Human Models of Selective Insulin Resistance: Pancreatic Clamp

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorColumbia University

About this trial

This is a single-center, prospective, randomized, controlled (crossover) clinical study designed to investigate the impact of lowering insulin levels on hepatic glucose production (HGP) vs de novo lipogenesis (DNL) in people with insulin resistance. The investigators will recruit participants with a history of overweight/obesity and evidence of insulin resistance (i.e., fasting hyperinsulinemia plus prediabetes and/or impaired fasting glucose and/or Homeostasis Model Assessment of Insulin Resistance \[HOMA-IR\] score \>=2.73), and with evidence of metabolic dysfunction-associated steatotic liver disease (MASLD). Participants will undergo two pancreatic clamp procedures -- one in which serum insulin levels are maintained near hyperinsulinemic baseline (Maintenance Hyperinsulinemia or "MH" Protocol) and the other in which serum insulin levels are lowered by 50% (Reduction toward Euinsulinemia or "RE" Protocol). In both clamps the investigators will use stable-isotope tracers to monitor hepatic glucose and triglyceride metabolism. The primary outcome will be the impact of steady-state clamp insulinemia on HGP vs DNL.

Eligibility criteria

Qualifiers

Men and women, ages 18-65 years

Body mass index of 27-50 kg/m2

Able to understand written and spoken English and/or Spanish

Prediabetes: Hemoglobin A1c 5.7-6.4%

Disqualifiers

Unable to provide informed consent in English or Spanish

Unwillingness to use only bedpan or urinal to void or to refrain from non-emergent mobile device use during the clamp

Documented weight loss of ≥ 5% of baseline within the previous 3 months

Abnormal blood pressure (including on treatment, if prescribed)

Trial design

Treatments tested in this trial

  • Insulin human
  • Octreotide Acetate
  • Glucagon
  • Growth Hormone, Human
  • 20% D-glucose (aq)
  • [6,6-2H2] D-glucose
  • [1-13C1] sodium acetate
  • Nestle BOOST Plus
  • KIND Bar
  • Harvard Apparatus PHD ULTRA CP syringe pump
  • Yellow Springs Instruments (YSI) 2500 Biochemistry Glucose/Lactate Analyzer

Treatment groups

36 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Columbia University

Lead sponsor

University of California, Berkeley

Collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator