Evidence map›Paper›PMID 30279272›Full record

ArticleJournal of the American Society of Nephrology : JASN2018

Inhibitory Anti-Peroxidasin Antibodies in Pulmonary-Renal Syndromes.

A Scott McCall, Gautam Bhave, Vadim Pedchenko, Jacob Hess, Meghan Free, Dustin J Little, Thomas P Baker, William F Pendergraft, Ronald J Falk, Stephen W Olson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Anti-glomerular basement membrane disease-treatment standard.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Review
  3. Perlecan is a novel target of autoantibodies in anti-glomerular basement membrane disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Article
  4. The multiple autoantibodies in anti-GBM disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Article
  5. Basement membranes in lung development, disease, and repair.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. ANCA-associated vasculitis.Nature reviews. Disease primers · 2020
    Review
  14. Review
  15. Article
  16. Biallelic Deletion ofInternational journal of molecular sciences · 2019
    Article
  17. Article
  18. Peroxidasin-a Novel Autoantigen in Anti-GBM Disease?Journal of the American Society of Nephrology : JASN · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

A Scott McCallDepartment of Nephrology and Hypertension, scott.mccall@vanderbilt.edu billy.hudson@vanderbilt.edu.
Gautam BhaveDepartment of Nephrology and Hypertension.
Vadim PedchenkoDepartment of Nephrology and Hypertension.
Jacob HessUniversity of North Carolina Kidney Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Meghan FreeUniversity of North Carolina Kidney Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Dustin J LittleDepartment of Nephrology, Walter Reed Army Medical Center, Bethesda, Maryland.ORCID 0000-0002-4201-0237
Thomas P BakerDepartment of Nephrology, Walter Reed Army Medical Center, Bethesda, Maryland.
William F PendergraftUniversity of North Carolina Kidney Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Ronald J FalkUniversity of North Carolina Kidney Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Stephen W OlsonDepartment of Nephrology, Walter Reed Army Medical Center, Bethesda, Maryland.
Billy G HudsonDepartment of Nephrology and Hypertension, scott.mccall@vanderbilt.edu billy.hudson@vanderbilt.edu.
University of North Carolina at Chapel Hill · USHypertension Institute · USBreast Cancer Research Foundation · USVanderbilt University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Translation of Knowledge on the Pathogenesis of ANCA Disease into NovelP01DK058335 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NACHMAN, PATRICK H · 2000 to 2019
$25.9M
STUDIES ON THE STRUCTURE OF BASEMENT MEMBRANESR01DK018381 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Sergey Petrovich Budko, BILLY GERALD HUDSON · 1986 to 2026
$12.4M
Role of Peroxidasin in Glomerular Matrix HomeostasisK08DK097306 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BHAVE, GAUTAM · 2013 to 2017
$739k
The role of peroxidasin in Goodpasture's diseaseF30DK100094 · NIDDK · VANDERBILT UNIVERSITY · PI MCCALL, ABRAHAM SCOTT · 2013 to 2016
$153k
NIDDK NIH HHS F30 DK100094NIDDK NIH HHS K08 DK097306NIDDK NIH HHS P01 DK058335NIDDK NIH HHS R01 DK018381NIGMS NIH HHS T32 GM007347Wellcome Trust
6 · The paper itself

Abstract

backgroundGoodpasture syndrome (GP) is a pulmonary-renal syndrome characterized by autoantibodies directed against the NC1 domains of collagen IV in the glomerular and alveolar basement membranes. Exposure of the cryptic epitope is thought to occur

methodsWe used ELISA and competitive binding assays to assess the presence and specificity of autoantibodies in serum from patients with GP and healthy controls. Peroxidasin activity was fluorometrically measured in the presence of partially purified IgG from patients or controls. Clinical disease severity was gauged by Birmingham Vasculitis Activity Score.

resultsWe detected anti-peroxidasin autoantibodies in the serum of patients with GP before and at clinical presentation. Enriched anti-peroxidasin antibodies inhibited peroxidasin-mediated hypobromous acid production

conclusionsAnti-peroxidasin antibodies, which would previously have been mischaracterized, are associated with pulmonary-renal syndromes, both before and during active disease, and may be involved in disease activity and pathogenesis in some patients.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, Antineutrophil CytoplasmicAntibody SpecificityAnti-Glomerular Basement Membrane DiseaseAutoantibodiesAutoantigensChildCohort StudiesCollagen Type IVExtracellular Matrix ProteinsFemaleGlomerulonephritisHemorrhageAntibodies, Antineutrophil CytoplasmicAutoantibodiesAutoantigensCollagen Type IVExtracellular Matrix ProteinsMPO protein, humanPeroxidasePeroxidasesPeroxidasinPXDN protein, humantype IV collagen alpha3 chainANCAanti-GBM diseaseextracellular matrixglomerulonephritisGoodpasture-s syndromevasculitis

Identifiers

PMID30279272
PMCPMC6218858
OpenAlexW2894609186

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.