Contribution of a genetic risk score to clinical prediction of hepatic steatosis in obese children and adolescents

被引:34
作者
Zusi, Chiara [1 ,2 ]
Mantovani, Alessandro [2 ]
Olivieri, Francesca [1 ]
Morandi, Anita [1 ]
Corradi, Massimiliano [1 ]
Del Giudice, Emanuele Miraglia [3 ]
Dauriz, Marco [2 ]
Valenti, Luca [4 ,5 ]
Byrne, Christopher D. [6 ,7 ]
Targher, Giovanni [2 ]
Matteis, Claudio [1 ]
机构
[1] Univ Hosp Verona, Pediat Diabet & Metab Disorders Unit, Dept Surg Dent Pediat & Gynaecol, Verona, Italy
[2] Univ Hosp Verona, Div Endocrinol Diabet & Metab, Dept Med, Verona, Italy
[3] Univ Campania Luigi Vanvitelli, Dept Woman Child & Gen & Specialized Surg, Naples, Italy
[4] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy
[5] Policlin Milano, Fdn IRCCS Ca Granda, Osped Maggiore, Translat Med & Hepatol Transfus Onal Ctr, Milan, Italy
[6] Univ Southampton, Nutr & Metab, Fac Med, Southampton, Hants, England
[7] Univ Hosp Southampton, Southampton Gen Hosp, Southampton Natl Inst, Hlth Res Biomed Res Ctr, Southampton, Hants, England
关键词
Genetics; NAFLD; Nonalcoholic fatty liver disease; Obesity; Pediatrics; FATTY LIVER-DISEASE; DIAGNOSIS; NAFLD; STEATOHEPATITIS; HERITABILITY; ASSOCIATION; OVERWEIGHT; MANAGEMENT; VARIANT; PNPLA3;
D O I
10.1016/j.dld.2019.05.029
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Nonalcoholic fatty liver disease (NAFLD) is the commonest liver disease in children and adolescents in Western countries. Complex traits arise from the interplay between environmental and genetic factors in the pathogenesis of NAFLD. Aims: We examined the association between NAFLD and eleven single nucleotide polymorphisms (SNPs) at genetic loci potentially associated with liver damage (GCKR, MBOAT7, GPR120), oxidative stress (SOD2), lipid metabolism (PNPLA3, TM6SF2, LPIN1, ELOVL2, FADS2, MTTP) and fibrogenesis (KLF6) in a paediatric population. A genetic risk score (GRS) was performed taking into account both these SNPs and clinical risk factors. Methods: We recruited a cohort of 514 obese children and adolescents (mean age [+/- SD]: 11.2 +/- 2.8 years, z-BMI 3.3 +/- 0.8). NAFLD was identified by ultrasonography. Genotyping was performed by TaqMan-based RT-PCR system. Results: The overall prevalence of NAFLD was 67.5% (347 patients). Among the eleven genotyped SNPs, the genetic variants in TM6SF2 rs58542926 (OR = 4.13, p = 0.002), GCKR rs1260326 (OR = 1.53, p = 0.003), PNPLA3 rs738409 (OR = 1.58, p = 0.004) and ELOVL2 rs2236212 (OR = 1.34, p = 0.047) were significantly associated with a higher risk of NAFLD. Addition of a 11-polymorphism GRS to established clinical risk factors significantly (albeit modestly) improved the discriminatory capability of the regression model for predicting the risk of NAFLD (with SNPs C-statistic 0.81 [95%CI 0.75-0.88] vs. 0.77 [0.70-0.84] without SNPs; p = 0.047). Conclusions: NAFLD was strongly associated with three genetic variants, TM6SF2 rs58542926, PNPLA3 rs738409 and GCKR rs1260326, and more slightly with ELOVL2 rs2236212, in obese children and adolescents. Addition of a 11-polymorphism GRS to clinical risk factors improved the predictability of NAFLD. (C) 2019 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1586 / 1592
页数:7
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