Evidence map›Paper›PMID 35013245›Full record

ArticleNature communications2022

Maternal regulation of biliary disease in neonates via gut microbial metabolites.

Jai Junbae Jee, Li Yang, Pranavkumar Shivakumar, Pei-Pei Xu, Reena Mourya, Unmesha Thanekar, Pu Yu, Yu Zhu, Yongkang Pan, Haibin Wang and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. The bile acid-gut microbiota-vitamin D axis: new insights into biliary atresia.Frontiers in cellular and infection microbiology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The gut microbiota-bile acid axis in cholestatic liver disease.Molecular medicine (Cambridge, Mass.) · 2024
    Review
  10. Biliary atresia.Nature reviews. Disease primers · 2024
    Review
  11. GutJHEP reports : innovation in hepatology · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Biliary atresia: the role of gut microbiome, and microbial metabolites.Frontiers in cellular and infection microbiology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Biliatresone: progress in biliary atresia study.World journal of pediatrics : WJP · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 9 institutions in 4 countries.

Jai Junbae Jee *Divisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Li Yang *Divisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Pranavkumar Shivakumar *Divisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.ORCID http://orcid.org/0000-0002-2095-0623
Pei-Pei Xu *Department of Pediatric Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430022, Wuhan, Hubei, China.
Reena MouryaDivisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Unmesha ThanekarDivisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.ORCID http://orcid.org/0000-0002-6118-825X
Pu YuDepartment of Neonatal Surgery, Xi'an Children's Hospital, 710003, Xi'an, Shaanxi, China.
Yu ZhuDepartment of Pediatrics, Western China Second Hospital, Sichuan University, 610041, Chengdu, Sichuan, China.
Yongkang PanDepartment of Neonatal Surgery, Xi'an Children's Hospital, 710003, Xi'an, Shaanxi, China.
Haibin WangDepartment of Pediatric Surgery, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430015, Wuhan, Hubei, China.
Xufei DuanDepartment of Pediatric Surgery, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430015, Wuhan, Hubei, China.
Yongqin YeDepartment of General Surgery, Shenzhen Children's Hospital, 518038, Shenzhen, Guangdong, China.
Bin WangDepartment of General Surgery, Shenzhen Children's Hospital, 518038, Shenzhen, Guangdong, China.
Zhu JinDepartment of Pediatric General Thoracic and Urology Surgery, The Affiliated Hospital of Zunyi Medical University, 563000, Zunyi, Guizhou, China.
Yuanmei LiuDepartment of Pediatric General Thoracic and Urology Surgery, The Affiliated Hospital of Zunyi Medical University, 563000, Zunyi, Guizhou, China.
Zhiqing CaoDepartment of Pediatric Surgery, Jiangmen Maternity and Child Health Care Hospital, 529000, Jiangmen, Guangdong, China.
Miki Watanabe-ChaillandDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Lindsey E Romick-RosendaleDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Michael WagnerDepartment of Pediatric Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430022, Wuhan, Hubei, China.
Lin FeiDepartment of Pediatric Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430022, Wuhan, Hubei, China.ORCID http://orcid.org/0000-0002-8187-6295
Zhenhua LuoDivisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Nicholas J OllberdingDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Shao-Tao TangDepartment of Pediatrics, University of Cincinnati, College of Medicine, Cincinnati, OH, 45267, USA. tshaotao83@hust.edu.cn.
Jorge A BezerraDivisions of Gastroenterology, Hepatology and Nutrition and The Liver Care Center at Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA. jorge.bezerra@cchmc.org.ORCID http://orcid.org/0000-0001-9667-7742
Cincinnati Children's Hospital Medical Center · USWuhan Children's Hospital · CNXi’an Children’s Hospital · CNZunyi Medical University · CNJiangmen Central Hospital · CNShenzhen Children's Hospital · CNSichuan University · CNUnion Hospital · CNUniversity of Cincinnati Medical Center · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
Immunologic Dysfunction in Biliary AtresiaR01DK064008 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI DENSON, LEE ARMISTEAD · 2003 to 2022
$6.7M
Biological Basis of Phenotypes and Clinical Outcomes in Biliary AtresiaR01DK083781 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BEZERRA, JORGE A. · 2009 to 2023
$6.1M
NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK064008NIDDK NIH HHS R01 DK083781
6 · The paper itself

Abstract

Maternal seeding of the microbiome in neonates promotes a long-lasting biological footprint, but how it impacts disease susceptibility in early life remains unknown. We hypothesized that feeding butyrate to pregnant mice influences the newborn's susceptibility to biliary atresia, a severe cholangiopathy of neonates. Here, we show that butyrate administration to mothers renders newborn mice resistant to inflammation and injury of bile ducts and improves survival. The prevention of hepatic immune cell activation and survival trait is linked to fecal signatures of Bacteroidetes and Clostridia and increases glutamate/glutamine and hypoxanthine in stool metabolites of newborn mice. In human neonates with biliary atresia, the fecal microbiome signature of these bacteria is under-represented, with suppression of glutamate/glutamine and increased hypoxanthine pathways. The direct administration of butyrate or glutamine to newborn mice attenuates the disease phenotype, but only glutamine renders bile duct epithelial cells resistant to cytotoxicity by natural killer cells. Thus, maternal intake of butyrate influences the fecal microbial population and metabolites in newborn mice and the phenotypic expression of experimental biliary atresia, with glutamine promoting survival of bile duct epithelial cells.

Indexed as

Gastrointestinal MicrobiomeAnimalsAnimals, NewbornBile DuctsBiliary AtresiaCholestasisDisease Models, AnimalEpithelial CellsFemaleHumansInfant, NewbornInflammationKiller Cells, NaturalLiverMiceMice, Inbred BALB C

Identifiers

PMID35013245
PMCPMC8748778
OpenAlexW4206596672

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.