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
About this trial
This is an interventional treatment trial for Metabolic Syndrome focused on measuring genistein, gut microbiota, AMPK, fatty acid oxidation
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
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
NCT ID
NCT04105023
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
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
Learn more about this trial
Genistein Stimulates Insulin Sensitivity Through Gut Microbiota
We'll reach out to this number within 24 hrs