Evidence map›Paper›PMID 36894566›Full record

ArticleNature communications2023

Gut microbiota alters host bile acid metabolism to contribute to intrahepatic cholestasis of pregnancy.

Bo Tang, Li Tang, Shengpeng Li, Shuang Liu, Jialin He, Pan Li, Sumin Wang, Min Yang, Longhui Zhang, Yuanyuan Lei and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 2 pooled it
24.6field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 2 syntheses or guidelines pooled it, 105 citations in OpenAlex.

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19 more citing papers are in PubMed but not listed here.

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

16 authors at 2 institutions in 1 country.

Bo Tang *Department of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.ORCID 0000-0003-4089-5155
Li Tang *Department of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.ORCID 0000-0002-7811-0854
Shengpeng LiDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Shuang LiuDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Jialin HeDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Pan LiDepartment of Obstetrics and Gynecology, First People's Hospital of Foshan, Foshan, Guangdong, China.ORCID 0000-0003-1645-6670
Sumin WangDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Min YangDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Longhui ZhangDepartment of Obstetrics and Gynecology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Yuanyuan LeiDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.ORCID 0000-0001-9900-2150
Dianji TuLaboratory Medicine Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
Xuefeng TangDepartment of Pathology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Hua HuDepartment of Obstetrics and Gynecology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Qin OuyangCollege of Pharmacy, Army Medical University, Chongqing, China.ORCID 0000-0002-1161-5102
Xia ChenDepartment of Obstetrics and Gynecology, First People's Hospital of Foshan, Foshan, Guangdong, China. 2676832333@qq.com.ORCID 0000-0002-7915-4568
Shiming YangDepartment of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China. Yangshiming@tmmu.edu.cn.ORCID 0000-0002-0000-4795
Army Medical University · CNFirst People's Hospital of Foshan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intrahepatic cholestasis of pregnancy (ICP) is a female pregnancy-specific disorder that is characterized by increased serum bile acid and adverse fetal outcomes. The aetiology and mechanism of ICP are poorly understood; thus, existing therapies have been largely empiric. Here we show that the gut microbiome differed significantly between individuals with ICP and healthy pregnant women, and that colonization with gut microbiome from ICP patients was sufficient to induce cholestasis in mice. The gut microbiomes of ICP patients were primarily characterized by Bacteroides fragilis (B. fragilis), and B. fragilis was able to promote ICP by inhibiting FXR signaling via its BSH activity to modulate bile acid metabolism. B. fragilis-mediated FXR signaling inhibition was responsible for excessive bile acid synthesis and interrupted hepatic bile excretion to ultimately promote the initiation of ICP. We propose that modulation of the gut microbiota-bile acid-FXR axis may be of value for ICP treatment.

Indexed as

Cholestasis, IntrahepaticGastrointestinal MicrobiomePregnancy ComplicationsAnimalsBile Acids and SaltsFemaleHumansMicePregnancyBile Acids and Salts

Identifiers

PMID36894566
PMCPMC9998625
OpenAlexW4323656790

What Socratic holds

Textmetadata
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 Socratic graph.