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Clinical Trials/NCT05420311
NCT05420311
Not yet recruiting
Not Applicable

Personalized or Precision Medicine in the Dietary Approach to Obesity

Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud1 site in 1 country450 target enrollmentOctober 31, 2022
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
Enrollment
450
Locations
1
Primary Endpoint
Changes in body weight after each intervention
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

The main objective of this project is to apply a precision medicine approach to try to explain the intra-individual variability of the response to different weight loss approaches: a balanced hypocaloric diet in macronutrients (MedDiet), a very low carbohydrate diet (KetoDiet) and an intermittent fasting (IF) approach, and try to establish in a personalized manner with the individual variability in genetics, metabolites, intestinal microbiome, and environmental factors the best dietary strategy for weight loss. As secondary objectives the investigators pretend to O1: To analyze whether individual variability in genetics, epigenetics, intestinal microbiome, and environmental factors determine the changes in insulin resistance, blood pressure, lipid levels and NASH markers after three different dietary interventions. O2: To analyze whether individual variability in genetics, epigenetics, intestinal microbiome, and environmental factors determine the changes in the body composition and the different ratio of free-fat/ fat mass loss after three different dietary interventions. O3: To determine the most effective intervention to increase the loss of fat mass, preserve the free-fat mass and trigger a better metabolic profile. O4: To follow-up changes in gut microbiota and DNA methylation after each of the cross-over dietary interventions. O5: To evaluate the transcriptional response of adipose tissue and elucidate its predictive value for the body-composition changes in patients subjected to the different dietary interventions.

O6: To evaluate the influence of D-ß-hydroxybutyrate as well as other short-chain acyl-CoA precursor metabolites in human adipocytes lipolysis by in vitro experimentation and elucidate the influence of metabolite-sensitive histone modifications in the shaping of adipose transcriptional program and lipolysis sensitivity. O7: To develop a machine learning algorithm based on genetics, epigenetics, intestinal microbiome, and environmental factors for the prediction of the best dietary approach for weight loss in a personalized manner. To try to respond to these objectives, the investigators will apply two models: a randomized cross-over study testing three different dietary weight-loss interventions: MedDiet, KetoDiet, and IF with wash-out periods before each intervention.

Detailed Description

The main objective of this project is to apply a precision medicine approach to try to explain the intra-individual variability of the response to different weight loss approaches: a balanced hypocaloric diet in macronutrients (MedDiet), a very low carbohydrate diet (KetoDiet) and an intermittent fasting (IF) approach, and try to establish in a personalized manner with the individual variability in genetics, metabolites, intestinal microbiome, and environmental factors the best dietary strategy for weight loss. As secondary objectives the investigators pretend to O1: To analyze whether individual variability in genetics, epigenetics, intestinal microbiome, and environmental factors determine the changes in insulin resistance, blood pressure, lipid levels and NASH markers after three different dietary interventions. O2: To analyze whether individual variability in genetics, epigenetics, intestinal microbiome, and environmental factors determine the changes in the body composition and the different ratio of free-fat/ fat mass loss after three different dietary interventions. O3: To determine the most effective intervention to increase the loss of fat mass, preserve the free-fat mass and trigger a better metabolic profile. O4: To follow-up changes in gut microbiota and DNA methylation after each of the cross-over dietary interventions. O5: To evaluate the transcriptional response of adipose tissue and elucidate its predictive value for the body-composition changes in patients subjected to the different dietary interventions. O6: To evaluate the influence of D-ß-hydroxybutyrate as well as other short-chain acyl-CoA precursor metabolites in human adipocytes lipolysis by in vitro experimentation and elucidate the influence of metabolite-sensitive histone modifications in the shaping of adipose transcriptional program and lipolysis sensitivity. O7: To develop a machine learning algorithm based on genetics, epigenetics, intestinal microbiome, and environmental factors for the prediction of the best dietary approach for weight loss in a personalized manner. To try to respond to these objectives, the investigators will apply two models: a randomized cross-over study testing three different dietary weight-loss interventions: MedDiet, KetoDiet, and IF with wash-out periods before each intervention in patients with obesity; and a second cellular approach with adipose tissue from the patients as well as with commercial cells.

Registry
clinicaltrials.gov
Start Date
October 31, 2022
End Date
December 1, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participants aged ≥ 18 and \<70 years old who were derived to the obesity-management unit of the Endocrinology and Nutrition Unit of the Virgen de la Victoria Hospital (Málaga).
  • BMI between 35 and 45 kg/m2.

Exclusion Criteria

  • Pregnant or lactating
  • Following a prescribed diet for any reason in the past 3 months
  • Celiac disease, Crohn's disease or any condition altering nutritional requirements.
  • Allergies or food intolerances, as well as antibiotics treatment or usual probiotics intake.

Outcomes

Primary Outcomes

Changes in body weight after each intervention

Time Frame: From baseline to 1 month

Weight in kg

Secondary Outcomes

  • DNA methylation.(From baseline to 1 month)
  • Changes in the degree of insulin resistance.(From baseline to 1 month)
  • Changes in lipid profile (cholesterol)(From baseline to 1 month)
  • Changes in the punctuation in neurocognitive test - WAISspan(From baseline to 1 month)
  • Changes in lipid profile (triglycerides)(From baseline to 1 month)
  • Changes in body composition and in the ratio of free-fat / fat mass loss after the three different dietary interventions.(From baseline to 1 month)
  • Changes in the systolic blood pressure(From baseline to 1 month)
  • Changes in the diastolic blood pressure(From baseline to 1 month)
  • Changes in the punctuation in neurocognitive test - Trailmaking Test (A - B)(From baseline to 1 month)
  • Changes in the degree of ketosis(From baseline to 1 month)
  • Changes in gut microbiota(From baseline to 1 month)
  • Changes in the punctuation in neurocognitive test - Stroop(From baseline to 1 month)
  • Changes in the punctuation in neurocognitive test - UPPS-P(From baseline to 1 month)

Study Sites (1)

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