Evidence map›Paper›PMID 39640486›Full record

ArticleFrontiers in pharmacology2024

ADRB2 serves as a novel biomarker and attenuates alcoholic hepatitis via the SIRT1/PGC-1α/PPARα pathway: integration of WGCNA, machine learning and experimental validation.

Li Song, Shuo Huang, Honghao Yan, Qing Ma, Qihan Luo, Jiang Qiu, Minxia Chen, Zongyuan Li, He Jiang, Yufan Chen and 6 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2024. 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

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

2 citing papers in PubMed.

  1. [Histone deacetylases and alcohol-related liver disease].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  2. 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

16 authors.

Li Song *Tongde Hospital of Zhejiang Province affiliated to Zhejiang Chinese Medical University, Analysis and Testing Center, Zhejiang Academy of Traditional Chinese Medicine, Hangzhou, China.
Shuo Huang *School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Honghao Yan *School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Qing MaThe First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Qihan LuoSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Jiang QiuDepartment of Medicine, Hangzhou Normal University, Hangzhou, China.
Minxia ChenSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Zongyuan LiSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
He JiangSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Yufan ChenSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Fangming ChenAcademy of Chinese Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Yu DuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Haozhe FuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Lisha ZhaoTongde Hospital of Zhejiang Province affiliated to Zhejiang Chinese Medical University, Analysis and Testing Center, Zhejiang Academy of Traditional Chinese Medicine, Hangzhou, China.
Kanglu ZhaoZhejiang Rehabilitation Medical Center, Rehabilitation Hospital Area of the Third Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Ping QiuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alcoholic hepatitis is a severe inflammatory liver disease. In recent years, the incidence of AH has been on the rise, leading to an increasingly severe disease burden. Currently, there is a lack of specific biomarkers for the diagnosis and prognosis of AH in clinical practice. Therefore, the main objective of this study is to identify biomarkers closely associated with the progression of AH, to address the shortcomings in pathological diagnosis, and to identify potential therapeutic targets. Methods: Bioinformatics and machine learning methods were used to comparatively study the differentially expressed genes (DEGs) between AH patients and healthy individuals by analyzing four mRNA microarray data sets obtained from the GEO database. Subsequently, the role of potential biomarkers in AH and their mechanism of action were further confirmed by AH patients and Results: Using differential analysis and WGCNA of the data set, a total of 167 key genes that may be related to AH were obtained. Among 167 genes, the LASSO logistic regression algorithm identified four potential biomarkers (KCNJ10, RPL21P23, ADRB2, and AC025279.1). Notably, ADRB2 showed biomarker potential in GSE28619, GSE94397, and E-MTAB-2664 datasets, and clinical liver samples. Furthermore, AH patients and Conclusion: This study points to ADRB2 as a promising biomarker with potential diagnostic and prognostic value in clinical cohort data. In addition, in AH patients,

Indexed as

ADRB2alcoholic hepatitisbiomarkerinflammationmachine learningoxidative stressSIRT1/PGC-1α/PPARα pathwayWGCNA

Identifiers

PMID39640486
PMCPMC11617210

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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.