ReviewHepatology forum2025
Role of micrornas in the pathophysiology and diagnosis of metabolic dysfunction-associated steatotic liver disease: A bibliometric review.
Review in Hepatology forum, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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.
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.
Who cites it
4 citing papers in PubMed.
- miR-34a and miR-223 as diagnostic biomarkers for the severity of non-alcoholic fatty liver disease.Journal, genetic engineering & biotechnology · 2026Article
- The Inflammaging-Redox-InflammamiR Axis in Metabolic Aging: From Diagnostic Clusters to Integrated Risk Phenotypes.Biomolecules · 2026Review
- MicroRNAs as Key Regulators in the Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease: A Bioinformatics Analysis.Biomedicines · 2026Article
- Loss of immunometabolic adaptability in MASH: gut-derived signals drive macrophage reprogramming and fibrosis.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Metabolic dysfunction-associated steatotic liver disease (MASLD) has become a public health problem, given its increasing incidence worldwide and strong association with metabolic syndrome components such as obesity, insulin resistance, and systemic inflammation. Recent studies have shown the relevance of microRNAs (miRNAs) as potential biomarkers and therapeutic targets in MASLD. This bibliometric review aimed to evaluate the scientific production of the last decade on miRNAs involved in the pathophysiology and diagnosis of MASLD. A total of 775 articles were initially retrieved from the PubMed database, with 51 meeting the inclusion criteria after a systematic screening process. Bibliometric analysis showed that China and the United States had the highest number of publications, with studies published mainly by the International Journal of Molecular Sciences and Hepatology. Among the most studied miRNAs were miR-122, miR-29a, miR-34a, and miR-223, which participate in lipid metabolism, inflammation, fibrosis, and insulin sensitivity. Co-authorship network analysis identified Gao Bin as the most influential author in the field. Keyword co-occurrence analysis showed growing interest in miRNAs in general, miR-29a, miR-34a, miR-122, miR-223, nonalcoholic fatty liver disease, lipogenesis, and mitochondrial stress in recent years. This review emphasizes the increasing scientific attention on miRNAs involved in MASLD and highlights their diagnostic and therapeutic potential. However, further studies are still needed for the identification and clinical validation of therapeutic targets that modulate miRNAs. Future perspectives include the integration of omics approaches and the exploration of nutritional or pharmacological strategies for miRNA modulation.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.