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Effects of Excess Energy Intake on Metabolic Risk (EXCESS)

Primary Purpose

Insulin Resistance

Status
Completed
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
Nutritional
Sponsored by
Garvan Institute of Medical Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Insulin Resistance

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Sedentary (<60 min formal exercise per week)
  • Aged 20-65 years

Exclusion Criteria:

  • Personal history of diabetes, cardiovascular disease or hypertension
  • Recent weight change (larger than 4kg in the past 3 months)
  • Smoking
  • Regular use of medications, except oral contraceptives
  • Individuals with alcoholism or other substance abuse
  • Pregnancy or lactation, women who are planning to become pregnant or who are not using adequate measures of birth control.

Sites / Locations

  • Garvan Institute of Medical Research

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Overfeeding

Arm Description

4 weeks of 1250 kcal added daily

Outcomes

Primary Outcome Measures

Insulin sensitiviy by hyperinsulinemic clamp

Secondary Outcome Measures

Fat oxidation (whole body RQ and C-14 palmitate), mitochondrial function

Full Information

First Posted
November 20, 2007
Last Updated
July 13, 2015
Sponsor
Garvan Institute of Medical Research
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1. Study Identification

Unique Protocol Identification Number
NCT00562393
Brief Title
Effects of Excess Energy Intake on Metabolic Risk
Acronym
EXCESS
Official Title
Effects of Excess Energy Intake on Metabolic Risk
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Garvan Institute of Medical Research

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The prevalence of obesity has reached epidemic proportions and is associated with the development of insulin resistance and type 2 diabetes (T2DM). A unifying theme has emerged over the past few years suggesting that lipid oversupply to metabolic organs responsible for glucose regulation leads to insulin resistance. Fitting with this, we and others have shown that increased lipid accumulation within skeletal muscle and/or liver is associated with impaired glucose uptake. However, the underlying mechanisms that mediate changes in muscle lipid metabolism are not yet known. The overall aim of this project is to examine metabolic effects of experimental weight gain in lean and overweight individuals with and without a genetic predisposition to type 2 diabetes. We hypothesise that lean subjects will increase fatty acid oxidation and upregulate mitochondrial oxidative capacity in muscle following overfeeding to protect against body weight gain and insulin resistance, but overweight subjects with a genetic predisposition to T2DM will have a defect in this ability.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
N/A
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Overfeeding
Arm Type
Experimental
Arm Description
4 weeks of 1250 kcal added daily
Intervention Type
Other
Intervention Name(s)
Nutritional
Intervention Description
Overfeeding high fat diet for 28 days
Primary Outcome Measure Information:
Title
Insulin sensitiviy by hyperinsulinemic clamp
Time Frame
28-days
Secondary Outcome Measure Information:
Title
Fat oxidation (whole body RQ and C-14 palmitate), mitochondrial function
Time Frame
28-days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Sedentary (<60 min formal exercise per week) Aged 20-65 years Exclusion Criteria: Personal history of diabetes, cardiovascular disease or hypertension Recent weight change (larger than 4kg in the past 3 months) Smoking Regular use of medications, except oral contraceptives Individuals with alcoholism or other substance abuse Pregnancy or lactation, women who are planning to become pregnant or who are not using adequate measures of birth control.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leonie K Heilbronn, PhD
Organizational Affiliation
Garvan Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lesley M Campbell, MBBS
Organizational Affiliation
Garvan Insititute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Garvan Institute of Medical Research
City
Darlinghurst
State/Province
New South Wales
ZIP/Postal Code
2010
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
20547978
Citation
Tam CS, Viardot A, Clement K, Tordjman J, Tonks K, Greenfield JR, Campbell LV, Samocha-Bonet D, Heilbronn LK. Short-term overfeeding may induce peripheral insulin resistance without altering subcutaneous adipose tissue macrophages in humans. Diabetes. 2010 Sep;59(9):2164-70. doi: 10.2337/db10-0162. Epub 2010 Jun 14.
Results Reference
result
PubMed Identifier
20461357
Citation
Samocha-Bonet D, Campbell LV, Viardot A, Freund J, Tam CS, Greenfield JR, Heilbronn LK. A family history of type 2 diabetes increases risk factors associated with overfeeding. Diabetologia. 2010 Aug;53(8):1700-8. doi: 10.1007/s00125-010-1768-y. Epub 2010 May 12.
Results Reference
result
PubMed Identifier
24792219
Citation
Sato K, Samocha-Bonet D, Handelsman DJ, Fujita S, Wittert GA, Heilbronn LK. Serum sex steroids and steroidogenesis-related enzyme expression in skeletal muscle during experimental weight gain in men. Diabetes Metab. 2014 Dec;40(6):439-44. doi: 10.1016/j.diabet.2014.03.006. Epub 2014 Apr 30.
Results Reference
result
PubMed Identifier
24356603
Citation
Samocha-Bonet D, Tam CS, Campbell LV, Heilbronn LK. Raised circulating fetuin-a after 28-day overfeeding in healthy humans. Diabetes Care. 2014;37(1):e15-6. doi: 10.2337/dc13-1728. No abstract available.
Results Reference
result
PubMed Identifier
23640727
Citation
Heilbronn LK, Coster AC, Campbell LV, Greenfield JR, Lange K, Christopher MJ, Meikle PJ, Samocha-Bonet D. The effect of short-term overfeeding on serum lipids in healthy humans. Obesity (Silver Spring). 2013 Dec;21(12):E649-59. doi: 10.1002/oby.20508. Epub 2013 Jul 29.
Results Reference
result
PubMed Identifier
24205333
Citation
Heilbronn LK, Campbell LV, Xu A, Samocha-Bonet D. Metabolically protective cytokines adiponectin and fibroblast growth factor-21 are increased by acute overfeeding in healthy humans. PLoS One. 2013 Oct 18;8(10):e78864. doi: 10.1371/journal.pone.0078864. eCollection 2013.
Results Reference
result
PubMed Identifier
22586466
Citation
Samocha-Bonet D, Campbell LV, Mori TA, Croft KD, Greenfield JR, Turner N, Heilbronn LK. Overfeeding reduces insulin sensitivity and increases oxidative stress, without altering markers of mitochondrial content and function in humans. PLoS One. 2012;7(5):e36320. doi: 10.1371/journal.pone.0036320. Epub 2012 May 7.
Results Reference
result
PubMed Identifier
29901727
Citation
Elshorbagy AK, Samocha-Bonet D, Jerneren F, Turner C, Refsum H, Heilbronn LK. Food Overconsumption in Healthy Adults Triggers Early and Sustained Increases in Serum Branched-Chain Amino Acids and Changes in Cysteine Linked to Fat Gain. J Nutr. 2018 Jul 1;148(7):1073-1080. doi: 10.1093/jn/nxy062.
Results Reference
derived

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Effects of Excess Energy Intake on Metabolic Risk

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