ICEECE2012 Poster Presentations Diabetes (248 abstracts)
Belorussian State Medical University, Minsk, Belarus.
The goal of this research was to analyze fasting glycemic variability in patients with DM1 depending on the type of basal insulin therapy - insulin NPH versus Glargine.
Material and methods: The glucose levels 24-hour monitoring was performed applying the CGMS. Glargine group - 19 and NPH group - 24 patients.
Results: In the glargine group there have been no episodes of severe fasting hypoglycemia (<2.8 mmol/L), LBGI=2.42±1.26; in the NPH group the relative duration of period of severe nocturnal hypoglycemia was 15.41±23.12%, LBGI=9.18±8.21. Intra-day variability indices: SD - 1.98±1.01 and 2.71±1.39 mmol\l; VC −24.32±15.49 and 31.51±16.21%; IQR −3.21±1.74 and 5.16±2.75 mmol\l; amplitude of glycemic excursions -7.31±3.42 and 11.24±5.58 mmol\l, CONGA1 - 1.60±0.72 and 2.71±1.62 mmol/l×h-1, P<0.05; for the glargine and NPH groups respectively. The predictors of high fasting glucose variability are frequent short-time (<1h) severe hypoglycemic episodes.
Both groups revealed a strong positive correlation between MODDf (analogous to MODD, but calculated for fasting period only) and difference of mean fasting blood glucose values: in the glargine group - rs=0.78; in the NPH - rs=0.895; P<0.001. Glargine group - MODDf=2.30±1.12; NPH group - MODDf=5.01±2.62, P<0.001.
In the NPH group only, high inter-day variability of blood glucose levels at 3 AM is a reliable predictor of high values of the difference of mean fasting blood glucose values (B=0.662; P<0.001). According to the equation of the linear regression with an increase of the difference of blood glucose values at 3 AM on 1 mmol/L, the difference of mean fasting blood glucose values increases by 0.662 mmol/L. In the Glargine group day-to-day blood glucose values at the control points - 3, 5 and 7 AM - were much more stable.
Conclusion: The use of glargine leads to a significant reduction in daily variability of fasting glycemia, minimizes the risk of hypoglycemia and provides a greater reserve in dosage increase in comparison with NPH insulin.
Declaration of interest: The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research project.
Funding: This research did not receive any specific grant from any funding agency in the public, commercial or not-for-profit sector.