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1 Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany
2 Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany; Department of Gastroenterology, Hepatology, and Endocrinology, Charite Campus Mitte, Berlin, Germany
3 Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany; Center for Liver, Digestive and Metabolic Diseases, University of Groningen Medical Center, Groningen, The Netherlands
* To whom correspondence should be addressed. E-mail: u_tietge{at}yahoo.com.
The adipokine resistin has been implicated in obesity and insulin resistance. Liver cirrhosis is associated with decreased body fat mass and insulin resistance. We determined plasma resistin levels in 57 patients with cirrhosis, 13 after liver transplantation, and 30 controls, and correlated these with a variety of hemodynamic as well as hepatic and systemic metabolic parameters. Patients with cirrhosis had dependent on the clinical stage an overall 86% increase in resistin levels (p<0.001) with hepatic venous resistin being higher than arterial levels (p<0.001). Plasma resistin was significantly correlated with plasma TNF-
levels (r=0.62, p<0.001). No correlation was observed between resistin and hepatic hemodynamics, body fat mass, systemic energy metabolism, and the degree of insulin resistance. However, plasma resistin in cirrhosis was negatively associated with hepatic glucose production (r= -0.47, p<0.01), and positively with circulating free fatty acids (r=0.40, p<0.01) and ketone bodies (r=0.48, p<0.001) as well as hepatic ketone body production (r=0.40, p<0.01). After liver transplantation plasma resistin levels remained unchanged, while insulin resistance was significantly improved (p<0.01). These data provide novel insights into the role of resistin in the pathophysiological background of a catabolic disease in humans, and also indicate that resistin inhibition might not represent a suitable therapeutic strategy for the treatment of insulin resistance and diabetes in patients with liver cirrhosis.
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