Larger effect size in composite kidney outcomes than in major cardiovascular events associated with sodium‐glucose cotransporter‐2 ( SGLT2) inhibitors compared with glucagon‐like peptide‐1 receptor agonists ( GLP ‐1 RAs) : A pooled analysis of type 2 diabetes trials

Author:

Diallo Alhassane1ORCID,Carlos‐Bolumbu Miguel2,Renard Pr Eric3ORCID,Galtier Florence1ORCID

Affiliation:

1. INSERM, CIC 1411, Clinical Investigation Center 1411 INSERM, CHU Montpellier, Univ Montpellier Montpellier Cedex 5 France

2. Department of Anaesthesia and Intensive Care Urgences réanimation centre hospitalier Sud Essonnes CHSE Paris France

3. Department of Endocrinology and Diabetes, Montpellier University Hospital; INSERM CIC 1411 Clinical Investigation Centre Institute of Functional Genomics, University of Montpellier, CNRS, INSERM Montpellier France

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference29 articles.

1. IDF Diabetes Atlas: Global estimates of the prevalence of diabetes for 2011 and 2030

2. Worldwide access to treatment for end-stage kidney disease: a systematic review

3. Association of Cardiometabolic Multimorbidity With Mortality

4. Department of Health and Human Services. Guidance for Industry on Diabetes Mellitus–Evaluating Cardiovascular Risk in New Antidiabetic Therapies to Treat Type 2 Diabetes; Availability. Food and Drug Administration [Docket No. FDA–2008–D–0118].

5. Sodium‐glucose cotransporter protein‐2 (SGLT‐2) inhibitors and glucagon‐like peptide‐1 (GLP‐1) receptor agonists for type 2 diabetes: systematic review and network meta‐analysis of randomised controlled trials;Palmer SC;BMJ,2021

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