Evidence map›Paper›PMID 41487453›Full record

ArticleGastro hep advances2026

Identification of Circulating MiR-4651 as Novel Biomarker for Metabolic Dysfunction-Associated Steatotic Liver Disease.

Mélanie Kirchmeyer, Anthoula Gaigneaux, Florence A Servais, Anita Arslanow, Claudia Rubie, Markus Casper, Matthias Glanemann, María L Martínez-Chantar, Marcin Krawczyk, Frank Lammert and 1 more

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Article in Gastro hep advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Mélanie KirchmeyerDepartment of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Anthoula GaigneauxDepartment of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Florence A ServaisDepartment of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Anita ArslanowDepartment of Medicine II, Saarland University Medical Center, Homburg, Germany.
Claudia RubieDepartment of Surgery, Saarland University Medical Center, Homburg, Germany.
Markus CasperDepartment of Medicine II, Saarland University Medical Center, Homburg, Germany.
Matthias GlanemannDepartment of Surgery, Saarland University Medical Center, Homburg, Germany.
María L Martínez-ChantarLiver Disease Lab, Center for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance, Derio, Spain.
Marcin KrawczykDepartment of Medicine II, Saarland University Medical Center, Homburg, Germany.
Frank LammertDepartment of Medicine II, Saarland University Medical Center, Homburg, Germany.
Iris BehrmannDepartment of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Metabolic dysfunction-associated steatotic liver disease (MASLD) affects >30% of adults and is becoming one of the leading causes of hepatocellular carcinoma (HCC). Reliable biomarkers are needed for the early diagnosis of HCC and detection of chronic liver diseases, like MASLD. Here we assessed the biomarker potential of circulating microRNAs in a cohort of patients genotyped for the risk allele of Methods: The cohort comprised 70 MASLD patients (40 with simple steatosis, 9 with metabolic dysfunction-associated steatohepatitis (MASH), 21 with cirrhosis), 47 HCC patients (32 with cirrhosis), and 14 healthy controls. Serum levels of miR-122-5p, miR-146a-5p, miR-146b-5p, miR-21-5p, miR-335-5p, miR-433-3p, miR-4530, miR-4651, miR-526a2, and miR-873-5p were quantified using custom qPCR plates. Their suitability for prediction of MASLD (steatosis/MASH/cirrhosis) or HCC was assessed by receiver operating characteristic curve analyses. Results: MiR-4651 and miR-21-5p were significantly reduced in sera from patients with MASLD, particularly in those with simple steatosis. Both microRNAs effectively distinguished MASLD patients with simple steatosis from healthy controls (area under the curve: 0.95 and 0.89, respectively). Moreover, miR-4651 emerged as the best predictor for differentiating "complicated" MASLD (i.e., MASH or cirrhosis) from simple steatosis; the predictive values could be increased by including additional parameters into the models (Fibroscan, thrombocytes, cytokines, or other miRNAs). miR-335-5p showed strong ability to differentiate HCC from healthy individuals (area under the curve: 0.86). The Conclusion: Serum microRNAs, in particular miR-4651, may serve as additional biomarkers in patients with steatotic liver disease.

Indexed as

circulating microRNAhepatocellular carcinomaliver cirrhosispatatin-like phospholipase domain-containing protein 3receiver operating characteristic curve analysis

Identifiers

PMID41487453
PMCPMC12756624

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