Evidence mapPaperPMID 39574069Full record

SynthesisBMC medicine2024

Strategic interventions in clinical randomized trials for metabolic dysfunction-associated steatotic liver disease (MASLD) and obesity in the pediatric population: a systematic review with meta-analysis and bibliometric analysis.

Isabel Omaña-Guzmán, Marisol Rosas-Diaz, Yoscelina Estrella Martínez-López, L Monserrat Perez-Navarro, Alvaro Diaz-Badillo, Anthony Alanis, Alejandra Bustamante, Octelina Castillo-Ruiz, Noemi Del Toro-Cisneros, Diego Armando Esquivel-Hernandez and 21 more

Registry-linked trialAbstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07731360 (A Non-Invasive Diagnostic Panel for MASLD in Children With Obesity), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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.

NCT07731360 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Non-Invasive Diagnostic Panel for MASLD in Children With Obesity: Evaluation of a Multiparametric Biomarker Panel and Genetic Risk Score Using LASSO-Regularized Logistic Regression - The PedMASLD-MultiOmics Pilot Study

TypeobservationalSponsorKayseri City HospitalRan2026 to 2027Enrolled180ConditionsMetabolic Dysfunction-Associated Steatotic Liver Disease, Pediatric Obesity, Insulin Resistance SyndromeArmsNon-Invasive Multi-Parameter Diagnostic Panel
3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Determinants of Liver Steatosis Progression in Chinese Children: A Prospective Cohort Study.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. The Microbiome and Metabolic Dysfunction-Associated Steatotic Liver Disease.International journal of molecular sciences · 2025
    Review
  11. Review
  12. 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

31 authors.

Isabel Omaña-GuzmánPediatric Obesity Clinic and Wellness Unit, Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico.
Marisol Rosas-DiazLaboratorio de Biologia Molecular, Universidad Autónoma de Tamaulipas, Tamaulipas, Mexico.
Yoscelina Estrella Martínez-LópezUT Health Science Center at Houston's School of Public Health, Brownsville, TX, USA.
L Monserrat Perez-NavarroServicio de Nefrologia. Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico.
Alvaro Diaz-BadilloDepartment of Health and Behavioral Sciences, Texas A&M University, San Antonio, TX, USA.
Anthony AlanisSchool of Medicine, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Alejandra BustamanteMedicina Interna, Hospital Angeles Clinica Londres, Mexico City, Mexico.
Octelina Castillo-RuizUniversidad Autónoma de Tamaulipas, Tamaulipas, Mexico.
Noemi Del Toro-CisnerosDepartamento de Nefrología y Metabolismo Mineral, Instituto Nacional de La Nutricion Salvador Zubiran, Mexico City, Mexico.
Diego Armando Esquivel-HernandezDepartamento de Procesos y Tecnología, Universidad Autónoma Metropolitana Cuajimalpa, Mexico City, Mexico.
Gloria Garcia-VillalobosServicio de Nefrologia. Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico.
Nayely Garibay-NietoPediatric Obesity Clinic and Wellness Unit, Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico.
Esperanza Milagros Garcia-OropesaLaboratorio de Biologia Molecular, Universidad Autónoma de Tamaulipas, Tamaulipas, Mexico.
Juan Carlos Hernandez-MartinezLaboratorio de Biologia Molecular, Universidad Autónoma de Tamaulipas, Tamaulipas, Mexico.
Elena Beatriz Lopez-SosaAngiologia y Cirugía Vascular, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado de México (ISSTE), Hospital 20 de Noviembre, Mexico City, Mexico.
Carlos MaldonadoInstituto Nacional de Enfermedaes Respiratorias, Mexico City, Mexico.
David MartinezDepartment of Biology, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Joshua MembrenoSchool of Medicine, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Oscar Omar Moctezuma-ChavezAsociación Odontológica Mexicana Para La Enseñanza y La Investigación, Mexico City, Mexico.
Claudia X Munguia-CisnerosCentro Especializado de Metabolismo y Diabetes (CEDIAMET), Universidad México Americana del Norte, Tamaulipas, Mexico.
Edna J Nava-GonzálezFacultad de Salud Pública y Nutrición, Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, México.
Adriana L Perales-TorresUniversidad Autónoma de Tamaulipas, Tamaulipas, Mexico.
Adolfo Pérez-GarcíaResearch Department, Hospital General de México "Dr. Eduardo Liceaga", Mexico City, Mexico.
Hector Rivera-MarreroSchool of Medicine, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Alisha ValdezSchool of Medicine, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Alfonso Alejandro Vázquez-ChávezUniversidad del Valle de México, Campus Hermosillo, Sonora, Mexico.
Carlos Ramirez-PfeifferEscuela de Medicina, Universidad México Americana del Norte, Reynosa, Tamaulipas, Mexico.
Kathleen V CarterSchool of Medicine, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Beatriz TapiaFaculty Affairs, Asst Dean Faculty Development, The University of Texas Rio Grande Valley, Edinburg, TX, USA.
Leonel VelaDivision of Population Health & Biostatistics, School of Medicine, University of Texas Rio Grande Valley, 2102 Treasure Hills Boulevard, Edinburg, TX, 78550, USA.
Juan Carlos Lopez-AlvarengaEscuela de Medicina, Universidad México Americana del Norte, Reynosa, Tamaulipas, Mexico. juan.lopezalvarenga@utrgv.edu.ORCID 0000-0002-0966-8766

