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Low-calorie Sweeteners and Adipose Signaling

Primary Purpose

Nutritional and Metabolic Diseases

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diet Soda
Sponsored by
George Washington University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Nutritional and Metabolic Diseases focused on measuring diet soda, low-calorie sweeteners, obesity

Eligibility Criteria

18 Years - 25 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Female
  2. 18-25 years of age
  3. Overweight and mild to moderate obesity (25 ≤ body mass index (BMI) <35 kg/m2)
  4. Consumption of <1 food/beverage with sucralose and/or acesulfame-potassium per month
  5. Able and willing to comply with all study procedures for the duration of the study

Exclusion Criteria:

  1. Overt diabetes
  2. Renal/gastrointestinal conditions
  3. Pregnant/lactating
  4. Recent significant weight change
  5. Acute illness (w/fever)
  6. Antibiotics in past 3 months
  7. Use of illegal drugs/condition limiting ability to give consent.

Sites / Locations

  • Milken Institute School of Public Health and GW Medical Faculty Associates

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Diet Soda

Arm Description

Subjects will be asked to consume a diet soda three times daily for eight weeks.

Outcomes

Primary Outcome Measures

Transcriptomics
Within-subjects changes in adipose gene expression will be evaluated using RNAseq

Secondary Outcome Measures

Full Information

First Posted
April 19, 2017
Last Updated
May 11, 2022
Sponsor
George Washington University
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1. Study Identification

Unique Protocol Identification Number
NCT03125356
Brief Title
Low-calorie Sweeteners and Adipose Signaling
Official Title
Low-calorie Sweeteners and Adipose Signaling
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
December 31, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
George Washington University

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
The purpose of this study is to determine whether eight weeks of low-calorie sweetener (LCS) exposure exerts cardiovascular and/or metabolic effects among LCS-naïve overweight and obese adolescents and young adults. We will examine changes in gene expression in subcutaneous fat and will correlate these molecular changes with plasma biochemistry.
Detailed Description
The proposed study will investigate LCS-induced changes in metabolically "at-risk" young adults, under conditions that reflect typical beverage consumption. We will first identify molecular pathways potentially affected by LCS (adipose transcriptomics via global RNAseq) and then identify links between LCS-induced gene expression changes and circulating levels of key metabolic biomarkers and clinical outcomes. We will perform subcutaneous adipose biopsies before and after consumption of 12 ounces of diet soda three times daily for eight weeks. Within-subjects changes in adipose gene expression will be evaluated using RNAseq. We will then correlate transcriptomic changes with circulating levels of key inflammatory and metabolic biomarkers, to provide mechanistic insight into which pathways drive clinically-relevant LCS-induced metabolic impairments. We will measure glucose, insulin, inflammatory markers and adipose-derived hormones before and after eight weeks of LCS exposure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nutritional and Metabolic Diseases
Keywords
diet soda, low-calorie sweeteners, obesity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Diet Soda
Arm Type
Experimental
Arm Description
Subjects will be asked to consume a diet soda three times daily for eight weeks.
Intervention Type
Other
Intervention Name(s)
Diet Soda
Intervention Description
Subjects will be asked to consume diet soda three times daily for eight weeks.
Primary Outcome Measure Information:
Title
Transcriptomics
Description
Within-subjects changes in adipose gene expression will be evaluated using RNAseq
Time Frame
Pre/post 8 weeks of diet soda

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Female 18-25 years of age Overweight and mild to moderate obesity (25 ≤ body mass index (BMI) <35 kg/m2) Consumption of <1 food/beverage with sucralose and/or acesulfame-potassium per month Able and willing to comply with all study procedures for the duration of the study Exclusion Criteria: Overt diabetes Renal/gastrointestinal conditions Pregnant/lactating Recent significant weight change Acute illness (w/fever) Antibiotics in past 3 months Use of illegal drugs/condition limiting ability to give consent.
Facility Information:
Facility Name
Milken Institute School of Public Health and GW Medical Faculty Associates
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20052
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Low-calorie Sweeteners and Adipose Signaling

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