Renal effects and safety of tirzepatide in subjects with and without diabetes: A systematic review and meta-analysis.
Summary
Across 15 RCTs, tirzepatide reduced UACR without harming eGFR in people with T2D and in those with obesity without diabetes, indicating potential renal benefit and reassuring safety in the short term.
Key Findings
- Meta-analysis of RCTs indicates tirzepatide reduces UACR compared with control conditions.
- No detrimental effect on eGFR was observed in short-term RCTs across T2D and obesity populations.
- Overall renal safety profile was reassuring; longer-term, hard renal outcomes remain to be established.
Clinical Implications
Clinicians can anticipate albuminuria improvements with tirzepatide without short-term eGFR penalty; monitoring UACR may aid risk stratification, while awaiting longer-term renal outcome data.
Why It Matters
Given tirzepatide’s rapid uptake in diabetes/obesity care, synthesized RCT evidence on renal outcomes informs drug choice and risk–benefit discussions pending dedicated renal outcome trials.
Limitations
- Short follow-up horizons preclude conclusions on hard renal endpoints (e.g., sustained eGFR decline, ESKD)
- Heterogeneity of comparators and trial populations; individual patient data were not analyzed
Future Directions
Conduct long-duration, dedicated renal outcome trials of tirzepatide and IPD meta-analyses to define effects on eGFR slope, CKD progression, and albuminuria regression.
Study Information
- Study Type
- Systematic Review/Meta-analysis
- Research Domain
- Treatment/Prognosis
- Evidence Level
- I - Meta-analysis of randomized controlled trials
- Study Design
- OTHER