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NCT Number: NCT06395246

Circulating Microvesicles Regulating Metabolic Homeostasis in Obesity After Caloric Restriction Programs

The main aim of the present study is to evaluate the effectiveness of two dietary protocols: Daily Caloric Restriction (DCR) and Early Time-Restricted Feeding + DCR (eTRE) on metabolic homeostasis and the influence of circulating extracellular vesicles (EVs) as inter-organ communication elements in obese patients.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitario de Tarragona Juan XXIII

Tarragona, 43005, Spain

Location status: Recruiting

Location contact

Juan Jose Vendrell Ortega, PhD, MD, Professor

CONTACT

[email protected]

+34 977295800

About this study

The specific objectives are:

  • To assess the effect of two dietary protocols on weight loss and metabolic benefits in non-morbidly obese subjects.
  • Influence of both protocols on energy signaling metabolites and the dynamics of enteroendocrine hormones.
  • Define the "digital footprint" of EVs as inter-organ communication elements influencing metabolic status in obese subjects.

The study design comprises a randomized parallel-arm design (n=40) with consecutive 1:1 allocation to a calorie restriction protocol for a healthy Mediterranean diet under Daily Caloric Restriction (DCR) (n=20) or an eTRE protocol (n=20) for 12 weeks. Clinical and analytical variables, adherence, satiety, chronotype, and brown fat content will be determined before and at the end of the follow-up. Derivatives of intestinal microbiota, short-chain fatty acids, bile acids, and circulating metabolites derived from host intermediary metabolism will be assessed through metabolomics. Glucagon-like peptide 1 (GLP1) and gastric inhibitory polypeptide (GIP) dynamics after a standard meal test. Metagenomics. Bioenergetic analysis of PBMC by SeaHorse. Total EV miRNA profile. Isolation of host and bacterial EVs. Characterization of the protein cargo of host and bacterial EVs.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age between 18 and 70 years old.
  • BMI ranges between 27 and 40 kg/ m2.
  • Absence of underlying pathology in medical and physical examination, except for those related to excess weight.
  • Signature of the informed consent for participation in the study.

Exclusion criteria

  • Serious systemic disease not related to obesity, such as cancer, kidney or severe liver disease.
  • Systemic diseases with intrinsic inflammatory activity (autoimmune diseases such as rheumatoid arthritis and asthma).
  • Pregnancy and lactation.
  • Vegetarians or subjects subjected to an irregular diet.
  • Patients with severe eating disorders.
  • Patients with clinical symptoms and signs of infection in the previous month.
  • Patients with chronic anti-inflammatory steroid treatments and/or nonsteroidal anti-inflammatory drugs.
  • Recent antibiotic treatment.
  • Uncontrolled alcoholism or drug abuse.
  • Rotating or nocturnal shift workers.

Treatment and study plan

Active Comparator: Continuous calorie restriction

Behavioral

Individualized continuous calorie restriction diet based on healthy Mediterranean diet recommendations aiming to achieve at least a 5% weight loss at the end of the intervention

eTRE

Behavioral

early (morning) time-restricted eating pluss individualized continuous calorie restriction diet based on healthy Mediterranean diet recommendations aiming to achieve at least a 5% weight loss at the end of the intervention

Primary outcomes

  1. Anthropometric measurements (I)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in weight (kg)

  2. Anthropometric measurements (II)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in body mass index (kg/m^2);

  3. Anthropometric measurements (III)

    Time frame: Before and after (12 weeks) of the intervention

    Changes waist circumference (cm)

  4. Anthropometric measurements (IV)

    Time frame: Before and after (12 weeks) of the intervention

    Changes hip circumference (cm)

  5. Anthropometric measurements (V)

    Time frame: Before and after (12 weeks) of the intervention

    Changes neck circumference (cm)

  6. Body composition (I)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in fat body mass (kg); assesed by bioimpedance monitoring device (Seca®)

  7. Body composition (II)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in lean body mass (kg); assesed by bioimpedance monitoring device (Seca®)

  8. Body composition (III)

    Time frame: Before and after (12 weeks) of the intervention

    Changes visceral adipose tissue (L); assesed by bioimpedance monitoring device (Seca®)

  9. Brown fat

    Time frame: Before and after (12 weeks) of the intervention

    Changes in brown fat volume (cm3); assessed by magnetic resonance image (MRI)

Secondary outcomes

  1. Gut and host microbiota-derived metabolites (I)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in circulating short-chain fatty acids levels [µM]; assesed by Gas Chromatography-Tandem Mass Spectrometry (GC-MS/MS)

  2. Gut and host microbiota-derived metabolites (II)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in circulating bile acids levels [nM]; Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)

  3. Gut and host microbiota-derived metabolites (III)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in circulating succinate levels [µM]; assesed by EnzyChrom™ Succinate Assay Kit

  4. Entero-endocrine incretin hormones (I)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in post-prandial response to a meal-tolerance test in serum levels of glucose [mg/dL]; assesed by ELISA kit

  5. Entero-endocrine incretin hormones (II)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in post-prandial response to a meal-tolerance test in serum levels of insulin levels [pmol/L] ]assesed by ELISA kit

  6. Entero-endocrine incretin hormones (III)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in post-prandial response to a meal-tolerance test in plasma levels of glucagon-like peptite 1 [GLP-1 ] (pmol/L); assesed by ELISA kit

  7. Entero-endocrine incretin hormones (IV)

    Time frame: Before and after (12 weeks) of the intervention

    Changes in post-prandial response to a meal-tolerance test in plasma levels of gastric inhibitory polypeptide (GIP) [pg/mL]; assesed by ELISA kit

  8. Microbial composition/metagenomic

    Time frame: Before and after (12 weeks) of the intervention

    Changes in alpha and beta diversity, relative abundance and functional metagenomics; assesed by Ilumina metagenomics

  9. Cellular energy metabolism

    Time frame: Before and after (12 weeks) of the intervention

    Changes in Cluster of Differentiation 14 positive (CD14+) monocytes isolated from peripheral blood mononuclear cells (PBMCs) will be used for bioenergetics analysis via an extracellular flux analyzer

Study contacts

Contact information is provided by the study sponsor or research team.

Juan José Vendrell Ortega, Professor

CONTACT

[email protected]

+34 619672912

Sponsors and collaborators

Lead sponsor

Institut Investigacio Sanitaria Pere Virgili

Other

Registry information

Official study title

The Usefulness of Circulating Microvesicles (host and Bacterial) in Regulating Metabolic Homeostasis in Obesity Randomized Study of Parallel Arms in Obese Patients Undergoing Caloric Restriction Diet Vs. Early Time-restricted Eating

Acronym: TREV

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
May 2, 2024
Registry last updated
Oct 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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