These data, therefore, support the view and join the growing body of evidence suggesting that CVD may be the major cause of death among individuals with NAFLD. In our opinion, because FLI was also independently associated with cancer mortality regardless of hepatic-related mortality, we should not forgot

that these data also suggest a link between NAFLD and mortality due to malignancies, which was also reported in diabetic patients of the Olmsted County study (but only as a trend).21 In our opinion, it is important to emphasize that in our study, FLI was more reliable than the glucose tolerance status (based on the OGTT procedure), metabolic syndrome (based on the Adult Treatment Panel III definition), and aminotransferases. The pathogenesis of diabetes and NAFLD RO4929097 mouse are closely related to insulin resistance and hyperinsulinemia.22 Consequently, we wanted to determine whether the association of FLI with mortality rates was independent of a surrogate index of insulin resistance, HOMA-IR, which is based on the product of the fasting plasma insulin concentration and is frequently used in population studies.23 HOMA-IR has been reported to be associated with CVD mortality in several

population studies,24-27 and we observed that HOMA-IR was also associated with cancer mortality in the population of the Cremona study (G. Perseghin, MD, G. Calori, MD, G. Lattuada, PhD, F. Ragogna, PhD, E. Dugnani, PhD, M. P. Garancini, this website MD, P. Crosignani, MD, M. Villa, MD, E. Bosi, MD, G. Ruotolo, MD, L. Piemonti, MD, unpublished data, 2011). In this set of data, FLI maintained its independent association with hepatic-related mortality; this suggests a specificity of this index that goes beyond the potential effects of other metabolic variables expressed by HOMA-IR. In contrast, FLI did not retain an independent association with CVD and cancer mortality rates when HOMA-IR was included in the analysis. The surrogate marker of insulin resistance appeared to be more important MCE公司 than FLI, and this suggests the primacy of the systemic insulin-resistant state over the fatty liver, which is the hepatic component

of metabolic syndrome. We feel that it is very difficult to determine the roles of HOMA-IR and FLI; from a statistical point of view, the correlation between the two variables is considerable, and from a pathophysiological point of view, it is well known that NAFLD not only may be a marker of insulin resistance syndrome but also may be involved in its pathogenesis. In particular, it was hypothesized for CVD that the pathogenic process may be mediated through the systemic release of pro-atherogenic mediators from the inflamed liver to peripheral tissues. Following this line of thinking, we noticed that FLI was correlated with surrogate markers of low-grade inflammation, such as fibrinogen, high-sensitivity C-reactive protein, and tumor necrosis factor α soluble receptor II.