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Omics Profiling of Weight Loss With Bariatric Surgery (Bariatric)

Primary Purpose

Obesity, Surgery

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Stable isotope infusion
Sponsored by
Texas A&M University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Obesity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria obese subjects:

  • Diagnosed with morbid obesity (defined as BMI > 40 kg/m2 or BMI > 35 kg/m2 with at least one serious comorbidity (1991 NIH compendium guidelines))
  • Scheduled for bariatric surgery
  • Age 18 years and older
  • Ability to lie in supine or elevated position for 9 hours
  • Willingness and ability to comply with the protocol

Inclusion criteria healthy subjects:

  • Healthy male or female according to the investigator's or appointed staff's judgment
  • Ability to walk, sit down and stand up independently
  • Age 18 years or older
  • Ability to lie in supine or elevated position for 9 hours
  • Willingness and ability to comply with the protocol

Exclusion Criteria

  • Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (for healthy control group only)
  • Presence of fever within the last 3 days
  • Untreated metabolic diseases including hepatic or renal disorder unrelated to the primary disease
  • Presence of acute illness or metabolically unstable chronic illness unrelated to the primary disease
  • (Possible) pregnancy
  • Any other condition according to the PI or nurse that would interfere with the study or safety of the patient
  • Failure to give informed consent
  • Use of protein or amino acid containing nutritional supplements within 3 days of first test day

Sites / Locations

  • Texas A&M University-CTRAL

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Healthy matched controls

Obese subjects

Arm Description

screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. study day: muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.

screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. 3 study days (one baseline, one pre-surgery, one post-surgery): muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.

Outcomes

Primary Outcome Measures

Net whole-body protein synthesis
Change in whole-body protein synthesis rate after intake of meal

Secondary Outcome Measures

Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS),
a fourteen item self-assessment scale. Seven of the items related to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression.
Executive Function-Adolescent/Adult Sensory Profile (ASP):
a standardized self-questionnaire that generates an individualized profile of sensory processing across four quadrants: low registration, sensation seeking, sensory sensitivity, and sensation avoiding.
Group differences in quality of life as measured by Short Form (36) Health Survey (SF36)
self administered questionnaire that measures each of the following eight health concepts: Physical Functioning (PF); Role-Physical (RP); Bodily Pain (BP); General Health (GH); Vitality (VT); Social Functioning (SF); Role-Emotional (RE); Mental Health (MH) as well as a reported Health Transition item (HT).
Group differences in activity as measured by Physical Activity Scale for the Elderly (PASE)
questionnaire is intended for use in an elderly population and focuses on 3 types of activities: leisure time activities, household activities and work-related activities.
Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT),
a word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match. The examinee reads the words or names the ink colors as quickly as possible within a time limit. Measures selective attention and inhibitory control. The total time in seconds was reported for each trial.
Group differences in state of mood as measured by the Profile of Mood State (POMS)
A psychological distress scale to measure mood disturbance in 6 domains - fatigue-inertia, vigor-activity, tension-anxiety, depression-dejection, anger-hostility, and confusion-bewilderment. Healthy populations take 3 to 7 minutes to complete, and others may take up a bit longer.
Group differences in learning and memory as measured by Controlled Oral Word Association Test (COWAT),
Controlled Oral Word Association Test (COWAT): The examinee is required to say as many words as they can think of in one minute that begin with a given letter of the alphabet. The task contains three trials. Measures phonetic verbal fluency. The raw score (total and mean words recorded across the three trials) was reported.
Group differences in learning and memory as measured by Auditory Verbal Learning Test (AVLT)
Auditory Verbal Learning Test (AVLT): a verbal episodic memory test that evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, retention and recognition of information.
Group differences in attention and executive functions as measured by PASAT
a measure of cognitive function that assesses auditory information processing speed and flexibility, as well as calculation ability.
Group differences in attention and executive functions as measured by Trail Making Test (TMT),
In Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy. In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy. Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility. The total time in seconds was reported for each measure.
Group differences in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA)
assesses several cognitive domains and is used for the screening of mild cognitive impairment. Total scores range from 0-30 with lower scores indicating decreased functioning.
Group differences in attention and executive functions as measured by Brief-A
a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment.
Skeletal muscle strength
handgrip and kin-com 1-leg test
diet recall
The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day.
Respiratory muscle strength
Maximum inhalation and exhalation pressure
Body Composition
Body composition as measured by Dual-Energy X-ray Absorptiometry on study day 1 and the change from day 2 and day 3 (obese only)
Gut function
Digestion of the stable tracers of amino acid

