氧化应激和胰岛素抵抗在非酒精性脂肪肝疾病严重程度中的作用

Emine Köroğlu, Billur Canbakan, Kadri Atay, İbrahim Hatemi, Murat Tuncer, Ahmet Dobrucalı, Abdullah Sonsuz, Ilhami Gültepe, Hakan Şentürk
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Malondialdehyde (MDA) and superoxide dismutase (SOD) activities were measured in tissue and serum specimens. Glutathione (GH) was measured in tissue homogenates. Nitric oxide (NO), vitamin E and C levels were measured in serum. RESULTS Patients with IR had significantly higher tissue MDA levels (p=0.001) and significantly decreased tissue SOD and GH levels (p=0.001 and 0.002, respectively) than those without IR. The steatosis grade, necroinflammatory grade and stage were significantly higher in patients with IR (p=0.035, 0.003 and 0.001, respectively). HOMA IR significantly correlated with the necroinflammatory grade, stage, tissue MDA, SOD and GH (p=0.013, 0.001, 0.008, 0.001 and 0.001, respectively). Serum MDA (β=1.88, p=0.002), serum SOD (β=0.57, p=0.006), tissue MDA (β=0.22, p=0.006), tissue SOD (β=1.48, p=0.071) and stage (β=2.81, p=0.003) were independently associated with increased HOMA IR. 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引用次数: 45

摘要

背景/目的:氧化应激和胰岛素抵抗(IR)是非酒精性脂肪性肝病(NAFLD)发病的主要因素。本研究的目的是发现有或无胰岛素抵抗(IR)的NAFLD患者氧化应激参数与组织病理学结果之间的关系。材料与方法:对32例无酒精摄入且活检证实诊断为NAFLD的患者进行研究(男/女:17/15;平均年龄(46.5±11.4岁)。21例NAFLD合并IR患者与11例非IR患者进行比较。测定空腹胰岛素水平,采用稳态模型评估法(HOMA)计算胰岛素抵抗指数。测定组织和血清中丙二醛(MDA)和超氧化物歧化酶(SOD)的活性。在组织匀浆中测定谷胱甘肽(GH)。测定血清一氧化氮(NO)、维生素E和C水平。结果:IR患者组织MDA水平显著高于未IR患者(p=0.001),组织SOD和GH水平显著低于未IR患者(p=0.001和0.002)。IR患者的脂肪变性分级、坏死炎症分级和分期明显高于IR患者(p分别为0.035、0.003和0.001)。HOMA IR与坏死炎症分级、分期、组织MDA、SOD、GH显著相关(p分别为0.013、0.001、0.008、0.001、0.001)。血清MDA (β=1.88, p=0.002)、血清SOD (β=0.57, p=0.006)、组织MDA (β=0.22, p=0.006)、组织SOD (β=1.48, p=0.071)和分期(β=2.81, p=0.003)与HOMA IR升高独立相关。MDA升高[OR: 1.51;95% ci: (1.03-2.22);p=0.034]是非酒精性脂肪性肝炎(NASH)的危险因素,SOD活性升高对NASH具有预防作用[OR: 0.008;95% ci: (0.001-0.98);p = 0.04)。结论:NAFLD患者胰岛素抵抗与氧化应激增强有关。组织病理学疾病严重程度与氧化应激参数显著相关。这些数据表明伴有IR的NAFLD患者可能会增加疾病进展的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of oxidative stress and insulin resistance in disease severity of non-alcoholic fatty liver disease.
BACKGROUND/AIMS Oxidative stress and insulin resistance (IR) are major contributors in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). The purpose of this study was to find the relation between oxidative stress parameters and histopathological findings in NAFLD patients with and without insulin resistance (IR). MATERIALS AND METHODS Thirty-two patients with no alcohol intake and biopsy-proven diagnosis of NAFLD were studied (M/F: 17/15; mean age 46.5±11.4 years). Twenty-one NAFLD patients with IR were compared with 11 patients without IR. The fasting insulin level was measured, and the insulin resistance index was calculated using the homeostasis model assessment (HOMA) method. Malondialdehyde (MDA) and superoxide dismutase (SOD) activities were measured in tissue and serum specimens. Glutathione (GH) was measured in tissue homogenates. Nitric oxide (NO), vitamin E and C levels were measured in serum. RESULTS Patients with IR had significantly higher tissue MDA levels (p=0.001) and significantly decreased tissue SOD and GH levels (p=0.001 and 0.002, respectively) than those without IR. The steatosis grade, necroinflammatory grade and stage were significantly higher in patients with IR (p=0.035, 0.003 and 0.001, respectively). HOMA IR significantly correlated with the necroinflammatory grade, stage, tissue MDA, SOD and GH (p=0.013, 0.001, 0.008, 0.001 and 0.001, respectively). Serum MDA (β=1.88, p=0.002), serum SOD (β=0.57, p=0.006), tissue MDA (β=0.22, p=0.006), tissue SOD (β=1.48, p=0.071) and stage (β=2.81, p=0.003) were independently associated with increased HOMA IR. Increased MDA [OR: 1.51; 95% CI: (1.03-2.22); p=0.034] was a risk factor for non-alcoholic steatohepatitis (NASH), and increased SOD activity had a preventive effect against NASH [OR: 0.008; 95% CI: (0.001-0.98); p=0.04]. CONCLUSION This study shows that insulin resistance in NAFLD correlates with enhanced oxidative stress. Histopathological disease severity significantly correlated with oxidative stress parameters. These data show that NAFLD patients with IR may have increased risk for disease progression.
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