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Gut Bifidobacterium longum is associated with better native liver survival in patients with biliary atresia.
Lee, Chee-Seng; Lin, Chia-Ray; Chua, Huey-Huey; Wu, Jia-Feng; Chang, Kai-Chi; Ni, Yen-Hsuan; Chang, Mei-Hwei; Chen, Huey-Ling.
Afiliação
  • Lee CS; Department of Pediatrics, National Taiwan University Hospital Hsin-Chu Branch, Hsin-Chu, Taiwan.
  • Lin CR; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chua HH; Department of Pediatrics, National Taiwan University College of Medicine and Children's Hospital, Taipei, Taiwan.
  • Wu JF; Department of Pediatrics, National Taiwan University College of Medicine and Children's Hospital, Taipei, Taiwan.
  • Chang KC; Department of Pediatrics, National Taiwan University College of Medicine and Children's Hospital, Taipei, Taiwan.
  • Ni YH; Department of Pediatrics, National Taiwan University College of Medicine and Children's Hospital, Taipei, Taiwan.
  • Chang MH; Department of Pediatrics, National Taiwan University College of Medicine and Children's Hospital, Taipei, Taiwan.
  • Chen HL; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
JHEP Rep ; 6(7): 101090, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39006502
ABSTRACT
Background &

Aims:

The gut microbiome plays an important role in liver diseases, but its specific impact on biliary atresia (BA) remains to be explored. We aimed to investigate the microbial signature in the early life of patients with BA and to analyze its influence on long-term outcomes.

Methods:

Fecal samples (n = 42) were collected from infants with BA before and after Kasai portoenterostomy (KPE). The stool microbiota was analyzed using 16S rRNA next-generation sequencing and compared with that of age-matched healthy controls (HCs). Shotgun metagenomic sequencing analysis was employed to confirm the bacterial composition in 10 fecal samples before KPE. The correlation of the microbiome signature with liver function and long-term outcomes was assessed.

Results:

In the 16S rRNA next-generation sequencing analysis of fecal microbiota, the alpha and beta diversity analyses revealed significant differences between HCs and patients with BA before and after KPE. The difference in microbial composition analyzed by linear discriminant analysis and random forest classification revealed that the abundance of Bifidobacterium longum (B. longum) was significantly lower in patients before and after KPE than in HCs. The abundance of B. longum was negatively correlated with the gamma-glutamyltransferase level after KPE (p <0.05). Patients with early detectable B. longum had significantly lower total and direct bilirubin 3 months after KPE (p <0.005) and had a significantly lower liver transplantation rate (hazard ratio 0.16, 95% CI 0.03-0.83, p = 0.029). Shotgun metagenomic sequencing also revealed that patients with BA and detectable B. longum had reduced total and direct bilirubin after KPE.

Conclusion:

The gut microbiome of patients with BA differed from that of HCs, with a notable abundance of B. longum in early infancy correlating with better long-term outcomes. Impact and implications Bifidobacterium longum (B. longum) is a beneficial bacterium commonly found in the human gut. It has been studied for its potential impacts on various health conditions. In patients with biliary atresia, we found that a greater abundance of B. longum in the fecal microbiome is associated with improved clinical outcomes. This suggests that early colonization and increasing B. longum levels in the gut could be a therapeutic strategy to improve the prognosis of patients with biliary atresia.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article