Maturity-Onset Diabetes of the Young (MODY) in a Racially/Ethnically Diverse Pediatric Population.

INTRODUCTION

Current practice guidelines recommend considering a diagnosis of maturity-onset diabetes of the young (MODY) in patients with diabetes with an affected parent but without typical features of type 1 diabetes (T1D) or type 2 diabetes (T2D).

OBJECTIVE

To test if these criteria apply to a real-world cohort of racially/ethnically diverse children with diabetes.

METHODS

We performed a retrospective case review of electronic medical records (EMR) of youth diagnosed with MODY in a large academic pediatric hospital in Southwestern U.S. Cases were ascertained based on the identification of a molecular diagnosis of MODY.

RESULTS

We studied 50 genetically confirmed cases of MODY: 60% GCK-MODY (MODY2, n=30), 16% HNF1A-MODY (MODY3, n=8), 18% HNF1B-MODY (MODY5, n=9), 4% HNF4A-MODY (MODY1, n=2), and 2% with a dual molecular diagnosis resulting from variants in more than one MODY gene (n=1). Race/ethnicity other than non-Hispanic White, lack of parental diabetes history, obesity/overweight at diagnosis, dyslipidemia and/or hypertension and acanthosis nigricans documented on physical exam were observed, respectively, in 52% (n=26), 24% (n=12), 22.2% (n =11), 30% (n=15), and 12% (n=6) of MODY cases. Furthermore, islet antibody positivity was observed in 8% of the cases GCK-MODY (n=4). The mean hemoglobin A1c at diabetes diagnosis was higher in patients with HNF4A-MODY (7.0%), HNF1A-MODY (6.7%), and HNF1B-MODY (6.7%), than in those with GCK-MODY (6.1%, p=0.005). Four (13.3%) GCK-MODY patients had persistent proteinuria of undetermined cause.

CONCLUSION

The current guidelines to consider a diagnosis of MODY may not apply to a racially/ethnically diverse U.S. population of children with diabetes.