Funding

NIA NIH HHS P30 AG059305
6 · The paper itself

Abstract

backgroundMetabolic dysfunction-associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty liver disease (NAFLD), is a prevalent hepatic condition linked to metabolic alterations. It gradually causes liver damage and potentially progresses to cirrhosis. Despite its significance, research, especially in the pediatric population, is limited, leading to contradictory findings in diagnosis and treatment. This meta-analysis aims to synthesize existing literature on therapeutic interventions for MASLD in children and adolescents.

methodsA comprehensive search of randomized controlled clinical trials yielded 634 entries from PubMed, Scopus, and Web of Science up to 2023. Interventions included medications, behavioral modifications, dietary changes, probiotics, supplements, surgical procedures, or combinations. The analysis focused on studies with treatment duration of at least 3 months, employing a random-effects REML meta-analysis model. Treatment effects on anthropometric measurements and biochemical components were examined and adjusted for heterogeneity factors analysis. A bibliometric analysis for insights into research contributors was performed.

resultsThe systematic review incorporated 31 clinical trials, with 24 meeting criteria for meta-analysis. These comprised 3 medication studies, 20 with supplements, 4 focusing on lifestyle, and 4 centered on diets. Significant overall treatment effects were observed for ALT, AST, BMI, and HOMA-IR mainly by supplements and lifestyle. Meta-regression identified age, BMI changes, and treatment duration as factors modifying ALT concentrations. Bibliometric analysis involving 31 linked studies highlighted contributions from 13 countries, with the USA, Spain, and Chile being the most influential.

conclusionsWe conclude that supplementation and lifestyle changes can effectively impact ALT and AST levels, which can help address liver issues in obese children. However, the evaluation of risk bias, the high heterogeneity, and the bibliometric analysis emphasize the need for more high-quality studies and broader inclusion of diverse child populations to provide better therapeutic recommendations.

trial registrationPROSPERO, CRD42023393952. Registered on January 25, 2023.

Indexed as

BibliometricsNon-alcoholic Fatty Liver DiseaseRandomized Controlled Trials as TopicAdolescentChildHumansPediatric ObesityLiver enzymesMASLD (metabolic dysfunction-associated steatotic liver disease)Meta-analysisPediatric NAFLDRandomized controlled trialsTherapeutic interventions

Identifiers

PMID39574069
PMCPMC11580631

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.