@article{16526,
  author = {de Galan Bastiaan and Kengne Andre and Zoungas Sophia and Poulter N. and Pillai A. and Marre M. and Harrap S. and Chalmers J. and Billot Laurent and Neal Bruce and Patel Anushka},
  title = {The efficacy of lowering glycated haemoglobin with a gliclazide modified release-based intensive glucose lowering regimen in the ADVANCE trial},
  abstract = {<p>
The aim of these analyses was to examine the efficacy of the intensive gliclazide MR-based glucose lowering regimen used in the ADVANCE trial in lowering the level of glycated haemoglobin (HbA1c). All 11,140 randomised patients were included in analyses of treatment efficacy. Treatment efficacy was also examined in subgroups defined by baseline characteristics and treatments. At the end of 5 years follow-up, the mean HbA1c was reduced from 7.5% at baseline to 6.5% in those on intensive glucose control and to 7.3% in those on standard glucose control. With intensive glucose lowering greater proportions achieved HbA1c levels of &lt; or =7.0%, &lt; or =6.5% and &lt; or =6.0%. With intensive glucose lowering substantial reductions in HbA1c were observed across subgroups defined by baseline age, sex, duration of diabetes, BMI, HbA1c or treatment regimen (p&lt;0.0001). The main independent predictors of reduction in HbA1c during follow-up were baseline HbA1c, duration of diabetes and BMI. There was no weight gain in the intensive glucose control group and severe hypoglycaemia was uncommon, though more frequent than in the standard control group. Intensive glucose control with a gliclazide MR-based regimen was well tolerated and consistently effective in lowering HbA1c across a broad range of patient with type 2 diabetes.
</p>
},
  year = {2010},
  journal = {Diabetes Research and Clinical Practice},
  volume = {89},
  edition = {2010/06/15},
  number = {2},
  pages = {126-33},
  isbn = {1872-8227 (Electronic)0168-8227 (Linking)},
  note = {Zoungas, SChalmers, JKengne, A PPillai, ABillot, Lde Galan, BMarre, MNeal, BHarrap, SPoulter, NPatel, ARandomized Controlled TrialResearch Support, Non-U.S. Gov'tIrelandDiabetes research and clinical practiceDiabetes Res Clin Pract. 2010 Aug;89(2):126-33. Epub 2010 Jun 11.},
  language = {eng},
}