Key result
Atrasentan reduces HOMA-IR ~13% vs placebo in T2D and CKD, especially in severe insulin resistance.
Why the study?
Patients with type 2 diabetes and high insulin resistance face an increased risk of chronic kidney disease, prompting an evaluation of whether atrasentan's effect on insulin resistance varies across different phenotypic clusters.
Does atrasentan improve insulin resistance in patients with type 2 diabetes and chronic kidney disease across different phenotypic clusters?
RCT (n=931)
placebo-controlled
randomized
Does atrasentan improve insulin resistance in patients with type 2 diabetes and chronic kidney disease across different phenotypic clusters?
Atrasentan significantly improves insulin sensitivity in patients with type 2 diabetes and chronic kidney disease, particularly those with a severe insulin-resistant phenotype.
Supports phenotype-specific insulin sensitization by atrasentan in T2D-CKD; hypothesis-generating pending randomized validation.
AIMS: Type 2 diabetes (T2D) patients with a clinical phenotype characterized by a high degree of insulin resistance are at increased risk of chronic kidney disease (CKD). We previously demonstrated that the endothelin receptor antagonist (ERA) atrasentan reduced insulin resistance in T2D. In this study, we compared the effect of atrasentan on insulin resistance across different phenotypic clusters of patients with T2D. MATERIALS AND METHODS: We performed a post hoc analysis of the SONAR trial, a randomized, placebo-controlled trial of the ERA atrasentan in patients with T2D and CKD. Patients were stratified into four previously identified phenotypic clusters: severe insulin-deficient diabetes (SIDD), severe insulin-resistant diabetes (SIRD), mild obesity-related diabetes (MOD) and mild age-related diabetes (MARD). Changes in insulin resistance, assessed by HOMA-IR, were compared between the phenotypic clusters using a mixed effects model. RESULTS: In total, 931 patients were included in the analysis. In the overall population, atrasentan compared to placebo reduced HOMA-IR by 12.9% [95%CI 3.5,21.4]. This effect of atrasentan was more pronounced in clusters characterized by insulin resistance or deficiency: (SIRD cluster 26.2% [95% CI 3.8,43.3] and SIDD cluster 18.5% [95%CI -3.8,35.9]), although the latter did not reach statistical significance. The effect of atrasentan compared to placebo was less pronounced in the other two clusters (MARD 12.2% [95% CI -1.7,24.12] and MOD -5.3% [95% CI -28.9,13.9]). CONCLUSIONS: Atrasentan significantly improved insulin sensitivity in patients with T2D and CKD, especially in those characterized by high insulin resistance (SIRD cluster). Further studies are warranted to investigate the long-term clinical outcomes of atrasentan treatment in these distinct phenotypic clusters.
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Smeijer et al. (2024) conducted an RCT in Type 2 diabetes and chronic kidney disease (n=931). atrasentan vs. placebo was evaluated on Changes in insulin resistance, assessed by HOMA-IR (12.9% reduction, 95% CI 3.5, 21.4). Atrasentan reduced HOMA-IR by 12.9% (95% CI 3.5-21.4) vs placebo in patients with type 2 diabetes and chronic kidney disease, with the greatest effect in the severe insulin-resistant cluster.
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