Evidence map›Paper›PMID 30006493›Full record

ArticleJournal of the American Heart Association2018

Endothelial Microparticles and Systemic Complement Activation in Patients With Chronic Kidney Disease.

Diana Jalal, Brandon Renner, Jennifer Laskowski, Erik Stites, James Cooper, Karissa Valente, Zhiying You, Loni Perrenoud, Moglie Le Quintrec, Ismaeel Muhamed and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02230202 (Endothelial Microparticles), which is not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.2field-weighted citation impact, top 4% 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.

NCT02230202 completednot on this map

Endothelial Microparticles: A Novel Marker of Vascular Dysfunction

Typeobservational_patient_registrySponsorUniversity of Colorado, DenverRan2014 to 2016Enrolled90ConditionsChronic Kidney DiseaseArmsFlow-mediated dilation, single blood draw
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
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  14. Review
  15. The role of complement in kidney disease.Nature reviews. Nephrology · 2023
    Review
  16. Article
  17. The complement system in pediatric acute kidney injury.Pediatric nephrology (Berlin, Germany) · 2023
    Review
  18. Article
  19. Alternative pathway diagnostics.Immunological reviews · 2023
    Review
  20. Article
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

16 authors at 5 institutions in 2 countries.

Diana JalalDivision of Nephrology, Carver College of Medicine University of Iowa, Iowa City, IA diana-jalal@uiowa.edu.
Brandon RennerDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Jennifer LaskowskiDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Erik StitesDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
James CooperDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Karissa ValenteDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Zhiying YouDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Loni PerrenoudDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
Moglie Le QuintrecDepartment of Nephrology and Renal Transplantation, Lapeyronnie Hospital and INSERM U1183 IRMB, Montpellier, France.
Ismaeel MuhamedJoint Department of Biomedical Engineering and Comparative Medicine Institute, North Carolina State University and University of North Carolina-Chapel Hill, NC.
Uwe ChristiansiC42 Clinical Research and Development, University of Colorado Anschutz Medical Campus, Aurora, CO.
Jelena KlawitteriC42 Clinical Research and Development, University of Colorado Anschutz Medical Campus, Aurora, CO.
Margaret A LindorferDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA.
Ronald P TaylorDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA.
V Michael HolersDivision of Rheumatology, University of Colorado Anschutz Medical Center, Aurora, CO.
Joshua M ThurmanDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Center, Aurora, CO.
University of Colorado Anschutz Medical Campus · USUniversity of Virginia · USHôpital Lapeyronie · FRUniversity of Iowa · USUniversity of North Carolina at Chapel Hill · US

Funding

The Complement System and Ischemic Acute Renal FailureR01DK076690 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Joshua M Thurman · 2008 to 2026
$6.6M
TRAINING IN RENAL &ELECTROLYTE DISEASE &HYPERTENSIONT32DK007135 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JOHNSON, RICHARD JOSEPH, KENDRICK, JESSICA B · 1986 to 2024
$5.3M
Immunologic Mechanisms of Progressive GlomerulosclerosisR01DK113586 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI THURMAN, JOSHUA M · 2017 to 2020
$1.4M
NIDDK NIH HHS R01 DK076690NIDDK NIH HHS R01 DK113586NIDDK NIH HHS T32 DK007135
6 · The paper itself

Abstract

backgroundEndothelial microparticles are associated with chronic kidney disease (CKD) and complement activation. We hypothesized that the complement pathway is activated in patients with CKD via endothelial microparticles and that complement activation correlates with endothelial dysfunction in CKD. METHODS AND

resultsWe analyzed complement data of 30 healthy subjects, 30 patients with stage III/IV CKD, and 30 renal transplant recipients with stage III/IV CKD, evaluating the potential correlation of complement fragments with brachial artery flow-mediated dilation, Chronic Kidney Disease Epidemiology Collaboration glomerular filtration rate, and urinary albumin/creatinine ratio. Endothelial microparticles were characterized via proteomic analysis and compared between study groups. Complement fragment Ba was significantly increased in CKD and post-kidney transplant CKD. Plasma Ba levels correlated significantly with lower brachial artery flow-mediated dilation, lower Chronic Kidney Disease Epidemiology Collaboration glomerular filtration rate, and higher urinary albumin/creatinine ratio. Factor D levels were significantly higher in the plasma microparticles of patients with CKD versus healthy controls. Plasma microparticles isolated from patients with CKD and containing factor D activated the alternative pathway in vitro.

conclusionThe alternative complement pathway is activated in CKD and correlates with endothelial dysfunction and markers of CKD. Future studies are needed to evaluate whether endothelial microparticles with increased factor D play a pathologic role in CKD-associated vascular disease. CLINICAL

trial registrationURL: http://www.clinicaltrials.gov. Unique identifier: NCT02230202.

Indexed as

Complement Pathway, AlternativeAdultAgedBrachial ArteryCase-Control StudiesCell-Derived MicroparticlesComplement ActivationComplement C4aComplement C5aComplement Factor BComplement Factor DComplement Membrane Attack ComplexComplement System ProteinsEndothelial CellsEndothelium, VascularFemaleComplement C4aComplement C5aComplement Factor BComplement Factor DComplement Membrane Attack ComplexComplement System Proteinschronic kidney diseaseMicroparticles complement activation

Identifiers

PMID30006493
PMCPMC6064828
OpenAlexW2884041267

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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.