Asian Indian Prediabetes Study (AIPS)

November 20, 2023 updated by: Jeannie Tay, Singapore Institute for Clinical Sciences

Diet and Lifestyle Intervention Strategies to Treat β-cell Dysfunction and Insulin Resistance in Asian Indians

Compared to other races, Indians have higher insulin resistance, poorer pancreatic function and a greater risk of developing diabetes, highlighting the importance of early strategies for improving insulin sensitivity and improving pancreatic function in Indians to prevent diabetes and lower the risk of heart disease.

A low carbohydrate diet can deplete fat from undesirable places, such as fat around organs in the abdominal cavity. In this study, we will determine if restriction of dietary carbohydrates will deplete fat in the pancreas and liver, and improve insulin sensitivity and early insulin secretion in Indians. These changes may prevent diabetes from developing. Hepatic and pancreatic fat will be measured using magnetic resonance imaging. Insulin sensitivity and secretion will be measured during an oral glucose tolerance test. In addition, this study will investigate if the higher insulin resistance in Indians is due to genes that cause the inability to store fat in the legs.

The results on the type of diet that is more effective for reducing pancreatic and hepatic fat is important for informing dietary guidelines on the use of low carbohydrate diets for diabetes prevention, particularly in Indians who have a higher risk of developing diabetes.

Study Overview

Status

Completed

Conditions

Detailed Description

Compared to other races, Indians have a greater risk of developing type 2 diabetes (T2D), increased insulin resistance (IR) and more rapid decline in β-cell function, highlighting the urgency and importance of early intervention strategies for improving insulin sensitivity and preserving/improving β-cell function to prevent T2D and mitigate against the increased vascular disease risk.

Preliminary findings show a reduction in glycemic load selectively depletes visceral and ectopic lipid and improves insulin sensitivity and β-cell function in non-diabetic adults. The proposed research will investigate if the phenotypic features increasing T2D risk in individuals of Indian ancestry (IR and impaired β-cell function) can be favorably modified by a low glycemic (LG) intervention, and if the increased IR is attributable to genetic factors regulating adipocyte differentiation and function.

These research objectives will be achieved through a 24-week randomized controlled trial (RCT) comparing isocaloric LG versus control diets in Indians with prediabetes. Compared to individuals in the control group, those on the LG diet are expected to have greater ectopic (pancreas, liver, visceral and intramyocellular) fat depletion assessed with MRI/MRS, and improvements in first phase insulin secretion and insulin sensitivity assessed with the C-peptide model and oral minimal model, respectively during an OGTT. Reductions in hepatic and pancreatic lipids will be associated with improvements in first-phase β-cell response. Individuals with a greater number of risk alleles from a 53-SNP IR genetic risk score will have lower insulin sensitivity and leg fat, supporting the notion that impaired adipocyte differentiation leading to limited peripheral adipose expansion capacity is an important etiological factor underpinning IR cardiometabolic disease in Indians.

The results will broaden the evidence base for effective prevention strategies in this high risk population by investigating the effect of the proposed diet intervention on underlying physiological and molecular mechanisms implicated in the pathophysiology of T2D in Indians.

Study Type

Interventional

Enrollment (Actual)

53

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

      • Singapore, Singapore, 117549
        • Singapore Institute for Clinical Sciences (SICS)

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

17 years to 46 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male or female
  • Asian Indian ethnicity
  • Age between 21-50 years
  • BMI not greater than 35 or less than 25
  • Prediabetes (based on results from an OGTT conducted in the last 3 months):

    • Impaired Fasting Glucose (IFG) which is a fasting blood glucose level of between 5.6 to 6.9 mmol/l and/or
    • Impaired Glucose Tolerance (IGT) which is a blood glucose level of 7.8 to 11.0 mmol/l, 2 hours after the OGTT but below 7.0 mmol/l in the fasting state.
  • Not have type 1 or type 2 diabetes
  • Not on any diabetes medications that affect insulin sensitivity e.g. metformin, glitazones
  • No abnormality of clinical significance on medical history
  • If female, not pregnant or breast feeding
  • No history of coronary artery disease or cardiac (heart) abnormalities
  • Participants must understand the procedures involved and agree to participate in the study by giving full informed, written consent

