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胰岛素抵抗与非酒精性脂肪性肝病:超越遗传学的危险关联。

Insulin Resistance and NAFLD: A Dangerous Liaison beyond the Genetics.

作者信息

Manco Melania

机构信息

Bambino Gesù Children's Hospital, Research Unit for Multifactorial Diseases, Via Ferdinando Baldelli 38, 00146 Rome, Italy.

出版信息

Children (Basel). 2017 Aug 14;4(8):74. doi: 10.3390/children4080074.

Abstract

Over the last decade, the understanding of the association between insulin resistance (IR) and non-alcoholic fatty liver disease (NAFLD) has dramatically evolved. There is clear understanding that carriers of some common genetic variants, i.e., the patatin-like phospholipase domain-containing 3 (PNPLA3) or the transmembrane 6 superfamily member 2 (TM6SF2) are at risk of developing severe forms of NAFLD even in the presence of reduced or absent IR. In contrast, there are obese patients with "metabolic" (non-genetically driven) NAFLD who present severe IR. Owing to the epidemic obesity and the high prevalence of these genetic variants in the general population, the number of pediatric cases with combination of genetic and metabolic NAFLD is expected to be very high. Gut dysbiosis, excessive dietary intake of saturated fats/fructose-enriched foods and exposure to some chemicals contribute all to both IR and NAFLD, adding further complexity to the understanding of their relationship. Once NAFLD is established, IR can accelerate the progression to the more severe form of liver derangement that is the non-alcoholic steatohepatitis.

摘要

在过去十年中,对胰岛素抵抗(IR)与非酒精性脂肪性肝病(NAFLD)之间关联的理解有了显著进展。人们清楚地认识到,一些常见基因变异的携带者,即含帕他汀样磷脂酶结构域3(PNPLA3)或跨膜6超家族成员2(TM6SF2),即使在IR降低或不存在的情况下,也有发展为严重形式NAFLD的风险。相比之下,有一些患有“代谢性”(非基因驱动)NAFLD的肥胖患者存在严重的IR。由于肥胖流行以及这些基因变异在普通人群中的高患病率,预计患有遗传性和代谢性NAFLD合并症的儿科病例数量会非常多。肠道微生物群失调、饮食中饱和脂肪/富含果糖食物的过量摄入以及接触某些化学物质都会导致IR和NAFLD,这进一步增加了理解它们之间关系的复杂性。一旦NAFLD形成,IR会加速疾病进展至更严重的肝脏紊乱形式,即非酒精性脂肪性肝炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810f/5575596/11772c30cd3e/children-04-00074-g001.jpg

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