Evidence map›Paper›PMID 22973538›Full record

ArticleG3 (Bethesda, Md.)2012

Quantitative trait loci affecting liver fat content in mice.

Olga Minkina, James M Cheverud, Gloria Fawcett, Clay F Semenkovich, Jane P Kenney-Hunt

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

5 authors at 2 institutions in 2 countries.

Olga MinkinaDepartment of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
James M Cheverud
Gloria Fawcett
Clay F Semenkovich
Jane P Kenney-Hunt
Institute of Neurobiology · BGWashington University in St. Louis · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
DE NOVO LIPOGENESIS AND METABOLIC DISEASER01DK076729 · NIDDK · WASHINGTON UNIVERSITY · PI SEMENKOVICH, CLAY F. · 2007 to 2015
$2.5M
Genetics Basis of Dietary Obesity in MiceR01DK055736 · NIDDK · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2000 to 2009
$2.1M
OBESITY, ADIPOGENESIS, AND LIPID LIGANDSR01DK088083 · NIDDK · WASHINGTON UNIVERSITY · PI SEMENKOVICH, CLAY F. · 2010 to 2013
$1.3M
GENETIC BASIS OF DIETARY OBESITY IN MICER56DK055736 · NIDDK · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2010 to 2010
$354k
NIDDK NIH HHS DK020579NIDDK NIH HHS DK055736NIDDK NIH HHS DK056341NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK056341NIDDK NIH HHS P60 DK020579NIDDK NIH HHS R01 DK055736NIDDK NIH HHS R01 DK076729NIDDK NIH HHS R01 DK088083NIDDK NIH HHS R56 DK055736
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease, a condition in which excess fat accumulates in the liver, is strongly associated with the metabolic syndrome, including obesity and other related conditions. This disease has the potential to progress from steatosis to steatohepatitis, fibrosis, and cirrhosis. The recent increase in the prevalence of the metabolic syndrome is largely driven by changes in diet and activity levels. Individual variation in the response to this obesogenic environment, however, is attributable in part to genetic variation between individuals, but very few mammalian genetic loci have been identified with effects on fat accumulation in the liver. To study the genetic basis for variation in liver fat content in response to dietary fat, liver fat proportion was determined using quantitative magnetic resonance imaging in 478 mice from 16 LG/J X SM/J recombinant inbred strains fed either a high-fat (42% kcal from fat) or low-fat (15% kcal from fat) diet. An analysis of variance confirmed that there is a genetic basis for variation in liver fat content within the population with significant effects of sex and diet. Three quantitative trail loci that contribute to liver fat content also were mapped.

Indexed as

Quantitative Trait LociAnimalsDiabetes MellitusDiet, Fat-RestrictedDiet, High-FatFatsFatty LiverFemaleLiverMaleMiceNon-alcoholic Fatty Liver DiseaseObesityFatsLG/JmouseNAFLDnonalcoholic fatty liver diseaseQTLSM/J

Identifiers

PMID22973538
PMCPMC3429915
OpenAlexW2159949570

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.