Effect of AT-derived miRNA on the Biology and Insulin Sensitivity of Skeletal Muscle in Humans
Status: | Active, not recruiting |
---|---|
Conditions: | Endocrine, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 2/17/2019 |
Start Date: | May 27, 2015 |
End Date: | April 2020 |
The purpose of this study is examine the effect of fat tissue-released miRNA on skeletal
muscle and if abnormal fat tissue-released miRNA contributes to insulin resistance in obese
individuals. This information will be important for our understanding of how the body's sugar
metabolism is regulated and why people who are obese become insulin resistant and are more
likely to develop type 2 diabetes.
muscle and if abnormal fat tissue-released miRNA contributes to insulin resistance in obese
individuals. This information will be important for our understanding of how the body's sugar
metabolism is regulated and why people who are obese become insulin resistant and are more
likely to develop type 2 diabetes.
Study Objectives:
1. To establish and optimize the methodology for measuring adipose tissue miRNA release.
2. To establish and optimize the methodology for measuring the effect of adipose
tissue-released miRNA on skeletal muscle biology and insulin sensitivity.
3. To profile adipose tissue-released miRNA in lean insulin-sensitive and obese
insulin-resistant healthy individuals.
4. To examine the effects of adipose tissue-released miRNA from lean insulin-sensitive
individuals and obese insulin-resistant individuals on skeletal muscle biology and
insulin sensitivity.
1. To establish and optimize the methodology for measuring adipose tissue miRNA release.
2. To establish and optimize the methodology for measuring the effect of adipose
tissue-released miRNA on skeletal muscle biology and insulin sensitivity.
3. To profile adipose tissue-released miRNA in lean insulin-sensitive and obese
insulin-resistant healthy individuals.
4. To examine the effects of adipose tissue-released miRNA from lean insulin-sensitive
individuals and obese insulin-resistant individuals on skeletal muscle biology and
insulin sensitivity.
Inclusion Criteria:
- Able to communicate meaningfully with the investigator and legally competent to
provide informed written consent
- 18-65 years of age
- BMI of 20-25 kg/m2 (lean subjects); 30-35 kg/m2 (obese subjects)
- Stable body weight (< 3 kg change in the last 8 weeks)
- homeostatic model assessment (HOMA)-insulin resistance <2.7 if lean; homeostatic model
assessment (HOMA)-insulin resistance ≥2.7 if obese
Exclusion Criteria:
- Lactation or pregnancy, current and/or within last 6 months, per participant's report
- Female subjects postmenopausal
- Cardiovascular disease (unstable angina, myocardial infarction or coronary
revascularization within 6 months)
- Liver disease (AST or ALT(alanine aminotransferase)>2.5 times the upper limit of
normal)
- Kidney disease (creatinine >1.6 mg/dl)
- Anemia (hemoglobin <12 g/dl in men, <11 g/dl in women)
- Thyroid dysfunction (abnormal TSH)
- HbA1c ≥6.5%
- Uncontrolled hypertension (systolic BP>160 mmHg, diastolic BP>100 mmHg)
- History of coagulopathies
- History (within the last 5 years) or presence of malignancy, (skin cancers, with the
exception of melanoma, may be acceptable)
- Current or history of drug abuse or alcohol abuse (>2 drinks/day)
- Prior treatment (within last 3 months) with systemic glucocorticoids (>2 weeks),
beta-blockers, drugs for weight loss, niacin or fibrates
- History of HIV, active Hepatitis B or C, or Tuberculosis (participant reported)
- Smoke > 5 cigarettes per day
We found this trial at
1
site
Orlando, Florida 32804
Principal Investigator: Christian Meyer, MD, PhD
Phone: 407-303-7100
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