Mealtime fast-acting insulin aspart versus insulin aspart for controlling postprandial hyperglycaemia in people with insulin-resistant Type 2 diabetes
Autor: | John N Harvey, Keith Bowering, J. W. Snyder, Bruce W. Bode, J. W. Kolaczynski |
---|---|
Rok vydání: | 2018 |
Předmět: |
Blood Glucose
Male medicine.medical_specialty endocrine system diseases Endocrinology Diabetes and Metabolism 030209 endocrinology & metabolism Type 2 diabetes Drug Administration Schedule law.invention Insulin aspart 03 medical and health sciences 0302 clinical medicine Endocrinology Randomized controlled trial Double-Blind Method law Diabetes mellitus Internal medicine Post-hoc analysis Internal Medicine medicine Humans 030212 general & internal medicine Meals Insulin Aspart Research Articles Aged Glycated Hemoglobin business.industry nutritional and metabolic diseases Middle Aged medicine.disease Postprandial Period Metformin Treatment Regimen Postprandial Diabetes Mellitus Type 2 Short Report: Treatment Delayed-Action Preparations Hyperglycemia Female business hormones hormone substitutes and hormone antagonists medicine.drug |
Zdroj: | Diabetic Medicine |
ISSN: | 1464-5491 |
Popis: | Aim This post hoc analysis explored whether mealtime fast‐acting insulin aspart treatment provided an advantage in postprandial plasma glucose (PPG) control vs. insulin aspart in people with Type 2 diabetes receiving high doses of bolus insulin. Methods A post hoc, post‐randomization, subgroup analysis of a 26‐week, randomized, double‐blind, treat‐to‐target trial (onset 2) that compared mealtime fast‐acting insulin aspart vs. mealtime insulin aspart, both in a basal–bolus regimen, in people with Type 2 diabetes uncontrolled on basal insulin therapy and metformin. At the end of trial, the impact of fast‐acting insulin aspart and insulin aspart on PPG control was assessed with a standard liquid meal test and participants were grouped into three post‐randomization subgroups: meal test bolus insulin dose ≤ 10 units per dose (n = 171), > 10–20 units per dose (n = 289) and > 20 units per dose (n = 146). Results A statistically significant treatment difference in favour of fast‐acting insulin aspart vs. insulin aspart was observed for the change in PPG increment at all post‐meal time points (from 1 to 4 h) for those in the > 20 units bolus insulin subgroup. There was no difference in the magnitude of change from baseline in HbA1c level between fast‐acting insulin aspart and insulin aspart in any of the bolus insulin dose subgroups (data herein). Conclusion Fast‐acting insulin aspart may hold promise as a more effective treatment compared with insulin aspart for controlling PPG in people with insulin‐resistant Type 2 diabetes. What's new? The results of this post hoc analysis indicate that fast‐acting insulin aspart may provide an advantage over conventional rapid‐acting insulin analogues in controlling postprandial hyperglycaemia in people with insulin‐resistant Type 2 diabetes requiring basal–bolus therapy. |
Databáze: | OpenAIRE |
Externí odkaz: |