Clinical features and metabolic complications for non-alcoholic fatty liver disease (NAFLD) in youth with obesity

被引:5
|
作者
Barbieri, Emiliano [1 ]
Santoro, Nicola [2 ,3 ,4 ]
Umano, Giuseppina Rosaria [5 ]
机构
[1] Univ Naples Federico II, Dept Pediat, Naples, Italy
[2] Kansas Univ, Dept Pediat, Med Ctr, Kansas City, KS 66045 USA
[3] V Tiberio Univ Molise, Dept Med & Hlth Sci, Campobasso, Italy
[4] Yale Sch Med, Dept Pediat, New Haven, CT 06510 USA
[5] Univ Campania Luigi Vanvitelli, Dept Woman the Child & Gen & Specialized Surg, Naples, Italy
来源
关键词
NAFLD; type; 2; diabetes; youth; insulin resistance; genetics; DE-NOVO LIPOGENESIS; INSULIN-RESISTANCE; CONFERS SUSCEPTIBILITY; GENETIC-VARIATION; COMMON VARIANT; HEPATIC FAT; CHILDREN; PNPLA3; ASSOCIATION; PATHOGENESIS;
D O I
10.3389/fendo.2023.1062341
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pediatric obesity has become in the last forty years the most common metabolic disease in children and adolescents affecting about 25% of the pediatric population in the western world. As obesity worsens, a whole-body insulin resistance (IR) occurs. This phenomenon is more pronounced during adolescence, when youth experience a high degree of insulin resistance due the production of growth hormone. As IR progresses, the blunted control of insulin on adipose tissue lipolysis causes an increased flux of fatty acids with FFA deposition in ectopic tissues and organs such as the liver, leading to the development of NAFLD. In this brief review, we will discuss the clinical implications of IR and NAFLD in the context of pediatric obesity. We will review the pathogenesis and the link between these two entities, the major pathophysiologic underpinnings, including the role of genetics and metagenomics, how these two entities lead to the development of type 2 diabetes, and which are the therapeutic options for NAFLD in youth.
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页数:5
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