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本文引用的文献

1
The Fatty Liver Index has limited utility for the detection and quantification of hepatic steatosis in obese patients.脂肪肝指数在检测和量化肥胖患者的肝脂肪变性方面效用有限。
Hepatol Int. 2013 Jun;7(2):592-9. doi: 10.1007/s12072-012-9401-4. Epub 2012 Sep 29.
2
Biomarkers of NAFLD progression: a lipidomics approach to an epidemic.非酒精性脂肪性肝病进展的生物标志物:一种针对流行病的脂质组学方法。
J Lipid Res. 2015 Mar;56(3):722-736. doi: 10.1194/jlr.P056002. Epub 2015 Jan 17.
3
Genomic medicine and risk prediction across the disease spectrum.基因组医学与疾病谱中的风险预测。
Crit Rev Clin Lab Sci. 2015;52(3):120-37. doi: 10.3109/10408363.2014.997930. Epub 2015 Jan 19.
4
Is aspartate aminotransferase-to-platelet ratio index a biomarker in the evaluation of advanced fibrosis in non-alcoholic fatty liver disease?天冬氨酸转氨酶与血小板比值指数是否为评估非酒精性脂肪性肝病晚期纤维化的生物标志物?
Gastroenterol Rep (Oxf). 2014 Nov;2(4):323-4. doi: 10.1093/gastro/gou063.
5
Carotid intima-media thickness is predicted by combined eotaxin levels and severity of hepatic steatosis at ultrasonography in obese patients with Nonalcoholic Fatty Liver Disease.在患有非酒精性脂肪性肝病的肥胖患者中,嗜酸性粒细胞趋化蛋白水平与肝脏脂肪变性严重程度相结合,可通过超声检查预测颈动脉内膜中层厚度。
PLoS One. 2014 Sep 30;9(9):e105610. doi: 10.1371/journal.pone.0105610. eCollection 2014.
6
Chronic permanent hypoxemia predisposes to mild elevation of liver stiffness.慢性持续性低氧血症易导致肝硬度轻度升高。
World J Gastroenterol. 2014 Aug 14;20(30):10564-9. doi: 10.3748/wjg.v20.i30.10564.
7
Role of liver biopsy in nonalcoholic fatty liver disease.肝活检在非酒精性脂肪性肝病中的作用。
World J Gastroenterol. 2014 Jul 21;20(27):9026-37. doi: 10.3748/wjg.v20.i27.9026.
8
Measurement of liver stiffness as a non-invasive method for diagnosis of non-alcoholic fatty liver disease.肝硬度测量作为一种非侵入性方法用于诊断非酒精性脂肪性肝病。
Hepatol Res. 2015 Jan;45(2):142-51. doi: 10.1111/hepr.12388. Epub 2014 Jul 29.
9
Treatment of non-alcoholic fatty liver disease.非酒精性脂肪性肝病的治疗
Dig Dis. 2014;32(5):597-604. doi: 10.1159/000360511. Epub 2014 Jul 14.
10
Proteomic and genomic studies of non-alcoholic fatty liver disease--clues in the pathogenesis.非酒精性脂肪性肝病的蛋白质组学和基因组学研究——发病机制中的线索
World J Gastroenterol. 2014 Jul 14;20(26):8325-40. doi: 10.3748/wjg.v20.i26.8325.

非酒精性脂肪性肝病谱的综合预后模型:在发展中国家的临床应用

Composite prognostic models across the non-alcoholic fatty liver disease spectrum: Clinical application in developing countries.

作者信息

Lückhoff Hilmar K, Kruger Frederik C, Kotze Maritha J

机构信息

Hilmar K Lückhoff, Maritha J Kotze, Division of Anatomical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, Bellville 7530, Cape Town, Western Cape, South Africa.

出版信息

World J Hepatol. 2015 May 28;7(9):1192-208. doi: 10.4254/wjh.v7.i9.1192.

DOI:10.4254/wjh.v7.i9.1192
PMID:26019735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4438494/
Abstract

Heterogeneity in clinical presentation, histological severity, prognosis and therapeutic outcomes characteristic of non-alcoholic fatty liver disease (NAFLD) necessitates the development of scientifically sound classification schemes to assist clinicians in stratifying patients into meaningful prognostic subgroups. The need for replacement of invasive liver biopsies as the standard method whereby NAFLD is diagnosed, graded and staged with biomarkers of histological severity injury led to the development of composite prognostic models as potentially viable surrogate alternatives. In the present article, we review existing scoring systems used to (1) confirm the presence of undiagnosed hepatosteatosis; (2) distinguish between simple steatosis and NASH; and (3) predict advanced hepatic fibrosis, with particular emphasis on the role of NAFLD as an independent cardio-metabolic risk factor. In addition, the incorporation of functional genomic markers and application of emerging imaging technologies are discussed as a means to improve the diagnostic accuracy and predictive performance of promising composite models found to be most appropriate for widespread clinical adoption.

摘要

非酒精性脂肪性肝病(NAFLD)在临床表现、组织学严重程度、预后和治疗结果方面存在异质性,因此有必要制定科学合理的分类方案,以帮助临床医生将患者分层为有意义的预后亚组。由于需要用组织学严重损伤的生物标志物取代侵入性肝活检作为诊断、分级和分期NAFLD的标准方法,因此开发了复合预后模型作为潜在可行的替代方法。在本文中,我们回顾了用于(1)确认未诊断的肝脂肪变性的存在;(2)区分单纯性脂肪变性和非酒精性脂肪性肝炎(NASH);以及(3)预测晚期肝纤维化的现有评分系统,特别强调NAFLD作为独立的心脑血管代谢危险因素的作用。此外,还讨论了功能基因组标记的纳入和新兴成像技术的应用,以此作为提高已发现最适合广泛临床应用的有前景的复合模型的诊断准确性和预测性能的一种手段。