Evidence map›Paper›PMID 25898945›Full record

ArticleBMC genomics2015

The uniform-score gene set analysis for identifying common pathways associated with different diabetes traits.

Hao Mei, Lianna Li, Shijian Liu, Fan Jiang, Michael Griswold, Thomas Mosley

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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 3 institutions in 2 countries.

Hao MeiCenter of Biostatistics & Bioinformatics, University of Mississippi Medical Center, Jackson, MS, USA. hmei@umc.edu.
Lianna LiDepartment of Biology, Tougaloo College, Jackson, MS, USA. lli@tougaloo.edu.
Shijian LiuShanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. arrow64@163.com.
Fan JiangShanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. riversailer@hotmail.com.
Michael GriswoldCenter of Biostatistics & Bioinformatics, University of Mississippi Medical Center, Jackson, MS, USA. mgriswold@umc.edu.
Thomas MosleyDepartment of Neurology, University of Mississippi Medical Center, Jackson, MS, USA. tmosley@umc.edu.
University of Mississippi Medical Center · USShanghai Children's Medical Center · CNTougaloo College · US

Funding

ARIC Neurocognitive Study (ARIC-NCS) Renewal 2 of 5U01HL096917 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI MOSLEY, THOMAS H · 2010 to 2018
$11.9M
FIELD CENTERN01HC055021 · HC · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI JONES, DANIEL W · 1985 to 2000
$617k
NHLBI NIH HHS N01 HC055021NHLBI NIH HHS N01-HC55021NHLBI NIH HHS U01 HL096917NHLBI NIH HHS U01-HL096917
6 · The paper itself

Abstract

backgroundGenetic heritability and expression study have shown that different diabetes traits have common genetic components and pathways. A computationally efficient pathway analysis of GWAS results will benefit post-GWAS study of SNP associations and identification of common genetic pathways from diabetes GWAS can help to improve understanding of the disease pathogenesis.

resultsWe proposed a uniform-score gene-set analysis (USGSA) with implemented package to unify different gene measures by a uniform score for identifying pathways from GWAS data, and use a pre-generated permutation distribution table to quickly obtain multiple-testing adjusted p-value. Simulation studies of uniform score for four gene measures (minP, 2ndP, simP and fishP) have shown that USGSA has strictly controlled family-wise error rate. The power depends on types of gene measure. USGSA with a two-stage study strategy was applied to identify common pathways associated with diabetes traits based on public dbGaP GWAS results. The study identified 7 gene sets that contain binding motifs at promoter region of component genes for 5 transcription factors (TFs) of FOXO4, TCF3, NFAT, VSX1 and POU2F1, and 1 microRNA of mir-218. These gene sets include 25 common genes that are among top 5% of the gene associations over genome for all GWAS. Previous evidences showed that nearly all of these genes are mainly expressed in the brain.

conclusionsUSGSA is a computationally efficient approach for pathway analysis of GWAS data with promoted interpretability and comparability. The pathway analysis suggested that different diabetes traits share common pathways and component genes are potentially regulated by common TFs and microRNA. The result also indicated that the central nervous system has a critical role in diabetes pathogenesis. The findings will be important in formulating novel hypotheses for guiding follow-up studies.

Indexed as

Genome, HumanGenome-Wide Association StudyBase SequenceDatabases, GeneticDiabetes MellitusHumansMicroRNAsPolymorphism, Single NucleotidePromoter Regions, GeneticTranscription FactorsMicroRNAsMIRN218 microRNA, humanTranscription Factors

Identifiers

PMID25898945
PMCPMC4415316
OpenAlexW2039593730

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LicenceCC BY
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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.