Evidence map›Paper›PMID 39166704›Full record

ArticleGut microbes

Machine learning-causal inference based on multi-omics data reveals the association of altered gut bacteria and bile acid metabolism with neonatal jaundice.

Wanling Chen, Peng Zhang, Xueli Zhang, Tiantian Xiao, Jianhai Zeng, Kaiping Guo, Huixian Qiu, Guoqiang Cheng, Zhangxing Wang, Wenhao Zhou and 2 more

Abstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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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

12 authors.

Wanling ChenDivision of Neonatology, Longgang Central Hospital of Shenzhen, Shenzhen, China.
Peng ZhangDivision of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Xueli ZhangDivision of Neonatology, Shenzhen Longhua People's Hospital, Shenzhen, China.
Tiantian XiaoDepartment of Neonatology, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Jianhai ZengDivision of Neonatology, Longgang Central Hospital of Shenzhen, Shenzhen, China.
Kaiping GuoDivision of Pediatric, Longgang Central Hospital of Shenzhen, Shenzhen, China.
Huixian QiuDivision of Neonatology, Longgang Central Hospital of Shenzhen, Shenzhen, China.
Guoqiang ChengDivision of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Zhangxing WangDivision of Neonatology, Shenzhen Longhua People's Hospital, Shenzhen, China.
Wenhao ZhouDivision of Neonatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Shujuan ZengDivision of Neonatology, Longgang Central Hospital of Shenzhen, Shenzhen, China.
Mingbang WangDepartment of Neonatology, Longgang Maternity and Child Institute of Shantou University Medical College (Longgang District Maternity & Child Healthcare Hospital of Shenzhen City), Shenzhen, China.ORCID 0000-0002-5989-5377

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early identification of neonatal jaundice (NJ) appears to be essential to avoid bilirubin encephalopathy and neurological sequelae. The interaction between gut microbiota and metabolites plays an important role in early life. It is unclear whether the composition of the gut microbiota and metabolites can be used as an early indicator of NJ or to aid clinical decision-making. This study involved a total of 196 neonates and conducted two rounds of "discovery-validation" research on the gut microbiome-metabolome. It utilized methods of machine learning, causal inference, and clinical prediction model evaluation to assess the significance of gut microbiota and metabolites in classifying neonatal jaundice (NJ), as well as the potential causal relationships between corresponding clinical variables and NJ. In the discovery stage, NJ-associated gut microbiota, network modules, and metabolite composition were identified by gut microbiome-metabolome association analysis. The NJ-associated gut microbiota was closely related to bile acid metabolites. By Lasso machine learning assessment, we found that the gut bacteria were associated with abnormal bile acid metabolism. The machine learning-causal inference approach revealed that gut bacteria affected serum total bilirubin and NJ by influencing bile acid metabolism. NJ-associated gut bile acids are potential biomarkers of NJ, and clinical prediction models constructed based on these biomarkers have some clinical effects and the model may be used for disease risk prediction. In the validation stage, it was found that intestinal metabolites can predict NJ, and the machine learning-causal inference approach revealed that bile acid metabolites affected NJ itself by affecting the total bilirubin content. Intestinal bile acid metabolites are potential biomarkers of NJ. By applying machine learning-causal inference methods to gut microbiome-metabolome association studies, we found NJ-associated intestinal bacteria and their network modules and bile acid metabolite composition. The important role of intestinal bacteria and bile acid metabolites in NJ was determined, which can predict the risk of NJ.

Indexed as

BacteriaBile Acids and SaltsGastrointestinal MicrobiomeJaundice, NeonatalMachine LearningBilirubinBiomarkersFemaleHumansInfant, NewbornMaleMetabolomeMetabolomicsMultiomicsBile Acids and SaltsBilirubinBiomarkers16S rRNA gene sequencingcausal inferenceLassoLC-MS/MSNeonatal jaundice

Identifiers

PMID39166704
PMCPMC11340767

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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.