Plasma visfatin levels and gene expression in morbidly obese women with associated fatty liver disease

ObjectivesThe few studies on the physiopathological role of visfatin in morbid obesity and the related metabolic diseases have led us to examine visfatin levels and its liver gene expression in morbidly obese women with non-alcoholic fatty liver disease (NAFLD).Design and methodsWe examined the circulating levels of visfatin by ELISA in serum samples from 95 morbidly obese women (MO) (BMI > 40 kg/m2) who underwent bariatric surgery and 38 normal weight control women (BMI < 25 kg/m2). We analysed visfatin liver and adipose tissue mRNA expression by RT-PCR. We evaluated the circulating levels and gene expression of adiponectin, resistin, RBP4, TNFα, IL6 and CRP.ResultsSerum visfatin was significantly higher in MO compared with controls, and also in MO with NAFLD was significantly higher than MO with normal liver. We found that NAFLD diabetic patients presented similar serum visfatin levels than non-diabetic. Serum visfatin correlated with IL6 (r = 0.496; p < 0.001) and CRP levels (r = 0.241; p = 0.049).Liver visfatin expression was significantly higher in MO compared to controls and was also significantly higher in MO with NAFLD than in MO with normal liver. Visfatin liver expression correlated positively with resistin (r = 0.436, p = 0.018) and TNFα expression (r = 0.328, p = 0.028).Visfatin expression in adipose tissues was similar among the MO groups analysed.ConclusionSerum visfatin and its liver expression are higher in MO women with NAFLD, irrespective of the presence of diabetes. Serum visfatin and its liver expression correlate positively with pro-inflammatory factors. These findings suggest that visfatin may be a molecule related with fat inflammation in morbid obesity and fatty liver disease.

► Visfatin levels and liver expression in morbidly obese are higher than in lean women.
► Visfatin levels and liver expression are higher in NAFLD versus normal liver.
► Visfatin levels and liver expression correlates with pro-inflammatory adipocytokines.