Related Experiment Video
Updated: May 7, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
Dipeptidyl peptidase-4 inhibitors in type 2 diabetes therapy--focus on alogliptin
Annalisa Capuano1, Liberata Sportiello, Maria Ida Maiorino
1Department of Experimental Medicine, University Hospital at the Second University of Naples, Piazza L Miraglia 2, Naples, Italy.
Abstract:
Type 2 diabetes mellitus is a complex and progressive disease that is showing an apparently unstoppable increase worldwide. Although there is general agreement on the first-line use of metformin in most patients with type 2 diabetes, the ideal drug sequence after metformin failure is an area of increasing uncertainty. New treatment strategies target pancreatic islet dysfunction, in particular gut-derived incretin hormones. Inhibition of the enzyme dipeptidyl peptidase-4 (DPP-4) slows degradation of endogenous glucagon-like peptide-1 (GLP-1) and thereby enhances and prolongs the action of the endogenous incretin hormones. The five available DPP-4 inhibitors, also known as 'gliptins' (sitagliptin, vildagliptin, saxagliptin, linagliptin, alogliptin), are small molecules used orally with similar overall clinical efficacy and safety profiles in patients with type 2 diabetes. The main differences between the five gliptins on the market include: potency, target selectivity, oral bioavailability, long or short half-life, high or low binding to plasma proteins, metabolism, presence of active or inactive metabolites, excretion routes, dosage adjustment for renal and liver insufficiency, and potential drug-drug interactions. On average, treatment with gliptins is expected to produce a mean glycated hemoglobin (HbA1c) decrease of 0.5%-0.8%, with about 40% of diabetic subjects at target for the HbA1c goal <7%. There are very few studies comparing DPP-4 inhibitors. Alogliptin as monotherapy or added to metformin, pioglitazone, glibenclamide, voglibose, or insulin therapy significantly improves glycemic control compared with placebo in adult or elderly patients with inadequately controlled type 2 diabetes. In the EXAMINE trial, alogliptin is being compared with placebo on cardiovascular outcomes in approximately 5,400 patients with type 2 diabetes. In clinical studies, DPP-4 inhibitors were generally safe and well tolerated. However, there are limited data on their tolerability, due to their relatively recent marketing approval. Alogliptin will be used most when avoidance of hypoglycemic events is paramount, such as in patients with congestive heart failure, renal failure, and liver disease, and in the elderly.
Insights
Dipeptidyl peptidase-4 (DPP-4) inhibitors, or gliptins, offer a new treatment option for type 2 diabetes management. Alogliptin shows promise, especially for patients needing to avoid hypoglycemia, with ongoing trials assessing cardiovascular outcomes.
Area of Science:
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) is a growing global health concern.
- Metformin is the standard first-line treatment, but effective second-line therapies remain uncertain.
- Incretin-based therapies, targeting glucagon-like peptide-1 (GLP-1) pathways, represent a novel approach.
Purpose of the Study:
- To review the role of dipeptidyl peptidase-4 (DPP-4) inhibitors in T2DM management.
- To compare the characteristics and clinical utility of available DPP-4 inhibitors (gliptins).
- To highlight the specific profile and potential applications of alogliptin.
Main Methods:
- Review of clinical efficacy and safety data for DPP-4 inhibitors.
- Comparison of pharmacokinetic and pharmacodynamic properties of gliptins.
- Analysis of alogliptin's performance in monotherapy and combination therapy, including cardiovascular outcome trials.
Main Results:
- DPP-4 inhibitors, including five gliptins, offer similar efficacy (0.5%-0.8% HbA1c reduction) and safety profiles.
- Key differences among gliptins exist in potency, selectivity, bioavailability, half-life, protein binding, metabolism, and excretion.
- Alogliptin demonstrates significant glycemic control improvement and is suitable for patients where hypoglycemia avoidance is critical.
Conclusions:
- DPP-4 inhibitors are valuable oral agents for T2DM, particularly after metformin failure.
- Alogliptin presents a favorable option for specific patient populations, including the elderly and those with comorbidities like heart, renal, or liver failure.
- Further comparative studies and long-term tolerability data are needed for DPP-4 inhibitors.
Related Concept Videos
Dipeptidyl Peptidase 4 Inhibitors
Glucagon-like Receptor Agonists
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 Glitazones
Oral Hypoglycemic Agents: Glinides
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are typically...
Diabetes: Management and Pharmacotherapy
Insulin remains the cornerstone of treatment for most patients with type 1 and many...