Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
被引:774
作者:
Zinman, Bernard
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机构:
Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, CanadaMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Zinman, Bernard
[1
]
Gerich, John
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机构:
Univ Rochester, Dept Med, Rochester, NY USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Gerich, John
[2
]
Buse, John B.
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Univ N Carolina, Chapel Hill, NC USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Buse, John B.
[3
]
Lewin, Andrew
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机构:
Natl Res Inst, Los Angeles, CA USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Lewin, Andrew
[4
]
Schwartz, Sherwyn
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机构:
Diabet & Glandular Dis Ctr, San Antonio, TX USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Schwartz, Sherwyn
[5
]
Raskin, Philip
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机构:
Univ Texas Dallas, Dept Med, Dallas, TX 75230 USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Raskin, Philip
[6
]
Hale, Paula M.
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机构:
Novo Nordisk AS, Copenhagen, DenmarkMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Hale, Paula M.
[7
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Zdravkovic, Milan
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Novo Nordisk AS, Copenhagen, DenmarkMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Zdravkovic, Milan
[7
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Blonde, Lawrence
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机构:
Ochsner Inst, New Orleans, LA USAMt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
Blonde, Lawrence
[8
]
机构:
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Univ Rochester, Dept Med, Rochester, NY USA
[3] Univ N Carolina, Chapel Hill, NC USA
[4] Natl Res Inst, Los Angeles, CA USA
[5] Diabet & Glandular Dis Ctr, San Antonio, TX USA
[6] Univ Texas Dallas, Dept Med, Dallas, TX 75230 USA
HUMAN GLP-1 ANALOG;
HOMEOSTASIS;
GLIMEPIRIDE;
INDUCTION;
D O I:
10.2337/dc08-2124
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
OBJECTIVE - To determine the efficacy and safety of liraglutide (a glucagon-like peptide-1 receptor agonist) when added to metformin and rosiglitazone in type 2 diabetes. RESEARCH DESIGN AND METHODS - This 26-week, double-blind, placebo-controlled, parallel-group trial randomized 533 subjects (1:1:1) to once-daily liraglutide (1.2 or 1.8 mg) or liraglutide placebo in combination with metformin (1 g twice daily) and rosiglitazone (4 mg twice daily). Subjects had type 2 diabetes, A1C 7-11% (previous oral antidiabetes drug [OAD] monotherapy 3 months) or 7-10% (previous OAD combination therapy 3 months), and BMI <= 45 kg/m(2). RESULTS - Mean A1C values decreased significantly more in the liraglutide groups versus placebo (mean +/- SE - 1.5 +/- 0.1% for both 1.2 and 1.8 mg liraglutide and -0.5 0.1% for placebo). Fasting plasma glucose decreased by 40, 44, and 8 mg/dl for 1.2 and 1.8 mg and placebo, respectively, and 90-min postprandial glucose decreased by 47, 49, and 14 mg/dl, respectively (P < 0.001 for all liraglutide groups vs. placebo). Dose-dependent weight loss occurred with 1.2 and 1.8 mg liraglutide (1.0 +/- 0.3 and 2.0 +/- 0.3 kg, respectively) (P < 0.0001) compared with weight gain With placebo (0.6 +/- 0.3 kg). Systolic blood pressure decreased by 6.7, 5.6, and 1.1 mmHg with 1.2 and 1.8 mg liraglutide and placebo, respectively. Significant increases in C-peptide and homeostasis model assessment of beta-cell function and significant decreases in the proinsulin-to-insulin ratio occurred with liraglutide versus placebo. Minor hypoglycemia occurred more frequently with liraglutide, but there was no major hypoglycemia. Gastrointestinal adverse events were more common with liraglutide, but Most occurred early and were trans ent. CONCLUSIONS - Liraglulide combined with metformin and a thiazolidinedione is a well-tolerated combination therapy for type 2 diabetes, providing significant improvements in glycemic control.