Nocturnal hypoxia-induced oxidative stress promotes progression of pediatric non-alcoholic fatty liver disease

JOURNAL OF HEPATOLOGY

卷:65

Article

Sundaram, Shikha S.^1,2,3  Halbower, Ann^3,4  Pan, Zhaoxing⁵  Robbins, Kristen^1,2,3  Capocelli, Kelley E.⁶  Klawitter, Jelena⁷  Shearn, Colin T.⁸  Sokol, Ronald J.^1,2,3 

[1] Childrens Hosp Colorado, Dept Pediat, Sect Gastroenterol Hepatol & Nutr, Aurora, CO USA

[2] Childrens Hosp Colorado, Digest Hlth Inst, 13123 E 16th Ave,B290, Aurora, CO 80045 USA

[3] Univ Colorado, Sch Med, Aurora, CO USA

[4] Childrens Hosp Colorado, Dept Pediat, Sect Pulm Med, Aurora, CO USA

[5] Colorado Sch Publ Hlth, Dept Biostat & Informat, Aurora, CO USA

[6] Univ Colorado, Sch Med, Dept Pathol, Pediat Pathol, Aurora, CO USA

[7] Univ Colorado, Sch Med, Dept Anesthesiol, Clin Res & Dev iC42, Aurora, CO USA

[8] Univ Colorado, Anschutz Med Ctr, Sch Pharm, Dept Pharmaceut Sci, Aurora, CO USA

关键词: Hypoxia;    NASH;    Sleep apnea;    Reactive oxygen species;    F (2)-isoprostanes;    Antioxidants;   

DOI  :  10.1016/j.jhep.2016.04.010

来源: Elsevier

【 摘 要 】

Background & Aims: Oxidative stress is proposed as a central mediator in NAFLD pathogenesis, but the specific trigger for reactive oxygen species generation has not been clearly delineated. In addition, emerging evidence shows that obesity related obstructive sleep apnea (OSA) and nocturnal hypoxia are associated with NAFLD progression in adults. The aim of this study was to determine if OSA/nocturnal hypoxia-induced oxidative stress promotes the progression of pediatric NAFLD. Methods: Subjects with biopsy proven NAFLD and lean controls were studied. Subjects underwent polysomnograms, liver histology scoring, laboratory testing, urine F(2)-isoprostanes (measure of lipid peroxidation) and 4-hydroxynonenal liver immunohistochemistry (in situ hepatic lipid peroxidation). Results: We studied 36 adolescents with NAFLD and 14 lean controls. The OSA/hypoxia group (69% of NAFLD subjects) had more severe fibrosis (64% stage 0-2; 36% stage 3) than those without OSA/hypoxia (100% stage 0-2), p = 0.03. Higher F(2)-isoprostanes correlated with apnea/hypoxia index (r = 0.39, p = 0.03), % time SaO(2) < 90% (r = 0.56, p = 0.0008) and inversely with SaO2 nadir (r = -0.46, p = 0.008). OSA/hypoxia was most severe in subjects with the greatest 4HNE staining (p = 0.03). Increasing F(2)-isoprostanes(r = 0.32, p = 0.04) and 4HNE hepatic staining (r = 0.47, p = 0.007) were associated with worsening steatosis. Greater oxidative stress occurred in subjects with definite NASH as measured by F(2)-isoprostanes (p = 0.06) and hepatic 4HNE (p = 0.03) compared to those with borderline/not NASH. Conclusions: These data support the role of nocturnal hypoxia as a trigger for localized hepatic oxidative stress, an important factor associated with the progression of NASH and hepatic fibrosis in obese pediatric patients. Lay summary: Obstructive sleep apnea and low nighttime oxygen are associated with NAFLD progression in adults. In this study, we show that adolescents with NAFLD who have OSA and low oxygen have significant scar tissue in their livers. NAFLD subjects affected by OSA and low oxygen have a greater imbalance between the production of free radicals and their body's ability to counteract their harmful effects than subjects without OSA and low oxygen. This study shows that low oxygen levels may be an important trigger in the progression of pediatric NASH. (C) 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

【 授权许可】

Free