Evidence map›Paper›PMID 42518540›Full record

ArticleFrontiers in endocrinology2026

Estradiol negatively associates with metabolic dysfunction-associated steatotic liver disease in children.

Judith Lubrecht, Robert Kleemann, Bjorn Winkens, Ger Koek, Annemieke Heijboer, Anita Vreugdenhil

Abstract read
In one paragraph

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

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Judith LubrechtCentre for Overweight Adolescent and Children's Healthcare (COACH), Maastricht University Medical Center+, MosaKids Children's Hospital, Maastricht, Netherlands.
Robert KleemannDepartment of Metabolic Health Research, The Netherlands Organization for Applied Scientific Research (TNO), Leiden, Netherlands.
Bjorn WinkensDepartment of Methodology and Statistics, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, Netherlands.
Ger KoekDepartment of Gastroenterology, Maastricht University Medical Center+, Maastricht, Netherlands.
Annemieke HeijboerEndocrine Laboratory, Department of Laboratory Medicine, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
Anita VreugdenhilCentre for Overweight Adolescent and Children's Healthcare (COACH), Maastricht University Medical Center+, MosaKids Children's Hospital, Maastricht, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is the leading cause of chronic liver disease in children and adolescents. Studies in adults indicate that MASLD is more prevalent in males compared to females and that sex hormones may play a significant role in MASLD development. However, limited pediatric research is available on the relation between sex hormones and MASLD. This study investigates associations between sex hormones and MASLD in children with overweight and obesity. Methods: A cross-sectional study was conducted in children with overweight and obesity in a tertiary care center (Maastricht UMC+). A comprehensive serum sex hormone panel, serum alanine aminotransferase (ALT) and hepatic steatosis on ultrasound (HS) were determined in 290 participants. Controlled Attenuation Parameter (CAP, measured with FibroScan) was available in 75 participants. Associations between sex hormones and MASLD parameters (ALT, HS and CAP) were investigated. Results: This study found that estradiol, Anti-Müllerian hormone (AMH) and sex hormone-binding globulin (SHBG) inversely associated with ALT (p=0.018, p=0.048 and p<0.001). Free (FT) and bioavailable (BT) testosterone and dehydroepiandrosterone sulfate (DHEAS) positively associated with ALT (both p=0.006). In addition to this, AMH and SHBG inversely associated with HS (p=0.028 and p<0.001), while FT, BioT and DHEAS positively associated with HS (p=0.024, p=0.024 and p=0.042). Lastly, AMH and SHBG inversely associated with CAP (p=0.04 and p<0.001), whereas follicle stimulating hormone, total testosterone (TT), FT, BioT, androstenedione and DHEAS positively associated (p=0.034, p=0.04, p=0.032, p=0.032, p=0.007 and p=0.003). Conclusions: Estradiol, AMH and SHGB inversely associate with MASLD parameters, while androgens, including TT, FT, BioT, and DHEAS, positively associate with MASLD parameters in children with overweight and obesity.

Indexed as

EstradiolFatty LiverMetabolic DiseasesNon-alcoholic Fatty Liver DiseaseAdolescentAlanine TransaminaseAnti-Mullerian HormoneChildCross-Sectional StudiesFemaleHumansMaleOverweightSex Hormone-Binding GlobulinAlanine TransaminaseAnti-Mullerian HormoneEstradiolSex Hormone-Binding GlobulinSHBG protein, humanadolescentchildestradiolfatty liverMASLDNAFLDobesitysex differences

Identifiers

PMID42518540
PMCPMC13381234

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.