The prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD)
is increasing worldwide. Uric acid (UA) is a well-known component of metabolic dysfunction
and also implicated as a risk factor for MASLD. Herein, elevated uric acid levels
can increase insulin resistance, inflammatory response and oxidative stress in the
liver, thereby promoting MASH progression. However, the role of uric acid in risk
stratification of MASLD patients remains unclear.
Uric acid levels were assessed in 96 MASLD patients and associated with established
non-invasive surrogates of liver fibrosis (e.g. FIB-4, VTCE/CAP). Patients on uric
acid-lowering therapy were excluded. Elevated UA was defined as≥360 μmol/l.
UA levels showed a linear correlation with increased CAP (r=0.27; p=0.0094) and median
values (r=0.23; p=0.032), suggesting greater hepatic steatosis and fibrosis. Among
patients at increased risk of fibrosis (FIB-4≥1.3 or median≥8 kPa), elevated UA was
associated with an increase in non-invasive tests. Patients above the 75th percentile
of UA (≥410 μmol/l) showed significantly higher FIB-4 and median in the at-risk population
compared to the 25th percentile. Interestingly, patients with elevated UA had significantly
higher triglycerides and lower HDL cholesterol. Of note, UA levels were independent
of diabetes status and body weight, but patients with elevated UA levels had higher
creatinine levels.
Conclusion: Uric acid levels significantly correlate with hepatological outcome in MASLD patients
at high fibrosis risk, suggesting a potential relevance for risk stratification. Further
longitudinal studies are needed to assess its prognostic value.