Exclusion Criteria:

  • BMI greater than 35 or less than 25
  • Weight gain or loss of more than 5% over the past 3 months
  • Have anaemia (low haemoglobin/ red blood cell levels), a malignancy (cancer), abnormal liver function, any significant endocrinopathy (e.g. thyroid problems), or a history of metabolic disease such as liver, kidney, cardiovascular, respiratory or gastrointestinal disease.
  • Have high uncontrolled hypertension (resting seated blood pressure >160/100 mmHg)
  • Taking medications that may affect glucose metabolism e.g. steroids, thiazide diuretics at doses>25mg/day.
  • History of smoking or using nicotine products during the 6 months prior to study
  • History of heavy alcohol consumption (> 5 standard drinks/day)
  • Inability to limit alcohol consumption for study duration
  • Lactose Intolerant or have a nut allergy
  • Have depression
  • Have a musculoskeletal injury, joint or peripheral vascular disease sufficient to impede exercise (such as hip arthritis, foot, ankle problems or pain)
  • Have severe exercise-induced asthma
  • Participating in a regular aerobic or resistance exercise program
  • Currently on a weight reducing diet or have an eating disorder
  • Contraindications for MRI e.g. if you have certain metallic implants/devices such as heart valves of a cardiac pacemaker which may be affected by the magnetic field
  • Unwilling to be randomized to either diet group
  • Extended absences due to travel or other commitments
  • Unable to comprehend or cope with study requirements

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Low Glycaemic Diet (LG)
Low carbohydrate, low saturated fat diet

The LG diet will comprise 20% carbohydrate, 30% protein, and 50% fat (<10% saturated fat). It will have a low glycaemic load; include plant and animal protein; non-starchy vegetables and salad greens; and some low-sugar fruit. Participants will be encouraged to incorporate a variety of foods rich in monounsaturated and polyunsaturated fats in their diet.

The control diet will comprise 50% carbohydrate, 20% protein and 30% total fat (<10% saturated fat). It will reflect the Health Promotion Board's (HPB) recommendations to reduce dietary fat, emphasize wholegrains and include a variety of fruits and vegetables. In contrast to the LG diet, the control diet will have a higher glycaemic load with a greater proportion of energy derived from unrefined carbohydrate foods.

Concurrent to the dietary intervention and consistent with physical activity guidelines, all participants will undertake a 60-min structured exercise program incorporating aerobic/ resistance exercises 3-4 days/week.

Active Comparator: Control Diet
High unrefined carbohydrate, low fat diet

The LG diet will comprise 20% carbohydrate, 30% protein, and 50% fat (<10% saturated fat). It will have a low glycaemic load; include plant and animal protein; non-starchy vegetables and salad greens; and some low-sugar fruit. Participants will be encouraged to incorporate a variety of foods rich in monounsaturated and polyunsaturated fats in their diet.

The control diet will comprise 50% carbohydrate, 20% protein and 30% total fat (<10% saturated fat). It will reflect the Health Promotion Board's (HPB) recommendations to reduce dietary fat, emphasize wholegrains and include a variety of fruits and vegetables. In contrast to the LG diet, the control diet will have a higher glycaemic load with a greater proportion of energy derived from unrefined carbohydrate foods.

