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Genistein Stimulates Insulin Sensitivity Through Gut Microbiota (GENISTEIN)

Primary Purpose

Metabolic Syndrome, Obesity

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
genistein
Placebo
Sponsored by
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome focused on measuring genistein, gut microbiota, AMPK, fatty acid oxidation

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults (men and women) between the ages of 18 and 50.
  • Patients with obesity (BMI ≥ 30 and ≤ 40 kg / m2) and with insulin resistance (HOMA - IR Index ≥ 2.5).
  • Mexican mestizos (parents and grandparents born in Mexico).
  • Patients who can read and write.

Exclusion Criteria:

  • • Patients with any type of diabetes.

    • Patients with kidney disease diagnosed by a medical or with creatinine> 1.3 mg / dL for men and > 1.1 mg / dL for women and / or BUN> 20 mg / dL.
    • Patients with acquired diseases that produce obesity and diabetes secondarily.
    • Patients who have suffered a cardiovascular event.
    • Patients with weight loss > 3 kg in the last 3 months.
    • Patients with any catabolic diseases.
    • Gravidity status
    • Positive smoking
    • Treatment with any medication

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    genistein

    placebo

    Arm Description

    Genistein capsules of 25 mg each, 50mg/day

    Maltodextrin capsules, administered orally once every 12 hours

    Outcomes

    Primary Outcome Measures

    intestinal microbiota
    Measurement of gut microbiota by sequencing using the Illumina platform

    Secondary Outcome Measures

    glucose metabolism profile
    serum glucose (mg/dL)
    Glucose metabolism profile
    serum insulin (µUI/ml)
    Triglycerides
    serum triglycerides (mg/dL)
    Total Cholesterol
    serum total cholesterol (mg/dL)
    LDL cholesterol
    serum LDL cholesterol (mg/dL)
    HDL cholesterol
    serum HDL cholesterol (mg/dL)
    Inflammatory profile
    plasma lipopolysaccharide (LPS) (ng/mL)
    Body weight
    body weight (kg)
    Blood pressure
    blood pressure (mmHg)

    Full Information

    First Posted
    September 20, 2019
    Last Updated
    September 24, 2019
    Sponsor
    Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
    Collaborators
    National Council of Science and Technology, Mexico
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04105023
    Brief Title
    Genistein Stimulates Insulin Sensitivity Through Gut Microbiota
    Acronym
    GENISTEIN
    Official Title
    Genistein Stimulates Insulin Sensitivity Through Gut Microbiota Reshaping and Skeletal Muscle AMPK Activation in Obese Subjects
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    September 15, 2013 (Actual)
    Primary Completion Date
    December 15, 2017 (Actual)
    Study Completion Date
    December 1, 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
    Collaborators
    National Council of Science and Technology, Mexico

    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
    There is evidence that genistein present in soy can improve insulin resistance in rodents and humans with metabolic syndrome (MetS). However, it is not known if this improvement is associated with changes in the gut microbiota. In the present study, the investigators show that the consumption of genistein for 2 months could have an effect on insulin resistance in subjects with MetS. This effect will be accompanied by a modification of the gut microbiota taxonomy. As a consequence, there will be a reduction in metabolic endotoxemia accompanied by an increase in AMP-activated protein kinase (AMPK) phosphorylation and the expression of genes of fatty acid oxidation in skeletal muscle.
    Detailed Description
    The investigators included 45 participants who met the following inclusion criteria: adults between 20 and 60 years of age with a diagnosis of MetS, HOMA index greater than 2.5, BMI ≥30 and ≤ 40 kg / m2 and who signed the consent letter. Patients who had any added pathology, pregnancy, smoking or consumed medications were excluded. Once the letter of informed consent was accepted, the patients were assigned to the respective treatment group. These individuals were advised to consume the recommended diet for subjects with MetS according to the guidelines of the ATPIII. Participants were randomly distributed to consume a) placebo treatment or b) genistein capsules (50 mg/day). The participants were followed for 2 months. In the previsit, informed consent letters were given, and blood samples were taken to evaluate glucose concentration, lipid profile, lipopolysaccharide and serum insulin. Also determined blood pressure, body weight, height, body composition and gut microbiota. The presence of insulin resistance was determined by means of the HOMA-IR index and by an oral glucose tolerance test. After 2 months, the same variables were assessed, and an expert surgeon in the operating room performed a vastus lateralis muscle biopsy, then RNA extraction and gene expression microarray assay was performed

