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World journal of gastroenterology : WJG, 2013-11, Vol.19 (41), p.6969-6978
2013
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Autor(en) / Beteiligte
Titel
PNPLA3 I148M polymorphism and progressive liver disease
Ist Teil von
  • World journal of gastroenterology : WJG, 2013-11, Vol.19 (41), p.6969-6978
Ort / Verlag
United States: Baishideng Publishing Group Co., Limited
Erscheinungsjahr
2013
Quelle
MEDLINE
Beschreibungen/Notizen
  • The 148 Isoleucine to Methionine protein variant (I148M) of patatin-like phospholipase domain-containing 3 (PNPLA3), a protein is expressed in the liver and is involved in lipid metabolism, has recently been identified as a major determinant of liver fat content. Several studies confirmed that the I148M variant predisposes towards the full spectrum of liver damage associated with fatty liver: from simple steatosis to steatohepatitis and progressive fibrosis. Furthermore, the I148M variant represents a major determinant of progression of alcohol related steatohepatitis to cirrhosis, and to influence fibrogenesis and related clinical outcomes in chronic hepatitis C virus hepatitis, and possibly chronic hepatitis B virus hepatitis, hereditary hemochromatosis and primary sclerosing cholangitis. All in all, studies suggest that the I148M polymorphism may represent a general modifier of fibrogenesis in liver diseases. Remarkably, the effect of the I148M variant on fibrosis was independent of that on hepatic steatosis and inflammation, suggesting that it may affect both the quantity and quality of hepatic lipids and the biology of non-parenchymal liver cells besides hepatocytes, directly promoting fibrogenesis. Therefore, PNPLA3 is a key player in liver disease progression. Assessment of the I148M polymorphism will possibly inform clinical practice in the future, whereas the determination of the effect of the 148M variant will reveal mechanisms involved in hepatic fibrogenesis.
Sprache
Englisch
Identifikatoren
ISSN: 1007-9327
eISSN: 2219-2840
DOI: 10.3748/wjg.v19.i41.6969
Titel-ID: cdi_swepub_primary_oai_gup_ub_gu_se_189278
Format
Schlagworte
Alcoholic liver disease, B-VIRUS INFECTION, Carcinoma, Hepatocellular, Cholangitis, Sclerosing - enzymology, Cholangitis, Sclerosing - genetics, Cholangitis, Sclerosing - pathology, Chronic hepatitis C virus hepatitis, CHRONIC HEPATITIS-C, Disease Progression, DOMAIN-CONTAINING 3, FATTY LIVER, Fatty Liver - complications, Fatty Liver - enzymology, Fatty Liver - genetics, Fatty Liver - pathology, Fatty Liver, Alcoholic - complications, Fatty Liver, Alcoholic - enzymology, Fatty Liver, Alcoholic - genetics, Fatty Liver, Alcoholic - pathology, Fibrogenesis, Gastroenterologi, Gastroenterology and Hepatology, Genetic Predisposition to Disease, GENETIC VARIANT, Genetics, GENOME-WIDE ASSOCIATION, GREATER-THAN-G, Hemochromatosis - enzymology, Hemochromatosis - genetics, Hemochromatosis - pathology, Hepatitis B, Chronic - enzymology, Hepatitis B, Chronic - genetics, Hepatitis B, Chronic - pathology, Hepatitis C, Chronic - complications, Hepatitis C, Chronic - enzymology, Hepatitis C, Chronic - genetics, Hepatitis C, Chronic - pathology, Hepatocellular, HEPATOCELLULAR-CARCINOMA, Humans, INSULIN-RESISTANCE, Lipase - genetics, Liver Cirrhosis - enzymology, Liver Cirrhosis - genetics, Liver Cirrhosis - pathology, Liver Cirrhosis, Alcoholic - enzymology, Liver Cirrhosis, Alcoholic - genetics, Liver Cirrhosis, Alcoholic - pathology, Liver Neoplasms - enzymology, Liver Neoplasms - genetics, Liver Neoplasms - pathology, Membrane Proteins - genetics, Non-alcoholic Fatty Liver Disease, NONALCOHOLIC STEATOHEPATITIS, Phenotype, Polymorphism, Genetic, Review, Risk Factors

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