Evidence mapPaperPMID 38281815Full record

ArticleClinical and molecular hepatology2024

Identification of signature gene set as highly accurate determination of metabolic dysfunction-associated steatotic liver disease progression.

Sumin Oh, Yang-Hyun Baek, Sungju Jung, Sumin Yoon, Byeonggeun Kang, Su-Hyang Han, Gaeul Park, Je Yeong Ko, Sang-Young Han, Jin-Sook Jeong and 10 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and molecular hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 1 country.

Sumin OhLaboratory of Biomedical Genomics, Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Yang-Hyun BaekLiver Center, Department of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Sungju JungLaboratory of Biomedical Genomics, Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Sumin YoonLaboratory of Biomedical Genomics, Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Byeonggeun KangDepartment of Biological Sciences and Institute of Molecular Biology and Genetics, Seoul National University, Seoul, Korea.
Su-Hyang HanLaboratory of Biomedical Genomics, Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Gaeul ParkDivision of Rare Cancer, Research Institute, National Cancer Center, Goyang, Korea.
Je Yeong KoDepartment of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Sang-Young HanLiver Center, On Hospital, Busan, Korea.
Jin-Sook JeongDepartment of Pathology, Dong-A University Medical Center, Busan, Korea.
Jin-Han ChoDepartment of Diagnostic Radiology, Dong-A University Medical Center, Busan, Korea.
Young-Hoon RohDepartment of Surgery, Dong-A University Medical Center, Busan, Korea.
Sung-Wook LeeLiver Center, Department of Internal Medicine, Dong-A University Medical Center, Busan, Korea.
Gi-Bok ChoiDepartment of Radiology, On Hospital, Busan, Korea.
Yong Sun LeeDivision of Rare Cancer, Research Institute, National Cancer Center, Goyang, Korea.
Won KimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea.
Rho Hyun SeongDepartment of Biological Sciences and Institute of Molecular Biology and Genetics, Seoul National University, Seoul, Korea.
Jong Hoon ParkDepartment of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Yeon-Su LeeDivision of Rare Cancer, Research Institute, National Cancer Center, Goyang, Korea.
Kyung Hyun YooLaboratory of Biomedical Genomics, Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Sookmyung Women's University · KRDong-A University · KRNational Cancer Center · KRSeoul National University · KRBusan Medical Center · KRBumin Hospital Group · KR

Funding

Ministry of Science and ICTNational Research Foundation of Korea -2017M3C9A6044199National Research Foundation of Korea 2017M3C9A6044517National Research Foundation of Korea 2017M3C9A6044519National Research Foundation of Korea 2022M3A9B6017654
6 · The paper itself

Abstract

BACKGROUND/

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by fat accumulation in the liver. MASLD encompasses both steatosis and MASH. Since MASH can lead to cirrhosis and liver cancer, steatosis and MASH must be distinguished during patient treatment. Here, we investigate the genomes, epigenomes, and transcriptomes of MASLD patients to identify signature gene set for more accurate tracking of MASLD progression.

methodsBiopsy-tissue and blood samples from patients with 134 MASLD, comprising 60 steatosis and 74 MASH patients were performed omics analysis. SVM learning algorithm were used to calculate most predictive features. Linear regression was applied to find signature gene set that distinguish the stage of MASLD and to validate their application into independent cohort of MASLD.

resultsAfter performing WGS, WES, WGBS, and total RNA-seq on 134 biopsy samples from confirmed MASLD patients, we provided 1,955 MASLD-associated features, out of 3,176 somatic variant callings, 58 DMRs, and 1,393 DEGs that track MASLD progression. Then, we used a SVM learning algorithm to analyze the data and select the most predictive features. Using linear regression, we identified a signature gene set capable of differentiating the various stages of MASLD and verified it in different independent cohorts of MASLD and a liver cancer cohort.

conclusionWe identified a signature gene set (i.e., CAPG, HYAL3, WIPI1, TREM2, SPP1, and RNASE6) with strong potential as a panel of diagnostic genes of MASLD-associated disease.

Indexed as

Fatty LiverLiver NeoplasmsAlgorithmsDisease ProgressionHumansBiomarkerMachine learningMASLDMulti-omicsSignature gene set

Identifiers

PMID38281815
PMCPMC11016492
OpenAlexW4391296847

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.