Biphasic Insulin Aspart-30 Reduces Glycemic Variability to a Greater Degree Than Insulin Detemir: A Randomized Controlled Trial of Once-daily Insulin Regimens Using Continuous Glucose Monitoring
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Introduction: We compared the efficacy of insulin detemir and biphasic insulin aspart-30 given in the morning as an add-on to oral hypoglycemic agents in type 2 diabetes patients.
Materials And Methods: The present study enrolled 30 patients with poorly controlled type 2 diabetes (8% ≤ glycated hemoglobin < 11%) being treated with oral hypoglycemic agent mono- or combination therapy with biguanides, sulfonylureas or thiazolidinediones. The patients were randomly assigned to insulin detemir (group D) or insulin aspart-30 (group A) given in the morning as add-on to oral hypoglycemic agents. After adjusting their insulin doses, the patients that underwent continuous glucose monitoring during a 3-day hospitalization and with day 2 continuous glucose monitoring data were subjected to analysis.
Results: There was no significant difference in patient background, baseline glycated hemoglobin levels and insulin doses during continuous glucose monitoring between the two groups. The percent coefficient of variation of 24-h glucose levels was significantly lower in group A (20.4 ± 7.6) than in group D (27.1 ± 6.5; P = 0.015). Similarly, mean amplitude of glycemic excursions was significantly smaller in group A (80 ± 32) than in group D (102 ± 14; P = 0.021). Postprandial glucose excursions were significantly smaller after breakfast in group A (65 ± 31 mg/dL) than in group D (106 ± 32 mg/dL; P = 0.002).
Conclusions: As once-daily insulin injection therapy given before breakfast in type 2 diabetes patients, the biphasic insulin analog might represent a better insulin option in significantly lowering the percent coefficient of variation and mean amplitude of glycemic excursions than the long-acting insulin preparation.
Jodar E, Romera I, Wang Q, Roche S, Garcia-Perez L Diabetes Obes Metab. 2021; 24(4):631-640.
PMID: 34866291 PMC: 9300025. DOI: 10.1111/dom.14615.
Breyton A, Lambert-Porcheron S, Laville M, Vinoy S, Nazare J Front Endocrinol (Lausanne). 2021; 12:666008.
PMID: 34566883 PMC: 8458933. DOI: 10.3389/fendo.2021.666008.