Failure to Preserve β-Cell Function With Mycophenolate Mofetil and Daclizumab Combined Therapy in Patients With New-Onset Type 1 Diabetes

被引:117
作者
Gottlieb, Peter A. [1 ]
Quinlan, Scott [2 ]
Krause-Steinrauf, Heidi [2 ]
Greenbaum, Carla J. [3 ]
Wilson, Darrell M. [4 ]
Rodriguez, Henry [5 ]
Schatz, Desmond A. [6 ]
Moran, Antoinette M. [7 ]
Lachin, John M. [2 ]
Skyler, Jay S. [8 ]
机构
[1] Univ Colorado Denver, Barbara Davis Ctr Childhood Diabet, Aurora, CO USA
[2] George Washington Univ, Ctr Biostat, Rockville, MD USA
[3] Benaroya Res Inst, Seattle, WA USA
[4] Stanford Univ, Pediat Endocrinol Dept, Stanford, CA 94305 USA
[5] Indiana Univ, Dept Pediat, Indianapolis, IN 46204 USA
[6] Univ Florida, Dept Pediat, Gainesville, FL USA
[7] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[8] Univ Miami, Diabet Res Inst, Miami, FL USA
关键词
PREVENTION; ANTI-CD25; MELLITUS;
D O I
10.2337/dc09-1349
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - This trial tested whether mycophenolate mofetil (MMF) alone or with daclizumab (DZB) could arrest the loss of insulin-producing beta-cells in subjects with new-onset type 1 diabetes. RESEARCH DESIGN AND METHODS - A multi-center, randomized, placebo-controlled, double-masked trial was initiated by Type 1 Diabetes TrialNet at 13 sites in North America and Europe. Subjects diagnosed with type 1 diabetes and with sufficient C-peptide within 3 months of diagnosis were randomized to either MMF alone, MMF plus DZB, or placebo, and then followed for 2 years. The primary outcome was the geometric mean area under the curve (AUC) C-peptide from the 2-h mixed meal tolerance test. RESULTS - One hundred and twenty-six subjects were randomized and treated during the trial. The geometric mean C-peptide AUC at 2 years was unaffected by MMF alone or MMF plus DZB versus placebo. Adverse events were more frequent in the active therapy groups relative to the control group, hut not significantly. CONCLUSIONS - Neither MMF alone nor MMF in combination with DZB had an effect on the loss of C-peptide in subjects with new-onset type 1 diabetes. Higher doses or more targeted immunotherapies may be needed to affect the autoimmune process.
引用
收藏
页码:826 / 832
页数:7
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