Hepatic tumor necrosis factor-α, leptin and adiponectin expression in morbid obese patients: Clinicopathological correlations

被引:0
|
作者
Liew, Phui-Ly [2 ,3 ]
Chen, Chi-Long [4 ]
Lee, Yi-Chih [5 ]
Huang, Ming-Te [6 ]
Wang, Weu [7 ]
Lee, Wei-Jei [1 ]
机构
[1] Min Sheng Gen Hosp, Dept Surg, Taoyuan Hsien, Taiwan
[2] Taipei Med Univ, Shuang Ho Hosp, Dept Pathol, Taipei, Taiwan
[3] Taipei Med Univ, Coll Med, Grad Inst Clin Med, Taipei, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Dept Pathol, Taipei, Taiwan
[5] Ching Yun Univ, Dept Int Business, Jhongli, Taiwan
[6] Taipei Med Univ, Shuang Ho Hosp, Dept Surg, Div Gen Surg, Taipei, Taiwan
[7] Taipei Med Univ, Taipei Med Univ Hosp, Dept Surg, Div Gen Surg, Taipei, Taiwan
关键词
Hepatic adipocytokines; Clinicopathology; Morbid obesity; NONALCOHOLIC FATTY LIVER; INSULIN-RESISTANCE; SERUM LEPTIN; STEATOHEPATITIS; DISEASE; FIBROSIS; PATHOGENESIS; RECEPTORS; WEIGHT; NASH;
D O I
10.1016/j.orcp.2011.04.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Nonalcoholic fatty liver disease (NAFLD) is associated with obesity. We retrospectively studied the clinicopathology and different hepatic adipocytokine expressions between nonalcoholic steatohepatitis (NASH) and non-NASH in morbid obesity. Methods: We enrolled 40 patients undergoing liver biopsy during bariatric surgery. We analyzed hepatic mRNA and immunohistochemistry of TNF-alpha, leptin, adiponectin and adiponectin receptor. Results: Thirty patients (75%) presented with NASH, including 11 with mild fibrosis and 19 with advanced fibrosis. The HbA1c (P = 0.000), AST (P = 0.000), ALT (P = 0.000), GGT (P = 0.016) and liver fibrosis (P = 0.028) have statistically difference between NASH and non-NASH groups. Steatosis was the only significant factor (r = 0.348, P < 0.05) associated with TNF-alpha mRNA level. Adiponectin mRNA was inversely associated with C-peptide (r = -0.416, P < 0.05) and uric acid level (r = -0.426, P < 0.05). The best predictors for TNF-alpha immunostain were hemoglobin (r = 0.432, P < 0.01), AST (r = 0.371, P < 0.05), lobular inflammation (r = 0.315, P < 0.05), portal inflammation (r = 0.331, P < 0.05), and NAS (r = 0.365, P < 0.05). Leptin immunostain was correlated with C-peptide (r = 0.356, P < 0.05) and portal inflammation (r = 0.334, P < 0.05). The AdipoRII immunoexpression was negatively correlated with systolic blood pressure (r = -0.481, P < 0.01). Multivariate linear regressions of adipocytokine profile related mostly to age, gender, systolic blood pressure, serum uric acid, steatosis, NAS and portal inflammation. Conclusion: Although different adipocytokines may be associated with NAFLD progression in morbid obesity, their major correlations in the pathogenesis of obesity-related NASH are not clear. Additional confirmatory studies are deserved. (C) 2011 Asian Oceanian Association for the Study of Obesity. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:E55 / E62
页数:8
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