Tirzepatide and injectable semaglutide deliver similar effectiveness against liver disease progression and major adverse liver outcomes (MALO) among adults with overweight or obesity and type 2 diabetes (T2D), a study has shown.
A team of investigators conducted a retrospective target trial emulation using the TriNetX global network to analyse new users of tirzepatide and semaglutide. The primary endpoint was time-to-first MALO (a composite of cirrhosis, decompensated events, and hepatocellular carcinoma). Baseline covariates were balanced via propensity score matching.
The risk of MALO over a median follow-up of about 17 months was not significantly different between tirzepatide and semaglutide initiators (estimated incidence rate [IR], 4.05 vs 4.04 per 1,000 person-year [PY]; hazard ratio [HR], 1.04, 95 percent confidence interval [CI], 0.88‒1.23).
The comparable risk profile persisted across sensitivity analyses, including individuals with metabolic dysfunction-associated liver disease (IR, 9.97 vs 10.03 per 1,000 PY; HR, 1.03, 95 percent CI, 0.75‒1.42) and “as treated” analysis (HR, 0.98, 95 percent CI, 0.80‒1.21). Notably, tirzepatide users achieved greater reduction in BMI (mean difference ~1.1 kg/m2; p<0.001).
“Internal validation confirmed both agents significantly outperformed sitagliptin,” the investigators said.