04084nam a22005537a 4500
170411s20162016 xxu||||| |||| 00| 0 eng d
1462-8902
Ovid MEDLINE(R)
26990378
Effect of adding insulin degludec to treatment in patients with type 2 diabetes inadequately controlled with metformin and liraglutide: a double-blind randomized controlled trial (BEGIN: ADD TO GLP-1 Study).[Erratum appears in Diabetes Obes Metab. 2016 Sep;18(9):952; PMID: 27546838]
Diabetes, Obesity & Metabolism. 18(7):663-70, 2016 Jul
Diabetes Obes Metab. 18(7):663-70, 2016 Jul
Diabetes, obesity & metabolism
2016
FY2017
2017-05-24
AIM: To evaluate the efficacy and safety of adding insulin degludec (IDeg) to treatment in patients with type 2 diabetes receiving liraglutide and metformin and qualifying for treatment intensification because of inadequate glycaemic control.
CONCLUSION: The addition of liraglutide and IDeg to patients sub-optimally treated with metformin and liraglutide and requiring treatment intensification was found to be effective and well-tolerated.
Copyright � 2016 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
METHODS: In this 26-week, double-blind trial, patients who still had inadequate glycaemic control after a 15-week run-in period with initiation and dose escalation of liraglutide to 1.8mg in combination with metformin (>1500mg) were randomized to addition of once-daily IDeg ('IDeg add-on to liraglutide' arm; n=174) or placebo ('placebo add-on to liraglutide' arm; n=172), with dosing of both IDeg and placebo based on titration guidelines.
RESULTS: At 26weeks, the mean change in glycated haemoglobin level was greater in the IDeg add-on to liraglutide arm (-1.04%) than in the placebo add-on to liraglutide arm (-0.16%; p<0.0001). Similarly, the mean fasting plasma glucose reduction was greater, and self-measured plasma glucose values were lower at all eight time points, with IDeg add-on versus placebo add-on (both p<0.0001). At 26weeks, the IDeg dose was 51U (0.54U/kg). During the run-in period with liraglutide, body weight decreased by ~3kg in both groups. After 26weeks, the mean change was +2.0kg (IDeg add-on to liraglutide) and -1.3kg (placebo add-on to liraglutide). Confirmed hypoglycaemia rates were low in both groups, although higher with IDeg than with placebo (0.57 vs. 0.12 episodes/patient-years of exposure; p=0.0002). Nocturnal confirmed hypoglycaemia was infrequent in both groups, with no episodes of severe hypoglycaemia, and no marked differences in adverse events with either treatment approach.
English
*Diabetes Mellitus, Type 2/dt [Drug Therapy]
*Hypoglycemic Agents/ad [Administration & Dosage]
*Insulin, Long-Acting/ad [Administration & Dosage]
*Liraglutide/ad [Administration & Dosage]
*Metformin/ad [Administration & Dosage]
Blood Glucose/me [Metabolism]
Double-Blind Method
Drug Therapy, Combination
Fasting/bl [Blood]
Female
Hemoglobin A, Glycosylated/me [Metabolism]
Humans
Hypoglycemia/ci [Chemically Induced]
Hypoglycemic Agents/ae [Adverse Effects]
Insulin, Long-Acting/ae [Adverse Effects]
Liraglutide/ae [Adverse Effects]
Male
Metformin/ae [Adverse Effects]
Middle Aged
Treatment Outcome
MedStar Health Research Institute
Journal Article
Aroda, Vanita R
Andersen TH, Aroda VR, Bailey TS, Cariou B, Kumar S, Leiter LA, Philis-Tsimikas A, Raskin P, Zacho J
https://dx.doi.org/10.1111/dom.12661
https://dx.doi.org/10.1111/dom.12661
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Article
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2017-05-24
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26990378
26990378
2017-09-26
2017-09-26
2017-05-24
ART
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2786