Poster Session 3.H - Pharmaceutical Sciences and Health Technologies
Rákóczi, Gabriella
Centre for Translational Medicine
Gabriella Rákóczi1, Judit Nagy1, Shaghayegh Jozaee2, Shirin Jozaee2, Boglárka Lilla Szentes1, Jimin Lee1, Anett Rancz1, Péter Hegyi1, Gergely Agócs1, Emese Sipter1
1: Centre for Translational Medicine
2: Semmelweis University
Introduction
Prediabetes often remains undiagnosed until it progresses to type 2 diabetes mellitus (T2DM), particularly among individuals with obesity or a family history of diabetes. Conventional tests, including fasting plasma glucose (FPG), hemoglobin A1c (HbA1c), and the oral glucose tolerance test (OGTT), provide only static snapshots of glycemia and may fail to capture variability and postprandial excursions. Continuous glucose monitoring (CGM) offers dynamic insight into glucose regulation and may complement traditional diagnostic tools.
Aims
This study aimed to systematically evaluate differences in CGM-derived metrics between individuals with prediabetes and those with normoglycemia.
Methods
A systematic review and meta-analysis were conducted following PRISMA guidelines (PROSPERO: CRD42024608658). PubMed, EMBASE, and CENTRAL were searched from inception to September 3, 2025. Observational studies reporting CGM metrics in individuals without diabetes were included. The primary outcome was mean amplitude of glycemic excursions (MAGE), while secondary outcomes included time above range (TAR), 24-hour mean glucose, coefficient of variation (CV), and time in range (TIR).
Results
Sixteen studies were included in the systematic review, and ten (n = 1657 participants) in the meta-analysis. Prediabetes was associated with higher CGM-derived metrics than normoglycemia: MAGE (MD = 9.41 mg/dL, 95% CI: 4.31–15.31), TAR (MD = 5.68%, 1.04–10.32), and 24-hour mean glucose (MD = 7.91 mg/dL, 6.27–9.55).
Conclusion
These results provide the first quantitative evidence that CGM can discriminate between prediabetes and normoglycemia, supporting its potential as a complementary tool for refined metabolic risk assessment. Further prospective studies are needed to determine its predictive value for progression to T2DM.
Funding
This study was supported by the Centre for Translational Medicine, Semmelweis University, and the National Research, Development and Innovation Fund (TKP2021-EGA-23 to Péter Hegyi), as well as NKFIH project grants K131996 and K147265.