Yakaryilmaz Fahri, Guliter Sefa, Ozenirler Seren, Erdem Ozlem, Akyol Gulen
Departments of Gastroenterology, Gazi University School of Medicine, Ankara, Turkey.
Pathology, Gazi University School of Medicine, Ankara, Turkey.
Curr Ther Res Clin Exp. 2004 May;65(3):266-77. doi: 10.1016/S0011-393X(04)80077-8.
Free radicals have a pivotal role in the pathogenesis of nonalcoholic steatohepatitis (NASH). Decreasing oxidative stress might have beneficial effects on the biochemical and histologic progression of this disease.
We aimed to determine the therapeutic effect of vitamin E, a potent antioxidant, on liver enzymes and histology in NASH.
This 6-month, open-label study was conducted at the Departments of Gastroenterology and Pathology, Gazi University School of Medicine (Ankara, Turkey). Patients aged 18 to 70 years with biopsy-proven NASH were included in the study. All patients received vitamin E 800 U/d in 2 divided doses, orally (capsules) for 6 months. Patients were not advised to change their exercise or dietary habits. Body mass index (BMI) was calculated at months 0 (baseline) and 6. Histologic scoring of steatosis, necroinflammatory grade, and fibrosis stage was performed at 0 and 6 months. Liver enzyme activities (alanine aminotransferase [ALT], aspartate aminotransferase [AST], alkaline phosphatase [ALP], and gamma-glutamyltransferase [GGT]) were monitored monthly. Control biopsy specimens were obtained at the end of the treatment. All of the liver biopsies were read by a single pathologist (G.A.) who was blinded to the clinical, laboratory, and histopathologic data, as well as the sequence of liver biopsies. Assessments of compliance and tolerability of treatment were performed using a pill count and patient interview, respectively, at the end of each month.
Sixteen patients (12 men, 4 women; mean [SD] age, 45.5 [6.9] years [range, 37-60 years]) were enrolled. All patients completed 6 months of treatment. Mean BMI did not change significantly from baseline. Significant improvements in mean (SD) serum liver enzyme activities were observed at 6 months compared with baseline (ALT: 38.6 [16.3] U/L vs 84.8 [22.1] U/L, respectively, P = 0.001; AST: 29.8 [15.4] U/L vs 46.0 [16.0] U/L, respectively, P = 0.001; ALP: 154.6 [64.1] U/L vs 211.5 [70.4] U/L, respectively, P= 0.011; and GGT: 49.8 [38.5] U/L vs 64.7 [54.4] U/L, respectively, P = 0.002), as well as in total cholesterol level (176.2 [42.0] mg/dL vs 199.6 [60.6] mg/dL; P = 0.02). Posttreatment liver biopsy was available in 13 patients (81%). Significant improvements in the mean (SD) scores of steatosis (1.46 [0.66] vs 2.43 [0.62]; P = 0.002) and necroinflammatory grade (0.84 [0.24] vs 1.31 [0.51]; P= 0.006) were observed at 6 months compared with baseline, respectively. However, no significant change was noted in the mean (SD) score of fibrosis stage (0.77 [0.33] vs 1.12 [0.59], respectively). None of the patients reported any adverse effects.
In this small, 6-month, open-label study, vitamin E treatment was safe and well tolerated and led to potential biochemical and histologic improvements (except in fibrosis) in patients with NASH.
自由基在非酒精性脂肪性肝炎(NASH)的发病机制中起关键作用。降低氧化应激可能对该疾病的生化和组织学进展产生有益影响。
我们旨在确定强效抗氧化剂维生素E对NASH患者肝脏酶和组织学的治疗效果。
这项为期6个月的开放标签研究在加齐大学医学院(土耳其安卡拉)胃肠病学和病理学系进行。纳入年龄在18至70岁之间、经活检证实为NASH的患者。所有患者口服维生素E 800 U/d,分2次服用(胶囊),持续6个月。未建议患者改变其运动或饮食习惯。在第0个月(基线)和第6个月计算体重指数(BMI)。在第0个月和第6个月对脂肪变性、坏死性炎症分级和纤维化阶段进行组织学评分。每月监测肝脏酶活性(丙氨酸氨基转移酶[ALT]、天冬氨酸氨基转移酶[AST]、碱性磷酸酶[ALP]和γ-谷氨酰转移酶[GGT])。在治疗结束时获取对照活检标本。所有肝脏活检均由一位病理学家(G.A.)阅读,该病理学家对临床、实验室和组织病理学数据以及肝脏活检顺序均不知情。分别在每个月结束时通过药丸计数和患者访谈对治疗的依从性和耐受性进行评估。
纳入16例患者(12例男性,4例女性;平均[标准差]年龄为45.5[6.9]岁[范围37 - 60岁])。所有患者均完成了6个月的治疗。平均BMI与基线相比无显著变化。与基线相比,在6个月时观察到平均(标准差)血清肝脏酶活性有显著改善(ALT:分别为38.6[16.3]U/L和84.8[22.1]U/L,P = 0.001;AST:分别为29.8[15.4]U/L和46.0[16.0]U/L,P = 0.001;ALP:分别为154.6[64.1]U/L和211.5[70.4]U/L,P = 0.011;GGT:分别为49.8[38.5]U/L和64.7[54.4]U/L,P = 0.002),总胆固醇水平也有显著改善(176.2[42.0]mg/dL和199.6[60.6]mg/dL;P = 0.02)。13例患者(81%)有治疗后的肝脏活检结果。与基线相比,在6个月时观察到脂肪变性平均(标准差)评分(1.46[0.66]对2.43[0.62];P = 0.002)和坏死性炎症分级平均(标准差)评分(0.84[0.24]对1.31[0.51];P = 0.006)有显著改善。然而,纤维化阶段平均(标准差)评分无显著变化(分别为0.77[0.33]和1.12[0.59])。没有患者报告任何不良反应。
在这项小型、为期6个月的开放标签研究中,维生素E治疗安全且耐受性良好,并使NASH患者在生化和组织学方面(纤维化除外)有潜在改善。