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. 2019 Jul;37(3):250–259. doi: 10.2337/cd18-0040

TABLE 1.

FDA-Approved Pharmacological Interventions That Target Postprandial Hyperglycemia*

Agent Mode of Action A1C Reduction, % PPG Reduction, mmol/L (mg/dL) CV Benefit
AGIs
 Acarbose Inhibits carbohydrate digestion, delaying absorption 0.4–0.8 4.0 (72)
 Miglitol Inhibits carbohydrate digestion, delaying absorption; enhances GLP-1 activity 0.2–0.8 1.5–3.5 (27–63)
Amylin analogs
 Pramlintide Slows gastric emptying; suppresses glucagon activity; increases satiety 0.6 2.0 (36)
Glinides
 Repaglinide Stimulates insulin release 0.6–1.5 2.6 (47)
 Nateglinide Stimulates insulin release 0.5–0.8 2.6 (47)
Insulin
 Rapid-acting 1.5–2.5
SGLT2 inhibitors
 Canagliflozin Inhibition of glucose reuptake in the kidney; short-term inhibition of intestinal SLGT1 at higher doses 0.8–1.0 2.4–3.3 (43–59)
 Dapagliflozin Inhibition of glucose reuptake in the kidney 0.6–1.0 3.6–3.8 (65–68)
 Empagliflozin Inhibition of glucose reuptake in the kidney 0.7–0.8 2.0–2.6 (36–47)
Incretin-based agents
GLP-1 receptor agonists
 Exenatide Enhances insulin secretion; inhibits glucagon release after eating; delays gastric emptying; promotes satiety 0.5–1.0 3.6 (65)
Short-acting: predominant effect on PPG
Long-acting: predominant effect on FPG
 Liraglutide Enhances insulin secretion; inhibits glucagon release after eating 1.0–1.5 1.7–2.7 (31–49)
Predominant effect on FPG
 Lixisenatide Enhances insulin secretion; inhibits glucagon release after eating; delays gastric emptying; promotes satiety 0.5–0.9 3.1–5.9 (56–106)
Predominant effect on PPG
DPP-4 inhibitors
 Sitagliptin Inhibits DPP-4, increasing levels of GLP-1 0.6–0.8 2.8 (50)
 Saxagliptin Inhibits DPP-4, increasing levels of GLP-1 0.6–0.8 2.8 (50)
Combination agents
 iDegLira Complementary action of basal insulin on FPG and GLP-1 receptor agonist on PPG 0.8–1.9 Not reported
 iGlarLixi Complementary action of basal insulin on FPG and GLP-1 receptor agonist on PPG 1.1–1.6 4.7–5.7 (85–103)

Adapted from refs. 3, 96, and 97, with additional data from refs. 47–62.

*

Used as monotherapy or in combination with other antidiabetic agents.

Assuming starting value ≥8%.