Adipokines and Pathogenesis of Non Alcoholic Fatty Liver Disease - Jarrar, Mohammed
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Non alcoholic fatty liver disease is the hepatic manifestation of metabolic syndrome that may progress from simple steatosis to nonalcoholic steatohepatitis, cirrhosis and hepatocellular carcinoma. Expansion of omental adipose is accompanied by alteration in profiles of adipocytokines that contribute to NAFLD through enhanced steatogenesis in the liver and its inflammation. Gene transcription studies demonstrated a prominent adipose-specific deregulation of the inflammation and immune system related genes in NASH. Serum levels of soluble adipokines and cytokines can reliably predict NASH in…mehr

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Produktbeschreibung
Non alcoholic fatty liver disease is the hepatic manifestation of metabolic syndrome that may progress from simple steatosis to nonalcoholic steatohepatitis, cirrhosis and hepatocellular carcinoma. Expansion of omental adipose is accompanied by alteration in profiles of adipocytokines that contribute to NAFLD through enhanced steatogenesis in the liver and its inflammation. Gene transcription studies demonstrated a prominent adipose-specific deregulation of the inflammation and immune system related genes in NASH. Serum levels of soluble adipokines and cytokines can reliably predict NASH in the cohort of morbidly obese patients. Histologic fibrosis in patients with NASH could be predicted by TNF-a level. There is also strong connection between the HCV genotype 3, steatosis and increases in IL-8 serum levels. HCV genotype specific differences in soluble cytokine concentrations may help to elucidate pathogenesis of HCV hepatitis and potential triggers for HCV-related steatosis. These results should be of interest to the researchers of the clinical and fundamental aspects of human metabolism, obesity, diabetes, and hepatitis C.
Autorenporträt
Jarrar Mohammed§Mohammed H. Jarrar, PhD,MT. Assistant Professor of Biosciences at Biology Department, George Mason University, RAK-UAE. Studied CRA at George Washington University, Biotechnology at Johns Hopkins and George Mason universities. Worked as CLS at Hopkins Pathology for 10 years and for 2 years as Senior Researcher at KKI, Baltimore, USA.