Ghanem Amr Sayed, Tóth Ágnes, Takács Péter, Ulambayar Battamir, Móré Marianna, Nagy Attila Csaba
Department of Health Informatics, Faculty of Health Sciences, University of Debrecen, 4028 Debrecen, Hungary.
Department of Integrative Health Sciences, Faculty of Health Sciences, University of Debrecen, 4028 Debrecen, Hungary.
Int J Mol Sci. 2025 May 24;26(11):5057. doi: 10.3390/ijms26115057.
Non-alcoholic fatty liver disease (NAFLD) is a common metabolic liver disease linked to obesity and diabetes. This study aimed to assess whether serum GOT and GPT can predict NAFLD early in at-risk individuals. A retrospective cohort study was conducted using hospital records from the University of Debrecen (2012-2022), including 4886 NAFLD-free individuals at baseline. NAFLD incidence was tracked using ICD-10 codes, with transaminase levels (GOT and GPT) and key metabolic comorbidities analyzed as predictors in a longitudinal design. Survival analysis included Fleming-Harrington tests, Kaplan-Meier, and Nelson-Aalen estimators as well as restricted mean survival time. The Royston-Parmar flexible parametric model was used to assess the time-dependent effects of GOT, GPT, and metabolic risk factors on NAFLD incidence. An elevated GOT was significantly associated with an increased NAFLD hazard (HR = 2.71, 95% CI: 1.31-5.58), as was an elevated GPT (HR = 2.21, 95% CI: 1.09-4.43). Disorders of lipid metabolism showed the strongest association (HR = 3.29, 95% CI: 1.51-7.25). Elevated GOT and GPT levels, in combination with demographic and clinical factors, may serve as valuable prognostic biomarkers for NAFLD progression, underscoring the importance of routine liver enzyme monitoring and comprehensive metabolic management to improve long-term patient outcomes.
非酒精性脂肪性肝病(NAFLD)是一种与肥胖和糖尿病相关的常见代谢性肝病。本研究旨在评估血清谷草转氨酶(GOT)和谷丙转氨酶(GPT)是否能在高危个体中早期预测NAFLD。利用德布勒森大学(2012 - 2022年)的医院记录进行了一项回顾性队列研究,基线时纳入了4886名无NAFLD的个体。使用国际疾病分类第10版(ICD - 10)编码追踪NAFLD发病率,在纵向设计中分析转氨酶水平(GOT和GPT)及关键代谢合并症作为预测因素。生存分析包括弗莱明 - 哈林顿检验、卡普兰 - 迈耶法和纳尔逊 - 阿伦估计法以及受限平均生存时间。采用罗伊斯顿 - 帕尔马灵活参数模型评估GOT、GPT和代谢危险因素对NAFLD发病率的时间依赖性影响。GOT升高与NAFLD风险增加显著相关(风险比[HR] = 2.71,95%置信区间[CI]:1.31 - 5.58),GPT升高情况亦是如此(HR = 2.21,95% CI:1.09 - 4.43)。脂质代谢紊乱显示出最强的相关性(HR = 3.29,95% CI:1.51 - 7.25)。GOT和GPT水平升高,结合人口统计学和临床因素,可能作为NAFLD进展的有价值的预后生物标志物,强调了常规肝酶监测和全面代谢管理对改善患者长期预后的重要性。