Characteristics and diagnosis of NAFLD/NASH
- PMID: 24251707
- DOI: 10.1111/jgh.12271
Characteristics and diagnosis of NAFLD/NASH
Abstract
Non-alcoholic fatty liver disease (NAFLD) is considered to be a hepatic manifestation of metabolic syndrome. NAFLD has become an important public health issue because of its high prevalence. NAFLD consists of two clinicopathological entities: simple steatosis, which generally follows a benign non-progressive clinical course, and non-alcoholic steatohepatitis (NASH), which may progress to cirrhosis and hepatocellular carcinoma. The diagnosis of NAFLD is based on the following three criteria: non-alcoholic, detection of steatosis either by imaging or by histology, and appropriate exclusion of other liver diseases. Alcoholic liver disease can occur when daily alcohol consumption exceeds 20 g in women or 30 g in men. Thus, non-alcoholic indicates lower levels of these alcohol consumptions. However, there is still no clear consensus regarding the threshold alcohol consumption for defining non-alcoholic liver disease. Then, there is the strong recommendation for a change in the nomenclature, such as use of the term metabolic fatty liver and metabolic steatohepatitis. NASH has emerged as a clinicopathological entity, and even now, a liver biopsy remains the gold standard for making a definitive diagnosis. However, liver biopsy has several drawbacks. In general practice, NAFLD is a convenient-to-use term for the diagnosis and management of these patients, and serum biomarkers that indicate the severity of fibrosis serve as clinically useful tools for the identification of NAFLD in patients with bridging fibrosis or cirrhosis. In the future, improved understanding of the pathogenesis of NASH and new technologies may contribute to the diagnostic process and provide reliable, non-invasive alternatives to liver biopsy.
Keywords: diagnosis; non-alcoholic fatty liver diseases (NAFLD); non-alcoholic steatohepatitis (NASH).
© 2013 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.
Similar articles
-
[Diagnostic criteria for non-alcoholic steatohepatitis].Nihon Rinsho. 2006 Jun;64(6):1025-32. Nihon Rinsho. 2006. PMID: 16768105 Review. Japanese.
-
Hepatocarcinogenesis in non-alcoholic fatty liver disease in Japan.J Gastroenterol Hepatol. 2013 Dec;28 Suppl 4:88-92. doi: 10.1111/jgh.12239. J Gastroenterol Hepatol. 2013. PMID: 24251711 Review.
-
Metabolic disturbances in non-alcoholic fatty liver disease.Clin Sci (Lond). 2009 Apr;116(7):539-64. doi: 10.1042/CS20080253. Clin Sci (Lond). 2009. PMID: 19243311 Review.
-
[Non-alcoholic fatty liver disease--new view].Pol Merkur Lekarski. 2008 Jun;24(144):568-71. Pol Merkur Lekarski. 2008. PMID: 18702346 Review. Polish.
-
Non-alcoholic steatohepatitis in children.Pediatr Transplant. 2004 Dec;8(6):613-8. doi: 10.1111/j.1399-3046.2004.00241.x. Pediatr Transplant. 2004. PMID: 15598336 Review.
Cited by
-
Antifibrotic Effects of the Dual CCR2/CCR5 Antagonist Cenicriviroc in Animal Models of Liver and Kidney Fibrosis.PLoS One. 2016 Jun 27;11(6):e0158156. doi: 10.1371/journal.pone.0158156. eCollection 2016. PLoS One. 2016. PMID: 27347680 Free PMC article.
-
Tetrahydroxanthohumol, a xanthohumol derivative, attenuates high-fat diet-induced hepatic steatosis by antagonizing PPARγ.Elife. 2021 Jun 15;10:e66398. doi: 10.7554/eLife.66398. Elife. 2021. PMID: 34128467 Free PMC article.
-
Study on the independent effect of thyroid hormone based on uric acid level on NAFLD.J Health Popul Nutr. 2021 May 3;40(1):21. doi: 10.1186/s41043-021-00247-w. J Health Popul Nutr. 2021. PMID: 33941292 Free PMC article.
-
Comparison of hepatic steatosis index as noninvasive diagnostic tool and liver ultrasound for non-alcoholic steatosis in the adult population.Gastroenterol Hepatol Bed Bench. 2022;15(4):360-365. doi: 10.22037/ghfbb.v15i4.2480. Gastroenterol Hepatol Bed Bench. 2022. PMID: 36762218 Free PMC article.
-
Relationship between obstructive lung disease and non-alcoholic fatty liver disease in the Korean population: Korea National Health and Nutrition Examination Survey, 2007-2010.Int J Chron Obstruct Pulmon Dis. 2018 Aug 28;13:2603-2611. doi: 10.2147/COPD.S166902. eCollection 2018. Int J Chron Obstruct Pulmon Dis. 2018. PMID: 30214178 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources