Evidence map›Paper›PMID 34989650›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2022

Altered IGF-I activity and accelerated bone elongation in growth plates precede excess weight gain in a mouse model of juvenile obesity.

Allison L Machnicki, Cassaundra A White, Chad A Meadows, Darby McCloud, Sarah Evans, Dominic Thomas, John D Hurley, Daniel Crow, Habiba Chirchir, Maria A Serrat

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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 2 institutions in 1 country.

Allison L MachnickiDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Cassaundra A WhiteDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Chad A MeadowsDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Darby McCloudDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Sarah EvansDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Dominic ThomasDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
John D HurleyDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Daniel CrowDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.
Habiba ChirchirDepartment of Biological Sciences, Marshall University, Huntington, West Virginia.
Maria A SerratDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia.ORCID 0000-0001-9211-9508
Marshall University · USSmithsonian Institution · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sijin Wen · 2012 to 2026
$81.0M
WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
Regulation of Tight Junction Molecular Composition by Na/K-ATPaseP20GM121299 · NIGMS · MARSHALL UNIVERSITY · PI HAYNES, JENNIFER · 2018 to 2022
$10.6M
Heat enhanced molecular delivery to growth plates for targeted bone lengtheningR15AR067451 · NIAMS · MARSHALL UNIVERSITY · PI SERRAT, MARIA ANNE · 2014 to 2014
$383k
NASA 80NSSC20M0055NIAMS NIH HHS R15 AR067451NIAMS NIH HHS R15AR067451NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P20 GM121299NIGMS NIH HHS P20GM121299NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

Nearly one-third of children in the United States are overweight or obese by their preteens. Tall stature and accelerated bone elongation are characteristic features of childhood obesity, which cooccur with conditions such as limb bowing, slipped epiphyses, and fractures. Children with obesity paradoxically have normal circulating IGF-I, the major growth-stimulating hormone. Here, we describe and validate a mouse model of excess dietary fat to examine mechanisms of growth acceleration in obesity. We used in vivo multiphoton imaging and immunostaining to test the hypothesis that high-fat diet increases IGF-I activity and alters growth plate structure before the onset of obesity. We tracked bone and body growth in male and female C57BL/6 mice (

Indexed as

Growth PlatePediatric ObesityAnimalsChildDiet, High-FatFemaleHumansInsulin-Like Growth Factor IMaleMiceMice, Inbred C57BLWeight GainInsulin-Like Growth Factor Iendochondral ossificationgrowth platehigh-fat dietIGF binding proteinmultiphoton microscopy

Identifiers

PMID34989650
PMCPMC8836718
OpenAlexW4206105257

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.