دورية أكاديمية
Randomized Clinical Trial Comparing Basal Insulin Peglispro and Insulin Glargine in Patients With Type 2 Diabetes Previously Treated With Basal Insulin: IMAGINE 5
| العنوان: | Randomized Clinical Trial Comparing Basal Insulin Peglispro and Insulin Glargine in Patients With Type 2 Diabetes Previously Treated With Basal Insulin: IMAGINE 5 |
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| المؤلفون: | Buse, John B., Rodbard, Helena W., Serrano, Carlos Trescoli, Luo, Junxiang, Ivanyi, Tibor, Bue-Valleskey, Juliana, Hartman, Mark L., Carey, Michelle A., Chang, Annette M. |
| المصدر: | Diabetes Care, 39(1) |
| سنة النشر: | 2016 |
| المجموعة: | Carolina Digital Repository (UNC - University of North Carolina) |
| مصطلحات موضوعية: | Insulin Glargine, Blood Glucose, Humans, Glycated Hemoglobin A, Hypoglycemic Agents, Male, Hypoglycemia, Female, Diabetes Mellitus, Type 2, Aged, Middle Aged, Insulin Lispro |
| الوصف: | OBJECTIVE To evaluate the efficacy and safety of basal insulin peglispro (BIL) versus insulin glargine in patients with type 2 diabetes (hemoglobin A1c [HbA1c] ≤9% [75 mmol/mol]) treated with basal insulin alone or with three or fewer oral antihyperglycemic medications. RESEARCH DESIGN AND METHODS This 52-week, open-label, treat-to-target study randomized patients (mean HbA1c 7.42% [57.6 mmol/mol]) to BIL ( n = 307) or glargine ( n = 159). The primary end point was change from baseline HbA1c to 26 weeks (0.4% [4.4 mmol/mol] noninferiority margin). RESULTS At 26 weeks, reduction in HbA1c was superior with BIL versus glargine (−0.82% [−8.9 mmol/mol] vs. −0.29% [−3.2 mmol/mol]; least squares mean difference −0.52%, 95% CI −0.67 to −0.38 [−5.7 mmol/mol, 95% CI −7.3 to −4.2; P < 0.001); greater reduction in HbA1c with BIL was maintained at 52 weeks. More BIL patients achieved HbA1c <7% (53 mmol/mol) at weeks 26 and 52 ( P < 0.001). With BIL versus glargine, nocturnal hypoglycemia rate was 60% lower, more patients achieved HbA1c <7% (53 mmol/mol) without nocturnal hypoglycemia at 26 and 52 weeks ( P < 0.001), and total hypoglycemia rates were lower at 52 weeks ( P = 0.03). At weeks 26 and 52, glucose variability was lower ( P < 0.01), basal insulin dose was higher ( P < 0.001), and triglycerides and aminotransferases were higher with BIL versus glargine ( P < 0.05). Liver fat content (LFC), assessed in a subset of patients ( n = 162), increased from baseline with BIL versus glargine ( P < 0.001), with stable levels between 26 and 52 weeks. CONCLUSIONS BIL provided superior glycemic control versus glargine, with reduced nocturnal and total hypoglycemia, lower glucose variability, and increased triglycerides, aminotransferases, and LFC. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | https://doi.org/10.17615/d4gc-v603Test; https://cdr.lib.unc.edu/downloads/bk128h00c?file=thumbnailTest; https://cdr.lib.unc.edu/downloads/bk128h00cTest |
| DOI: | 10.17615/d4gc-v603 |
| الإتاحة: | https://doi.org/10.17615/d4gc-v603Test https://cdr.lib.unc.edu/downloads/bk128h00c?file=thumbnailTest https://cdr.lib.unc.edu/downloads/bk128h00cTest |
| حقوق: | http://rightsstatements.org/vocab/InC/1.0Test/ |
| رقم الانضمام: | edsbas.E8CE6E7D |
| قاعدة البيانات: | BASE |
| DOI: | 10.17615/d4gc-v603 |
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