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Journal article

Three-year efficacy of complex insulin regimens in type 2 diabetes.

Abstract:

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 pat ients who had sub-optimal 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%. Out come 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 glycat ed 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 pat ients who added a biphasic insulin-based regimen. Fewer hypoglycemic episodes and less weight gain occurred in patients adding basal insulin.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1056/nejmoa0905479

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
OCDEM
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Primary Care Health Sciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
OCDEM
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


Publisher:
Massachusetts Medical Society
Journal:
New England Journal of Medicine More from this journal
Volume:
361
Issue:
18
Pages:
1736-1747
Publication date:
2009-10-29
Acceptance date:
2009-10-22
DOI:
EISSN:
1533-4406
ISSN:
0028-4793


Language:
English
Keywords:
Pubs id:
pubs:1819
UUID:
uuid:ececa288-e4cc-4508-9570-0c9eb38a9166
Local pid:
pubs:1819
Source identifiers:
1819
Deposit date:
2012-12-19
ARK identifier:

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