Evidence map›Paper›PMID 30887029›Full record

ArticleBioinformatics (Oxford, England)2019

Differential network enrichment analysis reveals novel lipid pathways in chronic kidney disease.

Jing Ma, Alla Karnovsky, Farsad Afshinnia, Janis Wigginton, Daniel J Rader, Loki Natarajan, Kumar Sharma, Anna C Porter, Mahboob Rahman, Jiang He and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 30 citations in OpenAlex.

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  11. Present and future directions in diabetic kidney disease.Journal of diabetes and its complications · 2022
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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

17 authors at 13 institutions in 1 country.

Jing MaDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Alla KarnovskyDepartment of Computational Medicine & Bioinformatics, Ann Arbor, MI, USA.
Farsad AfshinniaDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Janis WiggintonMichigan Regional Comprehensive Metabolomics Resource Core, Ann Arbor, MI, USA.
Daniel J RaderDepartment of Medicine, Translational-Clinical Research, University of Pennsylvania, Philadelphia, PA, USA.
Loki NatarajanDepartment of Family Medicine and Public Health, University of California at San Diego, San Diego, CA, USA.
Kumar SharmaDepartment of Internal Medicine, University of Texas Health at San Antonio, San Antonio, TX, USA.
Anna C PorterDepartment of Internal Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Mahboob RahmanDepartment of Internal Medicine, Case-Western Reserve University, Cleveland, OH, USA.
Jiang HeDepartment of Epidemiology, Tulane University School of Medicine, Tulane University, New Orleans, LA, USA.
Lee HammSchool of Medicine, Division of Nephrology and Hypertension, Tulane University, New Orleans, LA, USA.
Tariq ShafiDepartment of Internal Medicine, Johns Hopkins University, Baltimore, MD, USA.
Debbie GipsonDepartment of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Crystal GadegbekuDepartment of Internal Medicine, Temple University, Philadelphia, PA, USA.
Harold FeldmanCenter for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, USA.
George MichailidisMichigan Regional Comprehensive Metabolomics Resource Core, Ann Arbor, MI, USA.
Subramaniam PennathurMichigan Regional Comprehensive Metabolomics Resource Core, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USTulane University · USCase Western Reserve University · USFred Hutch Cancer Center · USJohns Hopkins University · USMichigan Medicine · USTemple University · USThe University of Texas at San Antonio · USTranslational Therapeutics (United States) · USUniversity of California, San Diego · USUniversity of Florida · USUniversity of Illinois Chicago · USUniversity of Pennsylvania · US

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Scientific and Data Coordinating Center(SDCC) for the P*U01DK060990 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI FELDMAN, HAROLD I · 2001 to 2017
$50.1M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
Clinical and Translational Science Collaborative of ClevelandUL1TR002548 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI MCCOMSEY, GRACE A · 2018 to 2022
$35.5M
Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
Tulane COBRE in Cardiometabolic Diseases Clinical Research CoreP20GM109036 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI JING CHEN · 2016 to 2026
$25.3M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Zosuquidar trihydrochloride for acute myeloid leukemia &refractory anemiaM01RR000080 · NCRR · UNIVERSITY HOSPITALS OF CLEVELAND · PI DAVIS, PAMELA B · 1985 to 2007
$22.2M
Continuation of the Coordinating Center for the Chronic Renal Insufficiency Cohort (CRIC) StudyU24DK060990 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Amanda Hyre Anderson, Laura M Dember · 2018 to 2026
$21.5M
NCATS NIH HHS UL1 TR000003NCATS NIH HHS UL1 TR000424NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1 TR000439NCATS NIH HHS UL1 TR002003NCATS NIH HHS UL1 TR002240NCATS NIH HHS UL1 TR002548NCI NIH HHS R03 CA211817NCI NIH HHS U01 CA235487NCRR NIH HHS M01 RR000080NCRR NIH HHS M01 RR016500NCRR NIH HHS UL1 RR024131NCRR NIH HHS UL1 RR029879NIDDK NIH HHS K08 DK106523NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK081943NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK110541NIDDK NIH HHS R01 DK139225NIDDK NIH HHS R24 DK082841NIDDK NIH HHS U01 DK060902NIDDK NIH HHS U01 DK060963NIDDK NIH HHS U01 DK060980NIDDK NIH HHS U01 DK060984NIDDK NIH HHS U01 DK060990NIDDK NIH HHS U01 DK061021NIDDK NIH HHS U01 DK061022NIDDK NIH HHS U01 DK061028NIDDK NIH HHS U01 DK114920NIDDK NIH HHS U24 DK060990NIDDK NIH HHS U24 DK097153NIGMS NIH HHS P20 GM109036NIGMS NIH HHS R01 GM114029
6 · The paper itself

Abstract

motivationFunctional enrichment testing methods can reduce data comprising hundreds of altered biomolecules to smaller sets of altered biological 'concepts' that help generate testable hypotheses. This study leveraged differential network enrichment analysis methodology to identify and validate lipid subnetworks that potentially differentiate chronic kidney disease (CKD) by severity or progression.

resultsWe built a partial correlation interaction network, identified highly connected network components, applied network-based gene-set analysis to identify differentially enriched subnetworks, and compared the subnetworks in patients with early-stage versus late-stage CKD. We identified two subnetworks 'triacylglycerols' and 'cardiolipins-phosphatidylethanolamines (CL-PE)' characterized by lower connectivity, and a higher abundance of longer polyunsaturated triacylglycerols in patients with severe CKD (stage ≥4) from the Clinical Phenotyping Resource and Biobank Core. These finding were replicated in an independent cohort, the Chronic Renal Insufficiency Cohort. Using an innovative method for elucidating biological alterations in lipid networks, we demonstrated alterations in triacylglycerols and cardiolipins-phosphatidylethanolamines that precede the clinical outcome of end-stage kidney disease by several years. AVAILABILITY AND IMPLEMENTATION: A complete list of NetGSA results in HTML format can be found at http://metscape.ncibi.org/netgsa/12345-022118/cric_cprobe/022118/results_cric_cprobe/main.html. The DNEA is freely available at https://github.com/wiggie/DNEA. Java wrapper leveraging the cytoscape.js framework is available at http://js.cytoscape.org. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Renal Insufficiency, ChronicFemaleHumansLipidsMaleLipids

Identifiers

PMID30887029
PMCPMC6748777
OpenAlexW2913967880

What OpenQuestion holds

Textmetadata
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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.