Full Information

First Posted
February 1, 2016
Last Updated
May 27, 2020
Sponsor
Texas A&M University
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1. Study Identification

Unique Protocol Identification Number
NCT02757638
Brief Title
Omics Profiling of Weight Loss With Bariatric Surgery
Acronym
Bariatric
Official Title
Omics Profiling of the Response to Food and Variability of Weight Loss With Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 2015 (undefined)
Primary Completion Date
October 2020 (Anticipated)
Study Completion Date
October 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas A&M University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Understanding how foods and nutrients are digested, absorbed and metabolized when weight is stable and during weight loss induced by bariatric surgery procedure using the technologies of genomics, transcriptomics, proteomics, metabolomics and fluxomics ("omics") will enable generation of new hypotheses that could explain the inter-individual differences in weight loss and could lead to optimization and individualization of therapies designed to lose weight.
Detailed Description
The overarching hypothesis is that there are baseline, pre- and post-surgery combinations of 'omics' signatures in response to food and nutrients that explain the weight loss response of obese subjects to the pre-operative very low calorie (VLC) diet and to bariatric surgery. In order to address the general hypothesis the following specific aims will be addressed: Specific Aim 1: To test the hypothesis that there is a combination of 'omics' parameters in response to a defined meal that discriminate between morbidly obese subjects and normal weight subjects. Specific Aim 2: To test the hypothesis that variation in % weight loss to the VLC diet prior to bariatric surgery is related to baseline genomic markers, gene expression profile, proteomic and metabolomic signatures as well as baseline metabolic and substrates fluxomics response to a defined meal. Specific Aim 2: To test the hypothesis that variation in % weight loss 3 months after bariatric surgery is related to baseline genomic markers, gene expression profile, proteomic and metabolomic signatures as well as baseline metabolic and substrates fluxomics response to a defined meal. Specific Aim 3: To test whether there are "omics" characteristics post-surgery that track with variability in weight loss at 3 months. The benefit of these experiments will be the knowledge gained from understanding the variation in % weight loss to the medically required VLC diet prior to bariatric surgery, and to bariatric surgery, in relation to baseline genomic markers, gene expression profile, proteomic and metabolomic signatures as well as baseline metabolic and substrates fluxomics response to a defined meal in obese and healthy adults.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Surgery

