Three-Year Efficacy of Complex Insulin Regimens in Type 2 Diabetes

被引:498
作者
Holman, Rury R. [1 ,2 ]
Farmer, Andrew J. [2 ,3 ,4 ]
Davies, Melanie J. [5 ]
Levy, Jonathan C. [2 ]
Darbyshire, Julie L. [1 ,2 ]
Keenan, Joanne F. [1 ,2 ]
Paul, Sanjoy K. [1 ,2 ]
机构
[1] Univ Oxford, Diabet Trials Unit, Oxford, England
[2] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[3] Univ Oxford, Sch Primary Care Res, Dept Primary Hlth Care, Oxford, England
[4] Univ Oxford, Sch Primary Care Res, Natl Inst Hlth Res, Oxford, England
[5] Univ Leicester, Dept Cardiovasc Sci, Leicester, Leics, England
关键词
HUMAN NPH INSULIN; TO-TARGET TRIAL; HYPOGLYCEMIC AGENTS; GLUCOSE CONTROL; BASAL INSULIN; ORAL-THERAPY; GLARGINE; PEOPLE; TREAT; COMPLICATIONS;
D O I
10.1056/NEJMoa0905479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.)
引用
收藏
页码:1736 / 1747
页数:12
相关论文
共 31 条
[1]  
[Anonymous], 1996, INT C HARM TECHN REQ
[2]  
[Anonymous], 2000, Declaration of Helsinki: Ethical Principles for Medical Research Involving Human Subjects
[3]  
[Anonymous], COCHRANE DATABASE SY
[4]  
[Anonymous], 2009, TYP 2 DIAB MAN TYP 2
[5]   Statistical inference for a linear function of medians: Confidence intervals, hypothesis testing, and sample size requirements [J].
Bonett, DG ;
Price, RM .
PSYCHOLOGICAL METHODS, 2002, 7 (03) :370-383
[6]  
Bretzel RG, 2008, LANCET, V372, P718
[7]   Once-daily basal insulin glargine versus thrice-daily prandial insulin lispro in people with type 2 diabetes on oral hypoglycaemic agents (APOLLO): an open randomised controlled trial [J].
Bretzel, Reinhard G. ;
Nuber, Ulrike ;
Landgraf, Wolfgang ;
Owens, David R. ;
Bradley, Clare ;
Linn, Thomas .
LANCET, 2008, 371 (9618) :1073-1084
[8]   The management of people with type 2 diabetes with hypoglycaemic agents in primary care: retrospective cohort study [J].
Calvert, Melanie J. ;
McManus, Richard J. ;
Freemantle, Nick .
FAMILY PRACTICE, 2007, 24 (03) :224-229
[9]   Initiation of insulin glargine therapy in type 2 diabetes subjects suboptimally controlled on oral antidiabetic agents:: results from the AT.LANTUS trial [J].
Davies, M. ;
Lavalle-Gonzalez, F. ;
Storms, F. ;
Gomis, R. .
DIABETES OBESITY & METABOLISM, 2008, 10 (05) :387-399
[10]  
Demidenko E., 2004, Mixed Models: Theory and Applications