Department of Pediatrics, San Paolo Hospital, University of Milan, Milan, Italy.
Department of Health Sciences, University of Milan, Milan, Italy.
J Transl Med. 2015 Apr 2;13:109. doi: 10.1186/s12967-015-0471-7.
Non-alcoholic fatty liver disease represents the most common chronic liver disease in obese children of industrialized countries. Nowadays the first line of treatment of pediatric non-alcoholic fatty liver disease is based on dietary and lifestyle intervention; however compliance to these interventions is very difficult to maintain in long term period. This editorial discusses about docosahexaenoic acid treatment as possible novel approach for non-alcoholic fatty liver disease in obese children. Docosahexaenoic acid may modulate the inflammatory response, improve insulin sensitivity and could be effective in enhancing intestinal barrier integrity, essential to protect a healthy gut-liver axis. Indeed alteration of gut microbiota composition and increased intestinal permeability may rise the exposure of liver to gut-derived bacterial products, causing activation of signalling pathways implicated in liver inflammation and fibrogenesis. This mechanism has been observed in vitro and animal models of non-alcoholic fatty liver disease but also in a clinical study in adults. While evidence suggests that n-3 long-chain polyunsaturated fatty acids supplementation may decrease liver fat in adults, in pediatric population only a study examined this topic. In obese children with non-alcoholic fatty liver disease well designed randomized controlled trials are needed to better clarify the possible efficacy of docosahexaenoic acid treatment, and underlying mechanisms, to identify the optimal required dose and to evaluate if the docosahexaenoic acid effect is limited to the duration of the treatment or it may continue after the end of treatment.
非酒精性脂肪性肝病是工业化国家肥胖儿童中最常见的慢性肝病。如今,儿科非酒精性脂肪性肝病的一线治疗方法基于饮食和生活方式干预;然而,长期坚持这些干预措施非常困难。这篇社论讨论了二十二碳六烯酸(DHA)治疗肥胖儿童非酒精性脂肪性肝病的可能性。二十二碳六烯酸可能调节炎症反应,改善胰岛素敏感性,并可能有效增强肠道屏障完整性,这对于保护健康的肠道-肝脏轴至关重要。事实上,肠道微生物群组成的改变和肠道通透性的增加可能会增加肝脏对肠道来源的细菌产物的暴露,从而导致涉及肝脏炎症和纤维化的信号通路的激活。这种机制在非酒精性脂肪性肝病的体外和动物模型中观察到,也在成人的临床研究中观察到。虽然有证据表明 n-3 长链多不饱和脂肪酸补充可能会减少成年人的肝脏脂肪,但在儿科人群中,只有一项研究对此进行了研究。在患有非酒精性脂肪性肝病的肥胖儿童中,需要进行精心设计的随机对照试验,以更好地阐明二十二碳六烯酸治疗的可能疗效及其潜在机制,确定最佳所需剂量,并评估二十二碳六烯酸的作用是否仅限于治疗期间,还是在治疗结束后仍会继续。