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Dietary Intervention Modifies Gut Microbiota in Type 2 Diabetes.

Primary Purpose

Type 2 Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
dietary portfolio
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 Type 2 Diabetes Mellitus focused on measuring gut microbiota, functional foods, branched chain amino acids, TMAO, type 2 diabetes

Eligibility Criteria

30 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • clinical diagnosis of type 2 diabetes
  • Male or female.
  • Adults between 30 and 60 years old.
  • BMI of 25 to 39.9 kg / m².
  • Pharmacological treatment with metformin, a combination of metformin and glibenclamide.
  • Evolution of the type 2 diabetes of 4 ± 3 years.
  • Patients who knew how to read and write.
  • Signature of informed consent.

Exclusion Criteria:

  • Diseases that produce secondary obesity.
  • Cardiovascular event.
  • Weight loss> 3 kg in the last 3 months after the evaluation of the criteria.
  • Catabolic diseases such as cancer and acquired immunodeficiency syndrome.
  • Gravidity status.
  • Positive smoking.
  • Treatment with antihypertensive drugs
  • Treatment with other hypoglycemic agents that were not metformin
  • Treatment with statins, fibrates or other drugs to control dyslipidemia, 6 months before the start of the protocol.
  • Any drug or medication that activates intestinal motility
  • Use of laxatives or antispasmodics 4 weeks before the study
  • Treatment with antibiotics 6 months before the study
  • Use of steroids, chemotherapy, immunosuppressant or radiotherapy.
  • Uncontrolled type 2 diabetes, ( HbA1c concentration ≥ 9.9%)
  • Fasting glucose ≥ 220 mg / dL
  • Fasting cholesterol ≥ 240 mg / dL
  • Fasting triglycerides ≥ 350 mg / dL
  • Serum creatinine in women> 1.2 mg / dL in men> 1.3 mg / d

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    1. Dietary portfolio (DP)

    2. placebo (P)

    Arm Description

    the dietary portfolio was given daily in the breakfast and dinner for 2.5 months

    the placebo (P) was based was given daily in the breakfast and dinner for 2.5 months

    Outcomes

    Primary Outcome Measures

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

    Secondary Outcome Measures

    Glucose metabolism profile
    serum glucose (mg/dl)
    Glucose metabolism profile
    serum insulin (µUI/ml)
    Glucose metabolism profile
    plasma glycated hemoglobin (HbA1c) (%)
    Lipid metabolism profile
    serum triglycerides (mg/dl)
    Lipid metabolism profile
    serum total cholesterol (mg/dl)
    Lipid metabolism profile
    serum LDL cholesterol (mg/dl)
    Lipid metabolism profile
    serum HDL cholesterol (mg/dl)
    Lipid metabolism profile
    plasma free fatty acids (FFA) (mmol/L)
    metabolomic profile
    plasma betaine (µmol/L)
    metabolomic profile
    plasma choline (µmol/L)
    metabolomic profile
    plasma trimethylamine oxide (TMAO) (µmol/L)
    metabolomic profile
    plasma branched chain amino acids (BCAA) (µmol/L)
    inflammatory profile
    plasma lipopolysaccharide (LPS) (ng/ml)
    inflammatory profile
    serum C reactive protein (CRP) (mg/dl)

    Full Information

    First Posted
    January 17, 2018
    Last Updated
    January 29, 2018
    Sponsor
    Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
    Collaborators
    University of Connecticut
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03421301
    Brief Title
    Dietary Intervention Modifies Gut Microbiota in Type 2 Diabetes.
    Official Title
    A Dietary Intervention With Functional Foods Reduce Metabolic Endotoxemia and Attenuates Biochemical Abnormalities in Subjects With Type 2 Diabetes by Modifying the Gut Microbiota.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    August 7, 2014 (Actual)
    Primary Completion Date
    September 28, 2016 (Actual)
    Study Completion Date
    December 28, 2016 (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
    University of Connecticut

