Evidence map›Paper›PMID 37935884›Full record

ArticlePediatric research2024

Metabolic and fecal microbial changes in adult fetal growth restricted mice.

Stephanie P Gilley, Miguel A Zarate, Lijun Zheng, Purevsuren Jambal, Deaunabah N Yazza, Sree V Chintapalli, Paul S MacLean, Clyde J Wright, Paul J Rozance, Kartik Shankar

Open access · hybridAbstract read
In one paragraph

Article in Pediatric research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 13% of its field
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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Microbe on the move:Journal of bacteriology · 2026
    Review
  3. Article
  4. 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

10 authors at 3 institutions in 1 country.

Stephanie P GilleyDepartment of Pediatrics, Section of Nutrition, University of Colorado School of Medicine, Aurora, CO, USA. Stephanie.Gilley@cuanschutz.edu.ORCID 0000-0003-0304-5514
Miguel A ZarateDepartment of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
Lijun ZhengDepartment of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
Purevsuren JambalDepartment of Pediatrics, Section of Nutrition, University of Colorado School of Medicine, Aurora, CO, USA.
Deaunabah N YazzaDepartment of Pediatrics, Section of Nutrition, University of Colorado School of Medicine, Aurora, CO, USA.
Sree V ChintapalliArkansas Children's Nutrition Center, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Paul S MacLeanDepartment of Medicine, Division of Endocrinology, Metabolism, and Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Clyde J WrightDepartment of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
Paul J RozanceDepartment of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
Kartik ShankarDepartment of Pediatrics, Section of Nutrition, University of Colorado School of Medicine, Aurora, CO, USA.
University of Colorado Denver · USArkansas Children's Nutrition Center · USUniversity of Colorado Anschutz Medical Campus · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS · 1995 to 2026
$32.6M
Training Program in Perinatal Biology and MedicineT32HD007186 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Paul Joseph Rozance · 1985 to 2026
$6.5M
NIDDK National Research Service Award (NRSA) T32 Diversity Administrative SupplementT32DK007658 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Kristen Elizabeth Boyle, Ihuoma U Eneli · 1991 to 2026
$6.0M
Physiological Ramifications of Chorionic Somatomammotropin DeficiencyR01HD093701 · NICHD · UNIVERSITY OF COLORADO DENVER · PI ANTHONY, RUSSELL V, ROZANCE, PAUL JOSEPH · 2018 to 2022
$2.9M
Fetal glucagon links fetal metabolism with uterine blood flow and placental nutrient transfer by inhibiting placental lactogen secretionR01HD111557 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Paul Joseph Rozance · 2023 to 2026
$2.5M
NICHD NIH HHS R01 HD093701NICHD NIH HHS R01 HD111557NICHD NIH HHS T32 HD007186NIDDK NIH HHS T32 DK007658
6 · The paper itself

Abstract

backgroundFetal growth restriction (FGR) increases risk for development of obesity and type 2 diabetes. Using a mouse model of FGR, we tested whether metabolic outcomes were exacerbated by high-fat diet challenge or associated with fecal microbial taxa.

methodsFGR was induced by maternal calorie restriction from gestation day 9 to 19. Control and FGR offspring were weaned to control (CON) or 45% fat diet (HFD). At age 16 weeks, offspring underwent intraperitoneal glucose tolerance testing, quantitative MRI body composition assessment, and energy balance studies. Total microbial DNA was used for amplification of the V4 variable region of the 16 S rRNA gene. Multivariable associations between groups and genera abundance were assessed using MaAsLin2.

resultsAdult male FGR mice fed HFD gained weight faster and had impaired glucose tolerance compared to control HFD males, without differences among females. Irrespective of weaning diet, adult FGR males had depletion of Akkermansia, a mucin-residing genus known to be associated with weight gain and glucose handling. FGR females had diminished Bifidobacterium. Metabolic changes in FGR offspring were associated with persistent gut microbial changes.

conclusionFGR results in persistent gut microbial dysbiosis that may be a therapeutic target to improve metabolic outcomes. IMPACT: Fetal growth restriction increases risk for metabolic syndrome later in life, especially if followed by rapid postnatal weight gain. We report that a high fat diet impacts weight and glucose handling in a mouse model of fetal growth restriction in a sexually dimorphic manner. Adult growth-restricted offspring had persistent changes in fecal microbial taxa known to be associated with weight, glucose homeostasis, and bile acid metabolism, particularly Akkermansia, Bilophilia and Bifidobacteria. The gut microbiome may represent a therapeutic target to improve long-term metabolic outcomes related to fetal growth restriction.

Indexed as

Diabetes Mellitus, Type 2Fetal Growth RetardationAdultDiet, High-FatFemaleFetal DevelopmentGlucoseHumansInfantMaleWeight GainGlucose

Identifiers

PMID37935884
PMCPMC10899111
OpenAlexW4388453640

What OpenQuestion holds

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LicenceCC BY
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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.