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Growth Hormone Resistance of Beta-cells in Women and People

Recruiting
Conditions
Obesity
Healthy
Registration Number
NCT06571500
Lead Sponsor
University of Missouri-Columbia
Brief Summary

The purpose of the research study is to better understand how beta-cells (cells in the pancreas that make insulin and help regulate blood sugar) respond to growth hormone in people with a family history of type 2 diabetes at the University of Missouri. Our aim is to advance understanding of how growth hormone affects beta-cells and risk factors for developing gestational diabetes and type 2 diabetes.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • 18 to 45 years old
  • hemoglobin HbA1c ≤5.6% and fasting blood glucose <100 mg/dl
  • body mass index ≥30.0 kg/m2 and <45.0 kg/m2

Additional, group-specific inclusion criteria:

  • Family history of type 2 diabetes: first degree relative with type 2 diabetes
  • Control group: no family history of type 2 diabetes
Exclusion Criteria
  • Pregnant, planning to become pregnant during the study, or breastfeeding
  • Current diagnosis or history of type 1 or type 2 diabetes
  • Use of medications that can impact the study outcomes (e.g., GLP-1 receptor agonists)
  • History of bariatric surgery
  • Known hypothyroidism or use of thyroid medications
  • History of intracranial hypertension, including papilledema, or a condition that increases the risk of developing intracranial hypertension, such as Turner Syndrome, Prader-Willi Syndrome, or renal impairment
  • Current cancer or cancer that has been in remission less than 5 years
  • First degree relative with type 1 diabetes diagnosis
  • Evidence of significant anemia or significant end organ dysfunction (e.g., liver, kidney, heart disease)
  • Alcohol use disorder, use of controlled substances, or smoking >2 cigarettes per day
  • Greater than 3% weight loss within three months of screening or engaged in regular (≥3 days per week), continuous moderate- or high-intensity exercise of ≥30 min duration
  • Mentally disabled persons, prisoners, and persons with inability to grant voluntary informed consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Beta-cell function15, 30, 60, 120, 240, and 360 min and 7 days after rhGH administration

Insulin secretion rate in relationship to plasma glucose

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Missouri School of Medicine

🇺🇸

Columbia, Missouri, United States

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