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Table 3 Therapeutic considerations of selected US FDA-approved antidiabetes agents [20, 21, 25, 30–35]

From: Therapies for type 2 diabetes: lowering HbA1c and associated cardiovascular risk factors

Intervention

HbA1c Reduction (%)

Effect on Weight

Effect on Lipids

Effect on Blood Pressure

Safety

Oral

     

SFUs

0.9-2.5

Increased

Small improvements; mainly in TG

Poorly quantified

Increased risk of hypoglycemia

Metformin

1.1-3.0

Neutral or slightly decreased

Improved

Neutral

Contraindicated in patients with renal insufficiency

Glinides

0.4-0.6

Neutral (poorly quantified)

Poorly quantified

Poorly quantified

Caution in patients with hepatic or renal impairment (nateglinide)

TZDs

1.5-1.6

Increased

Improved HDL and TG

Small improvements

Fluid retention, CHF, bone fractures, potential increase in MI (rosiglitazone)

DPP-4 inhibitors

0.8

Neutral

Poorly quantified

Small improvements in non-diabetics

Long-term safety not established

α-Glucosidase inhibitors

0.5-1.0

Suggested decrease

Poorly quantified

Poorly quantified

Frequent flatulence

Parenteral

     

Insulin

Up to 4.9

Increased

Improved

Neutral

Increased risk of hypoglycemia

GLP-1 receptor agonists

0.8-1.5

Decreased

Improved

Lowered

Nausea and vomiting; hypoglycemia with sulfonylureas; rare pancreatitis and renal dysfunction; thyroid C-cell tumors in rodents

Amylin analog

0.4-0.6

Slightly decreased

Small improvements

Small improvements

Contraindicated in patients with gastroparesis

  1. BID, twice daily; CHF, congestive heart failure; DPP-4, dipeptidyl peptidase-4; GLP-1, glucagon like peptide-1; HbA1c, glycated hemoglobin; HDL, high-density lipoprotein; MI, myocardial infarction; SFUs, sulfonylureas; TG, triglyceride; TZDs, thiazolidinediones; US FDA, United States Food and Drug Administration.