Evidence map›Paper›PMID 36658452›Full record

ArticleWorld journal of pediatrics : WJP2023

Poly-hydroxylated bile acids and their prognostic roles in Alagille syndrome.

Meng-Xuan Wang, Jun Han, Teng Liu, Ren-Xue Wang, Li-Ting Li, Zhong-Die Li, Jun-Cong Yang, Lang-Li Liu, Yi Lu, Xin-Bao Xie and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in World journal of pediatrics : WJP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

15 authors at 5 institutions in 2 countries.

Meng-Xuan WangDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, 201508, China.ORCID http://orcid.org/0000-0001-8935-6211
Jun HanUniversity of Victoria-Genome BC Proteomics Centre and Division of Medical Sciences, Victoria, British Columbia, Canada.
Teng LiuThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Ren-Xue WangBC Cancer Research Centre, Vancouver, British Columbia, Canada.
Li-Ting LiThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Zhong-Die LiThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Jun-Cong YangUniversity of Victoria-Genome BC Proteomics Centre and Division of Medical Sciences, Victoria, British Columbia, Canada.
Lang-Li LiuThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Yi LuThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Xin-Bao XieThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Jing-Yu GongDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, 201508, China.
Shi-Yu LiThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
Lei ZhangInstitutes of Biomedical Sciences, Fudan University, Shanghai, 201199, China.
Victor LingBC Cancer Research Centre, Vancouver, British Columbia, Canada.
Jian-She WangThe Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China. jshwang@shmu.edu.cn.
Children's Hospital of Fudan University · CNJinshan Hospital of Fudan University · CNUniversity of Victoria · CAFudan University · CNShanghai Veterinary Research Institute · CN

Funding

Key Technologies Research and Development Program 2021YFC 2700800National Natural Science Foundation of China 81741056National Natural Science Foundation of China 81873543Natural Science Foundation of Shanghai 20YF1402900
6 · The paper itself

Abstract

backgroundThe liver manifestations of Alagille syndrome (ALGS) are highly variable, and factors affecting its prognosis are poorly understood. We asked whether the composition of bile acids in ALGS patients with good clinical outcomes differs from that in patients with poor outcomes and whether bile acids could be used as prognostic biomarkers.

methodsBlood for bile acid profiling was collected from genetically confirmed JAG1-associated ALGS patients before one year of age. A good prognosis was defined as survival with native liver and total bilirubin (TB) < 85.5 μmol/L, while a poor prognosis was defined as either liver transplantation, death from liver failure, or TB ≥ 85.5 μmol/L at the last follow-up.

resultsWe found that the concentrations of two poly-hydroxylated bile acids, tauro-2β,3α,7α,12α-tetrahydroxylated bile acid (THBA) and glyco-hyocholic acid (GHCA), were significantly increased in patients with good prognosis compared to those with poor prognosis [area under curve (AUC) = 0.836 and 0.782, respectively] in the discovery cohort. The same trend was also observed in the molar ratios of GHCA to glyco- chenodeoxycholic acid (GCDCA) and tetrahydroxylated bile acid (THCA) to tauro-chenodeoxycholic acid (TCDCA) (both AUC = 0.836). A validation cohort confirmed these findings. Notably, tauro-2β,3α,7α,12α-THBA achieved the highest prediction accuracy of 88.00% (92.31% sensitivity and 83.33% specificity); GHCA at > 607.69 nmol/L was associated with native liver survival [hazard ratio: 13.03, 95% confidence interval (CI): (2.662-63.753), P = 0.002].

conclusionsWe identified two poly-hydroxylated bile acids as liver prognostic biomarkers of ALGS patients. Enhanced hydroxylation of bile acids may result in better clinical outcomes.

Indexed as

Alagille SyndromeBile Acids and SaltsBiomarkersChenodeoxycholic AcidHumansPrognosisBile Acids and SaltsBiomarkersChenodeoxycholic AcidAlagille syndromeBile acid profilePoly-hydroxylated bile acidsPrognostic biomarkers

Identifiers

PMID36658452
OpenAlexW4317567103

What OpenQuestion holds

Textmetadata
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.