Cited by 53Chronic Kidney Disease and DiabetesDiabetes Treatment and ManagementDiabetes Management and Research

Effects of tirzepatide versus insulin glargine on cystatin C-based kidney function: a SURPASS-4 post hoc analysis

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Heerspink, Hiddo J.L., Sattar, Naveed, Pavo, Imre, Haupt, Axel, Duffin, Kevin L., Yang, Zhengyu, Wiese, Russell J., Wilson, Jonathan M. +3 more·2023·Diabetes Care

Published version of a preprint

Abstract

OBJECTIVE: Tirzepatide reduces HbA1c and body weight, and creatinine-based estimated glomerular filtration rate (eGFR) decline. Unlike creatine-derived eGFR (eGFR-creatinine), cystatin C–derived eGFR (eGFR-cystatin C) is unaffected by muscle mass changes. We assessed effects of tirzepatide on eGFR-creatinine and eGFR-cystatin C. RESEARCH DESIGN AND METHODS: Our primary outcome was eGFR change from baseline at 52 weeks with pooled tirzepatide (5, 10, and 15 mg) and titrated insulin glargine in adults with type 2 diabetes and high cardiovascular risk (SURPASS-4). RESULTS: Least squares mean (SE) eGFR-creatinine (mL/min/1.73 m2) changes from baseline with tirzepatide and insulin glargine were −2.5 (0.38) and −3.9 (0.38) (between-group difference, 1.4 [95% CI 0.3–2.4]) and −3.5 (0.37) and −5.3 (0.37) (between-group difference, 1.8 [95% CI 0.8–2.8]) for eGFR-cystatin C. Baseline, 1-year, and 1-year change from baseline values significantly correlated between eGFR-cystatin C and eGFR-creatinine. Measures of eGFR changes did not correlate with body weight changes. CONCLUSIONS: Tirzepatide slows the eGFR decline rate, supporting a kidney-protective effect.

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  • Treatment with the GIP/GLP-1 receptor agonist, tirzepatide was associated with reduced albuminuria in patients with T2D or obesity, although most patients in these studies had normal albuminuria and did not have CKD.

    “Treatment with the GIP/GLP-1 receptor agonist, tirzepatide was associated with reduced albuminuria in patients with T2D or obesity, although most patients in these studies had normal albuminuria and did not have CKD.22,23”

    From The Effect of Retatrutide on Kidney Parameters in Participants With Type 2 Diabetes Mellitus and/or Obesity (2025) · cites this paper as [22]

    The Results (Table 1; page unavailable) show that 63–64% of SURPASS-4 participants had no albuminuria at baseline. However, this analysis studied adults with type 2 diabetes, not an obesity-only population, and reports slower eGFR decline rather than a reduction in albuminuria. The copy does not establish that most participants did not have CKD. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • Preliminary data from the SURPASS program indicate that tirzepatide slowed eGFR decline in comparison with both placebo and comparator drugs including insulin glargine.

    “Preliminary data point toward beneficial effects of GIP agonism, as reported in findings from the SURPASS program that tirzepatide reduced UACR and slowed down eGFR declined in comparison with both placebo (53) and comparator drugs including insulin glargine (74, 75).”
  • Preliminary data from the SURPASS program indicate that tirzepatide reduced UACR in comparison with both placebo and comparator drugs including insulin glargine.

    “Preliminary data point toward beneficial effects of GIP agonism, as reported in findings from the SURPASS program that tirzepatide reduced UACR and slowed down eGFR declined in comparison with both placebo (53) and comparator drugs including insulin glargine (74, 75).”

    From GLP-1 agonists in the treatment of chronic kidney disease in type 2 diabetes and obesity (2025) · cites this paper as [75]

    The Results report baseline UACR values, but no change in UACR with tirzepatide versus insulin glargine or placebo. The Conclusions say a future study will provide data on UACR; this paper instead reports slower eGFR decline versus insulin glargine. Searched the indexed copy for UACR reduction and placebo comparisons. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

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Authors
Heerspink, H. J. L., Sattar, N., Pavo, I., Haupt, A., Duffin, K. L., Yang, Z., Wiese, R. J., Wilson, J. M., Hemmingway, A., Cherney, D. Z. I., & Tuttle, K. R.
Affiliations
  • University Medical Center Groningen (NL)
  • University of Glasgow (GB)
  • Eli Lilly (United States) (US)
  • University Health Network (CA)
  • University of Washington (US)
Corresponding author
Heerspink, Hiddo J.L.
Venue
Diabetes Care
Published
2023-06-02
Volume
46
Issue
8
Pages
1501-1506
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W4379113768
Cited by
53
References
21
Citations by year
2026: 15 · 2025: 18 · 2024: 15 · 2023: 5
FWCI
10.24
Type
journal article
Language
en
Open access
Locations
  • Diabetes Care (publishedVersion, other-oa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
Funders
Eli Lilly and Company
Topics
  • Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
Keywords
tirzepatide, insulin glargine, cystatin C, estimated glomerular filtration rate, renal function, type 2 diabetes, renal function decline, renal protection, high cardiovascular risk, body weight
MeSH terms
Insulin Glargine, Tirzepatide, Adult, Body Weight, Creatinine, Diabetes Mellitus, Type 2, Glomerular Filtration Rate, Humans, Kidney, Cystatin C

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