Primary-care observational database study of the efficacy of GLP-1 receptor agonists and insulin in the UK

被引:25
作者
Hall, G. C. [1 ]
McMahon, A. D. [2 ]
Dain, M. -P. [3 ]
Wang, E. [4 ]
Home, P. D. [5 ]
机构
[1] Grimsdyke House, London, England
[2] Univ Glasgow, Sch Dent, Glasgow, Lanark, Scotland
[3] Sanofi Aventis, Diabet Metab Franchise, Paris, France
[4] Sanofi Aventis, Diabet Metab Franchise, Bridgewater, NJ USA
[5] Newcastle Univ, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
EXENATIDE; GLARGINE;
D O I
10.1111/dme.12137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims We investigated use and efficacy of glucagon-like peptide-1 (GLP-1) receptor agonists in UK practice. Methods People starting a GLP-1 receptor agonist (exenatide, liraglutide) or insulin (glargine, detemir, NPH) after a regimen of two or three oral glucose-lowering agents were identified from The Health Information Network observational primary care database (20072011). Mean change in HbA1c and body weight were compared at 1year between cohorts, adjusting for baseline characteristics. Results Baseline characteristics of GLP-1 receptor agonist (n=1123) vs. insulin (n=1842) users were HbA1c 78 vs. 84mmol/mol (9.3 vs. 9.8%) and BMI 38.2 vs. 30.9kg/m2. The GLP-1 receptor agonist cohort was younger, had shorter diabetes duration and follow-up, less microvascular disease and heart failure, higher estimated glomerular filtration rate and more use of oral glucose-lowering agents. Lower HbA1c reduction on GLP-1 receptor agonist [7 vs. 13mmol/mol (0.6 vs. 1.2%) (n=366 vs. 892)] was not statistically significant [adjusted mean difference 1.4 (95% CI 4.1, 1.2) mmol/mol], except in the highest HbA1c quintile [>96mmol/mol (>10.9%); adjusted mean difference 17.8 (28.6, 7.0) mmol/mol]. GLP-1 receptor agonist users lost weight [4.5 vs. +1.5kg; adjusted mean difference 4.7 (3.7, 5.8) kg; n=335 vs. 634]. A UK 6-month target reduction for GLP-1 receptor agonists of 11mmol/mol (1.0%) HbA1c and 3% weight was reached by 24.9% of those continuing treatment. Conclusions Those starting GLP-1 receptor agonists are heavier with better glycaemic control than those starting basal insulin. Subsequently, they have improved weight change, with similar HbA1c reduction unless baseline HbA1c is very high. The UK 6-month GLP-1 receptor agonist target is usually not reached.
引用
收藏
页码:681 / 686
页数:6
相关论文
共 14 条
[1]  
[Anonymous], 2009, NICE SHORT CLIN GUID
[2]   One-year Treatment With Exenatide Improves β-Cell Function, Compared With Insulin Glargine, in Metformin-Treated Type 2 Diabetic Patients A randomized, controlled trial [J].
Bunck, Mathijs C. ;
Diamant, Michaela ;
Corner, Anja ;
Eliasson, Bjorn ;
Malloy, Jaret L. ;
Shaginian, Rimma M. ;
Deng, Wei ;
Kendall, David M. ;
Taskinen, Marja-Riitta ;
Smith, Ulf ;
Yki-Jarvinen, Hannele ;
Heine, Robert J. .
DIABETES CARE, 2009, 32 (05) :762-768
[3]   Liraglutide once a day versus exenatide twice a day for type 2 diabetes: a 26-week randomised, parallel-group, multinational, open-label trial (LEAD-6) [J].
Buse, John B. ;
Rosenstock, Julio ;
Sesti, Giorgio ;
Schmidt, Wolfgang E. ;
Montanya, Eduard ;
Brett, Jason H. ;
Zychma, Marcin ;
Blonde, Lawrence .
LANCET, 2009, 374 (9683) :39-47
[4]   Exenatide compared with long-acting insulin to achieve glycaemic control with minimal weight gain in patients with type 2 diabetes: results of the Helping Evaluate Exenatide in patients with diabetes compared with Long-Acting insulin (HEELA) study [J].
Davies, M. J. ;
Donnelly, R. ;
Barnett, A. H. ;
Jones, S. ;
Nicolay, C. ;
Kilcoyne, A. .
DIABETES OBESITY & METABOLISM, 2009, 11 (12) :1153-1162
[5]   Once weekly exenatide compared with insulin glargine titrated to target in patients with type 2 diabetes (DURATION-3): an open-label randomised trial [J].
Diamant, Michaela ;
Van Gaal, Luc ;
Stranks, Stephen ;
Northrup, Justin ;
Cao, Dachuang ;
Taylor, Kristin ;
Trautmann, Michael .
LANCET, 2010, 375 (9733) :2234-2243
[6]  
Guerci B, 2011, DIABETES, V60, pA283
[7]   Macrovascular and microvascular outcomes after beginning of insulin versus additional oral glucose-lowering therapy in people with type 2 diabetes: an observational study [J].
Hall, Gillian C. ;
McMahon, Alex D. ;
Carroll, Dawn ;
Home, Philip D. .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2012, 21 (03) :305-313
[8]  
Heine RJ, 2005, ANN INTERN MED, V143, P559, DOI 10.7326/0003-4819-143-8-200510180-00006
[9]  
Joint Formulary Committee, 2010, BRIT NAT FORM 60
[10]  
Loh J, 2008, EFFICACY EXENATIDE T, P105