Evidence map›Paper›PMID 40510350›Full record

Observational studyFrontiers in immunology2025

Causal relationship between hepatic function indicators and thrombocytopenia risk in early-stage hepatitis B virus infection: evidence from clinical observational studies and mendelian randomization analyses.

Tian-Bin Chen, Jian-Wei Jiang, Hong-Yan Guo, Xiao-Tong Chen, Shuai Zhi, Yu-Hai Hu, Ya Fu, Yong-Bing Zeng, Can Liu, Qi-Shui Ou and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. 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

11 authors.

Tian-Bin Chen *The First Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Jian-Wei Jiang *Department of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, Institute of Precision Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Hong-Yan Guo *The School of Public Health, Fujian Medical University, Fuzhou, China.
Xiao-Tong ChenDepartment of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, Institute of Precision Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Shuai ZhiDepartment of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, Institute of Precision Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Yu-Hai HuDepartment of Hepatopancreatobiliary Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Ya FuThe First Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Yong-Bing ZengThe First Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Can LiuThe First Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Qi-Shui OuThe First Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.
Shi-Tao RaoDepartment of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, Institute of Precision Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Thrombocytopenia is a common occurrence in patients with hepatitis B virus (HBV) infection, particularly in those with liver cirrhosis. However, it can also manifest in the early stages of HBV infection, before the onset of liver cirrhosis. Despite its prevalence, the molecular mechanisms underlying thrombocytopenia in this context are not well understood. Therefore, the primary aim of this study was to investigate whether common hepatic function indicators have a significant causal role in this mechanism. Methods: We conducted a retrospective examination of the association between HBV infection and thrombocytopenia risk in apparently healthy participants who underwent health screening examinations. Subsequently, we investigated the causal relationship between multiple hepatic function indicators and thrombocytopenia risk by integrating clinical observational studies and univariate/multivariate Mendelian randomization (MR) analyses. Results: Among 16,464 participants who underwent health screening examinations, 2,730 subjects (16.58%) tested positive for HBsAg. The prevalence of thrombocytopenia was significantly higher in HBsAg-positive subjects compared to healthy controls ( Conclusions: This study identified multiple hepatic function indicators as independent factors associated with thrombocytopenia risk. Notably, our findings provided the first dual confirmation of the causal effect of the injury indicator ALT on thrombocytopenia risk, as evidenced by both clinical observational studies and genetics-based MR analyses, prior to the development of liver cirrhosis.

Indexed as

Hepatitis BHepatitis B virusLiverThrombocytopeniaAdultAlanine TransaminaseBiomarkersFemaleHumansLiver CirrhosisLiver Function TestsMaleMendelian Randomization AnalysisMiddle AgedPrevalenceRetrospective StudiesAlanine TransaminaseBiomarkersHBV: hepatitis B virusHCV: hepatitis C virusIV: instrumental variableMR: mendelian randomizationRCT: randomized controlled trialsingle-nucleotide polymorphismssnpsTPO: thrombopoietin

Identifiers

PMID40510350
PMCPMC12158931

What Socratic holds

Textmetadata
LicenceCC BY
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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.