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Effect of once-weekly exenatide on estimated glomerular filtration rate slope depends on baseline renal risk: A post hoc analysis of the EXSCEL trial
Authors:Annemarie B van der Aart-van der Beek PharmD  Lindsay E Clegg PhD  Robert C Penland PhD  David W Boulton PhD  C David Sjöström MD  Robert J Mentz MD  Rury R Holman FRCP  Hiddo J L Heerspink PhD
Institution:1. Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands;2. Clinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland, USA;3. Clinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Boston, Massachusetts, USA;4. Late-Stage Development CVRM, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden;5. Duke University and Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA;6. Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK
Abstract:The effects of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on renal outcomes in patients with type 2 diabetes at high cardiovascular risk are modest or neutral. However, GLP-1RAs may confer clinical benefits in those at high risk of progressive renal function loss. We examined the effects of once-weekly exenatide (EQW) on estimated glomerular filtration rate (eGFR) slope and urinary albumin:creatinine ratio (UACR) as a function of baseline UACR in 3503 EXSCEL participants (23.7%) with eGFR data available and 2828 participants (19.2%) with UACR change data available. EQW improved eGFR slope assessed via mixed model repeated measures, compared with placebo, in participants with baseline UACR >100 mg/g (0.79 mL/min/1.73 m2/year 95% confidence interval {CI} 0.24–1.34]) and UACR >200 mg/g (1.32 mL/min/1.73 m2/year 95% CI 0.57–2.06]), but not at lower UACR thresholds. EQW reduced UACR, compared with placebo, assessed via analysis of covariance, consistently across subgroups with baseline UACR >30 mg/g (28.2% reduction), baseline UACR >100 mg (22.5% reduction) and baseline UACR >200 mg (34.5% reduction). This post hoc EXSCEL analysis suggests that EQW reduces UACR, with improvement in eGFR slope specifically in participants with elevated baseline UACR.
Keywords:diabetic kidney disease  exenatide  GLP-1RA  glucagon-like peptide-1 receptor agonists  pooled analysis
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