    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
    Aim: To study the effect of a dietary intervention with functional foods on gut microbiota in subjects with type 2 diabetes Materials and methods: Patients with type 2 diabetes were enrolled in a double-blind, parallel-arm, placebo-control study were randomized to receive a dietary portfolio (DP) or placebo (P) treatment for 3 mo. The primary endpoint was the effect of a dietary portfolio based on functional foods on gut microbiota. Secondary endpoints were biochemical parameters, branched chain amino acids, TMAO
    Detailed Description
    This study was a single-center, randomized, controlled, double-blind, parallel versus placebo that consisted of six visits. The first visit was a screening evaluation to determine whether subjects meet the inclusion criteria. The selected subjects were invited to a second visit that consisted of a medical history, 2-h oral glucose tolerance test (OGTT), collection of stool samples for DNA isolation and collection of 5 ml blood sample. The participants received the first stage dietary strategy for 15 days. In the third visit and second stage of dietary treatment, subjects were randomized to received the dietary portfolio (DP) or placebo (P) treatment accompanied of the reduced energy diet for 1 mo. In the fourth and fifth visits, with a 1 mo interval, dietary assessment and compliance to the DP or P was evaluated. During each follow-up visit, a 24-h dietary recall was collected, a physical activity questionnaire was filled out and anthropometric and clinical parameters were assessed. In the sixth visit, a 2-h oral glucose tolerance test (OGTT) was performed, and a stool sample for DNA isolation and 5 ml blood were collected. Dietary Intervention In the first stage, the participants consumed a reduced-energy diet tailored to provide a 500-kcal/d deficit as recommended by NIH (8) the with respect to their habitual diet for 15 days. The diet plan consisted in 45-55% carbohydrates, 15-20% protein, 25-35% fat, <7% saturated fat, 200 mg/d cholesterol, 20-35g fiber, 2000-3000 mg/d sodium based on total energy. In the second stage the participants continued to consume the reduced energy diet with the addition of a combination of functional foods (dietary portfolio; DP). The DP provided 200 kcal that were subtracted from the diet. The DP consisted of a mixture of 14g of dehydrated nopal, 4g of chia seed, 30g of soy protein, 4g of inulin,) and 1g of flavoring. The placebo (P) consisted of 28 g of calcium caseinate, 15g of maltodextrin and 1g of flavoring. The kcal, appearance and flavor were similar in DP and P. The DP and P was given in a package in dehydrated form ready to be dissolved in water. The DP was divided into two packages, the first package contained 17.3 g of DP or P given in the breakfast and dissolved in 250 ml and the second package was given at the dinner time (15:00-16:00 h) and contained 34.7g of P and DP dissolved in 300 mL of water. Dietary compliance Dietary compliance was assessed with a 24-h dietary recall and 3-d food record (food log), during each visit that were analyzed by Food Processor Nutrition Analysis Software. The compliance of the consumption of the DP or P was evaluated with the number of empty packages returned at the following visit. Physical activity was assessed using the International physical activity questionnaire (IPAQ).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Type 2 Diabetes Mellitus
    Keywords
    gut microbiota, functional foods, branched chain amino acids, TMAO, type 2 diabetes

