Low and high birth weights are risk factors for nonalcoholic fatty liver disease in children

KP Newton, HS Feldman, CD Chambers, L Wilson… - The Journal of …, 2017 - Elsevier
KP Newton, HS Feldman, CD Chambers, L Wilson, C Behling, JM Clark, JP Molleston…
The Journal of pediatrics, 2017Elsevier
Objectives To examine the distribution of birth weight in children with nonalcoholic fatty liver
disease (NAFLD) compared with the general US population, and to investigate the
relationship between birth weight and severity of NAFLD. Study design A multicenter, cross-
sectional study of children with biopsy-proven NAFLD enrolled in the Nonalcoholic
Steatohepatitis Clinical Research Network Database. Birth weight was categorized as low
birth weight (LBW), normal birth weight (NBW), or high birth weight (HBW) and compared …
Objectives
To examine the distribution of birth weight in children with nonalcoholic fatty liver disease (NAFLD) compared with the general US population, and to investigate the relationship between birth weight and severity of NAFLD.
Study design
A multicenter, cross-sectional study of children with biopsy-proven NAFLD enrolled in the Nonalcoholic Steatohepatitis Clinical Research Network Database. Birth weight was categorized as low birth weight (LBW), normal birth weight (NBW), or high birth weight (HBW) and compared with the birth weight distribution in the general US population. The severity of liver histology was assessed by birth weight category.
Results
Children with NAFLD (n = 538) had overrepresentation of both LBW and HBW compared with the general US population (LBW, 9.3%; NBW, 75.8%; HBW, 14.9% vs LBW, 6.1%; NBW, 83.5%; HBW 10.5%; P < .0001). Children with HBW had significantly greater odds of having more severe steatosis (OR, 1.82, 95% CI. 1.15-2.88) and nonalcoholic steatohepatitis (OR, 2.03; 95% CI, 1.21-3.40) compared with children with NBW. In addition, children with NAFLD and LBW had significantly greater odds of having advanced fibrosis (OR, 2.23; 95% CI, 1.08-4.62).
Conclusion
Birth weight involves maternal and in utero factors that may have long-lasting consequences. Children with both LBW and HBW may be at increased risk for developing NAFLD. Among children with NAFLD, those with LBW or HBW appear to be at increased risk for more severe disease.
Elsevier