Evidence map›Paper›PMID 21211013›Full record

ArticleBMC medical genetics2011

Lack of association between genetic polymorphisms within DUSP12 - ATF6 locus and glucose metabolism related traits in a Chinese population.

Cheng Hu, Rong Zhang, Congrong Wang, Xiaojing Ma, Jie Wang, Yuqian Bao, Kunsan Xiang, Weiping Jia

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. The Association of a Genetic Variant inJournal of diabetes research · 2017
    Article
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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

8 authors at 2 institutions in 1 country.

Cheng HuDepartment of Endocrinology and Metabolism, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Clinical Center for Diabetes, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, PR China.
Rong Zhang
Congrong Wang
Xiaojing Ma
Jie Wang
Yuqian Bao
Kunsan Xiang
Weiping Jia
Shanghai Sixth People's Hospital · CNShanghai Jiao Tong University · CN

Funding

The international 1q type 2 diabetes consortiumR01DK073490 · NIDDK · UNIVERSITY OF OXFORD · PI MCCARTHY, MARK IAN · 2006 to 2010
$5.9M
NIDDK NIH HHS R01-DK073490
6 · The paper itself

Abstract

backgroundGenome-wide linkage studies in multiple ethnic populations found chromosome 1q21-q25 was the strongest and most replicable linkage signal in the human chromosome. Studies in Pima Indian, Caucasians and African Americans identified several SNPs in DUSP12 and ATF6, located in chromosome 1q21-q23, were associated with type 2 diabetes.

methodsWe selected 19 single nucleotide polymorphisms (SNPs) that could tag 98% of the SNPs with minor allele frequencies over 0.1 within DUSP12-ATF6 region. These SNPs were genotyped in a total of 3,700 Chinese Han subjects comprising 1,892 type 2 diabetes patients and 1,808 controls with normal glucose regulation.

resultsNone of the SNPs and haplotypes showed significant association to type 2 diabetes in our samples. No association between the SNPs and quantitative traits was observed either.

conclusionsOur data suggests common SNPs within DUSP12-ATF6 locus may not play a major role in glucose metabolism in the Chinese.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticActivating Transcription Factor 6Asian PeopleBlood GlucoseCase-Control StudiesChromosomes, Human, Pair 1Diabetes Mellitus, Type 2Dual-Specificity PhosphatasesFemaleGene FrequencyHaplotypesHumansMalePolymorphism, Single NucleotideActivating Transcription Factor 6ATF6 protein, humanBlood Glucosedual specificity phosphatase 12Dual-Specificity Phosphatases

Identifiers

PMID21211013
PMCPMC3022799
OpenAlexW1981719381

What OpenQuestion holds

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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.