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    In the first stage, the participants with type 2 diabetes consumed a reduced-energy diet tailored to provide a 500-kcal/d deficit as recommended by NIH (8) the with respect to their habitual diet for 15 days. In the second stage the participants continued to consume the reduced energy diet with the addition of a combination of functional foods (dietary portfolio; DP). The DP provided 200 kcal that were subtracted from the diet. The DP consisted of a mi The kcal, appearance and flavor were similar in DP and P. The DP and P was given in a package in dehydrated form ready to be dissolved in water. The DP was divided into two packages, the first package contained 17.3 g of DP or P given in the breakfast and dissolved in 250 ml and the second package was given at the dinner time (15:00-16:00 h) and contained 34.7g of P and DP dissolved in 300 mL of water.
    Masking
    ParticipantInvestigator
    Masking Description
    PD and placebo interventions were packaged identically in appearance, both the researcher and the participant did not know what type of maneuver was assigned. The envelopes were distributed by a person outside the study who was the same who performed the randomization. Study staff and participants were blinded during the assignment and execution of interventions in the study. The packages given to the participants were 2 per day, the placebo packages were matched in grams, calories, color, appearance, flavor to the PD.
    Allocation
    Randomized
    Enrollment
    81 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1. Dietary portfolio (DP)
    Arm Type
    Experimental
    Arm Description
    the dietary portfolio was given daily in the breakfast and dinner for 2.5 months
    Arm Title
    2. placebo (P)
    Arm Type
    Placebo Comparator
    Arm Description
    the placebo (P) was based was given daily in the breakfast and dinner for 2.5 months
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    dietary portfolio
    Intervention Description
    The dietary intervention was a combination of functional foods (dehydrated nopal, chia seed, soy protein and inulin) that was provided in dehydrated form in packages of 17.3 g dissolved in 250 ml water for breakfast and 34.7 g in 300 ml water for dinner.
    Primary Outcome Measure Information:
    Title
    intestinal microbiota
    Description
    Measurement of intestinal microbiota by sequencing using the Illumina platform
    Time Frame
    Change from baseline gut microbiota at three months after the dietary intervention
    Secondary Outcome Measure Information:
    Title
    Glucose metabolism profile
    Description
    serum glucose (mg/dl)
    Time Frame
    Change from baseline serum glucose at three months after dietary intervention
    Title
    Glucose metabolism profile
    Description
    serum insulin (µUI/ml)
    Time Frame
    Change from baseline serum insulin at three months after dietary intervention
    Title
    Glucose metabolism profile
    Description
    plasma glycated hemoglobin (HbA1c) (%)
    Time Frame
    Change from baseline plasma HbA1c at three months after dietary intervention
    Title
    Lipid metabolism profile
    Description
    serum triglycerides (mg/dl)
    Time Frame
    Change from baseline serum triglycerides at three months after dietary intervention
    Title
    Lipid metabolism profile
    Description
    serum total cholesterol (mg/dl)
    Time Frame
    Change from baseline serum total cholesterol at three months after dietary intervention
    Title
    Lipid metabolism profile
    Description
    serum LDL cholesterol (mg/dl)
    Time Frame
    Change from baseline serum LDL cholesterol at three months after dietary intervention
    Title
    Lipid metabolism profile
    Description
    serum HDL cholesterol (mg/dl)
    Time Frame
    Change from baseline serum HDL cholesterol at three months after dietary intervention
    Title
    Lipid metabolism profile
    Description
    plasma free fatty acids (FFA) (mmol/L)
    Time Frame
    Change from baseline plasma free fatty acids at three months after dietary intervention
    Title
    metabolomic profile
    Description
    plasma betaine (µmol/L)
    Time Frame
    Change from baseline plasma betaine at three months after dietary intervention
    Title
    metabolomic profile
    Description
    plasma choline (µmol/L)
    Time Frame
    Change from baseline plasma choline at three months after dietary intervention
    Title
    metabolomic profile
    Description
    plasma trimethylamine oxide (TMAO) (µmol/L)
    Time Frame
    Change from baseline plasma TMAO at three months after dietary intervention
    Title
    metabolomic profile
    Description
    plasma branched chain amino acids (BCAA) (µmol/L)
    Time Frame
    Change from baseline plasma BCAA at three months after dietary intervention
    Title
    inflammatory profile
    Description
    plasma lipopolysaccharide (LPS) (ng/ml)
    Time Frame
    Change from baseline plasma LPS at three months after dietary intervention
    Title
    inflammatory profile
    Description
    serum C reactive protein (CRP) (mg/dl)
    Time Frame
    Change from baseline serum CRP at three months after dietary intervention

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    30 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: clinical diagnosis of type 2 diabetes Male or female. Adults between 30 and 60 years old. BMI of 25 to 39.9 kg / m². Pharmacological treatment with metformin, a combination of metformin and glibenclamide. Evolution of the type 2 diabetes of 4 ± 3 years. Patients who knew how to read and write. Signature of informed consent. Exclusion Criteria: Diseases that produce secondary obesity. Cardiovascular event. Weight loss> 3 kg in the last 3 months after the evaluation of the criteria. Catabolic diseases such as cancer and acquired immunodeficiency syndrome. Gravidity status. Positive smoking. Treatment with antihypertensive drugs Treatment with other hypoglycemic agents that were not metformin Treatment with statins, fibrates or other drugs to control dyslipidemia, 6 months before the start of the protocol. Any drug or medication that activates intestinal motility Use of laxatives or antispasmodics 4 weeks before the study Treatment with antibiotics 6 months before the study Use of steroids, chemotherapy, immunosuppressant or radiotherapy. Uncontrolled type 2 diabetes, ( HbA1c concentration ≥ 9.9%) Fasting glucose ≥ 220 mg / dL Fasting cholesterol ≥ 240 mg / dL Fasting triglycerides ≥ 350 mg / dL Serum creatinine in women> 1.2 mg / dL in men> 1.3 mg / d
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nimbe Torres, PhD
    Organizational Affiliation
    Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Dietary Intervention Modifies Gut Microbiota in Type 2 Diabetes.

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