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Mechanism of Microbiome-induced Insulin Resistance in Humans (Aim 1)

Phase 2
Completed
Conditions
Insulin Sensitivity
Interventions
Other: High Fat diet
Other: Low Fat diet
Registration Number
NCT02124759
Lead Sponsor
The University of Texas Health Science Center at San Antonio
Brief Summary

The purpose of this study is to determine insulin sensitivity in individuals that are lean normal glucose tolerant subjects after consumption of a normal low fat diet and after a high fat diet and to explore the effects of high fat consumption on the intestinal microbiome, and metabolic endotoxemia.( Aim 1 of the protocol, a separate record is available for Aim 2)

Detailed Description

We will test the hypothesis that a high fat diet given to lean, normal glucose tolerant subjects will impair insulin signaling and sensitivity and modify gut microbiome composition and enhance intestinal permeability, which will increase plasma LPS concentration, induce an inflammatory response in peripheral tissues (skeletal muscle). Also we will test the hypothesis that the inflammatory response and insulin resistance caused by high fat ingestion can be ameliorated by administering

* a synbiotic (Bifidobacterium longum R0175 and oligofructose) which protects the intestinal epithelial barrier and decreases intestinal translocation of LPS; and

* sevelamer, an agent which sequesters lipopolysaccharide (LPS) in the gastrointestinal tract limiting its translocation into the circulation.

All subjects are fed both a low fat diet (considered a normal diet) and high fat diet, first one and then the other in no particular sequence. After a washout period participants are fed the other type of high or low fat diet, depending on which diet they were first assigned to in order to compare the effects of the intervention on insulin sensitivity during each diet.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Both genders. All races and ethnic groups.
  • Premenopausal women in the follicular phase, non-lactating, and with a negative pregnancy test. Postmenopausal women on stable dose of or not exposed to hormone replacement for ≥6 months.
  • Hematocrit (HCT)≥ 34%, serum creatinine ≤ 1.4 mg/dl, and normal serum electrolytes, urinalysis, and coagulation tests. Liver function tests (LFTs) up to 2 times normal.
  • Stable body weight (±2%) for ≥ 3 months
  • Two or less sessions of strenuous exercise/wk for last 6 months.
Exclusion Criteria
  • Presence of diabetes or impaired glucose tolerance based on ADA criteria.
  • Current treatment with drugs known to affect glucose and lipid homeostasis. If the subject has been on a stable dose for the past 3 months, the following agents will be permitted: calcium channel blockers, β-blockers, ACE inhibitors, angiotensin receptor blockers, and statins
  • History of allergy to sevelamer.
  • History of Non-steroidal anti-inflammatory drugs or systemic steroid use for more than a week within 3 months.
  • Current treatment with anticoagulants (warfarin). Aspirin (up to 325 mg) and clopidogrel will be permitted if these can be held for seven days prior to the biopsy in accordance with the primary physician.
  • Use of agents that affect gut flora (e.g. antibiotics, colestyramine, lactulose, PEG) within 3 months.
  • History of heart disease (New York Heart Classification greater than grade II; more than non-specific ST-T wave changes on the ECG), peripheral vascular disease, pulmonary disease, smokers.
  • Poorly controlled blood pressure (systolic BP>170, diastolic BP>95 mmHg).
  • Active inflammatory, autoimmune, hepatic, gastrointestinal, malignant, and psychiatric disease.
  • History of gastrointestinal surgery or gastrointestinal obstruction within two years.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SevelamerLow Fat dietSevelamer: (1.6 g sevelamer + 4.4 g maltodextrin three times a day)
PlaceboLow Fat dietPlacebo: maltodextrin, 6 g three times a day
SynbioticHigh Fat dietSynbiotic: 5g Oligofructose + 4x1010 Bifidobacterium longum CFU 3x daily during diet
PlaceboHigh Fat dietPlacebo: maltodextrin, 6 g three times a day
SevelamerHigh Fat dietSevelamer: (1.6 g sevelamer + 4.4 g maltodextrin three times a day)
SynbioticLow Fat dietSynbiotic: 5g Oligofructose + 4x1010 Bifidobacterium longum CFU 3x daily during diet
SynbioticSynbioticSynbiotic: 5g Oligofructose + 4x1010 Bifidobacterium longum CFU 3x daily during diet
PlaceboMaltodextrinPlacebo: maltodextrin, 6 g three times a day
SevelamerSevelamerSevelamer: (1.6 g sevelamer + 4.4 g maltodextrin three times a day)
Primary Outcome Measures
NameTimeMethod
Insulin Sensitivity Low Fat DietDay 28

Skeletal muscle insulin sensitivity measured after 28 days of low fat diet and drug intervention. The isocaloric low fat diet will provide 55% energy from carbohydrates, 20% from fat and 25% from protein.

Insulin Sensitivity High Fat DietDay 28

Skeletal muscle insulin sensitivity measured after 28 days of high fat diet. The High Fat diet consists of 60% energy from fat (50% saturated), 15% of energy as carbohydrate and 25% from protein consumed while study intervention is being administered.

Secondary Outcome Measures
NameTimeMethod
Gut Permeabilityon Day 24 of the intervention.

Gut permeability is measured using a lactulose/mannitol ingestion assay where urine samples are collected to analyse the ratio of excreted lactulose:mannitol.

Plasma Endotoxin LevelsAt baseline, on day 3, and 28 of the intervention.

Endotoxin is a bacterially derived product that we hypothesized would impact insulin sensitivity through pro inflammatory pathways.

Trial Locations

Locations (1)

Audie L. Murphy VA Hospital, STVHCS

🇺🇸

San Antonio, Texas, United States

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