Chang Zhe, Liu Zhe
Department of Ultrasound Medicine, Xi'an Fengcheng Hospital, Xi'an, 710016, China.
BMC Gastroenterol. 2025 Feb 20;25(1):94. doi: 10.1186/s12876-025-03666-9.
To evaluate the association between serum uric acid (SUA) levels and metabolic dysfunction-associated steatotic liver disease (MASLD), defined as excessive fat accumulation in the liver accompanied by at least one cardiometabolic risk factor, reflecting metabolic abnormalities associated with the condition, in a Chinese adult population.
This study included 3829 participants aged ≥ 18 years who underwent abdominal transient elastography and had complete SUA data. SUA was categorized into low, medium, and high tertiles. Hepatic steatosis was defined as a controlled attenuation parameter (CAP) ≥ 248 dB/m. MASLD diagnosis followed the latest definitions by relevant liver disease associations. Logistic regression analyzed the association between SUA and MASLD. Restricted cubic spline regression assessed non-linear relationships.
A total of 1737 participants were diagnosed with MASLD. SUA levels were higher in the MASLD group (5.79 ± 1.50 mg/dL) than in the non-MASLD group (5.03 ± 1.35 mg/dL). SUA was linearly related to MASLD (P for nonlinearity = 0.8451). Both medium and high SUA groups had increased MASLD risk compared to the low SUA group (P < 0.05). Each unit increase in SUA was associated with a 14% higher risk of MASLD (odds ratio [OR] = 1.14, P = 0.0004).
This study highlights the association between SUA levels and MASLD, suggesting that SUA may serve as a potential biomarker for MASLD risk assessment. Monitoring SUA levels could inform preventive strategies and facilitate early intervention, contributing to improved MASLD management.
在中国成年人群中,评估血清尿酸(SUA)水平与代谢功能障碍相关脂肪性肝病(MASLD)之间的关联。MASLD定义为肝脏脂肪过度蓄积,并伴有至少一种心血管代谢危险因素,反映了与该疾病相关的代谢异常。
本研究纳入了3829名年龄≥18岁且接受腹部瞬时弹性成像检查并拥有完整SUA数据的参与者。SUA被分为低、中、高三分位数。肝脂肪变性定义为受控衰减参数(CAP)≥248 dB/m。MASLD的诊断遵循相关肝病协会的最新定义。采用逻辑回归分析SUA与MASLD之间的关联。使用受限立方样条回归评估非线性关系。
共有1737名参与者被诊断为MASLD。MASLD组的SUA水平(5.79±1.50 mg/dL)高于非MASLD组(5.03±1.35 mg/dL)。SUA与MASLD呈线性相关(非线性P值=0.8451)。与低SUA组相比,中、高SUA组的MASLD风险均增加(P<0.05)。SUA每增加一个单位,MASLD风险增加14%(优势比[OR]=1.14,P=0.0004)。
本研究突出了SUA水平与MASLD之间的关联,表明SUA可能作为MASLD风险评估的潜在生物标志物。监测SUA水平可为预防策略提供依据并促进早期干预,有助于改善MASLD的管理。