Combination therapy with metformin plus vildagliptin in type 2 diabetes mellitus

被引:21
|
作者
Guarino, Elisa
Nigi, Laura
Patti, Aurora [2 ]
Fondelli, Cecilia
Dotta, Francesco [1 ,2 ]
机构
[1] Univ Siena, Dept Internal Med Endocrine & Metab Sci & Biochem, Diabet Unit, Policlin Le Scotte, I-53100 Siena, Italy
[2] Fdn Umberto Di Mario ONLUS, Siena, Italy
关键词
dipeptidyl peptidase-4 (DPP-4) inhibitors; metformin; type 2 diabetes treatment; vildagliptin; DIPEPTIDYL PEPTIDASE-IV; ACTIVATED PROTEIN-KINASE; GLUCAGON-LIKE PEPTIDE-1; TREATED PATIENTS; ADD-ON; INHIBITOR VILDAGLIPTIN; CLINICAL-TRIALS; EFFICACY; MONOTHERAPY; PHARMACOKINETICS;
D O I
10.1517/14656566.2012.667078
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Type 2 diabetes mellitus (T2DM) is pathophysiologically characterized by a combination of insulin resistance and beta-cell dysfunction. Consequently, a proper treatment of such a disease should target both of these defects. Dipeptidyl peptidase-4 (DPP-4) inhibitors are among the most recent additions to the therapeutic options for T2DM and are able to increase circulating levels of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), thus stimulating glucose-dependent insulin secretion. Areas covered: This paper provides an overview of the clinical results of combination therapy with metformin and the DPP-4 inhibitor vildagliptin in T2DM patients. Expert opinion: Vildagliptin-metformin single-tablet combination is indicated for the treatment of T2DM patients not achieving a sufficient glycemic control at their maximally tolerated dose of metformin. Results from clinical trials provide evidence of vildagliptin efficacy administered in addition to metformin, as either first-or second-line treatment. The vildagliptin-metformin association seems to have favorable effects on beta-cell function and is characterized by good safety and tolerability profiles when compared with other antidiabetic agents. Of note, data available suggest that administration of fixed-dose combination products, together with the low incidence of adverse gastrointestinal events, may improve compliance and adherence of patients to therapy, resulting in an improved metabolic control.
引用
收藏
页码:1377 / 1384
页数:8
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