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Systematic review with meta‐analysis: non‐invasive assessment of non‐alcoholic fatty liver disease – the role of transient elastography and plasma cytokeratin‐18 fragments

瞬态弹性成像 医学 脂肪性肝炎 脂肪肝 内科学 肝活检 纤维化 胃肠病学 人口 细胞角蛋白 疾病 病理 活检 免疫组织化学 环境卫生
作者
Raymond Kwok,Y K Tse,Grace Lai‐Hung Wong,Ye Jin Ha,A. U. Lee,M. C. Ngu,Henry Lik‐Yuen Chan,Vincent Wai‐Sun Wong
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:39 (3): 254-269 被引量:371
标识
DOI:10.1111/apt.12569
摘要

Summary Background Non‐alcoholic fatty liver disease ( NAFLD ) affects 15–40% of the general population. Some patients have non‐alcoholic steatohepatitis ( NASH ) and progressive fibrosis, and would be candidates for monitoring and treatment. Aim To review current literature on the use of non‐invasive tests to assess the severity of NAFLD . Methods Systematic literature searching identified studies evaluating non‐invasive tests of NASH and fibrosis using liver biopsy as the reference standard. Meta‐analysis was performed for areas with adequate number of publications. Results Serum tests and physical measurements like transient elastography ( TE ) have high negative predictive value (NPV) in excluding advanced fibrosis in NAFLD patients. The NAFLD fibrosis score comprises of six routine clinical parameters and has been endorsed by current American guidelines as a screening test to exclude low‐risk individuals. The pooled sensitivities and specificities for TE to diagnose F ≥ 2, F ≥ 3 and F4 disease were 79% and 75%, 85% and 85%, and 92% and 92% respectively. Liver stiffness measurement often fails in obese patients, but the success rate can be improved with the use of the XL probe. A number of biomarkers have been developed for the diagnosis of NASH , but few were independently validated. Serum/plasma cytokeratin‐18 fragments have been most extensively evaluated and have a pooled sensitivity of 66% and specificity of 82% in diagnosing NASH . Conclusions Current non‐invasive tests are accurate in excluding advanced fibrosis in NAFLD patients, and may be used for initial assessment. Further development and evaluation of NASH biomarkers are needed.

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