1. Intensifying Treatment Beyond Monotherapy in Type 2 Diabetes Mellitus: Where Do Newer Therapies Fit?
- Author
-
Vanita R. Aroda, Adline Ghazi, Alexander Kuhn, and Jean Park
- Subjects
medicine.medical_specialty ,030209 endocrinology & metabolism ,Type 2 diabetes ,Pharmacology ,Hypoglycemia ,Glucagon-Like Peptide-1 Receptor ,03 medical and health sciences ,0302 clinical medicine ,Sodium-Glucose Transporter 2 ,Weight loss ,Glucagon-Like Peptide 1 ,Diabetes mellitus ,medicine ,Humans ,Hypoglycemic Agents ,030212 general & internal medicine ,Intensive care medicine ,Sodium-Glucose Transporter 2 Inhibitors ,Glycemic efficacy ,Dipeptidyl-Peptidase IV Inhibitors ,business.industry ,Type 2 Diabetes Mellitus ,medicine.disease ,Clinical trial ,Sulfonylurea Compounds ,Tolerability ,Diabetes Mellitus, Type 2 ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - Abstract
Guidelines for a standard second diabetes medication for the treatment of type 2 diabetes (T2DM) have yet to be established. The rapid increase in the number of newer therapies available makes the choice more difficult. Thus, we reviewed clinical trial evidence evaluating newer therapies available for treatment intensification beyond monotherapy. Head-to-head studies comparing newer therapies versus traditional (i.e., sulfonylurea) approaches consistently find lower incidence of hypoglycemia and weight gain with newer therapies. Glucagon-like peptide-1 (GLP-1) receptor agonists and sodium-glucose co-transporter 2 (SGLT2) inhibitors demonstrate high glycemic efficacy, while merits of dipeptidyl peptidase-4 (DPP-4) inhibitors include their tolerability. Secondary effects (weight loss, cardiovascular outcomes, renal function) are of growing interest with newer therapies. Choices for treatment intensification in T2DM diabetes are numerous. Understanding the comparative evidence of newer treatment choices, as provided in this review, may help guide clinical decision making.
- Published
- 2017