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OxNASH score correlates with histologic features and severity of nonalcoholic fatty liver disease.OxNASH 评分与非酒精性脂肪性肝病的组织学特征和严重程度相关。
Dig Dis Sci. 2014 Jul;59(7):1617-24. doi: 10.1007/s10620-014-3031-8. Epub 2014 Jan 25.
2
The diagnosis and management of non-alcoholic fatty liver disease: practice Guideline by the American Association for the Study of Liver Diseases, American College of Gastroenterology, and the American Gastroenterological Association.非酒精性脂肪性肝病的诊断与管理:美国肝病研究协会、美国胃肠病学会和美国胃肠病协会实践指南
Hepatology. 2012 Jun;55(6):2005-23. doi: 10.1002/hep.25762.
3
Neutrophil to lymphocyte ratio: a new marker for predicting steatohepatitis and fibrosis in patients with nonalcoholic fatty liver disease.中性粒细胞与淋巴细胞比值:预测非酒精性脂肪性肝病患者脂肪性肝炎和纤维化的新标志物。
Liver Int. 2012 Feb;32(2):297-302. doi: 10.1111/j.1478-3231.2011.02639.x. Epub 2011 Sep 8.
4
Prospective biopsy-controlled evaluation of cell death biomarkers for prediction of liver fibrosis and nonalcoholic steatohepatitis.前瞻性活检对照评估细胞死亡生物标志物预测肝纤维化和非酒精性脂肪性肝炎。
Hepatology. 2012 Feb;55(2):455-64. doi: 10.1002/hep.24734. Epub 2011 Nov 29.
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Hepatology. 2012 Jan;55(1):77-85. doi: 10.1002/hep.24706. Epub 2011 Dec 6.
6
Complex non-invasive fibrosis models are more accurate than simple models in non-alcoholic fatty liver disease.复杂的非侵入性纤维化模型比简单模型在非酒精性脂肪性肝病中更准确。
J Gastroenterol Hepatol. 2011 Oct;26(10):1536-43. doi: 10.1111/j.1440-1746.2011.06774.x.
7
Endpoints and clinical trial design for nonalcoholic steatohepatitis.非酒精性脂肪性肝炎的终点和临床试验设计。
Hepatology. 2011 Jul;54(1):344-53. doi: 10.1002/hep.24376.
8
Apoptosis in nonalcoholic fatty liver disease: diagnostic and therapeutic implications.非酒精性脂肪性肝病中的细胞凋亡:诊断和治疗意义。
Expert Rev Gastroenterol Hepatol. 2011 Apr;5(2):201-12. doi: 10.1586/egh.11.6.
9
An apoptosis panel for nonalcoholic steatohepatitis diagnosis.用于非酒精性脂肪性肝炎诊断的凋亡panel。
J Hepatol. 2011 Jun;54(6):1224-9. doi: 10.1016/j.jhep.2010.08.023. Epub 2011 Feb 12.
10
A new composite model including metabolic syndrome, alanine aminotransferase and cytokeratin-18 for the diagnosis of non-alcoholic steatohepatitis in morbidly obese patients.一种包含代谢综合征、丙氨酸氨基转移酶和细胞角蛋白-18 的新复合模型,用于诊断病态肥胖患者的非酒精性脂肪性肝炎。
Aliment Pharmacol Ther. 2010 Dec;32(11-12):1315-22. doi: 10.1111/j.1365-2036.2010.04480.x. Epub 2010 Oct 7.

非酒精性脂肪性肝病范围内非酒精性脂肪性肝炎和肝纤维化的无创诊断

Noninvasive Diagnosis of NASH and Liver Fibrosis Within the Spectrum of NAFLD.

作者信息

Alkhouri Naim, McCullough Arthur J

机构信息

Dr. Alkhouri and Dr. McCullough are affiliated with the Department of Gastroenterology and Hepatology and the Digestive Disease Institute at The Cleveland Clinic in Cleveland, Ohio.

出版信息

Gastroenterol Hepatol (N Y). 2012 Oct;8(10):661-8.

PMID:24683373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3969008/
Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most common type of chronic liver disease in the United States, affecting an estimated 70 million Americans. The histologic spectrum of NAFLD ranges from simple steatosis to nonalcoholic steatohepatitis (NASH), fibrosis, and eventually cirrhosis. Patients with NASH and significant fibrosis seen on liver biopsy have an increased risk for liver-related morbidity and mortality compared to patients with simple steatosis. Due to the high prevalence of NAFLD, there has been an urgent need to develop reliable noninvasive markers and tests that can accurately predict the presence of advanced disease without the need for liver biopsy. These tests can be divided into 2 groups: those that predict the presence of NASH (such as markers of hepatocyte apoptosis, oxidative stress, and inflammation, as well as predictive models based on clinical variables) and those that predict the presence of fibrosis (such as simple and complex predictive models). This paper provides an overview of various noninvasive methods for detecting NAFLD and suggests a diagnostic algorithm that can be used in clinical practice.

摘要

非酒精性脂肪性肝病(NAFLD)是美国最常见的慢性肝病类型,估计影响7000万美国人。NAFLD的组织学谱范围从单纯性脂肪变性到非酒精性脂肪性肝炎(NASH)、纤维化,最终发展为肝硬化。与单纯性脂肪变性患者相比,肝活检显示有NASH和显著纤维化的患者发生肝脏相关发病和死亡的风险增加。由于NAFLD的高患病率,迫切需要开发可靠的非侵入性标志物和检测方法,能够在无需肝活检的情况下准确预测晚期疾病的存在。这些检测方法可分为两类:一类预测NASH的存在(如肝细胞凋亡、氧化应激和炎症标志物,以及基于临床变量的预测模型),另一类预测纤维化的存在(如简单和复杂的预测模型)。本文概述了检测NAFLD的各种非侵入性方法,并提出了一种可用于临床实践的诊断算法。