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本文引用的文献

1
Effects of excess high-normal alanine aminotransferase levels in relation to new-onset metabolic dysfunction-associated fatty liver disease: Clinical implications.高正常范围内丙氨酸氨基转移酶水平升高与新发代谢功能障碍相关脂肪性肝病的关系及临床意义
World J Gastroenterol. 2024 Jul 21;30(27):3264-3267. doi: 10.3748/wjg.v30.i27.3264.
2
Development and validation of a nomogram model for predicting the risk of MAFLD in the young population.用于预测年轻人群中MAFLD风险的列线图模型的开发与验证
Sci Rep. 2024 Apr 23;14(1):9376. doi: 10.1038/s41598-024-60100-y.
3
Cumulative effects of excess high-normal alanine aminotransferase levels in relation to new-onset metabolic dysfunction-associated fatty liver disease in China.中国人群中高水平丙氨酸氨基转移酶与新发代谢相关脂肪性肝病的累积效应。
World J Gastroenterol. 2024 Mar 14;30(10):1346-1357. doi: 10.3748/wjg.v30.i10.1346.
4
Non-invasive testing and risk-stratification in patients with MASLD.非侵入性检测和 MASLD 患者的风险分层。
Eur J Intern Med. 2024 Apr;122:11-19. doi: 10.1016/j.ejim.2024.01.013. Epub 2024 Jan 20.
5
Reply: A multi-society Delphi consensus statement on new fatty liver disease nomenclature.回复:关于新的脂肪性肝病命名的多学会德尔菲共识声明。
Hepatology. 2024 Mar 1;79(3):E93-E94. doi: 10.1097/HEP.0000000000000696. Epub 2023 Nov 20.
6
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.全基因组关联荟萃分析确定了 17 个与非酒精性脂肪性肝病相关的位点。
Nat Genet. 2023 Oct;55(10):1640-1650. doi: 10.1038/s41588-023-01497-6. Epub 2023 Sep 14.
7
Liver Fat Scores for Noninvasive Diagnosis and Monitoring of Nonalcoholic Fatty Liver Disease in Epidemiological and Clinical Studies.用于非酒精性脂肪性肝病流行病学和临床研究中无创诊断及监测的肝脏脂肪评分
J Clin Transl Hepatol. 2023 Oct 28;11(5):1212-1227. doi: 10.14218/JCTH.2022.00019. Epub 2023 May 31.
8
One ALT Is Not Like the Other.一种丙氨酸氨基转移酶与另一种不同。
Gastroenterology. 2023 Aug;165(2):320-323. doi: 10.1053/j.gastro.2023.04.009. Epub 2023 Apr 23.
9
Comparative Accuracy of Clinical Fibrosis Markers, Hepascore and Fibroscan® to Detect Advanced Fibrosis in Patients with Nonalcoholic Fatty Liver Disease.临床纤维化标志物、Hepascore 和 Fibroscan®对非酒精性脂肪性肝病患者诊断肝纤维化的准确性比较。
Dig Dis Sci. 2023 Jun;68(6):2757-2767. doi: 10.1007/s10620-023-07896-3. Epub 2023 Mar 22.
10
Machine learning classifiers for screening nonalcoholic fatty liver disease in general adults.机器学习分类器在一般成年人中非酒精性脂肪性肝病筛查中的应用。
Sci Rep. 2023 Mar 3;13(1):3638. doi: 10.1038/s41598-023-30750-5.

代谢相关脂肪性肝病:长期高正常丙氨酸氨基转移酶作为筛查试验的问题。

Metabolic dysfunction-associated steatotic liver disease: The question of long-term high-normal alanine aminotransferase as a screening test.

机构信息

Department of Pathology and Laboratory Medicine, University of Ottawa and The Ottawa Hospital, Ottawa K1H 8L6, Ontario, Canada.

出版信息

World J Gastroenterol. 2024 Nov 14;30(42):4576-4582. doi: 10.3748/wjg.v30.i42.4576.

DOI:10.3748/wjg.v30.i42.4576
PMID:39563746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11572615/
Abstract

The growing prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) is being driven by the obesity epidemic. The quest for solutions continues particularly with regard to early detection. This editorial comments on the utility of long-term high-normal alanine aminotransferase (ALT) in screening for MASLD. Chen found that new onset MASLD can be detected by repetitively high normal ALT. Implicit in this concept is the question of what should be the accepted upper limit of normal (ULN) for ALT. It was previously set at 40 IU/L based on studies that included people with subclinical liver disease but the new consensus is 30/19 U/L in healthy males/females. Thus, when Chen defines the ULN as 40 U/L, others may view it as excessively high. It is important to recognize the variables affecting ULN instrumentation, diurnal variations, exercise and ageing. These variables matter when the distinctions are subtle normal high-normal. In this regard, the utility of long-term high normal ALT as a disease marker could be enhanced by combining it with other biomarkers, imaging and MASLD genetics to create machine learning classifiers. All in all, Chen 's work on long-term high normal ALT as a marker of new-onset MASLD deserves merit.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)的患病率不断上升,主要与肥胖症的流行有关。人们一直在寻找解决方法,特别是在早期检测方面。这篇社论评论了长期高正常丙氨酸氨基转移酶(ALT)在 MASLD 筛查中的作用。Chen 发现,通过反复出现的高正常 ALT 可以检测到新发 MASLD。这一概念隐含的问题是,ALT 的正常上限(ULN)应该是多少。以前,基于包括亚临床肝病患者的研究,将其设定为 40IU/L,但新的共识是健康男性/女性的 ALT ULN 为 30/19U/L。因此,当 Chen 将 ULN 定义为 40U/L 时,其他人可能会认为它过高。重要的是要认识到影响 ULN 的变量,包括仪器、昼夜变化、运动和老化。当区分正常和高正常值时,这些变量很重要。在这方面,通过将长期高正常 ALT 与其他生物标志物、影像学和 MASLD 遗传学相结合,创建机器学习分类器,可以提高其作为疾病标志物的效用。总的来说,Chen 关于长期高正常 ALT 作为新发 MASLD 标志物的研究值得肯定。