英国生物银行的血浆代谢组衍生模型预测了非酒精性脂肪肝疾病的严重肝脏结局。

IF 5.4 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Xiaoqin Xu, Jiang Li, Yanqi Fu, Jie Li, Wenqi Shen, Xiao Tan, Ningjian Wang, Bin Wang, Yingli Lu
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引用次数: 0

摘要

目的:严重肝脏疾病(SLD)在非酒精性脂肪性肝病(NAFLD)中往往诊断较晚,因为进行性纤维化的无症状期较长。我们的目的是确定与SLD相关的代谢组学特征,并建立一个预测模型来改善风险分层。材料和方法:我们招募了59579名英国生物银行参与者,他们的脂肪肝指数(≥60)和血浆代谢组学特征呈阳性,评估肝硬化、失代偿性肝病、肝细胞癌和/或肝移植的发生率。应用Cox回归模型评估个体代谢物与SLD风险之间的关系。使用可解释的机器学习框架,开发了代谢组学集成的nomogram预测模型,并与传统评分系统进行了比较。结果:经Bonferroni校正后,在Cox回归模型中,249种代谢物中有110种与SLD发生风险显著相关。其中,11种代谢物最终被优先作为预测因子,基于最优机器学习算法构建代谢组学评分。综合代谢组学评分、谷氨酰转移酶、血小板计数、腰臀比、糖尿病和性别的nomogram对10年SLD风险的预测能力(受试者工作特征下面积0.841 [95% CI: 0.800-0.881])优于验证队列中纤维化-4指数(0.712,0.662-0.763)、NAFLD纤维化评分(0.659,0.609-0.709)和天冬氨酸转氨酶-血小板比值指数(0.705,0.652-0.759)。根据选择的截止点对参与者进行分类,显示出明显的SLD累积风险,与低风险组相比,高风险组的风险比为25.71 (95% CI: 17.10-38.66)。结论:血浆代谢组学与常规指标的结合增强了NAFLD严重肝脏结局的预测能力,在疾病风险分层和精准干预方面显示出潜在的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A plasma metabolome-derived model predicts severe liver outcomes of nonalcoholic fatty liver disease in the UK Biobank.

Aims: Severe liver disease (SLD) in nonalcoholic fatty liver disease (NAFLD) is often diagnosed late due to the long asymptomatic period of progressive fibrosis. We aimed to identify metabolomic profiles associated with SLD and develop a predictive model to improve risk stratification.

Materials and methods: We enrolled 59 579 UK Biobank participants with a positive fatty liver index (≥60) and plasma metabolomic profiles, evaluating the incidence of cirrhosis, decompensated liver disease, hepatocellular carcinoma and/or liver transplantation. Cox regression models were applied to evaluate the associations between individual metabolites and SLD risk. Using an interpretable machine-learning framework, a metabolomics-integrated nomogram prediction model was developed and compared with conventional scoring systems.

Results: After Bonferroni correction, 110 of 249 metabolites were significantly associated with the risk of incident SLD in the Cox regression model. Among them, 11 metabolites were ultimately prioritised as predictors to construct the metabolomic score based on the optimal machine learning algorithm. The nomogram integrating metabolomic score, gamma glutamyltransferase, platelet count, waist/hip ratio, diabetes and sex showed better predictive capacity of 10-year SLD risk (area under the receiver operating characteristic 0.841 [95% CI: 0.800-0.881]) than the fibrosis-4 index (0.712, 0.662-0.763), NAFLD fibrosis score (0.659, 0.609-0.709) and aspartate aminotransferase-to-platelet ratio index (0.705, 0.652-0.759) in the validation cohort. Categorisation of participants according to selected cutoffs revealed a distinct cumulative risk of SLD, with a hazard ratio of 25.71 (95% CI: 17.10-38.66) for the high-risk group compared with the low-risk group.

Conclusions: Integrating plasma metabolomics with routine indicators enhanced the predictive capacity for severe liver outcomes of NAFLD, which shows the potential benefits in disease risk stratification and precise interventions.

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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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