Diabetologie und Stoffwechsel 2025; 20(S 01): S99
DOI: 10.1055/s-0045-1807554
Abstracts | DDG 2025
Poster
Posterwalk 15: Sonstige Themen

Effect of Tirzepatide on Kidney Parameters in People with Excess Body Weight and Type 2 Diabetes: A Post-Hoc Analysis of the SURMOUNT-2 Trial

HJ L Heerspink
1   University of Groningen, University Medical Center Groningen, Department of Clinical Pharmacy and Pharmacology, Groningen, Netherlands
,
A N Friedman
2   Indiana University School of Medicine, DaVita Metro Pointe Dialysis Medical Director, Indiana, United States
,
P Bjornstad
3   University of Colorado School of Medicine, Pediatrics-Endocrinology, Colorado, United States
,
D H van Raalte
4   Amsterdam University Medical Center, Diabetes & Metabolism, Amsterdam, Netherlands
,
D Cao
5   Eli Lilly and Company, Statistics – RWA2 – Medical Affairs, Indianapolis, United States
,
L E García-Pérez
6   Eli Lilly and Company, Obesity/NILEX, Indianapolis, United States
,
A Stefanski
7   Eli Lilly and Company, CWM Development, Indianapolis, United States
,
I Turfanda
8   Eli Lilly and Company, Next Generation Incretins (NILEX), Indianapolis, United States
,
M Bunck
9   Eli Lilly and Company, Incretin Platform Outcomes, Indianapolis, United States
,
I Benabbad
10   Eli Lilly and Company, benabbad_imane@lilly.com, Indianapolis, United States
,
C Piras de Oliveira
11   Eli Lilly and Company, Incretin Platform NILEX, Indianapolis, United States
,
R Griffin
12   Eli Lilly and Company, Global Medical Affairs-Obesity, Indianapolis, United States
,
T Ebert
13   Universitätsklinikum Leipzig, Klinik und Poliklinik für Endokrinologie, Nephrologie und Rheumatologie, Leipzig, Germany
,
C Geiß
13   Lilly Deutschland GmbH
› Institutsangaben
 

What was the potential impact of tirzepatide (TZP) vs. placebo (PBO) on kidney parameters in people with obesity or overweight with type 2 diabetes, based on a post-hoc analysis of the SURMOUNT-2 trial (SM-2)?

Methods: Data from all participants randomly assigned to treatment were included (pooled TZP [10 and 15 mg], N=623; PBO, N=315). Assessments included CKD-EPI creatinine-cystatin-C-based eGFR (Cr-Cys-C-eGFR), and urine albumin-to-creatinine ratio (UACR). The change from baseline to week 72 was analyzed using mixed models for repeated measures with on-treatment data.

Results: Baseline mean Cr-Cys-C-eGFR was 91.3±19.5 mL/min/1.73 m ^ 2. The estimated treatment difference (ETD) between pooled TZP groups and PBO on the change from baseline in Cr-Cys-C-eGFR was 0.0 mL/min/1.73 m ^ 2 (95% confidence interval [CI] -1.7, 1.7; p=0.993). TZP compared to placebo did not change Cr-Cys-C-eGFR at week 72 in participants with baseline Cr-Cys-C-eGFR<60 ml/min/1.73m ^ 2 (p=0.180) or≥60 ml/min/1.73m ^ 2 (p=0.714). Baseline median UACR was 13.0 mg/g (interquartile range 6.0–35.0 mg/g). UACR significantly decreased with TZP vs. PBO (ETD -31.1%, 95% CI -40.9, -19.7, p<0.001) and for those with baseline UACR≥30 mg/g, the ETD was -55.2% (95% CI -68.5, -36.4; p<0.001).

Conclusion: In this post-hoc analysis SM-2 trial population of participants with obesity or overweight with T2D and preserved eGFR at baseline, TZP reduced albuminuria without adversely affecting eGFR.

^ denotes &apos;square root of&apos; in this abstract



Publikationsverlauf

Artikel online veröffentlicht:
28. Mai 2025

© 2025. Thieme. All rights reserved.

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany