Evidence map›Paper›PMID 24156295›Full record

ArticleBMC medical genetics2013

Studies of association of AGPAT6 variants with type 2 diabetes and related metabolic phenotypes in 12,068 Danes.

Lena Sønder Snogdal, Niels Grarup, Karina Banasik, Mette Wod, Torben Jørgensen, Daniel R Witte, Torsten Lauritzen, Aneta A Nielsen, Ivan Brandslund, Cramer Christensen and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 35% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

16 authors at 6 institutions in 1 country.

Lena Sønder Snogdal
Niels Grarup
Karina Banasik
Mette Wod
Torben Jørgensen
Daniel R Witte
Torsten Lauritzen
Aneta A Nielsen
Ivan Brandslund
Cramer Christensen
Oluf Pedersen
Knud Yderstræde
Henning Beck-Nielsen
Jan Erik Henriksen
Torben Hansen
Kurt Højlund
Odense University Hospital · DKNovo Nordisk Foundation · DKVejle Sygehus · DKUniversity of Copenhagen · DKAarhus University · DKSteno Diabetes Center · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 2 diabetes, obesity and insulin resistance are characterized by hypertriglyceridemia and ectopic accumulation of lipids in liver and skeletal muscle. AGPAT6 encodes a novel glycerol-3 phosphate acyltransferase, GPAT4, which catalyzes the first step in the de novo triglyceride synthesis. AGPAT6-deficient mice show lower weight and resistance to diet- and genetically induced obesity. Here, we examined whether common or low-frequency variants in AGPAT6 associate with type 2 diabetes or related metabolic traits in a Danish population.

methodsEleven variants selected by a candidate gene approach capturing the common and low-frequency variation of AGPAT6 were genotyped in 12,068 Danes from four study populations of middle-aged individuals. The case-control study involved 4,638 type 2 diabetic and 5,934 glucose-tolerant individuals, while studies of quantitative metabolic traits were performed in 5,645 non-diabetic participants of the Inter99 Study.

resultsNone of the eleven AGPAT6 variants were robustly associated with type 2 diabetes in the Danish case-control study. Moreover, none of the AGPAT6 variants showed association with measures of obesity (waist circumference and BMI), serum lipid concentrations, fasting or 2-h post-glucose load levels of plasma glucose and serum insulin, or estimated indices of insulin secretion or insulin sensitivity.

conclusionsCommon and low-frequency variants in AGPAT6 do not significantly associate with type 2 diabetes susceptibility, or influence related phenotypic traits such as obesity, dyslipidemia or indices of insulin sensitivity or insulin secretion in the population studied.

Indexed as

Polymorphism, Single NucleotideBody Mass IndexCase-Control StudiesDenmarkDiabetes Mellitus, Type 2Genetic Predisposition to DiseaseGenotypeGlycerol-3-Phosphate O-AcyltransferaseHumansInsulinInsulin ResistanceLinkage DisequilibriumLipidsObesityOdds RatioPhenotypeGlycerol-3-Phosphate O-AcyltransferaseGPAT4 protein, humanInsulinLipids

Identifiers

PMID24156295
PMCPMC4231429
OpenAlexW2050726407

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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.