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首页> 外文期刊>European journal of gastroenterology and hepatology >How adiponectin, leptin, and ghrelin orchestrate together and correlate with the severity of nonalcoholic fatty liver disease
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How adiponectin, leptin, and ghrelin orchestrate together and correlate with the severity of nonalcoholic fatty liver disease

机译:脂联素,瘦素和生长素释放肽如何协调并与非酒精性脂肪肝疾病的严重程度相关

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摘要

BACKGROUND: Adipose tissue contributes to nonalcoholic fatty liver disease (NAFLD), being a source of fatty acids and cytokines such as leptin and adiponectin, and regulating ghrelin production. Their role in NAFLD pathogenesis remains controversial. We aimed to study the influence of those cytokines on the severity of NAFLD. METHODS: Morbidly obese individuals with biopsy-proven NAFLD were recruited. The NAFLD activity score was applied to liver histology. Serum concentrations of adiponectin, leptin, and ghrelin were determined. RESULTS: Eighty-two patients were included, 13% with nonalcoholic steatohepatitis (NASH). Hypertriglyceridemia (P=0.018) and metabolic syndrome (P=0.040) were independent factors associated with NASH. Leptin associated positively and ghrelin associated negatively with BMI; adiponectin associated negatively with the waist to hip ratio. Adiponectin associated negatively with insulin resistance, hypertension, and metabolic syndrome; ghrelin associated positively with diabetes mellitus. Adiponectin below 23 ng/ml associated with NASH (odds ratio 12.95, P<0.001). Leptin increased progressively (P=0.032) and adiponectin decreased (P=0.004) with increasing severity of steatosis. Also, leptin increased progressively with more severe fibrosis (P=0.053). A formula incorporating the three cytokines yielded an AUROC of 0.789 (P=0.002), a sensitivity of 81.8%, and a specificity of 76.1% for NASH. CONCLUSION: An imbalance in adiponectin, leptin, and ghrelin seems to be associated with more severe NAFLD. A formula combining the three cytokines showed good accuracy for NASH.
机译:背景:脂肪组织是非酒精性脂肪肝疾病(NAFLD)的来源,是脂肪酸和细胞因子(如瘦素和脂联素)的来源,并调节ghrelin的产生。它们在NAFLD发病机理中的作用仍存在争议。我们旨在研究这些细胞因子对NAFLD严重程度的影响。方法:招募经活检证实为NAFLD的病态肥胖个体。将NAFLD活性评分应用于肝脏组织学。测定血清脂联素,瘦素和生长素释放肽的浓度。结果:包括82例患者,其中13%患有非酒精性脂肪性肝炎(NASH)。高甘油三酯血症(P = 0.018)和代谢综合征(P = 0.040)是与NASH相关的独立因素。瘦素与BMI呈正相关,而生长素释放肽与BMI呈负相关。脂联素与腰臀比负相关。脂联素与胰岛素抵抗,高血压和代谢综合征呈负相关; ghrelin与糖尿病呈正相关。脂联素低于23 ng / ml与NASH相关(比值比为12.95,P <0.001)。随着脂肪变性严重程度的增加,瘦素逐渐增加(P = 0.032),脂联素减少(P = 0.004)。同样,随着更严重的纤维化,瘦素逐渐增加(P = 0.053)。包含这三种细胞因子的配方产生的AUROC为0.789(P = 0.002),对NASH的敏感性为81.8%,特异性为76.1%。结论:脂联素,瘦素和生长素释放肽的失衡似乎与更严重的NAFLD有关。结合了三种细胞因子的公式显示了NASH的良好准确性。

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