ArticleFrontiers in endocrinology2025
Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Cardiovascular-Kidney-Metabolic Syndrome and Its Hepatic Dimension: A Narrative Review.Medicina (Kaunas, Lithuania) · 2026Review
- Metabolic Dysfunction-Associated Steatotic Liver Disease in Childhood: From Disease Heterogeneity to Personalized Care.Journal of personalized medicine · 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: With the rising global prevalence of childhood obesity, the incidence of metabolic dysfunction-associated steatotic liver disease (MASLD) in pediatric and adolescent populations is also increasing. The genetic mechanisms underlying MASLD remain incompletely elucidated. This study aimed to investigate the roles of eight genetic loci- Methods: A total of 350 children and adolescents aged 7-17 years were enrolled, including 196 with MASLD (case group) and 154 healthy controls. Demographics, medical history, anthropometric measurements, and hepatic B-ultrasound data were collected. Fasting morning blood samples were obtained for biochemical analysis and genotyping. Statistical analyses included chi-square tests, Fisher's exact tests, and multivariate logistic regression to identify predictive factors for pediatric MASLD. Results: The allele frequencies of Conclusion: The
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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 OpenQuestion graph.