# Circulating Bilirubin Levels, but Not Their Genetic Determinants, Are Inversely Associated with Steatotic Liver Disease in Adolescents

**Authors:** José Patricio Miranda, Juan Cristóbal Gana, Gigliola Alberti, Karen Galindo, Ana Pereira, José Luis Santos

PMC · DOI: 10.3390/ijms26072980 · International Journal of Molecular Sciences · 2025-03-25

## TL;DR

Higher bilirubin levels in adolescents are linked to lower risk of fatty liver disease, but this may not be due to genetics.

## Contribution

This study explores bilirubin's role in protecting against fatty liver disease in adolescents, finding no causal genetic link.

## Key findings

- Higher bilirubin levels are associated with a 30% lower likelihood of steatotic liver disease in adolescents.
- Genetic determinants of bilirubin, like rs887829 and polygenic scores, are not significantly associated with steatotic liver disease.
- The observed association may be due to unmeasured confounding factors rather than a causal relationship.

## Abstract

Epidemiologic studies suggest that elevated plasma unconjugated bilirubin confer protection against steatotic liver disease (SLD) in adults. However, evidence supporting this protective role in adolescents remains limited. We aimed to assess the association between serum bilirubin levels and their genetic determinants in protecting against SLD in Chilean adolescents. We conducted a cross-sectional study with 704 adolescents aged 15.4 ± 1 years (52% girls) of the Chilean Growth and Obesity Cohort Study. Ultrasonography echogenicity was used to diagnose SLD. We measured Z-scores of body mass index (z-BMI), total bilirubin (TB), and the genetic determinants of bilirubin (including rs887829 genotypes of UGT1A1 and bilirubin polygenic scores). Multiple logistic regression models evaluated the associations between standardized TB and its genetic determinants with SLD. We found that 1-SD of standardized plasma TB was significantly associated with a 30% reduction in the likelihood of SLD after adjustment by sex, age, z-BMI, and ethnicity (OR = 0.7; 95% CI = 0.50–0.96; p = 0.03). No significant associations were found among the rs887829 genotypes, bilirubin polygenic scores, and SLD in logistic regression models adjusted by covariates. Increased circulating bilirubin levels are unlikely causally associated with protection against SLD, and the cross-sectional association could be due to unmeasured confounding.

## Linked entities

- **Genes:** UGT1A1 (UDP glucuronosyltransferase family 1 member A1) [NCBI Gene 54658]

## Full-text entities

- **Genes:** UGT1A1 (UDP glucuronosyltransferase family 1 member A1) [NCBI Gene 54658] {aka BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT 1-1, UGT1}
- **Diseases:** SLD (MESH:D008107), Obesity (MESH:D009765)
- **Chemicals:** Bilirubin (MESH:D001663)
- **Mutations:** rs887829

## Full text

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## References

80 references — full list in the complete paper: https://tomesphere.com/paper/PMC11988633/full.md

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Source: https://tomesphere.com/paper/PMC11988633