Evidence map›Paper›PMID 20459604›Full record

ArticleBMC medical genetics2010

Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes.

Vesna Boraska, Nigel W Rayner, Christopher J Groves, Timothy M Frayling, Mahamadou Diakite, Kirk A Rockett, Dominic P Kwiatkowski, Aaron G Day-Williams, Mark I McCarthy, Eleftheria Zeggini

Abstract read
In one paragraph

Article in BMC medical genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 6 pooled it
–field-weighted citation impact
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

19 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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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

10 authors.

Vesna BoraskaDepartment of Medical Biology, University of Split School of Medicine, Split, Croatia. vboraska@mefst.hr
Nigel W Rayner
Christopher J Groves
Timothy M Frayling
Mahamadou Diakite
Kirk A Rockett
Dominic P Kwiatkowski
Aaron G Day-Williams
Mark I McCarthy
Eleftheria Zeggini

Funding

Medical Research Council G0000934Medical Research Council G0600230Medical Research Council G19/9Wellcome Trust 068545/Z/02Wellcome Trust 076113Wellcome Trust WT088885/Z/09/Z
6 · The paper itself

Abstract

backgroundThe TNF/LTA locus has been a long-standing T2D candidate gene. Several studies have examined association of TNF/LTA SNPs with T2D but the majority have been small-scale and produced no convincing evidence of association. The purpose of this study is to examine T2D association of tag SNPs in the TNF/LTA region capturing the majority of common variation in a large-scale sample set of UK/Irish origin.

methodsThis study comprised a case-control (1520 cases and 2570 control samples) and a family-based component (423 parent-offspring trios). Eleven tag SNPs (rs928815, rs909253, rs746868, rs1041981 (T60N), rs1800750, rs1800629 (G-308A), rs361525 (G-238A), rs3093662, rs3093664, rs3093665, and rs3093668) were selected across the TNF/LTA locus and genotyped using a fluorescence-based competitive allele specific assay. Quality control of the obtained genotypes was performed prior to single- and multi-point association analyses under the additive model.

resultsWe did not find any consistent SNP associations with T2D in the case-control or family-based datasets.

conclusionsThe present study, designed to analyse a set of tag SNPs specifically selected to capture the majority of common variation in the TNF/LTA gene region, found no robust evidence for association with T2D. To investigate the presence of smaller effects of TNF/LTA gene variation with T2D, a large-scale meta-analysis will be required.

Indexed as

Genetic Association StudiesPolymorphism, Single NucleotideDiabetes Mellitus, Type 2FemaleGenetic LociGenotypeHumansLinkage DisequilibriumLymphotoxin-alphaMaleMiddle AgedPedigreeLymphotoxin-alpha

Identifiers

PMID20459604
PMCPMC2873325

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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.