Related Experiment Videos

Sitagliptin: a novel drug for the treatment of type 2 diabetes

Mary Choy1, Sum Lam

  • 1Department of Clinical Pharmacy Practice, College of Pharmacy and Allied Health Professions, St. John's University, Jamaica, New York 11439, USA. choym@stjohns.edu

Cardiology in Review
|August 19, 2007
PubMed

Insights

Sitagliptin, a dipeptidyl peptidase-4 inhibitor, effectively lowers blood glucose in type 2 diabetes patients. It offers a well-tolerated treatment option, alone or with other antidiabetic drugs, with manageable side effects.

Area of Science:

  • Endocrinology and Metabolism
  • Pharmacology
  • Internal Medicine

Background:

  • Type 2 diabetes mellitus (T2DM) is a global health challenge requiring effective glycemic control.
  • Current antidiabetic agents have limitations regarding safety and tolerability.
  • Sitagliptin represents a novel therapeutic class, dipeptidyl peptidase-4 (DPP-4) inhibitors.

Purpose of the Study:

  • To evaluate the efficacy and safety of sitagliptin in managing type 2 diabetes.
  • To assess sitagliptin's role as monotherapy and in combination with other oral antidiabetic agents.
  • To determine sitagliptin's place in therapy for patients with contraindications or intolerance to existing treatments.

Main Methods:

  • Randomized, placebo-controlled trials (up to 6 months) and a 52-week clinical trial.
  • Assessment of glycosylated hemoglobin (HbA1c) levels as a primary efficacy endpoint.
  • Evaluation of safety and tolerability profiles, including adverse events and hypoglycemia rates.

Main Results:

  • Sitagliptin demonstrated significant reductions in HbA1c levels (0.5-0.8%) compared to placebo.
  • Sitagliptin was noninferior to glipizide as an add-on therapy in patients inadequately controlled on metformin.
  • The drug was well-tolerated, with gastrointestinal complaints being the most common side effect; hypoglycemia and weight gain rates were similar to placebo.

Conclusions:

  • Sitagliptin is an effective treatment option for type 2 diabetes, improving glycemic control.
  • It can be used as monotherapy or in combination with metformin or thiazolidinediones.
  • Sitagliptin offers a valuable alternative for patients with contraindications or intolerance to other antidiabetic medications.

Related Concept Videos

Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a significant...
Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood glucose levels...
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively manages...
Oral Hypoglycemic Agents: Sulfonylureas01:17

Oral Hypoglycemic Agents: Sulfonylureas

Sulfonylureas are oral hypoglycemic agents utilized in treating type 2 diabetes. They are characterized by their unique sulfonylurea chemical structure. The family of sulfonylureas is divided into generations. First-generation sulfonylureas, including tolbutamide (Orinase), chlorpropamide (Diabinese), and tolazamide (Tolinase), trigger insulin release from pancreatic β cells and enhance peripheral tissues' insulin sensitivity. The second-generation members, such as glipizide (Glucotrol),...
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are typically...