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Isoleucine Intake and Intermediary Metabolism in Type 2 Diabetes

Primary Purpose

Type 2 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Oral Supplement
Placebo
Sponsored by
Texas A&M University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Type 2 Diabetes focused on measuring Isoleucine intake

Eligibility Criteria

45 Years - 84 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria:

  • Age: 45-84 years old, inclusive
  • Clinical diagnosis with type-II diabetes (Diabetics subjects only) and oral glucose lowering medication or insulin
  • Stable body-weight (± 5%) for the past 3 months
  • Body Mass Index (BMI): 28 kg/m2 or higher
  • Subject is judged to be in satisfactory health based on medical history, physical examination, and laboratory screening evaluations.
  • Ability to walk, sit down and stand up independently
  • Ability to lie in supine or elevated position for up to 10 hours
  • Willingness and ability to comply with the protocol

Exclusion criteria:

  • Subject is expected to have surgery within one-month of screening
  • Subject is currently participating or has participated in a study with an investigational compound or device within 30 days of signing the informed consent.
  • Active dependence of alcohol or drugs
  • Diagnosed and active treatment of Type 1 Diabetes Mellitus
  • Medication: Use of substances known to influence protein metabolism: antibiotics within 3 weeks prior to the study visit, current use of corticosteroids, growth hormone, testosterone, estrogen, immunosuppressant, blood thinners, or insulin.
  • Adherence to a weight loss diet.
  • (Possible) pregnancy

Sites / Locations

  • Texas A&M University CTRALRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Isoleucine

Placebo

Healthy

Arm Description

Type 2 Diabetics randomized to isoleucine group

Type 2 Diabetics randomized to placebo group

gender-, age-, BMI-matched controls for baseline measurements only. No supplementation provided.

Outcomes

Primary Outcome Measures

Change in whole-body protein metabolism in type 2 diabetic obese subjects
Change in whole-body protein synthesis rate after 10 days of isoleucine supplementation

Secondary Outcome Measures

24-hour glucose levels in type 2 diabetic obese subjects
Blood glucose levels measured by continuous glucose monitor for 10 days of isoleucine supplementation
Group differences in fat metabolism between type 2 diabetics and non-diabetic subjects
Whole-body production rate of glycerol in postabsorptive state
Group differences in glucose metabolism between type 2 diabetics and non-diabetic subjects
Whole-body production rate of glucose in postabsorptive state
Changes in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS) in type 2 diabetics obese subjects
Measured by a validated questionnaire on 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.
Changes in state of mood as measured by the Profile of Mood State (POMS) in type 2 diabetics obese subjects
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.
Changes in attention and executive functions as measured by Trail Making Test (TMT) in type 2 diabetics obese subjects
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.
Changes in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA) in type 2 diabetics obese subjects
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.
Changes in attention and executive functions as measured by Brief-A in type 2 diabetics obese subjects
Brief-A is a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment.
Changes in quality of life as measured by Short Form (36) Health Survey (SF36) in type 2 diabetics obese subjects
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)

Full Information

First Posted
June 22, 2020
Last Updated
December 10, 2021
Sponsor
Texas A&M University
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1. Study Identification

