandial state upon a challenge of a meal rich in SFAs, MUFAs, and ω3-LCPUFAs; 2) To analyse the contribution of postprandial triacylglyceride-rich lipoproteins (TRL) on EVs-mediated intercellular communication in a fatty acid-dependent manner; and 3) To determine the influence of diets rich in SFAs, MUFAs, and ω3-LCPUFAs on EVs in an animal model of atherosclerosis in the setting of MetS. Collectively, this project will provide fundamental insight into EV biology, and remarks the clinical and functional relevance and divergent consequences of dietary fatty acids in health and disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Metabolic Syndrome, Metabolic Disorder, Inflammation, Immune System and Related Disorders

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Metabolic Syndrome patients
Arm Type
Active Comparator
Arm Title
Healthy patients
Arm Type
Experimental
Intervention Type
Dietary Supplement
Intervention Name(s)
Oral lipid emulsions
Intervention Description
The oral lipid emulsions will contain water, sucrose, emulsifier, flavouring, and the corresponding fat (50 g/m2 of body surface area): milk cream (SFAs) or refined olive oil (MUFAs) with or without a dose of omega-3 PUFA, which will consist of 920 mg of EPA and 760 mg of DHA (ω3-LCPUFAs).
Primary Outcome Measure Information:
Title
Evolution of cytokines in postprandial state
Description
Pro-inflammatory and anti-inflammatory cytokines, including NFα, IL-1β, IL-6, IL-8, IL-10, ICAM-1, MCP-1, leptin, and adiponectin, in plasma will be measured using appropriate methods (EIA, ELISA, and/or Bioplex multiplex system) (mg/dl).
Time Frame
Up to 6 hours
Title
Evolution of inflammatory markers in postprandial state. [Time Frame: Up to 6 hours]
Description
The acute phase protein (hsCRP), PAI-1, fibrinogen, transferrin, albumin, and myeloperoxidase (MPO) will be measured using appropriate methods (EIA, ELISA, and/or Bioplex multiplex system) (mg/dl).
Time Frame
Up to 6 hours
Title
Effect of EVs on gene expression in PBMCs
Description
PBMCs will be isolated from the subjects' peripheral blood and treated with autologous circulating EVs for different times.
Time Frame
Up to 6 hours
Title
EV proteome
Description
The quantification of exosome-derived proteins will be performed by nLC-MS/MS
Time Frame
Up to 6 hours
Title
EV lipidome
Description
The analysis of intact lipids derived from exosomes will be performed by LC-MS
Time Frame
Up to 6 hours
Title
Ev microtranscriptome
Description
Enriched RNA and miRNA derived from exosomes will be determined by Next Generation Sequencing (NGS)
Time Frame
Up to 6 hours

10. Eligibility

Sex
All
Gender Based
Yes
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: • Clinical diagnosis of metabolic syndrome Exclusion Criteria: Allergy to dairy products Allergy to fish oil Vegetarian Tobacco smoker Current or recent (<4 wk) use of fish oil supplements or more than four times fish/week Received innoculations within 2 mo of starting the study or planned to during the study Donated or intended to donate blood from 2 mo before the study till 2 mo after the study Unstable body weight (no weight gain/loss >3 kg)
Facility Information:
Facility Name
University of Seville
City
Seville
ZIP/Postal Code
41009
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Deciphering the Role of Dietary Fatty Acids on Extracellular Vesicles-mediated Intercellular Communication

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