DPP-4 inhibitors, known as gliptins, are a class of oral diabetic medications approved by the Food and Drug Administration (FDA) for the treatment of type 2 diabetes mellitus in adults.
DPP-4 inhibitors which have been approved by the FDA include sitagliptin, saxagliptin, linagliptin, and alogliptin. Vildagliptin has approval from the European Medicines Agency (EMA), but not by the FDA.
These drugs act through incretin hormones, which are gut hormones responsible for glucose homeostasis after oral intake of food.
Apart from antihyperglycemic effects, this class of drugs possesses antihypertensive effects, anti-inflammatory effects, antiapoptotic effects and immunomodulatory effect on heart, kidneys and blood vessels independent of the incretin pathway. Some studies have shown that due to all these benefits this class of drugs could also be used in kidney and liver transplant recipients with new-onset diabetes after transplantation (NODAT).
DPP-4 is a ubiquitous enzyme that acts on incretin hormones, mainly GLP-1 (glucagon-like peptide-1) and GIP (gastric inhibitory peptide) which maintain glucose homeostasis by increasing insulin secretion and decreasing glucagon secretion.
GLP-1 is a hormone secreted by enteroendocrine L cells of the small intestine which lowers blood glucose through stimulation of insulin secretion, reduction in glucagon concentrations and delay in gastric emptying. It has a half-life of fewer than 2 minutes.
GIP is a hormone secreted in the stomach and proximal small intestine by neuroendocrine K-cells. Its half-life is approximately 7 minutes in healthy individuals and 5 minutes in individuals with type 2 diabetes.
These incretins get released within minutes of food intake, and DPP-4 degrades these hormones immediately owing to their short half-life.
DPP-4 inhibitors by inhibiting DPP-4 enzyme increase the levels of GLP-1 and GIP which in turn increase beta cell insulin secretion in the pancreas, thereby reducing postprandial and fasting hyperglycemia.
All the DPP-4 inhibitors are administered orally, once daily, before or after meals.
A study of oral and intravenous administration of sitagliptin in healthy individuals resulted in 87% oral bioavailability.
Gliptins are associated with a low incidence of adverse events including hypoglycemia and also have weight-neutral effects. However, the risk of hypoglycemia increases when used in conjunction with sulfonylureas.
The most common side effects noticed with the DPP-4 inhibitors sitagliptin and saxagliptin are upper respiratory tract infection, nasopharyngitis, headache, urinary tract infection, arthralgia.
There are also reports of hypersensitivity reactions such as anaphylaxis and angioedema in the prescribing information of most DPP-4 inhibitors. Sitagliptin was also associated with Stevens-Johnson syndrome in postmarketing reports.
Reports of acute pancreatitis including fatal and non-fatal hemorrhagic or necrotizing variants have correlations with the use of sitagliptin, vildagliptin, and saxagliptin in postmarketing data. However, a causal relationship remains unproven with the use of gliptins and pancreatitis.
There also has been a case series published in Japan of four patients who had acquired hemophilia A with use of DPP-4 inhibitors.
DPP-4 inhibitors (alogliptin, sitagliptin, saxagliptin, linagliptin) did not show an increased risk of cardiovascular death, non-fatal myocardial infarction or non-fatal stroke when compared to placebo in patients with type 2 diabetes, although saxagliptin had an association with an increased rate of hospitalization for heart failure.
Contraindications to gliptins include type 1 diabetes and diabetic ketoacidosis.
Sitagliptin is contraindicated in individuals who are sensitive to the drug or its components. Caution is necessary when using gliptins in patients with a history of pancreatitis; it would be reasonable to discontinue these drugs if pancreatitis is suspected.
Dose adjustments are necessary for patients with renal insufficiency taking sitagliptin and saxagliptin as these drugs undergo renal excretion; failure to adjust the dose could increase the chance of hypoglycemia.
DPP-4 inhibitors have minimal to no interactions with other drugs because of their pharmacokinetic properties, the exception being saxagliptin. Saxagliptin is metabolized to its active form by CYP3A4/5, hence the levels of drug and its active metabolite might be modified when administered along with drugs affecting CYP3A4/5 isoforms such as ketoconazole, diltiazem (inhibitors of CYP3A4/5) or rifampicin (inducer of CYP3A4/5). Dose adjustments of saxagliptin may be necessary for such instances.
The package insert of sitagliptin mentions about close monitoring when using in conjunction with digoxin as the former causes a small increase (11%) in the area under the curve (AUC) and plasma Cmax (18%) of digoxin. However, dose adjustment is not a recommendation.
Renal function requires monitoring after initiating therapy with either sitagliptin or saxagliptin in addition to glycemic control.
Clinical trials showed no adverse drug reactions using very high doses of saxagliptin, alogliptin, linagliptin. However, high doses of sitagliptin were associated with an 8.0-millisecond mean increase in QTc in controlled clinical trials as labeled by the FDA. In case of overdose, hemodialysis removes approximately 13% of sitagliptin and approximately 23% of saxagliptin but did not affect alogliptin or linagliptin.
A multidisciplinary approach is critical in controlling diabetes and its complications. It requires providers (primary care physician, endocrinologist, ophthalmologist, podiatrist), pharmacist, nurse practitioners, dieticians, and diabetes educator nurses to come together as a comprehensive team in providing care. Literature indicates that such a collaborative effect can improve diabetic management, lower the risk of chronic disease complications. [Level V]
Health care providers can emphasize the importance of metabolic control and other cardiovascular risk factors, promote healthy lifestyle practices including physical activity and healthful eating, and explain the benefits of comprehensive team care.
Diabetes educators and dieticians provide education to the patient in improving patient's weight loss and A1c values with ideal diet and nutrition.
Pharmacists can collaborate with patients and their physicians to improve clinical measures, lower health care costs and making sure that the drugs are in an affordable range to the patient by communicating with patient's insurance companies.
Recognizing danger signs of foot and eye problems and referral to an appropriate provider can be done by any member of the comprehensive team. Various health care providers achieve referral for regular screening.
Specialist providers such as podiatrists, ophthalmologists can help reduce lower extremity amputation rates in foot care clinics, prevent blindness respectively.
National Diabetes Education Program (NDEP), a federally sponsored initiative of National Institutes of Diabetes and Digestive and Kidney Diseases (NIDDK) is committed to work with public and private partners in preventing or delaying the onset of type 2 diabetes, promoting early diagnosis, improve treatment and outcomes for people with diabetes. It also offers resources to help healthcare professionals implement collaborative, multidisciplinary diabetes team care in a variety of settings.
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