Digestivo, Hospital Universitario Fundacion Alcorcon, España.
Digestivo, Hospital Clínico Universitario de Valladolid, España.
Rev Esp Enferm Dig. 2019 Apr;111(4):264-269. doi: 10.17235/reed.2019.5965/2018.
recent evidence suggests a causal link between serum uric acid and the metabolic syndrome, diabetes mellitus, arterial hypertension, and renal and cardiac disease. Uric acid is an endogenous danger signal and activator of the inflammasome, and has been independently associated with an increased risk of cirrhosis.
six hundred and thirty-four patients from the nation-wide HEPAMET registry with biopsy-proven NAFLD (53% NASH) were analyzed to determine whether hyperuricemia is related with advanced liver damage in patients with non-alcoholic fatty liver disease (NAFLD). Patients were divided into three groups according to the tertile levels of serum uric acid and gender.
the cohort was composed of 50% females, with a mean age of 49 years (range 19-80). Patients in the top third of serum uric acid levels were older (p = 0.017); they had a higher body mass index (p < 0.01), arterial blood pressure (p = 0.05), triglyceridemia (p = 0.012), serum creatinine (p < 0.001) and total cholesterol (p = 0.016) and lower HDL-cholesterol (p = 0.004). According to the univariate analysis, the variables associated with patients in the top third were more advanced steatosis (p = 0.02), liver fibrosis (F2-F4 vs F0-1; p = 0.011), NASH (p = 0.002) and NAS score (p = 0.05). According to the multivariate logistic regression analysis, the top third of uric acid level was independently associated with steatosis (adjusted hazard ratio 1.7; CI 95%: 1.05-2.8) and NASH (adjusted hazard ratio 1.8; CI 95%: 1.08-3.0) but not with advanced fibrosis (F2-F4) (adjusted hazard ratio 1.09; CI 95%: 0.63-1.87).
higher levels of serum uric acid were independently associated with hepatocellular steatosis and NASH in a cohort of patients with NAFLD. Serum uric acid levels warrants further evaluation as a component of the current non-invasive NAFLD scores of histopathological damage.
最近的证据表明,血清尿酸与代谢综合征、糖尿病、动脉高血压以及肾脏和心脏疾病之间存在因果关系。尿酸是一种内源性危险信号和炎症小体的激活剂,并且已经被独立地与肝硬化风险增加相关联。
对全国 HEPAMET 登记处的 634 名经活检证实的非酒精性脂肪性肝病 (NAFLD)(53% NASH)患者进行分析,以确定高尿酸血症是否与非酒精性脂肪性肝病 (NAFLD) 患者的肝损伤有关。根据血清尿酸和性别,将患者分为三组。
该队列由 50%的女性组成,平均年龄为 49 岁(19-80 岁)。血清尿酸水平最高的三分之一患者年龄较大(p=0.017);他们的体重指数较高(p<0.01)、动脉血压较高(p=0.05)、三酰甘油水平较高(p=0.012)、血清肌酐水平较高(p<0.001)、总胆固醇水平较高(p=0.016)和高密度脂蛋白胆固醇水平较低(p=0.004)。根据单因素分析,与第三组患者相关的变量包括更严重的脂肪变性(p=0.02)、肝纤维化(F2-F4 与 F0-1;p=0.011)、NASH(p=0.002)和 NAS 评分(p=0.05)。根据多变量逻辑回归分析,尿酸水平的前三分之一与脂肪变性(调整后的危险比 1.7;95%可信区间:1.05-2.8)和 NASH(调整后的危险比 1.8;95%可信区间:1.08-3.0)独立相关,但与晚期纤维化(F2-F4)无关(调整后的危险比 1.09;95%可信区间:0.63-1.87)。
在非酒精性脂肪性肝病患者队列中,血清尿酸水平升高与肝细胞脂肪变性和 NASH 独立相关。血清尿酸水平值得进一步评估,作为当前非酒精性脂肪性肝病组织病理学损伤无创评分的组成部分。