Efficacy of Modern Diabetes Treatments DPP-4i, SGLT-2i, and GLP-1RA in White and Asian Patients With Diabetes: A Systematic Review and Meta-analysis of Randomized Controlled Trials.
meta_analysis · Level I
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- Record sourced from PubMed, PMID 33534728.
- Also identified by DOI 10.2337/dc19-2419 and PMC identifier 7372059.
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Abstract
The pathophysiology of type 2 diabetes differs markedly by ethnicity. A systematic review and meta-analysis was conducted to assess the impact of ethnicity on the glucose-lowering efficacy of the newer oral agents, sodium-glucose cotransporter 2 inhibitors (SGLT-2i), glucagon-like peptide 1 receptor agonists (GLP-1RA), and dipeptidyl peptidase 4 inhibitors (DPP-4i), using evidence from randomized clinical trials (RCTs). A literature search was conducted in PubMed of all randomized, placebo-controlled trials of DPP-4i, SGLT-2i, and GLP-1RA. The search strategy was developed based on Medical Subject Headings (MeSH) terms and keywords. A total of 64 studies that qualified for meta-analysis after full-text review based on predefined inclusion and exclusion criteria-RCTs with at least 50 patients in each arm, >70% of population from Asian or white group, duration ≥24 weeks, and publication up to March 2019-were selected for systematic review and meta-analysis. Data extraction was done for aggregated study-level data by two independent researchers. Absolute changes in HbA<sub>1c</sub> (%) from baseline to 24 weeks between the drug and placebo were considered as the primary end point of the study. Change in HbA<sub>1c</sub> was evaluated by computing mean differences and 95% CIs between treatment and placebo arms. The study is based on summarized data and could not be separated based on East Asians and South Asians. The glucose-lowering efficacy of SGLT-2i, and to a lesser extent DPP-4i, was greater in studies of predominantly Asian ethnicity compared with studies of predominantly white ethnicity. There was no difference seen by ethnicity for GLP-1RA.
Medical subject headings
- Diabetes Mellitus
- Dipeptidyl-Peptidase IV Inhibitors
- Glucagon-Like Peptide Receptors
- Sodium-Glucose Transporter 2 Inhibitors