The reason for this research study is to better understand the use of liraglutide, a commonly prescribed Type 2 diabetes medication, in patients with a diagnosis of maturity-onset diabetes of the young (MODY). The investigators are interested in better understanding the way that this drug affects the metabolism and hormone levels of a person with MODY. Many people with MODY report having gastrointestinal (GI) issues such as an upset stomach. Investigators also are interested in finding out if this drug will help with GI issues. If liraglutide does help with this symptom of MODY, the investigators want to know why this happens. If this drug is effective for participants, the investigators will use participants cells to make human induced pluripotent stem cell (iPSC). This means that the investigators will use participant cells to create what are called stem cells, which are cells in the body that are able to be told what their job is. Investigators will use these cells to see what happens in gastrointestinal (GI) tract.
The objective of this study is to perform a comprehensive metabolic and hormonal evaluation of individuals with Maturity-onset diabetes of the young (MODY) at baseline and then assess response to initiation of liraglutide. Select individuals will be consented for human induced pluripotent stem cell (iPSC) generation to identify the cellular basis of enteroendocrine cell (EEC) dysfunction. The hypothesis is that heterozygous mutations in MODY-related genes contribute to a range of GI pathologies, including regional disruptions in epithelial identity and disturbances in the function of EECs. Thus, patients with MODY may experience improvement not only in HbA1c and BMI but also in GI symptoms with initiation of GLP-1 receptor agonists. Investigators plan to enroll approximately 50 patients with MODY and obtain baseline metabolic labs and imaging along with enteroendocrine labs before initiating liraglutide and assessing response with repeat labs and imaging. This project will provide further guidance for clinical care and treatment of patients with MODY.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Liraglutide will be prescribed following FDA approved packet insert for type 2 diabetes in our test population.
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, United States
RECRUITINGBlood sugar control - HbA1C
Hemoglobin A1c
Time frame: Baseline and 3 months after study treatment initiation
BMI
Body mass index; weight and height will be combined to report BMI in kg/m\^2
Time frame: baseline, 1 month, 2 months, and final study visit 3 months after study treatment initiation
Metabolic - Blood Sugar
Glycemic patterns observed utilizing a continuous glucose monitor
Time frame: Baseline through three months of study treatment
Enteroendocrine function - GI symptoms
ANMS Gastroparesis Cardinal Symptom Index Daily Diary (ANMS GCSI-DD)
Time frame: baseline, 1 month, 2 months, and final study visit 3 months after study treatment initiation
Enteroendocrine function - insulin
Fasting and post meal blood serum insulin levels will be assessed
Time frame: baseline and 3 months after study treatment initiation
Enteroendocrine function - c-peptide
Fasting and post meal blood serum c-peptide levels will be assessed
Time frame: baseline and 3 months after study treatment initiation
Body fat percentage
% body fat as identified by DXA
Time frame: baseline, 1 month, 2 months, and final study visit 3 months after study treatment initiation
Liver steatosis
MRI to determine liver health
Time frame: baseline and 3 months after treatment initiation
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