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 non-obese patients and in patients with decreased insulin secretion compared with the non-responder group.

Recently, beta cell dysfunction and reduction in maximal capacity to secrete insulin were demonstrated to be primary metabolic defects in patients with T2DM [11]. In particular, studies have suggested that beta cell dysfunction may be especially important in the development of T2DM in Korean patients [12]. These findings suggest that greater response to sitagliptin is expected in Korean T2DM patients with relative pancreatic secretory dysfunction in early phases of disease.

Sitagliptin is reported to be weight-neutral in clinical trials, and incidences of hypoglycemia and gastrointestinal adverse experiences in response to sitagliptin are similar to placebo [13]. In addition to its beneficial effects on glycemic control, sitagiptin, or combination treatment with sitagliptin and metformin, preserved beta cell function and beta cell integrity in Zucker diabetic fatty rats [14].

Kim et al.'s study was retrospective, and did not control for other factors that affect glucose control. Despite these limitations, their study is meaningful because it shows that early DPP-4 inhibitor initiation is a potential treatment option in younger, non-obese Korean T2DM patients whose glucose is not well controlled by metformin. As Kim et al. noted, further randomized, controlled prospective studies are needed.

We would like to express our gratitude to Kim et al. for conducting this study, and expect that expansion on these findings will yield even more useful results.