Cardiometabolic & kidney

Comprehensive Long-Term Changes in Cardiovascular Risk Biomarkers With Tirzepatide: A SURMOUNT-1 Post Hoc Analysis

J Am Coll CardiolPublished Post hoc analysis of the SURMOUNT-1 randomised trial

Authors' conclusion

In this post hoc analysis, tirzepatide was associated with improvements in biomarkers of metabolic/adiposity/hepatic stress and endothelial dysfunction, as well as selected biomarkers of inflammation and hemostasis/thrombosis.

Study context

Population
People with obesity or overweight in SURMOUNT-1 who completed treatmentafter low sample volumes excluded
Participants
392 people
Comparison
Tirzepatide 5, 10 or 15 mg vs placebo
Primary endpoint
Change in each log-transformed CV risk biomarker (% change in geometric means vs placebo)
Follow-up
72 weeks
Methodological detailsplacebo-controlled, 100 randomly selected participants per group
  • Placebo-controlled
  • 100 randomly selected participants per group

Primary result

As reported in the abstract

% change in biomarker geometric means vs placebo (5, 10, 15 mg) · Week 72
hs-CRP (5, 10, 15 mg)
−36.9%, −46.9%, −54.6%
Interleukin-6
−25.4%, −27.8%, −30.2%
Leukocytes
NS, −8.6%, −10.0%
HOMA-IR
−26.4%, −35.5%, −39.1%
Leptin
−44.4%, −59.3%, −61.4%
Gamma-glutamyl transferase
−18.6%, −21.6%, −32.7%
Fibroblast growth factor-21
−27.4%, −27.6%, −39.9%
Adiponectin
21.1%, 35.1%, 47.7%
Free fatty acids
NS, NS, −17.1%
Soluble ICAM-1
NS, −9.7%, −11.1%
E-selectin
−12.6%, −20.0%, −26.4%
PAI-1:Ag
−41.4%, −35.6%, −44.3%
Platelets
NS, NS, −6.0%

Original publication

Comprehensive Long-Term Changes in Cardiovascular Risk Biomarkers With Tirzepatide: A SURMOUNT-1 Post Hoc Analysis. J Am Coll Cardiol. Published 3 June 2026. doi:10.1016/j.jacc.2026.04.044

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