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儿科非酒精性脂肪性肝病的治疗选择:现状和未来方向。

Therapeutic options in pediatric non alcoholic fatty liver disease: current status and future directions.

机构信息

Medical School of the University of Salerno, Salerno, Italy.

出版信息

Ital J Pediatr. 2012 Oct 17;38:55. doi: 10.1186/1824-7288-38-55.

Abstract

The epidemics of overweight and obesity has resulted in a significant increase of non alcoholic fatty liver disease (NAFLD), a potentially progressive condition. Currently, obesity related hepatopathy represents therefore the main cause of pediatric chronic liver disease. The first choice treatment at all ages is weight loss and/or lifestyle changes, however compliance is very poor and a pharmacological approach has become necessary. In the present article we present a systematic literature review focusing on established pediatric NALFD drugs (ursodeoxycholic acid, insulin sensitizers, and antioxidants) and on innovative therapeutic options as well.Regarding the former ones, a pediatric pilot study highlighted that ursodeoxycholic acid is not efficient on transaminases levels and bright liver. Similarly, a recent large scale, multicenter randomized clinical trial (TONIC study) showed that also insulin sensitizers and antioxidant vitamin E have scarce effects on serum transaminase levels. Among a large series of novel therapeutic approaches acting on recently proposed different pathomechanisms, probiotics seem hitherto the most interesting and reasonable option for their safety and tolerability. Toll-like receptors modifiers, Pentoxifylline, and Farnesoid X receptors agonists have been still poorly investigated, and will need further studies before becoming possible promising innovative therapeutic strategies.

摘要

超重和肥胖的流行导致非酒精性脂肪性肝病(NAFLD)显著增加,这是一种潜在的进展性疾病。目前,肥胖相关肝疾病是小儿慢性肝病的主要原因。所有年龄段的首选治疗方法都是减肥和/或生活方式改变,但依从性很差,因此需要药物治疗。本文对已确立的儿科 NALFD 药物(熊去氧胆酸、胰岛素增敏剂和抗氧化剂)和创新的治疗选择进行了系统的文献综述。关于前者,一项儿科试点研究表明,熊去氧胆酸对转氨酶水平和肝脏亮度没有效果。同样,最近一项大规模、多中心随机临床试验(TONIC 研究)表明,胰岛素增敏剂和抗氧化维生素 E 对血清转氨酶水平也几乎没有影响。在一系列针对最近提出的不同发病机制的新型治疗方法中,益生菌似乎迄今为止是最安全、最耐受的选择。Toll 样受体调节剂、己酮可可碱和法尼醇 X 受体激动剂的研究仍较少,需要进一步研究才能成为有前途的创新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6637/3534557/4a6a6aa18383/1824-7288-38-55-1.jpg

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