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Comparative Effectiveness of Oral Hypoglycemic Agents for Glycemic Control and Glycemic Variability in Patients with
Poongothai Venkatachalapathy1, Karthik Kumar Dos Alagarswamy Mohandoss2, Murali Munisamy1,3
1Department of Pharmacy Practice, Karpagam College of Pharmacy, Coimbatore, Tamil Nadu, India.
Aim:
The study aimed to compare the effectiveness of oral hypoglycemic agents (OHAs) as monotherapy, dual and quadruple therapy for glycemic control (GC) and glycemic variability (GV) in patients with type 2 diabetes (T2DM) using flash glucose monitoring system (FGM).
Background:
Diabetes management largely relies on HbA1c monitoring. Glycemic variability has been an evolving glycemic target for preventing complications related to type 2 diabetes mellitus.
Objective:
The purpose of the study was to compare glycemic control measures and glycemic variability measures among study groups and to study the relationships between GC and GV indices.
Methods:
Retrospectively, FGM data were collected from 50 T2DM patients. The patients were classified based on prescribed number of OHAs as monotherapy [group 1: Dipeptidyl peptidase- 4 (DPP-4) inhibitors (n=10), group 2: Sodium-glucose co-transporter-2 (SGLT2) inhibitors (n=10), group 3: Sulphonylureas (n=10), group 4: Dual therapy (n=10), and group 5: Quadruple therapy (n=10)]. Measures of GC and GV were evaluated.
Results:
Significant differences between study groups were observed in GC and GV measurements. The SGLT2 inhibitors monotherapy group demonstrated optimal GC [eA1c (%): 6.5 ± 2.2; MBG: 140.80 ± 63.94; TIR: 60.60 ± 19.96] and GV (SD: 42.38 ± 34.57; CV: 27.85 ± 6.68; MAGE: 96.76 ± 52.47; MODD: 33.96 ± 22.91) in comparison to other study groups. On using Pearson correlation analysis, mean blood glucose (MBG) and mean amplitude of glycemic excursion (MAGE) showed moderate correlation (r = 0.742)(r2 = 0.551), depicting distinct glucose variabilities at the same mean blood glucose levels.
Conclusion:
The monotherapy group of SGLT2 inhibitors demonstrated glucose-lowering effects with reduced glycemic variability. Hence, optimum glycemic control is associated with decreased glycemic variability.
Insights
Sodium-glucose co-transporter-2 (SGLT2) inhibitor monotherapy in type 2 diabetes patients significantly improved glycemic control and reduced glycemic variability. Optimal glycemic control correlates with decreased glycemic variability.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Traditional diabetes management relies on HbA1c, but glycemic variability is an emerging target for preventing complications.
- Flash Glucose Monitoring (FGM) offers continuous data for assessing glycemic control and variability.
Purpose of the Study:
- To compare the effectiveness of oral hypoglycemic agents (OHAs) monotherapy, dual, and quadruple therapy for glycemic control (GC) and glycemic variability (GV) in type 2 diabetes (T2DM) patients.
- To analyze relationships between GC and GV indices using FGM data.
Main Methods:
- Retrospective analysis of FGM data from 50 T2DM patients.
- Patients categorized into monotherapy (DPP-4 inhibitors, SGLT2 inhibitors, Sulphonylureas), dual therapy, and quadruple therapy groups.
- Evaluation of GC (eA1c, MBG, TIR) and GV (SD, CV, MAGE, MODD) measures.
Main Results:
- SGLT2 inhibitor monotherapy group showed optimal GC (eA1c: 6.5 ± 2.2) and GV (MAGE: 96.76 ± 52.47).
- Significant differences in GC and GV measurements were observed across study groups.
- Pearson correlation revealed a moderate correlation (r=0.742) between mean blood glucose (MBG) and mean amplitude of glycemic excursion (MAGE).
Conclusions:
- SGLT2 inhibitor monotherapy effectively lowers glucose and reduces glycemic variability in T2DM.
- Achieving optimal glycemic control is linked to decreased glycemic variability.
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