Metabolic Effects of Birth Weight on Overweight and Obese Chinese Adults and Their Responses to Weight Loss

NCT ID: NCT01080378

Last Updated: 2010-03-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-04-30

Brief Summary

The overall objective of this study is to investigate in depth the impact of birth weight on the nature of metabolic physiology, body composition and epigenetic differences of the different phenotypes of overweight and obese individuals who are otherwise overtly healthy. We also aim to determine the efficacy of a weight loss intervention on the above mentioned metabolic parameters in these individuals.

Detailed Description

There is an exponential rise in the prevalence of type 2 diabetes and obesity in Singapore coincident with rapid nutritional and socioeconomic transition. Differing birth weights, even in the normal ranges, predisposes individuals to the risk of type 2 diabetes and obesity. We aim to examine the causal pathways, developmental contribution and effects of a weight loss intervention to this differential by evaluating the hypothesis that genomic, birth weight, developmental, lifestyle and environmental factors contribute to the variation in phenotype observed in adults with obesity and metabolic syndrome.

Although there are many large studies that examined the effect of birth weight on the expression of obesity and the metabolic syndrome phenotype, most of these studies usually lack in-depth physiological and epigenetic/genomic studies due to their large sample sizes. We therefore aim to explore such detailed aspects of physiological and epigenetic/genomic profiles on smaller but statistically powered samples, focusing on evaluating body composition, nutritional and metabolic phenotype in relationship to epigenetic/genetic markers and developmental history. In addition, we examine the effects of a weight loss intervention on these parameters. This will assist in weighing the importance of developmental and genetic pathways in contributing to individual risk and the response and efficacy to an intervention.

Conditions

Healthy; Overweight; Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Blinding Strategy: NONE

Study Groups

Higher Birth Weight

3447g to 3879g

Group Type: OTHER

Dietary and Exercise Intervention

Intervention Type: PROCEDURE

Participants will be enrolled into a 16 weeks weight loss programme that consists of (a) dietary interventions and (b) structured exercise sessions and (c) physical activity to achieve 7 - 10% decrease (more than 8 kg) in initial body weight in 16 weeks. They will be subjected to a caloric deficit of 40% of the subject's energy expenditure or 1000kcal, which ever it is higher. (allowance given for dietary control and physical activity).

Lower Birth Weight

2624g to 2964g

Group Type: OTHER

Dietary and Exercise Intervention

Intervention Type: PROCEDURE

Participants will be enrolled into a 16 weeks weight loss programme that consists of (a) dietary interventions and (b) structured exercise sessions and (c) physical activity to achieve 7 - 10% decrease (more than 8 kg) in initial body weight in 16 weeks. They will be subjected to a caloric deficit of 40% of the subject's energy expenditure or 1000kcal, which ever it is higher. (allowance given for dietary control and physical activity).

Normal Birth Weight

2965g to 3446g

Group Type: OTHER

Dietary and Exercise Intervention

Intervention Type: PROCEDURE

Participants will be enrolled into a 16 weeks weight loss programme that consists of (a) dietary interventions and (b) structured exercise sessions and (c) physical activity to achieve 7 - 10% decrease (more than 8 kg) in initial body weight in 16 weeks. They will be subjected to a caloric deficit of 40% of the subject's energy expenditure or 1000kcal, which ever it is higher. (allowance given for dietary control and physical activity).

Interventions

Dietary and Exercise Intervention

Participants will be enrolled into a 16 weeks weight loss programme that consists of (a) dietary interventions and (b) structured exercise sessions and (c) physical activity to achieve 7 - 10% decrease (more than 8 kg) in initial body weight in 16 weeks. They will be subjected to a caloric deficit of 40% of the subject's energy expenditure or 1000kcal, which ever it is higher. (allowance given for dietary control and physical activity).

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Ability to give informed consent

2. Chinese males (aged 21-40)

3. Body mass index between 23-30 kg/m2

4. Total body fat content >24%

5. Sedentary adults < 1 episode of exercise > =30 min/week

6. Birth weight between 5-95% percentiles

7. Fasting glucose < 7 mmol/L

8. Normotensive, defined as BP < 140/90 mmHg and not on any antihypertensive agents

Exclusion Criteria

1. Recent changes in weight of >5% over the past 6 months

2. Attempts to lose weight (weight not stable, exercises still changing and not in maintenance phase) over the past 6 months

3. Significant changes in diet over the past 6 months

4. Any use of weight reducing drugs in the past 6 months

5. Previous abdominal surgery (and bariatric surgery)

6. Any bleeding disorders which would preclude biopsies

7. Any use of investigational drugs in the past 6 months

8. Known allergy to insulin or local anaesthetics

9. Known allergy to milk or milk products (eg. Ensure, liquid meal)

10. Any serious illness requiring hospitalization or surgery in the past 6 months

11. Treatment with medications for hypertension, diabetes mellitus or dyslipidemia, epilepsy, ischemic heart disease

12. On anti-platelet agents, non-steroidal anti-inflammatory drugs (NSAIDs) or anticoagulants

13. Use of any prescription medication that cannot be safely discontinued within 14 days prior to study entry

14. Any use of corticosteroids in the past 6 months

15. Any other medications that could alter insulin resistance

16. History of surgery with metallic clips, staples or stents

17. Presence of cardiac pacemaker or other foreign body in any part of the body including tattoos

18. Mother no longer alive or unable to provide information on birth weight

19. Born premature (ie. not full term baby < 37 weeks of gestation age)

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

National Medical Research Council (NMRC), Singapore

OTHER_GOV

Sponsor Role: collaborator

National University Hospital, Singapore

OTHER

Sponsor Role: lead

Responsible Party

National University of Singapore (NUHS)

Principal Investigators

Yung Seng Lee

Role: PRINCIPAL_INVESTIGATOR

National University Hospital, Singapore

Locations

National University Hospital

Singapore, , Singapore

SGH Life Centre

Singapore, , Singapore

Countries

Singapore

Facility Contacts

Gladys Woon

Role: primary

obgwsmg@nus.edu.sg

Other Identifiers

DSRB C/09/604

Identifier Type: -

Identifier Source: org_study_id