Evidence map›Paper›PMID 42886740›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

Early-Life Betaine Supplementation Drives Sex-Specific Metabolic Programming in Rats, Affecting FGF21 Signaling and Energy Balance.

Rocío A Martín-Chamorro, Catalina A Pomar, Andreu Palou, Catalina Picó, Ana M Rodríguez

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Rocío A Martín-ChamorroLaboratory of Molecular Biology, Nutrition and Biotechnology (Group of Nutrigenomics, Biomarkers and Risk Evaluation, NUBE), University of the Balearic Islands (UIB), Palma, Spain.
Catalina A PomarLaboratory of Molecular Biology, Nutrition and Biotechnology (Group of Nutrigenomics, Biomarkers and Risk Evaluation, NUBE), University of the Balearic Islands (UIB), Palma, Spain.ORCID https://orcid.org/0000-0002-8113-761X
Andreu PalouLaboratory of Molecular Biology, Nutrition and Biotechnology (Group of Nutrigenomics, Biomarkers and Risk Evaluation, NUBE), University of the Balearic Islands (UIB), Palma, Spain.
Catalina PicóLaboratory of Molecular Biology, Nutrition and Biotechnology (Group of Nutrigenomics, Biomarkers and Risk Evaluation, NUBE), University of the Balearic Islands (UIB), Palma, Spain.
Ana M RodríguezLaboratory of Molecular Biology, Nutrition and Biotechnology (Group of Nutrigenomics, Biomarkers and Risk Evaluation, NUBE), University of the Balearic Islands (UIB), Palma, Spain.

Funding

Ministerio de Ciencia e Innovación (MCIN) PGC2018-097436-B-I00Ministerio de Ciencia e Innovación (MCIN) PID2022-138140NBI00
6 · The paper itself

Abstract

We aimed to evaluate the effects of maternal diet and betaine supplementation during the suckling period on Fgf21 expression and metabolic pathways related to FGF21 signaling and metabolic programming. Offspring of Wistar rats fed either a chow diet (CD) or a Western diet (WD) were studied at postnatal day 22 and at 7 months. During suckling, pups received betaine at a physiological dose corresponding to twice the average intake estimated from milk consumption, or a vehicle. After weaning onto a CD, all animals were switched to a WD from months four to seven. Biometric parameters, circulating markers, and gene expression in hypothalamus, retroperitoneal white adipose tissue (rWAT), and liver were analyzed, together with cecal Akkermansia muciniphila abundance. At day 22, a maternal WD reduced hepatic Fgf21 expression in both sexes; however, only males showed decreased Klb expression in rWAT, consistent with impaired FGF21 signaling. A maternal WD also reduced A. muciniphila abundance. Betaine increased Fgfr1 expression in rWAT of female offspring from control dams. By seven months, betaine supplementation in males born to WD dams increased adiposity, and insulin and leptin levels, whereas females exhibited an improved plasma lipid profile (lower NEFA and TG). Hypothalamic Drd2 and Fgfr1 expression further showed sex-specific modulation by the maternal diet and betaine. In conclusion, betaine supplementation during suckling exerts sex-specific long-term effects on metabolic programming. Females showed an improved lipid profile, whereas males, particularly those exposed to a maternal WD, developed increased adiposity and altered endocrine profiles. The findings suggest that early-life betaine supplementation can modulate long-term metabolic outcomes through sex-specific effects on FGF21-related pathways.

Indexed as

BetaineEnergy MetabolismFibroblast Growth FactorsSignal TransductionAnimalsDietary SupplementsFemaleHypothalamusMalePregnancyRatsRats, WistarBetainefibroblast growth factor 21Fibroblast Growth Factorsbetaineearly‐life nutritionFGF21 signalingmetabolic imprintingsex‐specific metabolism

Identifiers

PMID42886740
PMCPMC13674722

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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.