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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

Overview
Specialty Endocrinology
Date 2017 Sep 19
PMID 28921908
Citations 2
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Abstract

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.

Citing Articles

Glycaemic variability in patients with type 2 diabetes mellitus treated with dulaglutide, with and without concomitant insulin: Post hoc analyses of randomized clinical trials.

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.


CGMS and Glycemic Variability, Relevance in Clinical Research to Evaluate Interventions in T2D, a Literature Review.

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.

References
1.
Inzucchi S, Bergenstal R, Buse J, Diamant M, Ferrannini E, Nauck M . Management of hyperglycemia in type 2 diabetes, 2015: a patient-centered approach: update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2014; 38(1):140-9. DOI: 10.2337/dc14-2441. View

2.
. U.K. prospective diabetes study 16. Overview of 6 years' therapy of type II diabetes: a progressive disease. U.K. Prospective Diabetes Study Group. Diabetes. 1995; 44(11):1249-58. View

3.
Monnier L, Colette C, Dunseath G, Owens D . The loss of postprandial glycemic control precedes stepwise deterioration of fasting with worsening diabetes. Diabetes Care. 2007; 30(2):263-9. DOI: 10.2337/dc06-1612. View

4.
Liebl A, Davidson J, Mersebach H, Dykiel P, Tack C, Heise T . A novel insulin combination of insulin degludec and insulin aspart achieves a more stable overnight glucose profile than insulin glargine: results from continuous glucose monitoring in a proof-of-concept trial. J Diabetes Sci Technol. 2013; 7(5):1328-36. PMC: 3876378. DOI: 10.1177/193229681300700524. View

5.
Onishi Y, Ono Y, Rabol R, Endahl L, Nakamura S . Superior glycaemic control with once-daily insulin degludec/insulin aspart versus insulin glargine in Japanese adults with type 2 diabetes inadequately controlled with oral drugs: a randomized, controlled phase 3 trial. Diabetes Obes Metab. 2013; 15(9):826-32. DOI: 10.1111/dom.12097. View