Unique Protocol Identification Number
NCT04461236
Brief Title
Isoleucine Intake and Intermediary Metabolism in Type 2 Diabetes
Official Title
Isoleucine Intake and Intermediary Metabolism in Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 30, 2019 (Actual)
Primary Completion Date
May 30, 2022 (Anticipated)
Study Completion Date
May 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas A&M 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 primary objective of this study is to determine the mechanism of reduced branched-chain amino acid (BCAA) oxidation to propionyl CoA and isoleucine intake can affect TCA cycle function in obese insulin resistant T2D. We will test the hypotheses that isoleucine and valine oxidation to propionyl CoA is reduced and that week long oral administration of isoleucine in T2D subjects will increase propionyl CoA and succinyl CoA production in muscle. The secondary objectives of this study are to determine the extent to which type 2 diabetics are capable of controlling and coordinating complex patterns of force using the upper and lower limb. This line of research has functional significance as upper body coordination and fine motor control is important for many activities associated with daily living and may contribute to therapy protocols for individuals with type 2 diabetes. Functional performance via six-minute walk and balance board measurement will also be tested with and without sensory augmentation via electrical stimulation of foot. Changes in peripheral blood mononuclear cells (PBMCs) mitochondrial respiration values will also be assessed between subject types and for diabetic after the 10-day supplementation period.
Detailed Description
Defects in mitochondrial β-oxidation and branched chain amino acid (BCAA) oxidation are associated with type 2 diabetes (T2D) and other conditions such as Huntington's disease and maple syrup urine disease. Because of these defective mitochondrial pathways, production of TCA cycle intermediates can be limited and obesity worsen the condition of the disease. Interestingly, supplying precursors for the TCA cycle such as propionyl CoA can promote anaplerosis through a pathway that is independent of the defective pathway. Therefore, we hypothesize that providing oral isoleucine, a branched-chain amino acid, which is commonly used for other conditions, will promote anaplerosis by supplying the precursor, propionyl CoA for the TCA cycle intermediate succinyl CoA to muscle of T2D patients. This innovative approach is intended to improve TCA function and insulin resistance in obese T2D and could serve as a model for other nutritional interventions. Diabetes is a growing problem worldwide and has lead to 1.5 million deaths in 2012 and it's prevalence has increased to 9% in 2014, most like related to the steep increase in obesity rates. Research has shown that a combination of increased acetyl-carnitine and reduced propionyl- and isovaleryl-carnitine and elevated blood BCAA in T2D suggests reduced BCAA oxidation to propionyl-CoA, which can cause TCA cycle a malfunction. During homeostasis, transamination of valine and isoleucine leads to α-keto-isovalerate (KIV) and α-keto-methylvalerate (KMV) production, which can be further converted to propionyl CoA and the TCA cycle intermediate succinyl-CoA. Therefore, increased valine and isoleucine transamination can promote anaplerosis and stimulate mitochondrial energetic flux. Because of this, we believe that there is a critical need to identify therapies that can be used to restore TCA function in obese T2D. Furthermore, Type 2 diabetes causes and contributes to a variety of central nervous system (CNS) complications. CNS complications with type 2 diabetes include cognitive and motor dysfunction. There have been a number of studies investigating the association between diabetes and cognitive decline indicating deficits in psychomotor speed, executive function, memory, and attention. Research has also indicated motor deficits with complex motor skills, motor coordination, balance, and muscle strength in type 2 diabetics. However, the majority of research investigating motor dysfunction in type 2 diabetes has focused on lower body dysfunction (balance/gait) and muscular strength (grip) using gross motor control. It is not clear from the literature how type 2 diabetes influences upper body coordination and fine motor control. Chronic inflammatory states, such as obesity, congestive heart failure, diabetes, Alzheimer's disease are also linked to changes in peripheral blood mononuclear cells (PBMCs) mitochondrial respiration values]. PBMC isolation is a non-invasive way to measure mitochondrial function through high-resolution respirometry.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Isoleucine intake

