Evidence map›Paper›PMID 30666754›Full record

ArticleJournal of veterinary internal medicine2019

Evaluation of an HMGA2 variant for pleiotropic effects on height and metabolic traits in ponies.

Elaine M Norton, Felipe Avila, Nichol E Schultz, James R Mickelson, Ray J Geor, Molly E McCue

Open access · goldAbstract read
In one paragraph

Article in Journal of veterinary internal medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
8.8field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
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  15. HMGA Genes and Proteins in Development and Evolution.International journal of molecular sciences · 2020
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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 at 2 institutions in 2 countries.

Elaine M NortonVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota.ORCID https://orcid.org/0000-0001-9450-2893
Felipe AvilaVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota.
Nichol E SchultzVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota.
James R MickelsonVeterinary Biomedical Sciences Department, University of Minnesota, St. Paul, Minnesota.
Ray J GeorMassey University, College of Sciences, Palmerston North, New Zealand.
Molly E McCueVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota.
University of Minnesota · USMassey University · NZ

Funding

Foundation for the National Institutes of Health T32 OD010993Morris Animal Foundation D14EQ-033National Institute of Food and Agriculture 2009-55205-052542012-67015-19432
6 · The paper itself

Abstract

backgroundPonies are highly susceptible to metabolic derangements including hyperinsulinemia, insulin resistance, and adiposity. HYPOTHESIS/

objectivesGenetic loci affecting height in ponies have pleiotropic effects on metabolic pathways and increase the susceptibility to equine metabolic syndrome (EMS). ANIMALS: Two hundred ninety-four Welsh ponies and 529 horses.

methodsRetrospective study of horses phenotyped for metabolic traits. Correlations between height and metabolic traits were assessed by Pearson's correlation coefficients. Complementary genome-wide analysis methods were used to identify a region of interest (ROI) for height and metabolic traits, determine the fraction of heritability contributed by the ROI, and identify candidate genes.

resultsThere was an inverse relationship between height and baseline insulin (-0.26) in ponies. Genomic signature of selection and association analyses for both height and insulin identified the same ~1.3 megabase region on chromosome 6 that contained a shared ancestral haplotype between these traits. The ROI contributed ~40% of the heritability for height and ~20% of the heritability for insulin. High-mobility group AT-hook 2 was identified as a candidate gene, and Sanger sequencing detected a c.83G>A (p.G28E) variant associated with height in Shetland ponies. In our cohort of ponies, the A allele had a frequency of 0.76, was strongly correlated with height (-0.75), and was low to moderately correlated with metabolic traits including: insulin (0.32), insulin after an oral sugar test (0.25), non-esterified fatty acids (0.19), and triglyceride (0.22) concentrations. CONCLUSIONS AND CLINICAL IMPORTANCE: These data have important implications for identifying individuals at risk for EMS.

Indexed as

AnimalsBiometryFatty Acids, NonesterifiedFemaleGlucose Tolerance TestHorse DiseasesHorsesInsulinInsulin ResistanceMaleMetabolic SyndromePhenotypeRetrospective StudiesSpecies SpecificityTriglyceridesFatty Acids, NonesterifiedInsulinTriglyceridesequine metabolic syndromegeneticshorsesinsulin dysregulation

Identifiers

PMID30666754
PMCPMC6430908
OpenAlexW2912285156

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.