Evidence map›Paper›PMID 40839133›Full record

ArticleEuropean radiology2026

A novel multi-parameter MRI-based model for identification of high-risk metabolic dysfunction-associated steatohepatitis.

Wenxin Ma, Xutong Huang, Zhen Feng, Wenli Tan, Jinzhe Li, Huamei Yan, Yanxi Zheng, Zhiwei Qin, Fuhua Yan, Huimin Lin and 1 more

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Article in European radiology, 2026. 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. Review
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.

Wenxin MaDepartment of Radiology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Xutong HuangDepartment of Radiology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Zhen FengDepartment of Pathology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Wenli TanDepartment of Radiology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Jinzhe LiDepartment of Radiology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Huamei YanClinical Research Center, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yanxi ZhengDepartment of Liver, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Zhiwei QinMR Research Collaboration, Shanghai United Imaging Healthcare Co., Ltd., Shanghai, China.
Fuhua YanDepartment of Radiology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Huimin LinDepartment of Radiology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. lhm12362@rjh.com.cn.
Jie YuanDepartment of Radiology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China. yuanjie3352@shutcm.edu.cn.ORCID http://orcid.org/0000-0002-6471-6687

Funding

National Natural Science Foundation of China 81901694National Natural Science Foundation of China 82305184Shanghai Explorer Program 21TS1400600Shanghai Rising Stars of Medical Talents Youth Development Program SHWSRS(2024)_070
6 · The paper itself

Abstract

objectivesTo develop and evaluate a novel multi-parameter MRI-based model (EFT1) for identifying high-risk metabolic dysfunction-associated steatohepatitis (MASH) to improve diagnostic accuracy and efficiency. MATERIALS AND

methodsA prospective study included 118 patients (55 male; 48 ± 13 years) with hepatic steatosis and metabolic risk factors. Among these, 80 patients were classified as having high-risk MASH. Magnetic resonance elastography (MRE), T1 mapping, chemical-shift encoded MRI for quantification of proton density fat fraction (PDFF) and R2* were performed, followed by liver biopsy. MRI parameters were analyzed and correlated with histological features. The EFT1 model was developed using logistic regression and full subset regression analysis on a training cohort (70%) and validated on a test cohort (30%). The performance of the model was compared with traditional scoring systems.

resultsSignificant differences were observed in MRE, PDFF, and T1 between high-risk MASH and non-high-risk MASH groups. The EFT1 model, combining MRE, PDFF, and T1 showed strong diagnostic performance in both training (AUC 0.995, 95% CI 0.985-1.000) and test cohorts (AUC 0.995, 95% CI 0.979-1.000). At the optimal cut-off value of -0.431, the model achieved high sensitivity (98.2% training, 95.7% test) and specificity (96.3% training, 100% test). The EFT1 model outperformed traditional scoring systems (FIB-4, APRI, GPR) and showed comparable performance to the MAST score in identifying high-risk MASH.

conclusionThe novel EFT1 model demonstrates reasonable performance in non-invasive identification of high-risk MASH patients compared to other models, achieving an appropriate balance between sensitivity and specificity. CLINICAL

trial registrationThis study is registered with Chictr.org.cn (ChiCTR2400094017). KEY POINTS: Question Current non-invasive scoring systems for high-risk MASH have limitations. A novel multi-parameter MRI-based model is proposed to improve diagnostic accuracy and efficiency. Findings A novel multi-parameter MRI-based model (EFT1), incorporating MRE, PDFF, and T1 mapping, demonstrated higher accuracy in identifying high-risk MASH with an AUC of 0.995. Clinical relevance The EFT1 model provides a highly accurate, non-invasive tool for early identification of high-risk MASH, facilitating timely intervention and personalized treatment strategies, potentially reducing disease progression and improving patient outcomes.

Indexed as

Fatty LiverMagnetic Resonance ImagingNon-alcoholic Fatty Liver DiseaseAdultElasticity Imaging TechniquesFemaleHumansLiverMaleMiddle AgedProspective StudiesRisk FactorsSensitivity and SpecificityEFT1High-risk MASHIdentificationMRI

Identifiers

What Socratic holds

Textmetadata
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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.