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Vitamin E reduces liver stiffness in nonalcoholic fatty liver disease 被引量:1
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作者 Aiko Fukui Naoto Kawabe +10 位作者 Senju Hashimoto Michihito Murao Takuji Nakano Hiroaki Shimazaki Toshiki Kan Kazunori Nakaoka Masashi Ohki Yuka Takagawa Tomoki Takamura Hiroyuki Kamei Kentaro Yoshioka 《World Journal of Hepatology》 CAS 2015年第27期2749-2756,共8页
AIM: To evaluate the efficacy of vitamin E treatment on liver stiffness in nonalcoholic fatty liver disease(NAFLD).METHODS: Thirty-eight NAFLD patients were administered vitamin E for > 1 year. The doses of vitamin... AIM: To evaluate the efficacy of vitamin E treatment on liver stiffness in nonalcoholic fatty liver disease(NAFLD).METHODS: Thirty-eight NAFLD patients were administered vitamin E for > 1 year. The doses of vitamin E were 150, 300, or 600 mg; three times per day after each meal. Responses were assessed by liver enzyme levels [aspartate aminotransferase(AST), alanine aminotranferease(ALT), and γ-glutamyl transpeptidase(γ-GTP)], noninvasive scoring systems of hepatic fibrosis-4 [FIB-4 index and aspartate aminotransferaseto-platelet index(APRI)], and liver stiffness [velocity of shear wave(Vs)] measured by acoustic radiation force impulse elastography. Vs measurements were performed at baseline and 12 mo after baseline. The patients were genotyped for the patatin-like phospholipase domain containing 3(PNPLA3) polymorphisms and then divided into either the CC/CG or GG group to examine each group's responses to vitamin E treatment. RESULTS: We found marked differences in the platelet count, serum albumin levels, alkaline phosphatase levels, FIB-4 index, APRI, and Vs at baseline depending on the PNPLA3 polymorphism. AST, ALT, and γ-GTP levels(all P < 0.001); FIB-4 index(P = 0.035); APRI(P < 0.001); and Vs(P < 0.001) significantly decreased from baseline to 12 mo in the analysis of all patients. In the subset analyses of PNPLA3 genotypes, AST levels(P = 0.011), ALT levels(P < 0.001), γ-GTP levels(P = 0.005), APRI(P = 0.036), and Vs(P = 0.029) in genotype GG patients significantly improved, and AST and ALT levels(both P < 0.001), γ-GTP levels(P = 0.003), FIB-4 index(P = 0.017), and APRI(P < 0.001) in genotype CC/CG patients. CONCLUSION: One year of vitamin E treatment improved noninvasive fibrosis scores and liver stiffness in NAFLD patients. The responses were similar between different PNPLA3 genotypes. 展开更多
关键词 VITAMIN E ACOUSTIC RADIATION FORCE IMPULSE nonalco
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肠道微生物在非酒精性脂肪性肝病发病中的作用 被引量:3
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作者 卢伟娜 冯丽英 《世界华人消化杂志》 CAS 北大核心 2014年第3期340-344,共5页
肝脏和肠道不仅解剖学上而且在生物学功能上存在密切联系,即所谓"肠-肝轴"学说,其对某些疾病的影响越来越受到关注,其中肠道菌群在维持肠-肝轴的平衡方面起着重要作用.肠道菌群紊乱、肠道黏膜通透性改变、肠源性内毒素血症,... 肝脏和肠道不仅解剖学上而且在生物学功能上存在密切联系,即所谓"肠-肝轴"学说,其对某些疾病的影响越来越受到关注,其中肠道菌群在维持肠-肝轴的平衡方面起着重要作用.肠道菌群紊乱、肠道黏膜通透性改变、肠源性内毒素血症,这将破坏肝脏与肠道之间的正常关系进而导致多种肝脏疾病的发生,进而调整肠微生物成为一种治疗或预防慢性肝病的新手段.有研究表明其在非酒精性脂肪性肝病(nonalcoholic fatty liver disease,NAFLD)的发生发展中起到了重要作用,这里就肠道微生物对NAFLD的作用做一综述. 展开更多
关键词 肠道微生物 肠-肝轴 非酒精性脂肪性肝病 益生菌
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LPS/TLR4信号途径在非酒精性脂肪性肝病中的作用 被引量:6
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作者 殷小磊 卢伟娜 冯丽英 《世界华人消化杂志》 CAS 北大核心 2013年第28期2957-2962,共6页
脂多糖(lipopolysaccharide,LPS)/Toll样受体4(Toll-like receptor 4,TLR4)信号途径参与非酒精性脂肪性肝病的发生发展,非酒精性脂肪性肝病肝脏中LPS受体TLR4表达上调,诱导炎症反应,促使肝细胞损伤.非酒精性脂肪性肝病时肠道菌群失调,LP... 脂多糖(lipopolysaccharide,LPS)/Toll样受体4(Toll-like receptor 4,TLR4)信号途径参与非酒精性脂肪性肝病的发生发展,非酒精性脂肪性肝病肝脏中LPS受体TLR4表达上调,诱导炎症反应,促使肝细胞损伤.非酒精性脂肪性肝病时肠道菌群失调,LPS产生增多,肠壁通透性增强,形成肠源性内毒素血症,LPS上调Kupffer细胞TLR4的表达,分别通过MyD88-依赖途径和MyD88-不依赖途径,最终激活核因子B,诱导强力的炎症反应,从而介导肝损伤.本文就LPS/TLR4信号途径的构成、调节方式及与非酒精性脂肪性肝病的关系做一综述. 展开更多
关键词 LPS TLR4信号途径 非酒精性脂肪性肝病 KUPFFER细胞 肝损伤
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