DOI: 10.2337/dc05-1365 © 2006 by the American Diabetes Association
A 26-Week, Randomized, Parallel, Treat-to-Target Trial Comparing Insulin Detemir With NPH Insulin as Add-On Therapy to Oral Glucose-Lowering Drugs in Insulin-Naïve People With Type 2 Diabetes
1 Department of Endocrinology and Metabolism, Aarhus Sygehus THG, Aarhus University Hospital, Aarhus, Denmark Address correspondence and reprint requests to Professor Kjeld Hermansen, Department of Endocrinology and Metabolism, Aarhus Sygehus THG, Aarhus University Hospital, DK-8000 Aarhus C, Denmark. E-mail: kjeld.hermansen{at}as.aaa.dk OBJECTIVETo assess efficacy and tolerability of insulin detemir or NPH insulin added to oral therapy for type 2 diabetes in a treat-to-target titration protocol.
RESEARCH DESIGN AND METHODSIndividuals (n = 476) with HbA1c (A1C) 7.510.0% were randomized to addition of twice-daily insulin detemir or NPH insulin in a parallel-group, multicenter trial. Over 24 weeks, insulin doses were titrated toward prebreakfast and predinner plasma glucose targets of
RESULTSAt 24 weeks, A1C had decreased by 1.8 and 1.9% (from 8.6 to 6.8 and from 8.5 to 6.6%) for detemir and NPH, respectively (NS). In both groups, 70% of participants achieved an A1C CONCLUSIONSAddition of basal insulin to oral drug therapy in people with suboptimal control of type 2 diabetes achieves guideline-recommended A1C values in most people with aggressive titration. Insulin detemir compared with NPH insulin achieves this with reduced hypoglycemia and less weight gain.
Abbreviations: FPG, fasting plasma glucose ITT, intention-to-treat OGLD, oral glucose-lowering drug
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