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Healthy matched controls
Arm Type
Experimental
Arm Description
screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. study day: muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.
Arm Title
Obese subjects
Arm Type
Experimental
Arm Description
screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. 3 study days (one baseline, one pre-surgery, one post-surgery): muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.
Intervention Type
Other
Intervention Name(s)
Stable isotope infusion
Intervention Description
such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline
Primary Outcome Measure Information:
Title
Net whole-body protein synthesis
Description
Change in whole-body protein synthesis rate after intake of meal
Time Frame
0, 2, 5, 10, 15, 20, 30, 40, 50, 60, 90, 120, 150, 180, 210, 225, 240, 260, 280, 300, 320, 340, 360 ± 5 min
Secondary Outcome Measure Information:
Title
Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS),
Description
a fourteen item self-assessment scale. Seven of the items related to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Executive Function-Adolescent/Adult Sensory Profile (ASP):
Description
a standardized self-questionnaire that generates an individualized profile of sensory processing across four quadrants: low registration, sensation seeking, sensory sensitivity, and sensation avoiding.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in quality of life as measured by Short Form (36) Health Survey (SF36)
Description
self administered questionnaire that measures each of the following eight health concepts: Physical Functioning (PF); Role-Physical (RP); Bodily Pain (BP); General Health (GH); Vitality (VT); Social Functioning (SF); Role-Emotional (RE); Mental Health (MH) as well as a reported Health Transition item (HT).
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in activity as measured by Physical Activity Scale for the Elderly (PASE)
Description
questionnaire is intended for use in an elderly population and focuses on 3 types of activities: leisure time activities, household activities and work-related activities.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT),
Description
a word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match. The examinee reads the words or names the ink colors as quickly as possible within a time limit. Measures selective attention and inhibitory control. The total time in seconds was reported for each trial.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in state of mood as measured by the Profile of Mood State (POMS)
Description
A psychological distress scale to measure mood disturbance in 6 domains - fatigue-inertia, vigor-activity, tension-anxiety, depression-dejection, anger-hostility, and confusion-bewilderment. Healthy populations take 3 to 7 minutes to complete, and others may take up a bit longer.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in learning and memory as measured by Controlled Oral Word Association Test (COWAT),
Description
Controlled Oral Word Association Test (COWAT): The examinee is required to say as many words as they can think of in one minute that begin with a given letter of the alphabet. The task contains three trials. Measures phonetic verbal fluency. The raw score (total and mean words recorded across the three trials) was reported.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in learning and memory as measured by Auditory Verbal Learning Test (AVLT)
Description
Auditory Verbal Learning Test (AVLT): a verbal episodic memory test that evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, retention and recognition of information.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in attention and executive functions as measured by PASAT
Description
a measure of cognitive function that assesses auditory information processing speed and flexibility, as well as calculation ability.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in attention and executive functions as measured by Trail Making Test (TMT),
Description
In Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy. In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy. Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility. The total time in seconds was reported for each measure.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA)
Description
assesses several cognitive domains and is used for the screening of mild cognitive impairment. Total scores range from 0-30 with lower scores indicating decreased functioning.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Group differences in attention and executive functions as measured by Brief-A
Description
a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment.
Time Frame
Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3 (obese only)
Title
Skeletal muscle strength
Description
handgrip and kin-com 1-leg test
Time Frame
on study day 1 and the change from day 2 and day 3 (obese only)
Title
diet recall
Description
The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day.
Time Frame
on study day 1 and the change from day 2 and day 3 (obese only)
Title
Respiratory muscle strength
Description
Maximum inhalation and exhalation pressure
Time Frame
on study day 1 and the change from day 2 and day 3 (obese only)
Title
Body Composition
Description
Body composition as measured by Dual-Energy X-ray Absorptiometry on study day 1 and the change from day 2 and day 3 (obese only)
Time Frame
on study day 1 and the change from day 2 and day 3 (obese only)
Title
Gut function
Description
Digestion of the stable tracers of amino acid
Time Frame
In postabsorptive and prandial state every 20 minutes up to 6 hours before each sip feeding on study day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria obese subjects: Diagnosed with morbid obesity (defined as BMI > 40 kg/m2 or BMI > 35 kg/m2 with at least one serious comorbidity (1991 NIH compendium guidelines)) Scheduled for bariatric surgery Age 18 years and older Ability to lie in supine or elevated position for 9 hours Willingness and ability to comply with the protocol Inclusion criteria healthy subjects: Healthy male or female according to the investigator's or appointed staff's judgment Ability to walk, sit down and stand up independently Age 18 years or older Ability to lie in supine or elevated position for 9 hours Willingness and ability to comply with the protocol Exclusion Criteria Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (for healthy control group only) Presence of fever within the last 3 days Untreated metabolic diseases including hepatic or renal disorder unrelated to the primary disease Presence of acute illness or metabolically unstable chronic illness unrelated to the primary disease (Possible) pregnancy Any other condition according to the PI or nurse that would interfere with the study or safety of the patient Failure to give informed consent Use of protein or amino acid containing nutritional supplements within 3 days of first test day
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marielle Engelen, PhD
Organizational Affiliation
Texas A&M University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Texas A&M University-CTRAL
City
College Station
State/Province
Texas
ZIP/Postal Code
77843
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36166849
Citation
Wierzchowska-McNew RA, Engelen MPKJ, Thaden JJ, Ten Have GAM, Deutz NEP. Obesity- and sex-related metabolism of arginine and nitric oxide in adults. Am J Clin Nutr. 2022 Dec 19;116(6):1610-1620. doi: 10.1093/ajcn/nqac277.
Results Reference
derived

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Omics Profiling of Weight Loss With Bariatric Surgery

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