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Isoleucine
Arm Type
Experimental
Arm Description
Type 2 Diabetics randomized to isoleucine group
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Type 2 Diabetics randomized to placebo group
Arm Title
Healthy
Arm Type
No Intervention
Arm Description
gender-, age-, BMI-matched controls for baseline measurements only. No supplementation provided.
Intervention Type
Dietary Supplement
Intervention Name(s)
Oral Supplement
Intervention Description
Supplement provided in capsules. Half the capsules to be taken with lunch and the other half with dinner. All supplements are commercially available.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Change in whole-body protein metabolism in type 2 diabetic obese subjects
Description
Change in whole-body protein synthesis rate after 10 days of isoleucine supplementation
Time Frame
0, 10, 20, 40, 60, 120 ± 5 min after isotope infusion
Secondary Outcome Measure Information:
Title
24-hour glucose levels in type 2 diabetic obese subjects
Description
Blood glucose levels measured by continuous glucose monitor for 10 days of isoleucine supplementation
Time Frame
10 days
Title
Group differences in fat metabolism between type 2 diabetics and non-diabetic subjects
Description
Whole-body production rate of glycerol in postabsorptive state
Time Frame
0, 10, 20, 40, 60, 120 ± 5 min after isotope infusion
Title
Group differences in glucose metabolism between type 2 diabetics and non-diabetic subjects
Description
Whole-body production rate of glucose in postabsorptive state
Time Frame
0, 10, 20, 40, 60, 120 ± 5 min after isotope infusion
Title
Changes in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS) in type 2 diabetics obese subjects
Description
Measured by a validated questionnaire on 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 on study day 1 and study day 2
Title
Changes in state of mood as measured by the Profile of Mood State (POMS) in type 2 diabetics obese subjects
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 on study day 1 and study day 2
Title
Changes in attention and executive functions as measured by Trail Making Test (TMT) in type 2 diabetics obese subjects
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 on study day 1 and study day 2
Title
Changes in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA) in type 2 diabetics obese subjects
Description
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.
Time Frame
postabsorptive state on study day 1 and study day 2
Title
Changes in attention and executive functions as measured by Brief-A in type 2 diabetics obese subjects
Description
Brief-A is 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 on study day 1 and study day 2
Title
Changes in quality of life as measured by Short Form (36) Health Survey (SF36) in type 2 diabetics obese subjects
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 on study day 1 and study day 2
Other Pre-specified Outcome Measures:
Title
Group differences in skeletal muscle strength between type 2 diabetics and non-diabetic subjects
Description
Skeletal muscle strength measured by handgrip and Kin-Com 1-leg test
Time Frame
on study day 1 (baseline)
Title
Group differences in balance between type 2 diabetics and non-diabetic subjects
Description
Balance assessed by balance board test
Time Frame
on study day 1 (baseline)
Title
Group differences in exercise capacity between type 2 diabetics and non-diabetic subjects
Description
Functional exercise capacity assessed by 6-minute walk test
Time Frame
on study day 1 (baseline)
Title
Group differences in Reaction Time task between type 2 diabetics and non-diabetic subjects
Description
Participants attempt to match a position-time sinusoidal target with their right arm while reacting with their left arm.
Time Frame
on study day 1 (baseline)
Title
Group differences in Bi-manual Coordination Task between type 2 diabetics and non-diabetic subjects
Description
Participants attempt to coordinate both the right and left arm to match a visual pattern.
Time Frame
on study day 1 (baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
84 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: Age: 45-84 years old, inclusive Clinical diagnosis with type-II diabetes (Diabetics subjects only) and oral glucose lowering medication or insulin Stable body-weight (± 5%) for the past 3 months Body Mass Index (BMI): 28 kg/m2 or higher Subject is judged to be in satisfactory health based on medical history, physical examination, and laboratory screening evaluations. Ability to walk, sit down and stand up independently Ability to lie in supine or elevated position for up to 10 hours Willingness and ability to comply with the protocol Exclusion criteria: Subject is expected to have surgery within one-month of screening Subject is currently participating or has participated in a study with an investigational compound or device within 30 days of signing the informed consent. Active dependence of alcohol or drugs Diagnosed and active treatment of Type 1 Diabetes Mellitus Medication: Use of substances known to influence protein metabolism: antibiotics within 3 weeks prior to the study visit, current use of corticosteroids, growth hormone, testosterone, estrogen, immunosuppressant, blood thinners, or insulin. Adherence to a weight loss diet. (Possible) pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marielle Engelen, PhD
Phone
9792202282
Email
mpkj.engelen@ctral.org
First Name & Middle Initial & Last Name or Official Title & Degree
Agata McNew, MS
Phone
979-583-5800
Email
a.mcnew@ctral.org
Facility Information:
Facility Name
Texas A&M University CTRAL
City
College Station
State/Province
Texas
ZIP/Postal Code
77845-4253
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marielle Engelen
Phone
979-220-2282
Email
mpkj.engelen@ctral.org
First Name & Middle Initial & Last Name & Degree
Sofie deWandel, MS
Phone
979-422-1789
Email
research@ctral.org

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Description to be provided: Data may be shared upon request for up to 6 years beyond completion of the trial based on methods/proposal approved by both parties' institutional review committees. Individual participant data that underlie the results of the trial may be shared after de-identification (text, tables, figures, and appendices). Additional documents available per request include: study protocol, statistical analysis plan, and informed consent. Requests should be directed to Dr. Marielle Engelen (mpkj.engelen@ctral.org).
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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Isoleucine Intake and Intermediary Metabolism in Type 2 Diabetes

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