Authors
Victoria Chen, Cristina I Fernández Hernández, Megan Griff, Julia L Douvas, Micah Koss, Melton Fan, Will Marshall, Evelyn Greaux, Wyatt Pfau, Marjan Rezaei, Jeremy Graber, Vatsala Singh, Laura K Wiley, Sridharan Raghavan, Neda Rasouli, Miriam S Udler, Sara J Cromer, RADIANT Study Group
Published in
Diabetes, obesity, and cardiometabolic CARE. Volume 1. Issue 5. Pages 874-882. Epub Aug 27, 2026.
Abstract
To determine whether electronic health record (EHR)-based algorithms can identify individuals with atypical diabetes (AD) eligible for the Rare and Atypical Diabetes Network (RADIANT) study and whether these algorithms improve identification and enrollment of individuals from populations underrepresented in biomedical research (UBR).
Two RADIANT clinical sites independently developed EHR-based algorithms to identify AD phenotypes, including a lean type 2 diabetes-like physiology without features of metabolic syndrome (site 1) and concurrent diagnoses of type 1 and type 2 diabetes (site 2). Demographic characteristics were compared using χ2 tests between algorithm-identified individuals and RADIANT participants enrolled prior to the implementation of EHR-based algorithm recruitment.
Deployment of EHR-based algorithms identified 550 individuals in site 1 and 620 individuals in site 2, with 108 and 147 deemed eligible for RADIANT recruitment, respectively. Compared with prior RADIANT participants at these sites, EHR-identified, RADIANT-eligible individuals were more likely to self-identify as a race or ethnicity besides non-Hispanic White and prefer a language other than English. Of the 53 and 57 individuals who were successfully contacted at sites 1 and 2, respectively, 8 and 14 enrolled in RADIANT, representing meaningful contributions to total enrollment (21% and 22% at sites 1 and 2, respectively) compared with pre-EHR-based recruitment. However, demographics of newly enrolled individuals did not differ from traditionally recruited participants.
EHR-based algorithms successfully identified rare diabetes phenotypes and yielded greater representation of study-eligible individuals from UBR populations than traditional participant identification methods. However, additional strategies are needed to address persistent barriers to participation of UBR populations in AD research.
PMID:
42892882
Bibliographic data and abstract were imported from PubMed on 18 Oct 2026.
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