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十二指肠果糖载体葡萄糖转运蛋白-5 水平与非酒精性脂肪性肝病和肝纤维化的关系。

Association between higher duodenal levels of the fructose carrier glucose transporter-5 and nonalcoholic fatty liver disease and liver fibrosis.

机构信息

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

出版信息

J Intern Med. 2024 Feb;295(2):171-180. doi: 10.1111/joim.13729. Epub 2023 Oct 5.

Abstract

BACKGROUND

An increased dietary fructose intake has been shown to exert several detrimental metabolic effects and contribute to the pathogenesis of nonalcoholic fatty liver disease (NAFLD). An augmented intestinal abundance of the fructose carriers glucose transporter-5 (GLUT-5) and glucose transporter-2 (GLUT-2) has been found in subjects with obesity and type 2 diabetes. Herein, we investigated whether elevated intestinal levels of GLUT-5 and GLUT-2, resulting in a higher dietary fructose uptake, are associated with NAFLD and its severity.

METHODS

GLUT-5 and GLUT-2 protein levels were assessed on duodenal mucosa biopsies of 31 subjects divided into 2 groups based on ultrasound-defined NAFLD presence who underwent an upper gastrointestinal endoscopy.

RESULTS

Individuals with NAFLD exhibited increased duodenal GLUT-5 protein levels in comparison to those without NAFLD, independently of demographic and anthropometric confounders. Conversely, no difference in duodenal GLUT-2 abundance was observed amongst the two groups. Univariate correlation analyses showed that GLUT-5 protein levels were positively related with body mass index, waist circumference, fasting and 2 h post-load insulin concentrations, and insulin resistance (IR) degree estimated by homeostatic model assessment of IR (r = 0.44; p = 0.02) and liver IR (r = 0.46; p = 0.03) indexes. Furthermore, a positive relationship was observed between duodenal GLUT-5 abundance and serum uric acid concentrations (r = 0.40; p = 0.05), a product of fructose metabolism implicated in NAFLD progression. Importantly, duodenal levels of GLUT-5 were positively associated with liver fibrosis risk estimated by NAFLD fibrosis score.

CONCLUSION

Increased duodenal GLUT-5 levels are associated with NAFLD and liver fibrosis. Inhibition of intestinal GLUT-5-mediated fructose uptake may represent a strategy for prevention and treatment of NAFLD.

摘要

背景

研究表明,增加饮食中的果糖摄入量会产生多种有害的代谢作用,并导致非酒精性脂肪性肝病(NAFLD)的发病机制。在肥胖症和 2 型糖尿病患者中,发现肠道中果糖载体葡萄糖转运蛋白-5(GLUT-5)和葡萄糖转运蛋白-2(GLUT-2)的丰度增加。在此,我们研究了肠道中 GLUT-5 和 GLUT-2 水平升高,导致更高的饮食果糖摄取量是否与 NAFLD 及其严重程度相关。

方法

根据超声定义的 NAFLD 存在情况,将 31 名接受上消化道内镜检查的受试者分为 2 组,评估十二指肠黏膜活检中的 GLUT-5 和 GLUT-2 蛋白水平。

结果

与无 NAFLD 的受试者相比,患有 NAFLD 的个体的十二指肠 GLUT-5 蛋白水平升高,独立于人口统计学和人体测量学混杂因素。相反,两组之间十二指肠 GLUT-2 丰度没有差异。单变量相关分析显示,GLUT-5 蛋白水平与体重指数、腰围、空腹和 2 小时负荷后胰岛素浓度以及通过稳态模型评估的胰岛素抵抗(IR)程度(r=0.44;p=0.02)和肝 IR(r=0.46;p=0.03)指数相关。此外,还观察到十二指肠 GLUT-5 丰度与血清尿酸浓度呈正相关(r=0.40;p=0.05),尿酸是一种与 NAFLD 进展有关的果糖代谢产物。重要的是,十二指肠 GLUT-5 水平与通过 NAFLD 纤维化评分估计的肝纤维化风险呈正相关。

结论

十二指肠 GLUT-5 水平升高与 NAFLD 和肝纤维化有关。抑制肠道 GLUT-5 介导的果糖摄取可能是预防和治疗 NAFLD 的一种策略。

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