PMID- 26566714 OWN - NLM STAT- MEDLINE DCOM- 20170118 LR - 20221207 IS - 1742-1241 (Electronic) IS - 1368-5031 (Print) IS - 1368-5031 (Linking) VI - 70 IP - 1 DP - 2016 Jan TI - How much is too much? Outcomes in patients using high-dose insulin glargine. PG - 56-65 LID - 10.1111/ijcp.12747 [doi] AB - BACKGROUND AND OBJECTIVES: Many patients with type 2 diabetes mellitus (T2DM) do not achieve glycaemic control targets on basal insulin regimens. This analysis investigated characteristics, clinical outcomes and impact of concomitant oral antidiabetes drugs (OADs) in patients with T2DM treated with high-dose insulin glargine. METHODS: Patient-level data were pooled from 15 randomised, treat-to-target trials in patients with T2DM treated with insulin glargine +/- OADs for >/= 24 weeks. Data were stratified according to whether patients exceeded three insulin dose cut-off levels (> 0.5, > 0.7 and > 1.0 IU/kg). End-points included glycated haemoglobin A1c (A1C), fasting plasma glucose, body weight, and overall, nocturnal and severe hypoglycaemia. RESULTS: Data from 2837 insulin-naive patients were analysed. Patients with insulin titrated beyond the three doses investigated had significantly higher baseline A1C levels and were younger, with shorter diabetes duration than those at/below cut-offs (p < 0.05 for all cut-offs); they also had greater weight gain (p < 0.001 for the > 0.5 and > 0.7 IU/kg cut-offs) than those who did not exceed the cut-offs, regardless of concomitant OAD. Patients on concomitant metformin alone had higher insulin doses at Week 24, but achieved greater reductions in A1C, less weight gain and lower hypoglycaemia rates than patients on a concomitant sulfonylurea or metformin plus a sulfonylurea, regardless of whether cut-offs were exceeded. CONCLUSION: In patients with T2DM, increasing basal insulin doses above 0.5 IU/kg may not improve glycaemic control; treatment strategies targeting postprandial glucose control should be considered for such patients. CI - (c) 2015 Authors. International Journal of Clinical Practice Published by John Wiley & Sons Ltd. FAU - Reid, T AU - Reid T AD - Mercy Diabetes Center, Janesville, WI, USA. FAU - Gao, L AU - Gao L AD - Analysta Inc., Somerset, NJ, USA. FAU - Gill, J AU - Gill J AD - Sanofi US, Inc., Bridgewater, NJ, USA. FAU - Stuhr, A AU - Stuhr A AD - Sanofi US, Inc., Bridgewater, NJ, USA. FAU - Traylor, L AU - Traylor L AD - Sanofi US, Inc., Bridgewater, NJ, USA. FAU - Vlajnic, A AU - Vlajnic A AD - Sanofi US, Inc., Bridgewater, NJ, USA. FAU - Rhinehart, A AU - Rhinehart A AD - Johnstone Memorial Diabetes Care Center, Abingdon, VA, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20151113 PL - India TA - Int J Clin Pract JT - International journal of clinical practice JID - 9712381 RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) RN - 0 (Sulfonylurea Compounds) RN - 0 (hemoglobin A1c protein, human) RN - 2ZM8CX04RZ (Insulin Glargine) RN - 9100L32L2N (Metformin) SB - IM MH - Adult MH - Aged MH - Diabetes Mellitus, Type 2/blood/*drug therapy MH - Drug Therapy, Combination/adverse effects MH - Female MH - Glycated Hemoglobin/metabolism MH - Humans MH - Hypoglycemia/chemically induced MH - Hypoglycemic Agents/*administration & dosage/adverse effects MH - Insulin Glargine/*administration & dosage/adverse effects MH - Male MH - Metformin/therapeutic use MH - Middle Aged MH - Sulfonylurea Compounds/therapeutic use MH - Weight Gain/drug effects PMC - PMC4738456 EDAT- 2015/11/15 06:00 MHDA- 2017/01/19 06:00 PMCR- 2016/02/03 CRDT- 2015/11/15 06:00 PHST- 2015/11/15 06:00 [entrez] PHST- 2015/11/15 06:00 [pubmed] PHST- 2017/01/19 06:00 [medline] PHST- 2016/02/03 00:00 [pmc-release] AID - IJCP12747 [pii] AID - 10.1111/ijcp.12747 [doi] PST - ppublish SO - Int J Clin Pract. 2016 Jan;70(1):56-65. doi: 10.1111/ijcp.12747. Epub 2015 Nov 13.