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Updated: Aug 3, 2025

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Published on: February 24, 2023
Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes
Devin W Steenkamp1,2, Michael C Cheney1,2, Zhihui Ju1,2
1Department of Medicine, Section of Endocrinology, Diabetes and Nutrition, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Hepatocyte Nuclear Factor 1-alpha gene mutations (HNF1A-MODY) show lower glucose variability on continuous glucose monitoring (CGM) compared to type 1 diabetes (T1D). This suggests CGM may help identify atypical diabetes types.
Area of Science:
- Endocrinology
- Genetics
- Metabolism
Background:
- Monogenic diabetes, specifically Hepatocyte Nuclear Factor 1-alpha gene mutations (HNF1A-MODY), presents a distinct clinical profile.
- Type 1 diabetes (T1D) is the most common form of diabetes in younger individuals, characterized by autoimmune destruction of pancreatic beta cells.
Purpose of the Study:
- To investigate if HNF1A-MODY exhibits a unique continuous glucose monitoring (CGM) glucotype compared to T1D.
- To explore the potential of CGM metrics for differentiating diabetes phenotypes.
Main Methods:
- Continuous glucose monitoring (CGM) data from 5 HNF1A-MODY patients and 115 T1D patients were analyzed.
- Key glucose variability metrics, including hourly between-day coefficient of variation (CVb_1h), were calculated for both groups.
Main Results:
- HNF1A-MODY cohort demonstrated significantly lower minimum (11.3 ± 4.4% vs 18.0 ± 4.9%, P=.02) and maximum (33.9 ± 5.0% vs 50.3 ± 10%, P<.001) CVb_1h compared to T1D.
- All HNF1A-MODY subjects had %CVb_1h ≤ 17.3% (min) and ≤ 37.1% (max), thresholds met by only 12 T1D patients (P<.001).
Conclusions:
- HNF1A-MODY is characterized by reduced hourly, between-day glucose variability.
- CGM-derived metrics show promise for screening atypical diabetes phenotypes within the T1D population.
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