posted on 2012-10-24, 09:04authored byR. R. Holman, A. J. Farmer, M. J. Davies, J. C. Levy, J. Darbyshire, J. F. Keenan, S. K. Paul
Background
Evidence supporting the addition of specific insulin regimens to oral therapy in
patients with type 2 diabetes mellitus is limited.
Methods
In this 3-year open-label, multicenter trial, we evaluated 708 patients who had suboptimal
glycated hemoglobin levels while taking metformin and sulfonylurea therapy.
Patients were randomly assigned to receive biphasic insulin aspart twice daily,
prandial insulin aspart three times daily, or basal insulin detemir once daily (twice
if required). Sulfonylurea therapy was replaced by a second type of insulin if hyperglycemia
became unacceptable during the first year of the study or subsequently if
glycated hemoglobin levels were more than 6.5%. Outcome measures were glycated
hemoglobin levels, the proportion of patients with a glycated hemoglobin level of
6.5% or less, the rate of hypoglycemia, and weight gain.
Results
Median glycated hemoglobin levels were similar for patients receiving biphasic (7.1%),
prandial (6.8%), and basal (6.9%) insulin-based regimens (P=0.28). However, fewer
patients had a level of 6.5% or less in the biphasic group (31.9%) than in the prandial
group (44.7%, P=0.006) or in the basal group (43.2%, P=0.03), with 67.7%,
73.6%, and 81.6%, respectively, taking a second type of insulin (P=0.002). Median
rates of hypoglycemia per patient per year were lowest in the basal group (1.7),
higher in the biphasic group (3.0), and highest in the prandial group (5.7) (P<0.001
for the overall comparison). The mean weight gain was higher in the prandial
group than in either the biphasic group or the basal group. Other adverse event
rates were similar in the three groups.
Conclusions
Patients who added a basal or prandial insulin-based regimen to oral therapy had
better glycated hemoglobin control than patients who added a biphasic insulin-based
regimen. Fewer hypoglycemic episodes and less weight gain occurred in patients adding
basal insulin. (Current Controlled Trials number, ISRCTN51125379.)
History
Citation
New England Journal of Medicine, 2009, 361 (18), pp. 1736-1747