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Recruiting NCT07516509

Determining Cell- and Spatially-distinct Skeletal Muscle Transcriptional Aberrations in Insulin Resistance

Conditions: Insulin Resistance

Sex: All
Ages: 30 Years – 65 Years
Healthy volunteers: Yes
Enrollment: 36
Sponsor: AdventHealth Translational Research Institute

Location: AdventHealth Translational Research Institute Orlando Florida

Summary

The purpose of this study is to find new signs or signals in muscle cells that can help us understand when the body isn't responding well to insulin (a condition called insulin resistance).

Eligibility Criteria

Inclusion Criteria: * All Groups 1. 30 to 65 years of age 2. Stable weight (No Gain/Loss of \>10 lbs in 6 months) 3. Sedentary (≤ 1 continuous exercise/week) 4. Non-smoker 5. Resting Blood Pressure ≤ 150mmHg systolic and ≤ 95 mmHg diastolic Group A - Lean individuals with insulin sensitivity (IS-Lean) 1. BMI 18-25 kg/m2 2. Hemoglobin A1c ≤ 5.6% at screening 3. Blood glucose level ≤ 140 mg/dL 2hr after a 75g oral glucose tolerance test Group B - Individuals with obesity and insulin sensitivity (IS-Obesity) 1. BMI 30-40 kg/m2 2. Hemoglobin A1c ≤ 5.6% at screening 3. Blood glucose level ≤ 140 mg/dL 2hr after a 75g oral glucose tolerance test Group C - Individuals with obesity and insulin resistance (IR-Obesity) 1. BMI 30-40 kg/m2 2. Hemoglobin A1c ≤ 6.4 % at screening 3. Blood glucose level 140-199 mg/dL 2hr after a 75g oral glucose tolerance test Exclusion Criteria: 1. Clinically significant CVD including h/o MI, within the past year 2. Peripheral Vascular Disease 3. Diagnosed with Type I or Type II diabetes 4. Hepatic, renal, muscular/neuromuscular, or active hematologic/oncologic disease 5. Previous history of pulmonary emboli 6. Peripheral Neuropathy 7. Anemia (Hematocrit \190 mg/dL; total cholesterol \>300 mg/dL); 18. ALT \>80, AST\>80, Alk Phos \>240 if a participant presents with liver functions out of these ranges at screening the MI or PI can give discretion to participate 19. Proteinuria (defined as \> 1+) at screening 20. Kidney disease (creatinine \>1.6 mg/dl or estimated glomerular filtration rate \8) at screening or on thyroid replacement therapy 24. Abnormal bleeding or coagulopathy (self-report) or history of a bleeding disorder or clotting abnormality 25. History of cancer (other than non-melanoma skin cancer) within the last 5 years (not in remission); anti-hormonal therapy (e.g., for breast or prostate cancer) within the last 6 months; 26. Previous bariatric or other surgery for obesity 27. Females currently on hormone replacement therapy (HRT) less than 6 months 28. Females with an irregular menstrual cycle 29. Previous difficulty with lidocaine or other local anesthetic 30. ACS symptoms: * Positive ECG (\> 2mm ST segment depression) without PCP cardiologist permission to participate * Signs or symptoms of cardiovascular decomposition (eg. hypotensive response to exercise) * Onset of angina or angina like symptoms, shortness of breath, change in heart rhythm, signs of poor perfusion (light-headedness), tightness. 31. The following medication use is exclusionary; * Dose change for any chronic-use drug in the last 3 months; * Any medications that can alter glucose homeostasis (eg. steroids, glucocorticoids, nicotinic acid). Acute therapy (5-7 days) is not exclusionary however; participant must be agreeable to a washout period of 5-7 days prior to day of biopsy. * Blood thinners such as Coumadin, Lovenox etc. Aspirin is not exclusionary however; participant must be agreeable to a washout period of \> 10 days prior to day of biopsy * All Weight loss medications including but not limited toGLP-1 agonists- Wegovy, liraglutide, semaglutide, Trulicity (dulaglutide), Phentermine and Contrave * Cardiovascular: beta blockers and centrally acting anti-hypertensive drugs, anticoagulants, antiarrhythmics, and antiplatelet drugs (other than aspirin ≤100 mg/day); * Psychiatric: chronic use of medium- or long-acting sedatives and hypnotics, including all benzodiazepines (short-acting non-benzodiazepine sedative-hypnotics are allowed), mood stabilizers, antiepileptic drugs, stimulants, Attention-Deficit/Hyperactivity Disorder (ADHD) drugs, anti-psychotic drugs, anti-depressant medication (e.g. Bupropion, selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine re-uptake inhibitors (SNRIs)). * Pulmonary/Inflammation: chronic oral steroids (occasional use of inhaled steroids are allowed), burst/taper oral steroids more than once in the last 12 months, B2-agonists (allowed if on stable dose at least 3 months). * Genitourinary: 5-alpha reductase inhibitors, daily use of phosphodiesterase type 5 inhibitor. * Hormonal: androgenic anabolic steroids, anti-estrogens, anti-androgens, estrogens and/or progestins used for reasons other than birth control, growth hormone, insulin like growth factor-I, growth hormone releasing hormone, * any drugs used to treat diabetes mellitus or lower blood glucose including metformin, thiazolidinediones, SGLT-2 inhibits or insulin * any drugs used specifically to induce muscle growth/hypertrophy or augment exercise-induced muscle hypertrophy * Pain/Inflammation: narcotics and narcotic receptor agonists, regular use of non-steroidal anti-inflammatory drugs (NSAIDs) or acetaminophen, muscle relaxants ≥2 days per week * Other: chronic systemic antimicrobials (antibiotic, antiviral, antifungal, antiparasite, etc.) for any reason, high-potency topical steroids if ≥10% surface area using rule of 9s, continuous/chronic use of antibiotics or other anti-infectives for treatment or prevention, monoclonal antibodies, anti-rejection medications/immune suppressants. Participants can be re-screened after a 3 month washout period if antimicrobial use is only used acutely \< 2 weeks. 32. Presence of any condition that, in the opinion of the Investigator, compromises participant safety or data integrity or the participant's ability to complete the study.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07516509). StuddyBuddy aggregates publicly available trial information.