Department of Gastroenterology of the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Department of Infectious Diseases, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen 518107, China.
Nutrients. 2022 Aug 31;14(17):3587. doi: 10.3390/nu14173587.
Serum uric acid (SUA) is regarded as an independent risk factor for nonalcoholic fatty liver disease (NAFLD). However, the role of SUA in the new diagnosis flowchart of metabolic-associated fatty liver disease (MAFLD) remains unclear. A cross-sectional study enrolled consecutive individuals with ultrasonography and magnetic resonance imaging−based proton density fat fraction (MRI-PDFF) measurements in the First Affiliated Hospital of Sun Yat-sen University from January 2015 to December 2021. All patients were divided into four groups according to their baseline SUA levels and sex. Of the 3537 ultrasound-diagnosed and 1017 MRI-PDFF-diagnosed MAFLD patients included, the prevalence of severe steatosis determined with ultrasound or MRI-PDFF increased across the serum SUA quartiles. The SUA cutoffs were identified as ≥478 µmol/L and ≥423.5 µmol/L for severe steatosis in male and female MAFLD, respectively. Furthermore, using these cutoff values, patients with higher SUA levels in the NAFLD−non-MAFLD group had higher liver fat contents than those without (16.0% vs. 9.7%, p < 0.001). The lean/normal-weight NAFLD−non-MAFLD patients with higher SUA levels are still at high risk of severe steatosis. This study supports the rationale for SUA being established as another risk factor for metabolic dysfunctions in lean/normal-weight MAFLD.
血清尿酸(SUA)被认为是非酒精性脂肪性肝病(NAFLD)的独立危险因素。然而,SUA 在代谢相关脂肪性肝病(MAFLD)新诊断流程图中的作用尚不清楚。一项横断面研究纳入了 2015 年 1 月至 2021 年 12 月中山大学第一附属医院接受超声和磁共振成像质子密度脂肪分数(MRI-PDFF)测量的连续个体。所有患者根据其基线 SUA 水平和性别分为四组。在 3537 例超声诊断和 1017 例 MRI-PDFF 诊断的 MAFLD 患者中,根据超声或 MRI-PDFF 确定的严重脂肪变性的患病率随着血清 SUA 四分位数的增加而增加。确定的 SUA 截断值分别为男性和女性 MAFLD 中严重脂肪变性的≥478 µmol/L 和≥423.5 µmol/L。此外,使用这些截断值,在非 MAFLD-N AFLD 组中,SUA 水平较高的患者的肝脂肪含量高于 SUA 水平较低的患者(16.0%比 9.7%,p < 0.001)。SUA 水平较高的瘦/正常体重非 MAFLD-N AFLD 患者仍存在严重脂肪变性的高风险。本研究支持将 SUA 确立为瘦/正常体重 MAFLD 代谢功能障碍的另一个危险因素的原理。