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Endocrinology Research

Our division is dedicated to research that helps us understand why endocrine diseases happen in children and how to treat them effectively. Below, we have listed our current faculty-initiated studies and what they involve. We also work with industry partners to offer new therapies to our patients for endocrine conditions.

Clinical and Translational Research in areas of:

  • Type 1 Diabetes
  • Type 2 Diabetes
  • Pre-diabetes
  • Obesity
  • Growth Hormone Deficiency
  • Cystic Fibrosis
  • Congenital Adrenal Hyperplasia (CAH)
  • Hypophosphatemic Rickets
  • Lipodystrophy
  • Thyroid Cancer
  • Polycystic Ovarian Syndrome (PCOS)
  • Non-alcoholic fatty liver disease (NAFLD)
  • Precocious puberty
  • Lipodystrophy
  • Autosomal Dominant Hypocalcemia

Leadership

Christy Foster, MD
Director, Research Affairs


Research Coordinators

Pam Turner  
Email: prturner@uabmc.edu 
Phone: 205-638-5038
Clinical Research Nurse Coordinator

Tushima Fails Reeves
Email: TFails@uabmc.edu 
Phone: 205-638-9173
Clinical Research Coordinator

Meredith Snook 
Email:  macustred@uabmc.edu 
Phone: 205-638 5025
Clinical Research Coordinator

Current Studies

Children’s of Alabama/ UAB’s Division of Endocrinology and Diabetes and the Department of Nutrition Sciences is recruiting participants for the groundbreaking DISCOVERY study. This multi-center research initiative seeks to uncover why some children with a body mass index (BMI) above the 85th percentile develop type 2 diabetes while others do not.

Who can participate?
We are looking for children and teens who meet the following criteria:

  • Age: 9–13 for girls and 10-14 for boys
  • BMI: At or above the 85th percentile
  • HbA1c level: 5.5% or higher

What to expect?
Participants will receive comprehensive health evaluations, including:

  • In-person and phone visits
  • Lab tests
  • Physical exams
  • Glucose (blood sugar) monitoring
  • Questionnaires

Key details:

  • This study does not involve medications.
  • There is no cost to participate.
  • Participants will be compensated for their time.

By joining the DISCOVERY study, your child can contribute to important research that may help prevent type 2 diabetes in children and teens.

For more information, please contact us:

Learn more online: discovery.bsc.gwu.edu

Purpose: This study aims to understand changes in markers of pancreas function (beta cells/chromogranins) over time in adolescents with Type 2 diabetes.

Who can participate?

  • Newly diagnosed Type 2 diabetes within 3 months.
  • Age: 10–18 years.

What to Expect?

  • Participants will undergo bloodwork at baseline, 6 months, and 12 months.

Purpose: This study explores facilitators and barriers for a novel recruitment methodology using adolescent peer recruiters for genetic studies.

Who can participate? 

If affected:

  • Self-reported African American race.
  • Age: 12–18 years.
  • Diagnosis of Type 2 diabetes.
  • Tanner stage 4–5.
  • A1c > 6.5 at diagnosis.

If not affected:

  • Self-reported African American race.
  • Age: 12–18 years.
  • Tanner stage 4–5.
  • A1c < 5.6.

What to expect if you are a peer recruiter?

  • 1-hour training (in person or via Zoom).
  • Monthly phone check-ins with the study team for 6 months

What to expect for everyone?

  • Blood draw and surveys.
     

Purpose: This study investigates epigenetic changes in African American adolescents with Type 2 diabetes to understand underlying causes.

Who can participate?

If affected

  • Self-reported African American race.
  • Age: 12–18 years.
  • A1c > 6.5% or 2-hour glucose > 200 mg/dL (OGTT) at diagnosis.
  • Negative pancreatic antibodies.
  • Diagnosed within the last 12 months.

If not affected

  • Self-reported African American race.
  • Age: 12–18 years.
  • A1c < 5.6%.
  • No fasting glucose > 126 mg/dL or 2-hour glucose > 200 mg/dL (OGTT).
     

What to expect?

  • Participants will provide a blood draw and complete surveys.
     

Purpose: This protocol offers expanded access to tiratricol for patients with MCT8 deficiency who are not eligible for clinical trials or require continued treatment post-trial.

Who can participate?

  • Confirmed MCT8 deficiency via genetic testing.
  • Treatment-naïve or previously enrolled in the ReTRIACt study or prior IND.
  • Treating physician determines potential benefits outweigh risks.
  • Informed consent provided.
  • Approved for enrollment by RTT/Egetis Therapeutics AB.
     

For further information, please contact the Pediatric Endocrinology research team.