Camilla H N Thomsen, Simon L Cichosz, Thomas Kronborg, Stine Hangaard, Peter Vestergaard, Irl B Hirsch, David C Klonoff, Morten H Jensen
{"title":"Beyond the Mean: A Machine Learning-Based Trend Analysis of CGM Metrics for Improved HbA<sub>1C</sub> Estimation in Type 2 Diabetes.","authors":"Camilla H N Thomsen, Simon L Cichosz, Thomas Kronborg, Stine Hangaard, Peter Vestergaard, Irl B Hirsch, David C Klonoff, Morten H Jensen","doi":"10.1177/19322968261441312","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hemoglobin A<sub>1C</sub> (HbA<sub>1C</sub>) is the gold standard for assessing long-term glycemic control in people with diabetes. Increasing use of continuous glucose monitoring (CGM) has led to adoption of the glucose management indicator (GMI) as a CGM‑based HbA<sub>1C</sub> estimate, but GMI often differs from laboratory HbA<sub>1C</sub>, especially in type 2 diabetes. This discordance may be associated with the fact that GMI, as a measure of central tendency, fails to capture temporal glycemic trends and variability that relate to HbA<sub>1C</sub> formation.</p><p><strong>Objective: </strong>To evaluate whether combining CGM-derived metrics capturing variability, excursions, and temporal trends improves estimation of laboratory-measured HbA<sub>1C</sub> in type 2 diabetes.</p><p><strong>Methods: </strong>A machine learning framework was applied to CGM data from a three-month randomized trial, including 159 participants with type 2 diabetes. Participants had ≥70% CGM data coverage and valid end-of-trial HbA<sub>1C</sub>. From a standardized 90-day CGM window, 51 metrics were extracted. Benchmark models (mean glucose and GMI) were compared with models developed using forward and exhaustive feature selection with threefold cross-validated multiple linear regression.</p><p><strong>Results: </strong>Benchmark models yielded <i>R</i>-squared = 0.53. A forward selection model including five metrics (GMI at night, night-to-overall mean glucose ratio, glycemic risk assessment diabetes equation, time in tight range [3.0-7.8 mmol/L], time above range [13.9 mmol/L] at night) improved <i>R</i>-squared to 0.60. The best-performing model (substituting GRADE at night for GMI at night) achieved a similar <i>R</i>-squared (0.61). Nighttime and hyperglycemia‑related metrics were consistently selected.</p><p><strong>Conclusion: </strong>Continuous glucose monitoring‑based HbA<sub>1C</sub> estimation improves when variability and temporal patterns are included. Nighttime hyperglycemia adds notable predictive value, though further validation is needed.</p>","PeriodicalId":15475,"journal":{"name":"Journal of Diabetes Science and Technology","volume":" ","pages":"19322968261441312"},"PeriodicalIF":3.7000,"publicationDate":"2026-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Diabetes Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/19322968261441312","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Hemoglobin A1C (HbA1C) is the gold standard for assessing long-term glycemic control in people with diabetes. Increasing use of continuous glucose monitoring (CGM) has led to adoption of the glucose management indicator (GMI) as a CGM‑based HbA1C estimate, but GMI often differs from laboratory HbA1C, especially in type 2 diabetes. This discordance may be associated with the fact that GMI, as a measure of central tendency, fails to capture temporal glycemic trends and variability that relate to HbA1C formation.
Objective: To evaluate whether combining CGM-derived metrics capturing variability, excursions, and temporal trends improves estimation of laboratory-measured HbA1C in type 2 diabetes.
Methods: A machine learning framework was applied to CGM data from a three-month randomized trial, including 159 participants with type 2 diabetes. Participants had ≥70% CGM data coverage and valid end-of-trial HbA1C. From a standardized 90-day CGM window, 51 metrics were extracted. Benchmark models (mean glucose and GMI) were compared with models developed using forward and exhaustive feature selection with threefold cross-validated multiple linear regression.
Results: Benchmark models yielded R-squared = 0.53. A forward selection model including five metrics (GMI at night, night-to-overall mean glucose ratio, glycemic risk assessment diabetes equation, time in tight range [3.0-7.8 mmol/L], time above range [13.9 mmol/L] at night) improved R-squared to 0.60. The best-performing model (substituting GRADE at night for GMI at night) achieved a similar R-squared (0.61). Nighttime and hyperglycemia‑related metrics were consistently selected.
Conclusion: Continuous glucose monitoring‑based HbA1C estimation improves when variability and temporal patterns are included. Nighttime hyperglycemia adds notable predictive value, though further validation is needed.
期刊介绍:
The Journal of Diabetes Science and Technology (JDST) is a bi-monthly, peer-reviewed scientific journal published by the Diabetes Technology Society. JDST covers scientific and clinical aspects of diabetes technology including glucose monitoring, insulin and metabolic peptide delivery, the artificial pancreas, digital health, precision medicine, social media, cybersecurity, software for modeling, physiologic monitoring, technology for managing obesity, and diagnostic tests of glycation. The journal also covers the development and use of mobile applications and wireless communication, as well as bioengineered tools such as MEMS, new biomaterials, and nanotechnology to develop new sensors. Articles in JDST cover both basic research and clinical applications of technologies being developed to help people with diabetes.