Evidence map›Paper›PMID 40281461›Full record

ArticleBMC pediatrics2025

Metabolism-related hepatokines change in biliary atresia: ANGPTL6 as a potential biomarker.

Daiqiong Fang, Shuqi Hu, Jinfa Tou, Fengqin Dong, Shiqiao Peng

Abstract read
In one paragraph

Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. Review
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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

5 authors.

Daiqiong Fang *Department of Endocrinology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shuqi Hu *Department of Neonatal Surgery, The Children´s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, China.
Jinfa TouDepartment of Neonatal Surgery, The Children´s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, China.
Fengqin DongDepartment of Endocrinology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shiqiao PengDepartment of Endocrinology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. clearling405@163.com.

Funding

National Key Research and Development Program of China 2023YFC2506000
6 · The paper itself

Abstract

objectivesBiliary atresia (BA) is a severe obstructive cholangiopathy of early infancy that progresses to end-stage liver disease without any intervention. The aim of this study was to investigate the impact of drainage obstruction of bile on metabolism-related hepatokines and identify clinical biomarkers of BA.

methodsA total of 38 patients with BA and 12 age-matched controls were recruited. Blood samples were obtained for measuring liver function and hepatokine levels. Linear correlations between these changes in hepatokines and bilirubin/bile acid were subsequently examined to explore the hepatokines that may reflect the illness severity. Afterwards, ROC curve analysis was conducted to assess the diagnostic value of the hepatokines. Finally, prognostic analysis of the hepatokines was performed based on early cholangitis, the clearance of jaundice, native liver survival and liver transplantation.

resultsThe serum concentrations of TB, DB, ALT, AST, GGT, ALP and TBA in patients with BA were all increased compared with those in controls (P < 0.05). The plasma levels of ANGPTL4, HGF, FABP1, FGF21 and FGF23 were elevated in BA patients (P < 0.05), whereas the plasma ANGPTL6 level was decreased in BA patients (P < 0.05). The results of the correlation analysis revealed that ANGPTL6 was negatively linearly correlated with TB and DB and that FGF23 was positively linearly correlated with TBA. ROC curve analysis revealed that the AUC of ANGPTL6 for diagnosing BA was 0.9693, with a sensitivity of 0.8684 and a specificity of 1.0 at an optimal cut-off value of 1140.76 ng/ml. Prognostic analysis revealed that a lower plasma level of ANGPTL6 at KPE was associated with the occurrence of early cholangitis after KPE (P < 0.05).

conclusionsAmong all of the hepatokines that were measured in this study, ANGPTL6 may be a potential diagnostic biomarker of BA and may be able to predict the occurrence of early cholangitis. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Angiopoietin-like ProteinsBiliary AtresiaAngiopoietin-Like Protein 6Bile Acids and SaltsBilirubinBiomarkersCase-Control StudiesFemaleFibroblast Growth FactorsHumansInfantMalePrognosisROC CurveAngiopoietin-Like Protein 6Angiopoietin-like ProteinsANGPTL6 protein, humanBile Acids and SaltsBilirubinBiomarkersFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsANGPTL6Biliary atresiaBiomarkerEarly cholangitisHepatokine

Identifiers

PMID40281461
PMCPMC12032793

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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.