The Rare and Atypical Diabetes Network (RADIANT) Study: Design and Early Results.
RADIANT Study Group
https://pubmed.ncbi.nlm.nih.gov/37104866/Actively Recruiting
Led by University of South Florida · Updated on 2025-08-14
2000
Participants Needed
13
Research Sites
N/A
Total Duration
Researchers are investigating rare and atypical forms of diabetes to better understand their unique causes and mechanisms. This study, conducted through the RADIANT network of 14 clinical sites and laboratories, aims to identify individuals and families with undiagnosed rare diabetes types, determine the underlying causes, and explore the diseases effects on the body. The study has three stages. In Stage 1, participants complete a consent form and questionnaire to identify possible atypical diabetes, followed by blood tests for autoantibodies and further questionnaires. Selected participants move to Stage 2, which involves genetic screening, family history assessments, and whole genome sequencing of DNA samples. Stage 3 includes in-depth testing such as an Oral Glucose Tolerance Test, more blood collection, physical exams, and detailed questionnaires. The Discovery Team reviews all data to understand novel genetic variants and may enroll family members for similar testing or recommend additional procedures. Participants provide samples, complete questionnaires, and attend clinic visits for physical exams and glucose tolerance testing. Researchers collect and analyze genetic and metabolic data to characterize new diabetes types. The main outcome is phenotypic and genetic characterization over about three years. Family members may also participate if needed. The study is observational, with no treatment given, and aims to improve understanding of atypical diabetes.
CONDITIONS
Rare and Atypical Diabetes Network
J
Jeffrey Krischer, PhD
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University of South Florida
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Variable depending on eligibility determination
Participants complete consent and questionnaires to identify potential atypical diabetes forms. Blood samples are collected for islet autoantibody testing and further questionnaires are completed.
1 to 2 visits depending on assessments
Duration - Variable based on sequencing and analysis timelines
Participants consent again, complete a family history questionnaire, and provide blood for DNA and RNA extraction. Whole Genome Sequencing and RNA sequencing are performed as needed to identify monogenic diabetes variants.
1 visit for blood collection and questionnaires
Duration - 1 day
Participants visit a study clinic to consent and undergo detailed phenotyping including an Oral Glucose Tolerance Test, additional blood collection, physical exam, and questionnaires.
1 clinic visit
Duration - Up to study completion (average of 3 years)
Ongoing iterative analysis of collected data may lead to enrollment of family members for similar procedures and additional optional testing to better characterize diabetes forms.
Additional visits may occur depending on family enrollment and optional procedures
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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RADIANT Study Group
https://pubmed.ncbi.nlm.nih.gov/37104866/University of South Florida
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor