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Abstract
Over a median 4.3-year follow-up, new users of GLP-1 receptor agonists had a lower hazard of major adverse liver outcomes (HR 0.91).
- GLP-1 receptor agonists may lead to a lower risk of major adverse liver outcomes compared to SGLT-2 inhibitors.
- The association with lower hazard appeared stronger when considering on-treatment analysis (HR 0.78) and hospital diagnoses (HR 0.77).
- Benefits were observed for liver cirrhosis (HR 0.88), decompensation events (HR 0.91), and hepatocellular carcinoma (HR 0.76).
- No significant difference was found for all-cause mortality (HR 1.04).
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