The Genetics of Pediatric Nonalcoholic Fatty Liver Disease

被引:29
|
作者
Goyal, Nidhi P. [1 ,2 ]
Schwimmer, Jeffrey B. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Gilman Dr, La Jolla, CA 92993 USA
[2] Rady Childrens Hosp, Dept Gastroenterol, Childrens Way, San Diego, CA 92123 USA
关键词
Nonalcoholic steatohepatitis; Children; Liver; Steatosis; PNPLA3; TM6SF2; Obesity; Alanine aminotransferase; PLASMA ALT LEVELS; CONFERS SUSCEPTIBILITY; COMMON VARIANT; NORMAL-WEIGHT; PNPLA3; GENE; CHILDREN; ASSOCIATION; POLYMORPHISM; NUTRITION; RECOMMENDATIONS;
D O I
10.1016/j.cld.2017.08.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in children. Severe fibrosis and cirrhosis are potential consequences of pediatric NAFLD and can occur within a few years of diagnosis. Observations suggest that genetics may be a strong modifying factor in the presentation, severity, and natural history of the disease. There is increasing interest in determining at-risk populations based on genetics in the hope of finding genotypes that correlate to NAFLD phenotype. Ultimately, the hope is to be able to tailor therapeutics to genetic predispositions and decrease disease morbidity in children with NAFLD.
引用
收藏
页码:59 / +
页数:14
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