Candidate Dipeptidyl Peptidase-4 Inhibitors for the Treatment of Type 2 Diabetes

Corresponding author: Dong-Lim Kim Division of Endocrinology and Metabolism, Department of Internal Medicine, Konkuk University School of Medicine, 4-12 Hwayang-dong, Gwangjin-gu, Seoul 143-729, Korea E-mail: [email protected] Type 2 diabetes mellitus (T2DM) is a progressive disease that is characterized by insulin resistance and decreased insulin secretion [1]. Based on data from the UK Prospective Diabetes Study (UKPDS), there is consensus regarding the importance of glycemic control in patients with T2DM [2]. The American Diabetes Association (ADA) considers general glycemic control to be represented by HbA1c below 7.0% [3]. The ADA and European Association for the Study of Diabetes (EASD) statement on the management of hyperglycemia in T2DM patients recommends metformin intervention at the time of diagnosis in combination with lifestyle changes, and continuing timely augmentation of therapy with additional agents to achieve and maintain the recommended levels of glycemic control [4]. Sitagliptin is an oral, selective dipeptidyl peptidase-4 (DPP-4) inhibitor that is used for the treatment of patients with T2DM [5]. Sitagliptin delays the enzymatic degradation and inactivation of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP), the major incretins involved in glucose homeostasis, thereby increasing insulin release and lowering glucagon secretion in a glucose-dependent manner [5,6]. Incretin-based therapies are currently recommended as add-on therapy, when metformin treatment alone is not sufficient to reach the ADA/EASD HbA1c target. Treatment with sitagliptin 100 mg once daily leads to improvements in glycemic control in patients with T2DM, including reductions in HbA1c 0.6 to 0.7% [7]. The combined use of sitagliptin and metformin is an effective method of lowering glucose levels in T2DM. The reduction in HbA1c was 1.1% with metformin (2,000 mg/day) alone, and 1.9% with sitagliptin/metformin (100 mg/2,000 mg) [8]. When sitagliptin (100 mg) was added to ongoing sulfonylurea therapy alone or to a combination of sulfonylurea/metformin, HbA1c levels were reduced by only 0.3% and 0.6%, respectively, whereas only 11% and 23% of patients, respectively, achieved HbA1c <7% at the end of 24 weeks [9]. However, some studies have attempted to identify which patients respond to sitagliptin with better glycemic control among Korean T2DM patients. In this issue, ‘Predictive clinical parameters for the therapeutic efficacy of sitagliptin in Korean type 2 diabetes mellitus’ by Kim et al. [10] evaluates clinical factors associated with the therapeutic efficacy of sitagliptin when added to on oing metformin or metformin and sulfonylurea combination therapies. Kim et al. found that patients with more than a 20% decrease in fasting glucose and over 10% decrease in glycated hemoglobin after 24 weeks of sitagliptin administration, were younger and had lower body mass index (BMI) compared to non-responders. Treatment with 100 mg sitagliptin with metformin, or metformin and sulfonyurea for 24 weeks, led to additional reduction of mean HbA1c to 1.23±1.15%. This glycemic lowering effect is more potent than that observed in other previous studies [8,9]. In addition, the HbA1c lowering effect of sitagliptin was better in Editorial