Table 1.

Pharmacological Treatment Choices for Patients with Type 2 Diabetes

Pharmacologic Treatment ClassesMechanism of ActionEffects/CharacteristicsAdverse Events
Biguanide (metformin)
  • Decrease hepatic glucose production

  • Decrease intestinal glucose absorption

  • Increase glucose uptake by skeletal muscle and fat

  • Reduce blood glucose concentration

  • Increase sensitivity to insulin

  • Reduce blood lipid levels

  • Oral administration

  • Diarrhea

  • Nausea

  • Vomitting

  • May cause lactic acidosis

Sulfonylureas
  • Stimulate pancreatic β-cell insulin secretion

  • Reduce blood glucose concentration

  • Lower risk of hypoglycemia than insulin

  • Oral administration

  • Hypoglycemia

  • Weight gain

  • Nausea

  • Vomiting

Thiazolidinediones
  • Improve target cell response to insulin

  • Decrease hepatic glucose output

  • Increase insulin-dependent glucose uptake in skeletal muscle and fat

  • Reduce blood glucose concentration

  • Beneficial alteration of blood lipid levels

  • Possible beneficial effects on pancreas and cardiovascular risk factors

  • Oral administration

  • Alteration in liver function indicators

  • Anemia

  • Detrimental cardiac effects

  • Edema

  • Weight gain

Meglitinides and d-phenylalanine derivatives
  • Stimulate glucose-mediated insulin secretion

  • Reduce blood glucose concentration

  • Reduce postprandial glucose excursions

  • Stimulates insulin secretion

  • Oral administration

  • Hypoglycemia

  • Diarrhea

  • Weight gain

α-Glucosidase inhibitors
  • Inhibit pancreatic α-amylase and membrane-bound α-glucosidase enzymes

  • Inhibit intestinal disaccharide metabolism, delaying glucose absorption

  • Reduce blood glucose concentration

  • Reduce postprandial glucose excursions

  • Level out daytime glucose concentrations

  • Disperse calories over time

  • Weight neutral

  • Oral administration

  • Abdominal pain

  • Diarrhea

  • Flatulence

  • Possible elevated liver enzymes

Insulin and insulin analogues
  • Replace/supplement endogenous insulin hormone to correct deficiency

  • Reduce blood glucose concentration

  • Subcutaneous injection

  • Hypoglycemia

  • Weight gain

Potential therapeutics discussed in this article
Incretin mimetics: Exenatide (others in clinical testing)
  • Replace/supplement endogenous incretin hormone(s) glucoregulatory activity

  • Adjunctive therapy with metformin and/or sulfonylureas

  • Reduce blood glucose concentration

  • Reduce postprandial glucose excursions

  • Enhance glucose-dependent insulin secretion

  • Suppress inappropriately elevated glucagon secretion

  • Reduce food intake

  • Slow gastric emptying

  • Weight reduction or weight neutral

  • Possible beneficial effects on pancreas (preclinical diabetes models)

  • Subcutaneous injection

  • Nausea

  • Vomiting

  • Increased hypoglycemia when administered with sulfonylureas

  • Awaiting clinical data for combination with other antidiabetic treatments

DPP-IV inhibitors (clinical testing)
  • Inhibit peptide hormone metabolism by DPP-IV enzyme, thus increasing blood concentations of endogenous, bioactive forms of GLP-1 and other peptides

  • Reduce blood glucose concentration

  • Reduce postprandial glucose excursions

  • Weight neutral

  • Possible beneficial effects on pancreas and insulin sensitivity (preclinical diabetes models)

  • Oral administration

  • Status of disease progression may impact efficacy

  • Adverse events data not yet publicly available. Phase 3 clinical trials in progress for full efficacy & safety profile