Calorie Restriction Intervention Induces Enterotype-associated BMI Loss in Nonobese Individuals (CRDI)

July 31, 2019 updated by: BGI-Shenzhen

Calorie restriction (CR), which has the potential effect on weight loss and blood amino acids, has been demonstrated to associate with gut microbiota in humans, especially in obese individuals. However, studies for simultaneously evaluating enterotype-dependent impacts of CR on the gut microbiota and blood amino acids in nonobese individuals are still limited.

Here, 41 nonobese individuals received a 3-week CR diet with approximately 50% fewer calories than a normal diet. The investigators measured individuals' BMI and blood amino acid concentration, along with the gut microbiota before and after the intervention. In this trial, 28 Enterotype Bacteroides (ETB) subjects and 13 Enterotype Prevotella (ETP) subjects were identified before the intervention.

The purpose of this intervention study is to evaluate the effect of calorie restriction on BMI loss, amino acid, and gut microbiota in healthy volunteers of two different enterotypes and provide useful insights for potential application of gut microbiome stratification in personalized nutrition intervention.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

  1. Volunteer Recruitment

    Volunteer-wanted posters were propagated at the China National Gene Bank in Shenzhen from March to April 2017. A non-obese healthy volunteer was considered if his/her BMI less than 28 kg/m2. 50 individuals met all the criteria and were recruited in this study, and 41 individuals (24 females and 17 males aged 30 ± 6 years old) completed the whole intervention. The study was approved by the institutional review board on bioethics and biosafety of BGI-Shenzhen, Shenzhen (NO. BGI-IRB 17020). All participates were fully informed of the design and purpose of this intervention study and signed a written informed consent letter.

  2. Experiment Process

    The study included a one-week run-in period (baseline) and a three-week CR dietary intervention period. During the first week (run-in period), all healthy volunteers consumed their usual diet and were encouraged to avoid yogurt, high-fat foods, and alcohol. The CR diet was comprised of ~50% calories of a normal-calorie diet (female, 1000kcal/day; male, 1200kcal/day). It was designed with carbohydrate, fat, and protein as approximately 55%, 30% and 15% of the total energy intake respectively, according to the Dietary Guidelines for Chinese Residents (2016) and nutritionally balanced and a recent large nutritional study in China. Common foods in low-calorie diets such as rice, vegetables, eggs, pork, and beef were prepared in the investigators' study center to control experimental variables introduced by different foods and calorie estimation errors.

    Traditional Chinese cooking style - boiled, stir-fried and stewed, were applied for the foods. For each meal, digital scales were used to measure the nutritional and caloric values of different foods and total meal for males and females respectively.

  3. Sample and Data Collection

BMI, blood and fecal samples of each volunteer were collected at the investigators' study center at baseline and after the 3-week CR intervention. BMI was measured via the clinic scale. The concentrations of 31 amino acids and derivatives in the fasting serum samples were measured by LC-MS/MS. The gut microbial composition was determined using shotgun metagenomics sequencing of fecal DNA.

Study Type

Interventional

Enrollment (Actual)

41

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Guangdong
      • ShenZhen, Guangdong, China, 518083
        • BGI-Shenzhen, Guangdong, China

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

22 years to 53 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • BMI less than 28 kg/m2 and more than 18 kg/m2;
  • without antibiotics in the recent 2 months;
  • regular eating and lifestyle patterns;
  • no international travel in the recent 3 month;
  • without hypertension, diabetes mellitus, gastrointestinal disease and other severe auto-immune disease;
  • without prebiotic or probiotic supplements in the recent 2 months;

Exclusion Criteria:

  • with antibiotics in the recent 2 months;
  • Failure to comply with experimental requirement;

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Caloric Restriction
3-week low calorie diet
Low Calorie Diet consisted of ~50% calories of a normal-calorie diet (female, 1000kcal/day; male, 1200kcal/day)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in BMI of all volunteers (n=41) following calorie restriction dietary intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
BMI was be measured via clinic scale.
at baseline and after 3-week calorie restriction dietary intervention
different changes in BMI between enterotype Bacteroides (n=28) and enterotype Prevotella (n=13) follow calorie restriction dietary intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
BMI was be measured via clinic scale.
at baseline and after 3-week calorie restriction dietary intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in concentration of amino acids of 36 volunteers following calorie restriction dietary intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
Fasting blood sample for measurement of 31 amino acids
at baseline and after 3-week calorie restriction dietary intervention
different changes in concentration of 31 amino acids (fasting status) between enterotype Bacteroides (n=25) and enterotype Prevotella (n=11) follow calorie restriction dietary intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
Fasting blood sample for measurement of 31 amino acids
at baseline and after 3-week calorie restriction dietary intervention
change in gut microbiota of all volunteers (n=41) following calorie restriction intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
faecal bacterial composition determined from microbiological cultures and deep metagenomic next-generation sequencing of bacterial DNA in fece
at baseline and after 3-week calorie restriction dietary intervention
different changes in gut microbiota between enterotype Bacteroides (n=28) and enterotype Prevotella (n=13) follow calorie restriction dietary intervention
Time Frame: at baseline and after 3-week calorie restriction dietary intervention
faecal bacterial composition determined from microbiological cultures and deep metagenomic next-generation sequencing of bacterial DNA in fece
at baseline and after 3-week calorie restriction dietary intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2017

Primary Completion (Actual)

April 30, 2017

Study Completion (Actual)

February 4, 2018

Study Registration Dates

First Submitted

July 24, 2019

First Submitted That Met QC Criteria

July 31, 2019

First Posted (Actual)

August 5, 2019

Study Record Updates

Last Update Posted (Actual)

August 5, 2019

Last Update Submitted That Met QC Criteria

July 31, 2019

Last Verified

July 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • BGI-20170204

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Study Protocol, Statistical analysis plan and analytic code will release

IPD Sharing Time Frame

analytic code will be available for all the time

IPD Sharing Access Criteria

analytic code will be available at github

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Study Data/Documents

  1. Individual Participant Data Set
    Information comments: cohort description including sex, weigt, weight, age
  2. Analytic Code
    Information comments: The Rmd files are used for this study in each directory
  3. gut microbiota and amino acids profiles
    Information comments: the relative abundance profie of gut micorbiota and the concertration profiles of blood amino acids profile

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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