Evidence map›Paper›PMID 26885899›Full record

ArticleOncotarget2016

Integrative analysis of genome-wide association studies and gene expression analysis identifies pathways associated with rheumatoid arthritis.

Mingming Zhang, Hongbo Mu, Hongchao Lv, Lian Duan, Zhenwei Shang, Jin Li, Yongshuai Jiang, Ruijie Zhang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 9 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

8 authors at 2 institutions in 1 country.

Mingming ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Hongbo MuCollege of Science, Northeast Forestry University, Harbin, China.
Hongchao LvCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Lian DuanCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Zhenwei ShangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Jin LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Yongshuai JiangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Ruijie ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Harbin Medical University · CNNortheast Forestry University · CN

Funding

Medical Research Council G1001799Medical Research Council MR/N01104X/1
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a complex and systematic autoimmune disease, which is usually influenced by both genetic and environmental factors. Pathway analyses based on a single data type such as microarray data or SNP data have successfully revealed some biology pathways associated with RA. However, we found that the pathway analysis based on a single data type only provide limited understanding about the pathogenesis of RA. Gene-disease association is usually caused by many ways, such as genotype, gene expression and so on. Therefore, the integrative analysis method combining multiple levels of evidence can more precisely and comprehensively identify the pathway associations. In this study, we performed a pathway analysis by integrating GWAS and gene expression analysis to detect the RA-related pathways. The integrative analysis identified 28 pathways associated with RA. Among these pathways, 18 pathways were also found by both GWAS and gene expression analysis, 7 pathways are novel RA-related pathways, such as B cell receptor signaling pathway, Toll-like receptor signaling pathway, Fc gamma R-mediated phagocytosis and so on. Compared with pathway analyses using only one type genomic data, we found integrative analysis can increase the power to identify the real associations and provided more stable and accurate results. We believe these results will contribute to perform future genetic studies in RA pathogenesis and may promote the development of new therapeutic strategies by targeting these pathways.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyArthritis, RheumatoidBiomarkersComputational BiologyGenomicsGenotypeHumansPolymorphism, Single NucleotideSignal TransductionSystems BiologyBiomarkersgene expressionPathology Sectionpathway analysisrheumatoid arthritissingle nucleotide polymorphism

Identifiers

PMID26885899
PMCPMC4890988
OpenAlexW2282555216

What OpenQuestion holds

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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.