Concurrent to the dietary intervention and consistent with physical activity guidelines, all participants will undertake a 60-min structured exercise program incorporating aerobic/ resistance exercises 3-4 days/week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in β-cell Function [First-phase β-cell response (PhiD)]
Time Frame: Week 0, 8 and 24
First-phase β-cell response (PhiD) will be calculated from blood glucose and C-peptide data during a 3h 75g oral glucose tolerance test (OGTT) using the C-peptide minimal model.
Week 0, 8 and 24
Change in Insulinogenic index (ΔC-peptide/∆glucose during the first 30 minutes of the OGTT)
Time Frame: Week 0, 8 and 24
ΔC-peptide/∆glucose during the first 30 minutes of the OGTT will be calculated as an index of early insulin secretion (Insulinogenic index).
Week 0, 8 and 24
Change in Incremental AUC
Time Frame: Week 0, 8 and 24
Incremental AUC over 180 minutes of the OGTT will be calculated for glucose, insulin, and C-peptide.
Week 0, 8 and 24
Change in Insulin sensitivity (Oral Minimal model)
Time Frame: Week 0, 8 and 24
Insulin sensitivity will be calculated from blood glucose, insulin and C-peptide during a 3h 75g oral glucose tolerance test (OGTT) using both the oral minimal model
Week 0, 8 and 24
Change in Matsuda index for whole body insulin sensitivity
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Body fat distribution
Time Frame: Week 0, 8 and 24
Body fat distribution will be imaged and quantified using MRI and MRS. Abdominal fat will be segmented to identify and quantify subcutaneous (deep and superficial) and visceral fat compartments. Lower body gluteal fat compartment will also be imaged and quantified. Fat within liver, pancreas and skeletal muscle fibers will be determined by MRI / MRS.
Week 0, 8 and 24
Change in Weight (kg)
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in Blood Pressure
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in Body Composition- Total body fat
Time Frame: Week 0, 8 and 24
Total body fat (kg) will be assessed using DXA
Week 0, 8 and 24
Change in Body Composition- Total lean mass
Time Frame: Week 0, 8 and 24
Total lean mass (kg) will be assessed using DXA
Week 0, 8 and 24
Genotyping analyses
Time Frame: Week 0
Genomic DNA isolated from blood samples will be analysed
Week 0
Change in Blood Lipids (total cholesterol, HDL-C, TAG, lipoprotein subfractions)
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in liver enzymes
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in inflammatory markers (e.g. IL-6, TNFα and CRP)
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in satiety hormones (e.g. leptin, ghrelin, GIP and GLP-1).
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Lipidomics
Time Frame: Week 0, 8 and 24
Lipidomics evaluation of several lipid classes including sphingolipids (sphingomyelins, ceramides and glycosphingolipids) in plasma
Week 0, 8 and 24
Change in Plasma phospholipid fatty acid (FA) profile
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24
Change in Gut microbiota composition
Time Frame: Week 0, 8 and 24
Gut microbiota composition will be assessed by 16S or shotgun metagenomic sequencing
Week 0, 8 and 24
Change in Faecal characteristics- including short chain fatty acids (SCFAs).
Time Frame: Week 0, 8 and 24
Week 0, 8 and 24

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in respiratory quotient (RQ)
Time Frame: Week 0, 8 and 24
Respiratory quotient (RQ) to assess substrate utilization by indirect calorimetry.
Week 0, 8 and 24
Change in blood ketone (β-hydroxybutyrate, βHB) concentrations
Time Frame: Week 0, 8 and 24
A marker of carbohydrate intake
Week 0, 8 and 24
Change in 24-h urinary urea to creatinine ratio
Time Frame: Week 0, 8 and 24
A marker of protein intake
Week 0, 8 and 24
Change in Physical activity levels
Time Frame: Week 0, 8 and 24
Assessed with 7 consecutive days of triaxial accelerometry
Week 0, 8 and 24
Change in Exercise Classes attendance
Time Frame: 24 weeks
24 weeks
Change in dietary intake (diet checklists)
Time Frame: 24 weeks
24 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jeannie Tay, PhD, Singapore Institute for Clinical Sciences

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)

October 19, 2020

Primary Completion (Actual)

January 27, 2023

Study Completion (Actual)

February 1, 2023

Study Registration Dates

First Submitted

August 6, 2020

First Submitted That Met QC Criteria

August 9, 2020

First Posted (Actual)

August 11, 2020

Study Record Updates

Last Update Posted (Estimated)

November 22, 2023

Last Update Submitted That Met QC Criteria

November 20, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

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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