Evidence map›Paper›PMID 39082696›Full record

ArticleEndocrinology2024

Changes in the Bile Acid Pool and Timing of Female Puberty: Potential Novel Role of Hypothalamic TGR5.

Heidi Vanden Brink, Doris Vandeputte, Ilana L Brito, Oline K Ronnekleiv, Mark S Roberson, Alejandro Lomniczi

Abstract read
In one paragraph

Article in Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
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  8. Muricholic acid mediates puberty initiation via the hypothalamic TGR5 signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  10. Review
  11. Article
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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.

Heidi Vanden BrinkDepartment of Nutrition, Texas A&M University, College Station, TX 77840, USA.
Doris VandeputteMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Ilana L BritoMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Oline K RonnekleivDepartment of Chemical Physiology and Biochemistry, Oregon Health and Sciences University, Portland, OR 97239, USA.
Mark S RobersonDepartment of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0001-5317-810X
Alejandro LomnicziDepartment of Physiology and Biophysics, Dalhousie School of Medicine, Halifax, NS B3H 4R2, Canada.ORCID 0000-0003-4535-0103

Funding

Metabolic Control of Puberty: Epigenetic LinksR01HD084542 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI LOMNICZI, ALEJANDRO · 2015 to 2019
$2.6M
Epigenetic Signaling in the Aging HypothalamusR21AG061141 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI LOMNICZI, ALEJANDRO, URBANSKI, HENRYK F · 2020 to 2021
$481k
Trajectory of ovarian morphology during the adolescent reproductive transition.R21HD095372 · NICHD · CORNELL UNIVERSITY · PI LUJAN, MARLA E · 2019 to 2020
$436k
CIHREunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health R21HD095372European Union's Horizon 2020 research 895167NIA NIH HHS R21 AG061141NICHD NIH HHS R01 HD084542NICHD NIH HHS R21 HD095372NIH HHS 5R01HD084542Packard FoundationPew Charitable TrustsTexas A&M and AgriLife ResearchWeill Cornell-Cornell Multi-Investigator Seed Grant
6 · The paper itself

Abstract

contextThe regulation of pubertal timing and reproductive axis maturation is influenced by a myriad of physiologic and environmental inputs yet remains incompletely understood.

objectiveTo contrast differences in bile acid isoform profiles across defined stages of reproductive maturity in humans and a rat model of puberty and to characterize the role of bile acid signaling via hypothalamic expression of bile acid receptor populations in the rodent model.

methodsSecondary analysis and pilot studies of clinical cohorts, rodent models, ex vivo analyses of rodent hypothalamic tissues. Bile acid concentrations is the main outcome measure.

resultsLower circulatory conjugated:deconjugated bile acid concentrations and higher total secondary bile acids were observed in postmenarcheal vs pre-/early pubertal adolescents, with similar shifts observed in infantile (postnatal day [PN]14) vs early juvenile (PN21) rats alongside increased tgr5 receptor mRNA expression within the mediobasal hypothalamus of female rats. 16S rRNA gene sequencing of the rodent gut microbiome across postnatal life revealed changes in the gut microbial composition predicted to have bile salt hydrolase activity, which was observed in parallel with the increased deconjugated and increased concentrations of secondary bile acids. We show that TGR5-stimulated GnRH release from hypothalamic explants is mediated through kisspeptin receptors and that early overexpression of human-TGR5 within the arcuate nucleus accelerates pubertal onset in female rats.

conclusionBile acid isoform shifts along stages of reproductive maturation are conserved across rodents and humans, with preclinical models providing mechanistic insight for the neuroendocrine-hepatic-gut microbiome axis as a potential moderator of pubertal timing in females.

Indexed as

Bile Acids and SaltsHypothalamusReceptors, G-Protein-CoupledSexual MaturationAdolescentAdultAnimalsChildFemaleGastrointestinal MicrobiomeHumansPubertyRatsRats, Sprague-DawleyYoung AdultBile Acids and SaltsGPBAR1 protein, humanGpbar1 protein, ratReceptors, G-Protein-Coupledbile acidshypothalamusneuroendocrinepituitarypubertyTGR5

Identifiers

PMID39082696
PMCPMC11334072

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LicenceCC BY-NC-ND
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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.