Postprandial Metabolites of Meal Challenge Test in Diabetes State

January 15, 2020 updated by: Barakatun Nisak Bt Mohd Yusof, Universiti Putra Malaysia

Metabolomics Determinant of Postprandial Metabolism Following Meal-Challenge Test in Diabetes State Using NMR-based Metabolomics Approach

Postprandial hyperglycemia is a hallmark feature of Type 2 Diabetes Mellitus (T2D), and persistent elevated glycemic level has shown to be strongly associated with oxidative stress, and a risk factor for cardiovascular disease (CVD). In Malaysia, the glycemic control is poor and patients with T2D commonly experiencing persistent postprandial hyperglycemia (12.7 mmol/L). A low glycemic index (GI) meal has been reported to reduce postprandial glycemia and insulin concentration in patients with T2D. Metabolomics technique can be used to identify comprehensive metabolites in response to different diet. Till date, local scientific data documented on the role and interaction between diet and metabolites for the Malaysian patients with T2D is unknown. This study is to determine the postprandial metabolomic effect of low and high GI meals in patients with T2D using the NMR-based metabolomics approach. Then, patients with T2D will be assigned for 14 days of chronic feeding trial intervention. This study will help to establish local baseline data and understand the impact of meal-patterns on metabolic and metabolite at postprandial responses.

Study Overview

Detailed Description

Despite targeting to optimize fasting blood glucose and lowering HbA1c level, postprandial hyperglycemia needs to be highlighted in the management of Type 2 Diabetes Mellitus (T2D). Postprandial hyperglycemia is the rapid and significant rise in blood glucose level above 7.8 mmol/L 2 hour after meal ingestion. It is strongly associated with oxidative stress and a risk factor for cardiovascular disease (CVD).

In Malaysia, the glycemic control is poor, and patients with T2D commonly experiencing persistent hyperglycemia (12.7 mmol/L), which is the highest concentration in South East Asia region. Nonetheless, a low glycemic index (GI) meal has been reported to reduce postprandial glycemia and insulin concentration in patients with T2D but the metabolite responsiveness following low GI meal is not studied yet. The study of the postprandial state is imperative as it reveals multiple aspects of metabolic health that would not be apparent from solely studying the fasting parameters.

Hence, the objective of this study is to determine the postprandial metabolomic effects of low and high GI meals in patients with T2D using the NMR-based metabolomics approach. Then, the postprandial metabolic response and metabolomic profiles before and after the 14 days chronic feeding trial intervention will be determined and compared. The calculated sample size was 24 patients with T2D and 24 healthy individuals. The study design for meal challenge test (MCT) is a single-blinded, randomized crossover trial with 1-week washout period; whereas a case-control design will be used to compare metabolomic profiles of patients with T2D and healthy individuals.

The MCT model is designed to be high GI (63) and low GI (46) with similar caloric value. During the test day, participants are required to consume the meal within 15 minutes and the blood sample will be taken at the following time points: 0min (fasting), 30, 60, 120, 180 and 240 min. Meanwhile, the urine sample will also be collected at 0, 60 and 240 min accordingly.

The blood sample will be analyzed for blood glucose, insulin, GLP-1, and metabolites; while the urine sample will be analyzed for metabolites. The findings of this study are able to provide fundamental data on metabolic responsiveness of T2D patients following specific meal-plan tailored to Malaysian meal pattern using NMR-based metabolomics approach. Besides, this study is able to establish a local baseline data of postprandial metabolite profiles of patients with T2D following a specific meal plan. At the same time, this study contributes insight to improve diabetes meal-plan that is friendly to postprandial metabolic perturbations.

Study Type

Interventional

Enrollment (Anticipated)

48

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

    • Selangor
      • Serdang, Selangor, Malaysia, 43400
        • Universiti Putra Malaysia

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

35 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • BMI 18.5-35.0 kg/m²
  • Glycemic control (HbA1c level 6.5 - 10.0%)
  • On stabilised oral-antidiabetic drug (OAD) : metformin, sulphonylureas, SGLT2 inhibitors
  • Estimated glomerular filtration rate (GFR) >60ml/min
  • No clinically significant cardiovascular, renal or liver disease

Exclusion Criteria:

  • Smokers
  • Pregnant and lactating women
  • Food allergies or intolerances
  • On weight loss diet
  • On insulin therapy
  • On OAD: DPP-4 inhibitors, GLP-1 receptor agonists, acarbose
  • Anemia (Hb <10g/dL)
  • On regular use of hormones or anti-inflammatory medication (aspirin, corticosteroid)
  • Suggestive indicators for impaired thyroid (high T2H level) or liver function

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: T2D patients
T2D patients (n=24) will be randomized to high GI and low GI MCT randomly.
T2D patients will undergo a 14-day chronic feeding trial intervention where the strategies to lower postprandial hyperglycemia will be educated. For example, to control portion of carbohydrate, incorporate low GI food and diabetes-specific formula, promote physical activity and practice consistent meal timing. After that, patients will undergo MCT again to evaluate the difference before and after the intervention.
Active Comparator: Healthy individuals
Healthy individuals (n=24) will be randomized to high GI MCT only.
Assess nutritional status and no active intervention is conducted.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postprandial glucose
Time Frame: Change from baseline and after 14-days intervention
Between low GI and high GI meal challenge measured by blood plasma using Abbott Architect c16000 analyser
Change from baseline and after 14-days intervention
Postprandial insulin
Time Frame: Change from baseline and after 14-days intervention
Between low GI and high GI meal challenge measured by blood serum using COBAS e411 analyzer
Change from baseline and after 14-days intervention
Postprandial GLP-1
Time Frame: Change from baseline and after 14-days intervention
Between low GI and high GI meal challenge measured by blood plasma using total ELISA kit
Change from baseline and after 14-days intervention
1H-NMR metabolites
Time Frame: Change from baseline and after 14-days intervention
Between low GI and high GI meal challenge measured by blood plasma using 1H-NMR spectrometer
Change from baseline and after 14-days intervention
Postprandial 1H-NMR metabolites
Time Frame: During the 4 hour meal challenge
Between T2D and healthy individuals measured by blood plasma using 1H-NMR spectrometer
During the 4 hour meal challenge

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body mass index (BMI)
Time Frame: Before and after the 14-days intervention
Measured by weight change using Tanita digital weighing scale
Before and after the 14-days intervention
Waist circumference
Time Frame: Before and after the 14-days intervention
Using measuring tape
Before and after the 14-days intervention
Lipid profile
Time Frame: Before and after the 14-days intervention
Measured by blood plasma using Abbott Architect c16000 analyser
Before and after the 14-days intervention
Dietary glycemic index (GI)
Time Frame: Before and after the 14-days intervention
Between T2D and healthy individuals measured using Dietary History Questionnaire
Before and after the 14-days intervention
Dietary Glycemic load(GL)
Time Frame: Before and after the 14-days intervention
Between T2D and healthy individuals measured using Dietary History Questionnaire
Before and after the 14-days intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Assoc. Prof. Dr. Barakatun Nisak, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia

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)

August 1, 2019

Primary Completion (Anticipated)

January 1, 2020

Study Completion (Anticipated)

June 1, 2020

Study Registration Dates

First Submitted

December 3, 2019

First Submitted That Met QC Criteria

January 15, 2020

First Posted (Actual)

January 21, 2020

Study Record Updates

Last Update Posted (Actual)

January 21, 2020

Last Update Submitted That Met QC Criteria

January 15, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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