Evidence map›Paper›PMID 39595599›Full record

ArticleBiomolecules2024

The Development of a Non-Invasive Screening Method Based on Serum microRNAs to Quantify the Percentage of Liver Steatosis.

Polina Soluyanova, Guillermo Quintás, Álvaro Pérez-Rubio, Iván Rienda, Erika Moro, Marcel van Herwijnen, Marcha Verheijen, Florian Caiment, Judith Pérez-Rojas, Ramón Trullenque-Juan and 2 more

Abstract read
In one paragraph

Article in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

12 authors.

Polina SoluyanovaUnidad Mixta de Investigación en Hepatología Experimental, IIS Hospital La Fe, 46026 Valencia, Spain.
Guillermo QuintásHealth and Biomedicine, LEITAT Technological Center, 08225 Terrassa, Spain.ORCID 0000-0002-4240-9846
Álvaro Pérez-RubioServicio de Cirugía General y Aparato Digestivo, Hospital Universitario Dr. Peset, 46017 Valencia, Spain.ORCID 0000-0001-8960-6145
Iván RiendaPathology Department, Hospital Universitario y Politécnico La Fe, 46026 Valencia, Spain.ORCID 0000-0002-3254-7372
Erika MoroUnidad Mixta de Investigación en Hepatología Experimental, IIS Hospital La Fe, 46026 Valencia, Spain.
Marcel van HerwijnenDepartment of Translational Genomics, Research Institute of Oncology and Developmental Biology (GROW), Maastricht University, 6229-ER Maastricht, The Netherlands.
Marcha VerheijenDepartment of Translational Genomics, Research Institute of Oncology and Developmental Biology (GROW), Maastricht University, 6229-ER Maastricht, The Netherlands.
Florian CaimentDepartment of Translational Genomics, Research Institute of Oncology and Developmental Biology (GROW), Maastricht University, 6229-ER Maastricht, The Netherlands.
Judith Pérez-RojasPathology Department, Hospital Universitario y Politécnico La Fe, 46026 Valencia, Spain.ORCID 0000-0002-6091-0888
Ramón Trullenque-JuanServicio de Cirugía General y Aparato Digestivo, Hospital Universitario Dr. Peset, 46017 Valencia, Spain.
Eugenia ParejaServicio de Cirugía General y Aparato Digestivo, Hospital Universitario Dr. Peset, 46017 Valencia, Spain.
Ramiro JoverUnidad Mixta de Investigación en Hepatología Experimental, IIS Hospital La Fe, 46026 Valencia, Spain.ORCID 0000-0002-4914-5804

Funding

European Commission under the Horizon 2020 Research and Innovation Framework program 963845 ONTOXFUNSECO (Fundación de la Sociedad Española de Cirugía de la Obesidad) 2022Instituto de Salud Carlos III (ISCIII) co-funded by the European Union PI20/00690MCIN/AEI/10.13039/501100011033 and "ERDF A way of making Europe" "European Union" PID2021- 125573OB-I00
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is often asymptomatic and underdiagnosed; consequently, there is a demand for simple, non-invasive diagnostic tools. In this study, we developed a method to quantify liver steatosis based on miRNAs, present in liver and serum, that correlate with liver fat. The miRNAs were analyzed by miRNAseq in liver samples from two cohorts of patients with a precise quantification of liver steatosis. Common miRNAs showing correlation with liver steatosis were validated by RT-qPCR in paired liver and serum samples. Multivariate models were built using partial least squares (PLS) regression to predict the percentage of liver steatosis from serum miRNA levels. Leave-one-out cross validation and external validation were used for model selection and to estimate predictive performance. The miRNAseq results disclosed (a) 144 miRNAs correlating with triglycerides in a set of liver biobank samples (

Indexed as

Fatty LiverMicroRNAsAdultBiomarkersFemaleHumansLiverMaleMiddle AgedBiomarkersMicroRNAsliver steatosisMetabolic dysfunction-associated steatotic liver diseasemicroRNApartial least squares regressionquantitative predictionserum biomarker

Identifiers

PMID39595599
PMCPMC11592063

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Registered trials

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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.