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Vildagliptin add-on to metformin produces similar efficacy and reduced hypoglycaemic risk compared with glimepiride, with no weight gain: results from a 2-year study
被引:155
作者:
Matthews, D. R.
[1
,2
]
Dejager, S.
[3
]
Ahren, B.
[4
]
Fonseca, V.
[5
]
Ferrannini, E.
[6
,7
]
Couturier, A.
[8
]
Foley, J. E.
[8
]
Zinman, B.
[9
]
机构:
[1] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
[2] Oxford Biomed Res Ctr, NIHR, Oxford, England
[3] Novartis Pharma SAS, Rueil Malmaison, France
[4] Lund Univ, Dept Clin Sci, Div Med, Lund, Sweden
[5] Tulane Univ, Hlth Sci Ctr, Dept Endocrinol, New Orleans, LA 70118 USA
[6] Univ Pisa, Dept Internal Med, Pisa, Italy
[7] Univ Pisa, CNR Inst Clin Physiol, Pisa, Italy
[8] Novartis Pharmaceut, E Hanover, NJ USA
[9] Univ Toronto, Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
关键词:
DPP-4;
inhibitor;
elderly;
glimepiride;
hypoglycaemia;
type 2 diabetes mellitus;
vildagliptin;
BETA-CELL FUNCTION;
DRUG-NAIVE PATIENTS;
IV INHIBITOR VILDAGLIPTIN;
ISLET FUNCTION;
DOUBLE-BLIND;
INSULIN SENSITIVITY;
GLYCEMIC CONTROL;
TYPE-2;
MONOTHERAPY;
24-WEEK;
D O I:
10.1111/j.1463-1326.2010.01233.x
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Methods: A randomized, double-blind, active-comparator study of patients with type 2 diabetes mellitus inadequately controlled (HbA1c 6.5-8.5%) by metformin monotherapy. Patients received vildagliptin (50 mg twice daily) or glimepiride (up to 6 mg/day) added to metformin. Results: In all, 3118 patients were randomized (vildagliptin, n = 1562; glimepiride, n = 1556). From similar baseline values (7.3%), after 2 years adjusted mean (s.e.) change in HbA1c was comparable between vildagliptin and glimepiride treatment: -0.1% (0.0%) and -0.1% (0.0%), respectively. The primary objective of non-inferiority was met. A similar proportion of patients reached HbA1c < 7% (36.9 and 38.3%, respectively), but with vildagliptin more patients reached this target without hypoglycaemia (36.0% vs. 28.8%; p = 0.004). The initial response (IR) was sustained for a mean (s.d.) of 309 (244) days with vildagliptin versus 270 (223) days for glimepiride (p < 0.001) (IR = nadir HbA1c where change from baseline >= 0.5% or HbA1c < 6.5% within the first six months of treatment. After IR was detected, sustained response = time between nadir and an increase of > 0.3% above IR). Independent of disease duration, age was a predictor of effect sustainability. Fewer patients experienced hypoglycaemia with vildagliptin (2.3% vs. 18.2% with glimepiride) with a 14-fold difference in the number of hypoglycaemic events (59 vs. 838). Vildagliptin had a beneficial effect on body weight [mean (s.e.) change from baseline -0.3 (0.1) kg; between-group difference -1.5 kg; p < 0.001]. Overall, both treatments were well tolerated and displayed similar safety profiles. Conclusions: Vildagliptin add-on has similar efficacy to glimepiride after 2 years' treatment, with markedly reduced hypoglycaemia risk and no weight gain.
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页码:780 / 789
页数:10
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