Type 2 Diabetes Clinical Trial
Official title:
Therapeutic Efficacy of Triple Combination of Metformin, DPP4 Inhibitor and Thiazolidinedione in Drug-naïve Korean Type 2 Diabetic Patients
Triple combination of metformin, DPP4 inhibitor and Thiazolidinedione would be a good option in the treatment of drug-naïve Korean type 2 diabetic patients.
Thiazolidionedione, a PPARgamman agonist, is an strong insulin sensitizer. It has shown that
durable glucose lowering effect and beta cell preservation. It is an important treatment
option in patients with type 2 diabetes.
It has been well established that inhibition of dipeptidyl peptidase-4 (DPP-4) reduces blood
glucose levels in both fasting and postprandial states, and preserves pancreatic β-cell
function in patients with type 2 diabetes. The mechanism of action of DPP-4 inhibitors is to
increase levels of active incretin, glucagon-like peptide-1 (GLP-1) and glucose-dependent
insulinotropic polypeptide (GIP), which stimulate insulin secretion as well as insulin
biosynthesis while inhibiting glucagon release from pancreatic islets.
DPP4 inhibitors also have better safety and tolerability profiles (e.g., weight neutrality
and less hypoglycemia) compared to other hypoglycemic agents. When considering combination
therapy with DPP-4 inhibitors, metformin is the most commonly used agent which has been shown
to be effective and well tolerated from previous studies. Besides the glucose lowering effect
by reducing hepatic glucose output and improving insulin resistance, metformin without
inhibiting DPP-4 activity,also increases active GLP-1 concentrations by 1.5- to 2-fold
following an oral glucose load in obese, nondiabetic subjects. Accordingly, this effect of
metformin may provide a unique benefit when combined with DPP-4 inhibitors through a
substantial enhancement of the incretin axis, which provides effective and potentially
additive glycemic improvement.
Because of its favorable pharmacological properties, combination of a DPP-4 inhibitor,
metformin, and thiazolidinedione has been increasingly used to achieve rapid glycemic goal
with low risk of hypoglycemia and no weight gain, and to delay the need for subsequent
regimen changes. DPP-4 inhibitors block DPP-4 enzyme and preserve endogenous incretins
whereas metformin increases the active form of GLP-1, both of which may enhance the secretory
function of pancreas. However, the response to DPP-4 inhibitors and metformin combination
therapy may be different in individuals according to their pancreatic function and insulin
resistance status. In fact, previous studies with DPP-4 inhibitors showed different potency
in glycemic controls depending on various patient characteristics including severity of
diabetes and the use of other antidiabetic drug.Consequently, it would be clinically
important to investigate effect of this triple combination therapy.
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