Postprandial Metabolites of Meal Challenge Test in Diabetes State
Primary Purpose
Type2 Diabetes, Postprandial Hyperglycemia
Status
Unknown status
Phase
Not Applicable
Locations
Malaysia
Study Type
Interventional
Intervention
Strategies to lower postprandial hyperglycemia in T2D patients
Control group
Sponsored by
About this trial
This is an interventional treatment trial for Type2 Diabetes focused on measuring Glycemic Index, NMR metabolomics, Postmeal glucose
Eligibility Criteria
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
Sites / Locations
- Universiti Putra Malaysia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
T2D patients
Healthy individuals
Arm Description
T2D patients (n=24) will be randomized to high GI and low GI MCT randomly.
Healthy individuals (n=24) will be randomized to high GI MCT only.
Outcomes
Primary Outcome Measures
Postprandial glucose
Between low GI and high GI meal challenge measured by blood plasma using Abbott Architect c16000 analyser
Postprandial insulin
Between low GI and high GI meal challenge measured by blood serum using COBAS e411 analyzer
Postprandial GLP-1
Between low GI and high GI meal challenge measured by blood plasma using total ELISA kit
1H-NMR metabolites
Between low GI and high GI meal challenge measured by blood plasma using 1H-NMR spectrometer
Postprandial 1H-NMR metabolites
Between T2D and healthy individuals measured by blood plasma using 1H-NMR spectrometer
Secondary Outcome Measures
Body mass index (BMI)
Measured by weight change using Tanita digital weighing scale
Waist circumference
Using measuring tape
Lipid profile
Measured by blood plasma using Abbott Architect c16000 analyser
Dietary glycemic index (GI)
Between T2D and healthy individuals measured using Dietary History Questionnaire
Dietary Glycemic load(GL)
Between T2D and healthy individuals measured using Dietary History Questionnaire
Full Information
NCT ID
NCT04234763
First Posted
December 3, 2019
Last Updated
January 15, 2020
Sponsor
Universiti Putra Malaysia
1. Study Identification
Unique Protocol Identification Number
NCT04234763
Brief Title
Postprandial Metabolites of Meal Challenge Test in Diabetes State
Official Title
Metabolomics Determinant of Postprandial Metabolism Following Meal-Challenge Test in Diabetes State Using NMR-based Metabolomics Approach
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2019 (Actual)
Primary Completion Date
January 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiti Putra Malaysia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes, Postprandial Hyperglycemia
Keywords
Glycemic Index, NMR metabolomics, Postmeal glucose
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
The meal challenge test (MCT) models are designed to be high glycemic index (GI) (GI=63, GL=25) and low GI meal (GI=46, GL=16), isocaloric (300kcal) with identical macronutrient distribution. The meals will be prepared on the morning of the test, portioned by weighing and served warm.
Masking
Participant
Allocation
Randomized
Enrollment
48 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
T2D patients
Arm Type
Experimental
Arm Description
T2D patients (n=24) will be randomized to high GI and low GI MCT randomly.
Arm Title
Healthy individuals
Arm Type
Active Comparator
Arm Description
Healthy individuals (n=24) will be randomized to high GI MCT only.
Intervention Type
Behavioral
Intervention Name(s)
Strategies to lower postprandial hyperglycemia in T2D patients
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Control group
Intervention Description
Assess nutritional status and no active intervention is conducted.
Primary Outcome Measure Information:
Title
Postprandial glucose
Description
Between low GI and high GI meal challenge measured by blood plasma using Abbott Architect c16000 analyser
Time Frame
Change from baseline and after 14-days intervention
Title
Postprandial insulin
Description
Between low GI and high GI meal challenge measured by blood serum using COBAS e411 analyzer
Time Frame
Change from baseline and after 14-days intervention
Title
Postprandial GLP-1
Description
Between low GI and high GI meal challenge measured by blood plasma using total ELISA kit
Time Frame
Change from baseline and after 14-days intervention
Title
1H-NMR metabolites
Description
Between low GI and high GI meal challenge measured by blood plasma using 1H-NMR spectrometer
Time Frame
Change from baseline and after 14-days intervention
Title
Postprandial 1H-NMR metabolites
Description
Between T2D and healthy individuals measured by blood plasma using 1H-NMR spectrometer
Time Frame
During the 4 hour meal challenge
Secondary Outcome Measure Information:
Title
Body mass index (BMI)
Description
Measured by weight change using Tanita digital weighing scale
Time Frame
Before and after the 14-days intervention
Title
Waist circumference
Description
Using measuring tape
Time Frame
Before and after the 14-days intervention
Title
Lipid profile
Description
Measured by blood plasma using Abbott Architect c16000 analyser
Time Frame
Before and after the 14-days intervention
Title
Dietary glycemic index (GI)
Description
Between T2D and healthy individuals measured using Dietary History Questionnaire
Time Frame
Before and after the 14-days intervention
Title
Dietary Glycemic load(GL)
Description
Between T2D and healthy individuals measured using Dietary History Questionnaire
Time Frame
Before and after the 14-days intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Assoc. Prof. Dr. Barakatun Nisak
Organizational Affiliation
Faculty of Medicine and Health Sciences, Universiti Putra Malaysia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universiti Putra Malaysia
City
Serdang
State/Province
Selangor
ZIP/Postal Code
43400
Country
Malaysia
12. IPD Sharing Statement
Plan to Share IPD
No
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