Evidence map›Paper›PMID 26299439›Full record

ArticleScientific reports2015

Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.

Wei-Dong Li, Hongxiao Jiao, Kai Wang, Fuhua Yang, Struan F A Grant, Hakon Hakonarson, Rexford Ahima, R Arlen Price

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 2 countries.

Wei-Dong LiResearch Center of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Hongxiao JiaoResearch Center of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Kai WangZilkha Neurogenetic Institute and Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA 90089, USA.
Fuhua YangResearch Center of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Struan F A GrantCenter for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Rexford AhimaDepartment of Medicine, Division of Endocrinology, Diabetes and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
R Arlen PriceCenter for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Tianjin Medical University · CNUniversity of Pennsylvania · USChildren's Hospital of Philadelphia · USUniversity of Southern California · US

Funding

GENETIC STUDIES OF OBESITYR01DK044073 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI PRICE, R ARLEN · 1991 to 2008
$3.8M
FINE LOCALIZATION OF GENES FOR HUMAN OBESITYR01DK056210 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI PRICE, R ARLEN · 2000 to 2004
$3.7M
An association scan for human obesity related genesR01DK076023 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI PRICE, R ARLEN · 2008 to 2011
$1.5M
Integrative statistical models for pathway analysis of GWAS dataR21HG006037 · NHGRI · VANDERBILT UNIVERSITY · PI WANG, LILY, ZHAO, ZHONGMING · 2013 to 2014
$445k
NHGRI NIH HHS HG006037NHGRI NIH HHS R21 HG006037NIDDK NIH HHS R01 DK044073NIDDK NIH HHS R01 DK056210NIDDK NIH HHS R01 DK076023NIDDK NIH HHS R01DK076023NIDDK NIH HHS R01DK44073NIDDK NIH HHS R01DK56210
6 · The paper itself

Abstract

Pathway-based analysis as an alternative and effective approach to identify disease-related genes or loci has been verified. To decipher the genetic background of plasma adiponectin levels, we performed genome wide pathway-based association studies in extremely obese individuals and normal-weight controls. The modified Gene Set Enrichment Algorithm (GSEA) was used to perform the pathway-based analyses (the GenGen Program) in 746 European American females, which were collected from our previous GWAS in extremely obese (BMI > 35 kg/m(2)) and never-overweight (BMI<25 kg/m(2)) controls. Rac1 cell motility signaling pathway was associated with plasma adiponectin after false-discovery rate (FDR) correction (empirical P < 0.001, FDR = 0.008, family-wise error rate = 0.008). Other several Rac1-centered pathways, such as cdc42racPathway (empirical P < 0.001), hsa00603 (empirical P = 0.003) were among the top associations. The RAC1 pathway association was replicated by the ICSNPathway method, yielded a FDR = 0.002. Quantitative pathway analyses yielded similar results (empirical P = 0.001) for the Rac1 pathway, although it failed to pass the multiple test correction (FDR = 0.11). We further replicated our pathway associations in the ADIPOGen Consortium data by the GSA-SNP method. Our results suggest that Rac1 and related cell motility pathways might be associated with plasma adiponectin levels and biological functions of adiponectin.

Indexed as

Genome-Wide Association StudyAdiponectinBody Mass IndexCase-Control StudiesHumansPolymorphism, Single Nucleotiderac1 GTP-Binding ProteinReproducibility of ResultsSignal TransductionWhite PeopleAdiponectinADIPOQ protein, humanrac1 GTP-Binding ProteinRAC1 protein, human

Identifiers

PMID26299439
PMCPMC4642532
OpenAlexW2432472560

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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.