2021
DOI: 10.1016/j.jpedsurg.2020.06.035
|View full text |Cite
|
Sign up to set email alerts
|

Alterations of gut microbiota and serum bile acids are associated with parenteral nutrition-associated liver disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
12
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 15 publications
(12 citation statements)
references
References 38 publications
0
12
0
Order By: Relevance
“…More exclusive KOs were found in the small intestines ( Figure 4 D), but the abundance of 16 KEGG pathways at the third levels were significant differences between large intestines and small intestines; there was a similar trend between AI and SI. Secondary bile acid is one of the major types of bacterial metabolites in the colon [ 74 ], gut bacteria expressing bile salt hydrolase include species in the genera Bacteroides , Bifidobacterium , Lactobacillus , and Clostridium [ 75 ]. Sphigolipid, are produced by the phylum Bacteroidetes (genera Bacteroides , Parabacteroides , Prevotella , Porphyromonas , Flectobacillus ) and the Chlorobi (genera Chlorobium ) [ 76 ].…”
Section: Discussionmentioning
confidence: 99%
“…More exclusive KOs were found in the small intestines ( Figure 4 D), but the abundance of 16 KEGG pathways at the third levels were significant differences between large intestines and small intestines; there was a similar trend between AI and SI. Secondary bile acid is one of the major types of bacterial metabolites in the colon [ 74 ], gut bacteria expressing bile salt hydrolase include species in the genera Bacteroides , Bifidobacterium , Lactobacillus , and Clostridium [ 75 ]. Sphigolipid, are produced by the phylum Bacteroidetes (genera Bacteroides , Parabacteroides , Prevotella , Porphyromonas , Flectobacillus ) and the Chlorobi (genera Chlorobium ) [ 76 ].…”
Section: Discussionmentioning
confidence: 99%
“…Microbial dysbiosis, including reduced microbial diversity and richness, is associated with changes in secondary bile acids and IFALD [23]; however, no studies have shown causality between dysbiosis and IFALD progression. There is ongoing research in animal models of neonatal rats on parenteral nutrition investigating microbiome changes [24], thus altering the gut microbiome may be a therapeutic target in the future.…”
Section: Microbiomementioning
confidence: 99%
“…Morin et al [ 17 ] also observed liver steatosis after 5 days of TPN in one-month-old guinea pigs. TPN feeding for 7 days to male one-month-old Sprague Dawley rats also led to the development of liver diseases [ 15 ]. Additionally, in humans, newborn infants (>1000 g) who received TPN for a longer period (>7 days) developed PNALD [ 14 ].…”
Section: In Vivo Impact Of Oxidized Tpn After Infusionmentioning
confidence: 99%
“…The oxidant load collectively generated in human neonates from various sources could lead to liver diseases, bronchopulmonary dysplasia (BPD), gut atrophy, necrotizing enterocolitis, and retinopathy [ 13 , 14 ]. Moreover, several animal experiments have demonstrated that the exogenous oxidized molecules from TPN could cause hepatocellular damage, cholestasis, apoptosis, and pulmonary fibrosis [ 15 , 16 , 17 , 18 , 19 ].…”
Section: Introductionmentioning
confidence: 99%