Cardiovascular and renal outcomes of GLP-1 receptor agonists vs. DPP-4 inhibitors and basal insulin in type 2 diabetes mellitus: A systematic review and meta-analysis

Author:

Evans Marc1,Kuodi Paul2,Akunna Chisom Joyqueenet3,McCreedy Nicole4ORCID,Donsmark Morten5,Ren Hongye5,Nnaji Chukwudi A3ORCID

Affiliation:

1. Department of Diabetes and Endocrinology, University Hospital Llandough, Penarth, UK

2. Department of Public Health, Faculty of Health Sciences, Lira University, Lira, Uganda

3. School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa

4. Last Mile P/S, Copenhagen, Denmark

5. Novo Nordisk A/S, Copenhagen, Denmark

Abstract

Objective To compare the cardiovascular and renal outcomes of GLP-1 RA versus DPP4i and basal insulin in the management of T2DM. Methods Data from 22 studies involving over 200,000 participants were pooled using the inverse variance method and random-effects meta-analysis. The review was reported in accordance with PRISMA. Results Compared with DPP4i, treatment with GLP-1 RA was associated with a greater benefit on composite cardiovascular outcomes (HR:0.77, 95% CI:0.69–0.87), myocardial infarction (HR:0.82, 95% CI:0.69–0.97), stroke (HR:0.83, 95% CI: 0.74–0.93), cardiovascular mortality (HR:0.76, 95% CI:0.68–0.85) and all-cause mortality (HR:0.65, 95% CI:0.48–0.90). There was no difference in effect on heart failure (HR:0.97, 95% CI:0.82–1.15). Compared with basal insulin, GLP-1 RA was associated with better effects on composite cardiovascular outcomes (HR:0.62, 95% CI:0.48–0.79), heart failure (HR:0.57, 95% CI:0.35–0.92), myocardial infarction (HR:0.70, 95% CI:0.58–0.85), stroke (HR:0.50, 95% CI:0.40–0.63) and all-cause mortality (HR:0.31, 95% CI:0.20–0.48). Evidence from a small number of studies suggests that GLP-1 RA had better effects on composite and individual renal outcomes, such as eGFR, compared with either DPP4i and basal insulin. Conclusion Available evidence suggests that treating T2DM with GLP-1 RA can yield better benefits on composite and specific cardiorenal outcomes than with DPP4i and basal insulin. PROSPERO Registration Number CRD42022335504.

Funder

Novo Nordisk

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

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