Endotoxin biomarkers, hepatic fat fraction, liver volume and liver stiffness among adolescents at high‐risk for non‐alcoholic fatty liver disease: The HEROES study

Author:

Perng Wei12ORCID,Salmon Kyle1,Schenker Rachel3,Janssen Rachel C.4,Friedman Jacob E.4,Goran Michael I.3

Affiliation:

1. Department of Epidemiology, Colorado School of Public Health University of Colorado Anschutz Medical Campus Aurora Colorado USA

2. Lifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center University of Colorado Anschutz Medical Campus Aurora Colorado USA

3. Department of Pediatrics Children's Hospital Los Angeles Los Angeles California USA

4. Harold Hamm Diabetes Center University of Oklahoma Health Sciences Center Oklahoma City Oklahoma USA

Abstract

SummaryBackgroundNon‐alcoholic fatty liver disease (NAFLD) is on the rise among youth. Identifying biomarkers of NAFLD progression/risk can aid in prevention efforts.AimsThis pilot study investigated associations of two endotoxin biomarkers—lipopolysaccharide‐binding protein (LBP) and anti‐endotoxin core immunoglobulin G (EndoCab)—with markers of NAFLD among 99 Latino/Latina adolescents (11–19 years) with obesity.Materials & MethodsWe used linear regression to examine associations of each endotoxin biomarker (per 1‐SD) with hepatic fat fraction (HFF), liver volume, and liver stiffness.ResultsWe found positive associations of LBP with HFF and liver volume. Each 1‐SD increment in LBP corresponded with 2.35% (95% CI: 0.46%, 4.23%) higher HFF and 0.14 (0.06, 0.23) L greater liver volume after adjusting for age, sex, and maternal education. Accounting for abdominal adiposity and Tanner stage did not change results. Excluding 72 participants with NAFLD attenuated associations of LBP with HFF but associations with liver volume persisted (0.11 [0.01, 0.21] L). EndoCab was not associated with any liver outcomes. Neither endotoxin biomarker predicted liver stiffness.Discussion/conclusionWhile additional research is warranted, our results support LBP as a biomarker of NAFLD risk/progression in high‐risk youth.

Funder

American Diabetes Association

Colorado Clinical and Translational Sciences Institute

National Institutes of Health

Publisher

Wiley

Subject

Public Health, Environmental and Occupational Health,Nutrition and Dietetics,Health Policy,Pediatrics, Perinatology and Child Health

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