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Metabolic Syndrome, Obesity
    Keywords
    genistein, gut microbiota, AMPK, fatty acid oxidation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    These individuals were advised to consume the recommended diet for subjects with MetS according to the guidelines of the ATPIII. Patients were randomly distributed to consume a) placebo treatment or b) genistein capsules (50 mg/day). The participants were followed for 2 months
    Masking
    ParticipantInvestigator
    Masking Description
    The interventions with genistein and placebo were identically encapsulated in appearance, both the researcher and the participant did not know what type of maneuver was assigned. The bottle with the capsules was distributed by a person outside the study who was the same one who performed the randomization. Study staff and participants were blinded during the assignment and execution of the interventions in the study. the capsules delivered to the participants were 2 per day, the capsules had the same color and appearance
    Allocation
    Randomized
    Enrollment
    45 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    genistein
    Arm Type
    Experimental
    Arm Description
    Genistein capsules of 25 mg each, 50mg/day
    Arm Title
    placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Maltodextrin capsules, administered orally once every 12 hours
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    genistein
    Intervention Description
    Administered orally once every 12 hours
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Placebo
    Intervention Description
    Administered orally once every 12 hours
    Primary Outcome Measure Information:
    Title
    intestinal microbiota
    Description
    Measurement of gut microbiota by sequencing using the Illumina platform
    Time Frame
    Baseline to 2 month
    Secondary Outcome Measure Information:
    Title
    glucose metabolism profile
    Description
    serum glucose (mg/dL)
    Time Frame
    Baseline to 2 month
    Title
    Glucose metabolism profile
    Description
    serum insulin (µUI/ml)
    Time Frame
    Baseline to 2 month
    Title
    Triglycerides
    Description
    serum triglycerides (mg/dL)
    Time Frame
    Baseline to 2 month
    Title
    Total Cholesterol
    Description
    serum total cholesterol (mg/dL)
    Time Frame
    Baseline to 2 month
    Title
    LDL cholesterol
    Description
    serum LDL cholesterol (mg/dL)
    Time Frame
    Baseline to 2 month
    Title
    HDL cholesterol
    Description
    serum HDL cholesterol (mg/dL)
    Time Frame
    Baseline to 2 month
    Title
    Inflammatory profile
    Description
    plasma lipopolysaccharide (LPS) (ng/mL)
    Time Frame
    Baseline to 2 month
    Title
    Body weight
    Description
    body weight (kg)
    Time Frame
    Baseline to 2 month
    Title
    Blood pressure
    Description
    blood pressure (mmHg)
    Time Frame
    Baseline to 2 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults (men and women) between the ages of 18 and 50. Patients with obesity (BMI ≥ 30 and ≤ 40 kg / m2) and with insulin resistance (HOMA - IR Index ≥ 2.5). Mexican mestizos (parents and grandparents born in Mexico). Patients who can read and write. Exclusion Criteria: • Patients with any type of diabetes. Patients with kidney disease diagnosed by a medical or with creatinine> 1.3 mg / dL for men and > 1.1 mg / dL for women and / or BUN> 20 mg / dL. Patients with acquired diseases that produce obesity and diabetes secondarily. Patients who have suffered a cardiovascular event. Patients with weight loss > 3 kg in the last 3 months. Patients with any catabolic diseases. Gravidity status Positive smoking Treatment with any medication

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    31451009
    Citation
    Guevara-Cruz M, Flores-Lopez AG, Aguilar-Lopez M, Sanchez-Tapia M, Medina-Vera I, Diaz D, Tovar AR, Torres N. Improvement of Lipoprotein Profile and Metabolic Endotoxemia by a Lifestyle Intervention That Modifies the Gut Microbiota in Subjects With Metabolic Syndrome. J Am Heart Assoc. 2019 Sep 3;8(17):e012401. doi: 10.1161/JAHA.119.012401. Epub 2019 Aug 27.
    Results Reference
    background
    PubMed Identifier
    31030168
    Citation
    Palacios-Gonzalez B, Vargas-Castillo A, Velazquez-Villegas LA, Vasquez-Reyes S, Lopez P, Noriega LG, Aleman G, Tovar-Palacio C, Torre-Villalvazo I, Yang LJ, Zarain-Herzberg A, Torres N, Tovar AR. Genistein increases the thermogenic program of subcutaneous WAT and increases energy expenditure in mice. J Nutr Biochem. 2019 Jun;68:59-68. doi: 10.1016/j.jnutbio.2019.03.012. Epub 2019 Mar 29.
    Results Reference
    background
    PubMed Identifier
    29979819
    Citation
    Lopez P, Sanchez M, Perez-Cruz C, Velazquez-Villegas LA, Syeda T, Aguilar-Lopez M, Rocha-Viggiano AK, Del Carmen Silva-Lucero M, Torre-Villalvazo I, Noriega LG, Torres N, Tovar AR. Long-Term Genistein Consumption Modifies Gut Microbiota, Improving Glucose Metabolism, Metabolic Endotoxemia, and Cognitive Function in Mice Fed a High-Fat Diet. Mol Nutr Food Res. 2018 Aug;62(16):e1800313. doi: 10.1002/mnfr.201800313. Epub 2018 Jul 29.
    Results Reference
    background
    PubMed Identifier
    30266575
    Citation
    Medina-Vera I, Sanchez-Tapia M, Noriega-Lopez L, Granados-Portillo O, Guevara-Cruz M, Flores-Lopez A, Avila-Nava A, Fernandez ML, Tovar AR, Torres N. A dietary intervention with functional foods reduces metabolic endotoxaemia and attenuates biochemical abnormalities by modifying faecal microbiota in people with type 2 diabetes. Diabetes Metab. 2019 Apr;45(2):122-131. doi: 10.1016/j.diabet.2018.09.004. Epub 2018 Sep 25.
    Results Reference
    background

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